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GABRB3

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297: 274: 196: 171: 548: 303: 202: 1447:, impacting neural differentiation, growth, and circuit organization. The expression of the beta-3 subunit reaches peak at different times in different locations of the brain, during development. The highest expression of Gabrb3 in mice, within the cerebral cortex and hippocampus are reached prenatally, while they are reached postnatally in the cerebellar cortex. After the highest peak of expression, Gabrb3 expression is down-regulated substantially in the 1556:
region displayed in autistic patients are almost always of maternal origin (not paternal) and account for 1–2% of diagnosed autism disorder cases. This gene is also a candidate for autism because of the physiological response that benzodiazepine has on the GABA-A receptor, when used to treat seizures and anxiety disorders.
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The Gabrb3 gene deficient mouse has been proposed as a model of autism spectrum disorder. These mice exhibit similar phenotypic symptoms such as non-selective attention, deficits in a variety of exploratory parameters, sociability, social novelty, nesting and lower rearing frequency as can be equated
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by cAMP-dependent protein kinase (PKA) has a regulatory effect dependent on the beta subunit involved. The mechanism by which the kinase is targeted towards the bata-3 subunit is unknown. AKAP79/150 binds directly to the GABRB3 subunit, which is critical for its own phosphorylation, mediated by PKA.
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Duplications of the Prader-Willi/Angelman syndrome region, also known as the imprinting region (15q11-13) that encompasses the GABRB3 gene are present in some patients diagnosed with Autism. These patients exhibit classic symptoms that are associated with the disorder. Duplications of the 15q11-13
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Defects in GABA transmission has often been implicated in epilepsy within animal models and human syndromes. Patients that are diagnosed with Angelman syndrome and have a deletion of the GABRB3 gene exhibit absence seizures. Reduced expression of the beta-3 subunit is a potential contributor to
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development. A disturbance in GABRB3 expression can be lined to the malformation of nonsyndromic cleft lip with or without cleft palate. Cleft lip and palate have also been observed in children who have inverted duplications encompassing the GABRB3 locus. Knockout of the beta-3 subunit in mice
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Deletion of the GABRB3 gene results in Angelman syndrome in humans, depending on the parental origin of the deletion. Deletion of the paternal allele of GABRB3 has no known implications with this syndrome, while deletion of the maternal GABRB3 allele results in development of the syndrome.
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and inferior olivary body of the mouse. By adulthood, the level of expression in the cerebral cortex and hippocampus drops below developmental expression levels, but the expression in the cerebellum does not change postnatally. The highest levels of Gabrb3 expression in the mature
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Brandon NJ, Jovanovic JN, Colledge M, Kittler JT, Brandon JM, Scott JD, Moss SJ (January 2003). "A-kinase anchoring protein 79/150 facilitates the phosphorylation of GABA(A) receptors by cAMP-dependent protein kinase via selective interaction with receptor beta subunits".
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Tanaka M, Olsen RW, Medina MT, Schwartz E, Alonso ME, Duron RM, Castro-Ortega R, Martinez-Juarez IE, Pascual-Castroviejo I, Machado-Salas J, Silva R, Bailey JN, Bai D, Ochoa A, Jara-Prado A, Pineda G, Macdonald RL, Delgado-Escueta AV (June 2008).
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In humans, the beta-3 subunit, as well as the subunits of its two neighbouring genes (GABRG3 and GABRA5), are bi-allelically expressed within the cerebral cortex, indicating that the gene is not subjected to imprinting within those cells.
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of a human β3 homopentamer was published in 2014. The study of the crystal structure of the human β3 homopentamer revealed unique qualities that are only observed in eukaryotic cysteine-loop receptors. The characterization of the
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of Gabrb3 causes severe neonatal mortality with the cleft palate phenotype present, the survivors experiencing hyperactivity, lack of coordination and suffering with epileptic seizures. These mice also exhibit changes to the
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Saitoh S, Kubota T, Ohta T, Jinno Y, Niikawa N, Sugimoto T, Wagstaff J, Lalande M (February 1992). "Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene".
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Wagstaff J, Chaillet JR, Lalande M (December 1991). "The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7".
310: 209: 1322:. GABRB3 was the first gene to be mapped to this particular region. It spans approximately 250kb and includes 10 exons within its coding region, as well as two additional alternative first exons that encode for 1472:
Due to the location of GABRB3 in the 15q11-13 imprinting region found in humans, this gene is subject to imprinting depending on the location and the cells developmental state. Imprinting is not present in the
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Buhr A, Bianchi MT, Baur R, Courtet P, Pignay V, Boulenger JP, Gallati S, Hinkle DJ, Macdonald RL, Sigel E (August 2002). "Functional characterization of the new human GABA(A) receptor mutation beta3(R192H)".
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beta-3 subunit sequences, there is a high level of genetic conservation. In mice the Gabrb3 gene is located on chromosome 7 of its genome in a similar gene cluster style with some of the other subunits of the
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Nurmi EL, Dowd M, Tadevosyan-Leyfer O, Haines JL, Folstein SE, Sutcliffe JS (July 2003). "Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13".
2052:"Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder" 1993:
Scapoli L, Martinelli M, Pezzetti F, Carinci F, Bodo M, Tognon M, Carinci P (January 2002). "Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate".
2757:"High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients" 1381:
of the nervous system. The two other genes in the gene cluster both encode for related subunits of the family. During development, when the GABRB3 subunit functions optimally, its role in the GABA
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receptor and subunits helps with the mechanistic determination of mutations within the subunits and what direct effect the mutations may have on the protein and its interactions.
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Mutations in this gene may be associated with the pathogenesis of Angelman syndrome, nonsyndromic orofacial clefts, epilepsy and autism. The GABRB3 gene has been associated with
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to characteristics found in patients diagnosed with autism spectrum disorder. When studying Gabrb3 deficient mice, significant hypoplasia of the cerebellar vermis was observed.
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Sarto I, Wabnegger L, Dögl E, Sieghart W (September 2002). "Homologous sites of GABA(A) receptor alpha(1), beta(3) and gamma(2) subunits are important for assembly".
2687:"gamma-Aminobutyric acidA receptors displaying association of gamma 3-subunits with beta 2/3 and different alpha-subunits exhibit unique pharmacological properties" 1931:"Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse" 1881:
Knoll JH, Cheng SD, Lalande M (January 1994). "Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region".
1781:"A Multifaceted GABAA Receptor Modulator: Functional Properties and Mechanism of Action of the Sedative-Hypnotic and Recreational Drug Methaqualone (Quaalude)" 2722:"A strong promoter element is located between alternative exons of a gene encoding the human gamma-aminobutyric acid-type A receptor beta 3 subunit (GABRB3)" 2652:"Mapping of the beta 2 subunit gene (GABRB2) to microdissected human chromosome 5q34-q35 defines a gene cluster for the most abundant GABAA receptor isoform" 2099:
Hosie AM, Dunne EL, Harvey RJ, Smart TG (April 2003). "Zinc-mediated inhibition of GABA(A) receptors: discrete binding sites underlie subtype specificity".
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region that spans the 15q11-13 region. Its sequence is considerably longer than the two other genes found within its gene cluster due to a large 150kb
882: 2246:"15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders" 132: 3275: 1497:. When the MECP2 gene is knocked out, the expression of Gabrb3 is reduced, suggesting a relationship of positive regulation between the two genes. 2883:
Buckley ST, Eckert AL, Dodd PR (September 2000). "Expression and distribution of GABAA receptor subtypes in human alcoholic cerebral cortex".
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Hammer H, Bader BM, Ehnert C, Bundgaard C, Bunch L, Hoestgaard-Jensen K, Schroeder OH, Bastlund JF, Gramowski-Voß A, Jensen AA (August 2015).
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receptor allows for proliferation, migration, and differentiation of precursor cells that lead to the proper development of the brain. GABA
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Wagstaff J, Knoll JH, Fleming J, Kirkness EF, Martin-Gallardo A, Greenberg F, Graham JM, Menninger J, Ward D, Venter JC (August 1991).
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DeLorey TM, Olsen RW (September 1999). "GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man".
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family. The encoded protein is one of at least 13 distinct subunits of a multisubunit chloride channel that serves as the receptor for
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within the ear, resulting in poor swimming skills, difficulty in walking on grid floors, and are found to run in circles erratically.
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The expression of GABRB3 is not constant among all cells or at all stages of development. The distribution of expression of the GABA
1148: 103:, ECA5, gamma-aminobutyric acid type A receptor beta3 subunit, EIEE43, gamma-aminobutyric acid type A receptor subunit beta3, DEE43 3170: 1867: 2617:"Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15" 1393:. The ions bind allosterically to the receptor, a mechanism that is critically dependent on the receptor subunit composition. 3925: 3013:"Unique assignment of inter-subunit association in GABA(A) alpha 1 beta 3 gamma 2 receptors determined by molecular modeling" 2382: 1543:
results in clefting of the secondary palate. Normal facial characteristics can be restored through the insertion of a Gabrb3
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Cook EH, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, Courchesne E (May 1998).
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Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH, Fang Y, Song CY, Vitale R (2002).
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Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH, Fang Y, Song CY, Vitale R (2002).
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or alter the kinetic properties of the channel. This results in the loss of the inhibitory properties of the receptor.
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of the brain at different points of development and maturity. GABRB3 deficiencies are implicated in many human
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There is an unknown association between autism and the 155CA-2 locus, located within an intron in GABRB3.
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is replicated later than the paternal allele. The reasoning and implications of this pattern are unknown.
2534:"A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity" 1267: 309: 208: 3641: 3598: 302: 201: 3935: 3441: 2142: 99: 3655: 3194: 3115: 3111: 1367: 1120: 1095: 1091: 1087: 1053: 1028: 1024: 1020: 120: 1371: 2227:"Crystal structure of a human gamma-aminobutyric acid receptor, the GABA(A)R-beta3 homopentamer" 1547:
into the mouse genome, making the Gabrb3 gene primarily responsible for cleft palate formation.
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within a highly conserved region of the GABRB3 gene can decrease the peak current amplitudes of
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transmitter-gated ion channel activity involved in regulation of postsynaptic membrane potential
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Glatt K, Glatt H, Lalande M (April 1997). "Structure and organization of GABRB3 and GABRA5".
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Glatt K, Glatt H, Lalande M (April 1997). "Structure and organization of GABRB3 and GABRA5".
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receptor subunits (GABRB3 included) during development indicates that GABA may function as a
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Russek SJ (February 1999). "Evolution of GABA(A) receptor diversity in the human genome".
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Meguro M, Mitsuya K, Sui H, Shigenami K, Kugoh H, Nakao M, Oshimura M (November 1997).
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Gabrb3 shows significantly reduced expression postnatally, when mice are deficient in
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Nicholls RD, Gottlieb W, Russell LB, Davda M, Horsthemke B, Rinchik EM (March 1993).
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it carries. A pattern is observed in GABRB3 gene replication, in humans the maternal
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The beta-3 subunit has very similar function to the human version of the subunit.
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with distinct signal peptides have been described. This gene is located within an
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National Center for Biotechnology Information, U.S. National Library of Medicine
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National Center for Biotechnology Information, U.S. National Library of Medicine
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Proceedings of the National Academy of Sciences of the United States of America
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and granule cells of the cerebellum, the hippocampus, and the piriform cortex.
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Sinnett D, Wagstaff J, Glatt K, Woolf E, Kirkness EJ, Lalande M (June 1993).
1457: 1223: 576: 2837: 2820: 1732:"Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers" 525: 403: 3863: 3096: 3067: 3038: 2995: 2955: 2912: 2875: 2803: 2668: 2651: 2559: 2518: 2460: 2425: 2359: 2315: 2279: 2212: 2120: 2085: 2015: 1955: 1814: 1796: 1701: 1401: 1311: 1287: 1259: 382: 161: 2946: 2929: 2846: 2811: 2782: 2747: 2712: 2677: 2642: 2599: 2416: 2399: 2143:"OMIM Entry - * 137192 - GAMMA-AMINOBUTYRIC ACID RECEPTOR, BETA-3; GABRB3" 1974: 1902: 1853: 1765: 1709: 1538:
There is a strong association between GABRB3 expression levels and proper
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Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM (March 2007).
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DeLorey TM, Sahbaie P, Hashemi E, Homanics GE, Clark JD (March 2008).
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brain, having an equal expression from maternal and paternal alleles.
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When comparing the human beta-3 subunit's genetic sequence with other
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Journal of the American Academy of Child and Adolescent Psychiatry
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15, within the q12 region in the human genome. It is located in a
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Overview of all the structural information available in the
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Urak L, Feucht M, Fathi N, Hornik K, Fuchs K (August 2006).
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Słopień A, Rajewski A, Budny B, Czerski P (2003). "".
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Tögel M, Mossier B, Fuchs K, Sieghart W (April 1994).
2400:"Association between a GABRB3 polymorphism and autism" 1566: 2576: 2531: 2098: 1729: 1214:. It is located within the 15q12 region in the human 537: 3854: 3017:Biochimica et Biophysica Acta (BBA) - Biomembranes 1626: 1624: 1622: 1605: 1603: 1601: 1533: 2882: 2789: 1880: 1687: 319: 218: 3917: 1924: 1922: 1920: 2045: 2043: 2041: 2039: 2037: 2035: 2033: 1988: 1986: 1984: 1826: 1824: 1619: 1598: 1201:Gamma-aminobutyric acid receptor subunit beta-3 717:negative regulation of neuron apoptotic process 605:extracellular ligand-gated ion channel activity 16:Protein-coding gene in the species Homo sapiens 2719: 2168: 2164: 2162: 1631:GRCm38: Ensembl release 89: ENSMUSG00000033676 1306:The GABRB3 gene is located on the long arm of 3171: 2171:"Crystal structure of a human GABAA receptor" 1917: 2438: 2330: 2286: 2030: 1981: 1821: 1683: 1681: 1679: 2159: 1725: 1723: 1721: 1719: 1610:GRCh38: Ensembl release 89: ENSG00000166206 1550: 3178: 3164: 3146:United States National Library of Medicine 2885:Annals of the New York Academy of Sciences 2649: 3114:at the U.S. National Library of Medicine 3028: 2985: 2945: 2836: 2772: 2737: 2702: 2667: 2632: 2549: 2508: 2415: 2269: 2202: 2075: 1964: 1954: 1804: 1755: 1676: 792:gamma-aminobutyric acid signaling pathway 620:transmembrane signaling receptor activity 3144:This article incorporates text from the 2720:Kirkness EF, Fraser CM (February 1993). 1716: 1500: 610:GABA-gated chloride ion channel activity 3010: 2372: 1389:receptor function is inhibited by zinc 1218:and spans 250kb. This gene includes 10 3918: 2853: 2169:Miller PS, Aricescu AR (August 2014). 1860: 1467: 737:regulation of neuron apoptotic process 3159: 661:integral component of plasma membrane 324: 285: 280: 223: 182: 177: 2296:Molecular and Cellular Neurosciences 1524: 1509:skills accompanying such disorders. 2726:The Journal of Biological Chemistry 2691:The Journal of Biological Chemistry 2650:Russek SJ, Farb DH (October 1994). 1567:Epilepsy/Childhood absence epilepsy 777:negative regulation of neuron death 757:inner ear receptor cell development 13: 2905:10.1111/j.1749-6632.2000.tb05183.x 2761:American Journal of Human Genetics 2621:American Journal of Human Genetics 2569: 2489:American Journal of Human Genetics 2352:10.1097/01.CHI.0000046868.56865.0F 1736:American Journal of Human Genetics 14: 3947: 3105: 1278:, nonsyndromic orofacial clefts, 1207:that in humans is encoded by the 732:inhibitory postsynaptic potential 442:lateral nuclear group of thalamus 807:regulation of membrane potential 787:chloride transmembrane transport 546: 308: 301: 295: 272: 207: 200: 194: 169: 2525: 2475: 2432: 2391: 2366: 2237: 2219: 2135: 2092: 1874: 1534:Nonsyndromic Orofacial Clefting 1366:GABRB3 encodes a member of the 1772: 1658: 1640: 1296:positive allosteric modulation 802:chemical synaptic transmission 782:cellular response to histamine 641:integral component of membrane 557:More reference expression data 526:More reference expression data 1: 3060:10.1016/S0028-3908(02)00160-0 3030:10.1016/S0005-2736(02)00512-6 2868:10.1016/S0378-1119(98)00594-0 2739:10.1016/S0021-9258(18)53626-7 2704:10.1016/S0021-9258(18)99974-6 2453:10.1016/s0920-1211(99)00046-7 2375:Fundamental Molecular Biology 2373:Allison, Lizabeth A. (2012). 2308:10.1016/S1044-7431(02)00017-9 1592: 1480: 1434: 1330:transcript variants encoding 293: 192: 3926:Genes on human chromosome 15 3011:Trudell J (September 2002). 2592:10.1016/0140-6736(92)91686-3 1846:10.1016/0888-7543(91)90034-C 1572:childhood absence epilepsy. 1417: 1294:are mediated through GABBR3 1268:neurodevelopmental disorders 1234:, all being subunits in the 686:cytoplasmic vesicle membrane 7: 1575: 1485:Phosphorylation of the GABA 1361: 817:inhibitory synapse assembly 797:ion transmembrane transport 10: 3952: 2501:10.1016/j.ajhg.2008.04.020 2056:Behavioural Brain Research 1230:, the gene codes for many 3841: 3801: 3738:Voltage- and ligand-gated 3736: 3666: 3654: 3632: 3482: 3432: 3258: 3210: 3201: 3195:ligand-gated ion channels 2978:10.1007/s00439-002-0766-7 2233:. RCSB. January 28, 2014. 2068:10.1016/j.bbr.2007.09.009 2008:10.1007/s00439-001-0639-5 1666:"Mouse PubMed Reference:" 1648:"Human PubMed Reference:" 1187: 1182: 1178: 1171: 1155: 1136: 1117: 1113: 1080: 1076: 1069: 1050: 1046: 1013: 1009: 1002: 989: 985: 970: 966: 957: 944: 940: 925: 921: 912: 899: 895: 880: 876: 867: 852: 845: 841: 825: 727:roof of mouth development 615:identical protein binding 600:chloride channel activity 575: 571: 554: 545: 536: 523: 472: 463: 410: 401: 371: 363: 359: 342: 329: 292: 271: 262: 258: 241: 228: 191: 168: 159: 155: 110: 107: 97: 90: 85: 66: 61: 44: 39: 34: 30: 26: 21: 3116:Medical Subject Headings 2825:Human Molecular Genetics 2538:Human Molecular Genetics 2250:Human Molecular Genetics 1551:Autism Spectrum Disorder 1368:ligand-gated ion channel 1314:, with two other genes, 1142:Chr 15: 26.54 – 26.94 Mb 666:chloride channel complex 590:GABA-A receptor activity 492:anterior amygdaloid area 3484:Nicotinic acetylcholine 1377:, the major inhibitory 1301: 1149:Chr 7: 57.07 – 57.48 Mb 676:GABA-A receptor complex 2804:10.1006/geno.1997.4639 2669:10.1006/geno.1994.1539 1956:10.1073/pnas.90.5.2050 1797:10.1124/mol.115.099291 1785:Molecular Pharmacology 1702:10.1006/geno.1997.4639 1587:Heritability of autism 1270:and syndromes such as 812:nervous system process 480:lateral septal nucleus 434:superior frontal gyrus 3191:cell surface receptor 3112:GABRB3+protein,+human 2947:10.1038/sj.mp.4001011 2838:10.1093/hmg/6.12.2127 2417:10.1038/sj.mp.4001011 1501:Clinical significance 1328:Alternatively spliced 1276:Prader-Willi syndrome 646:postsynaptic membrane 414:middle temporal gyrus 185:Chromosome 15 (human) 3856:Purinergic receptors 2934:Molecular Psychiatry 2404:Molecular Psychiatry 1228:alternative splicing 595:ion channel activity 484:ventromedial nucleus 326:7 B5|7 33.53 cM 287:Chromosome 7 (mouse) 62:List of PDB id codes 35:Available structures 2897:2000NYASA.914...58B 2697:(17): 12993–12998. 2195:10.1038/nature13293 2187:2014Natur.512..270M 2101:Nature Neuroscience 1947:1993PNAS...90.2050N 1468:Imprinting Patterns 1445:neurotrophic factor 772:signal transduction 722:cochlea development 691:cytoplasmic vesicle 446:islet of Langerhans 3624:β1δε - Muscle type 3203:Cys-loop receptors 3148:, which is in the 3085:Psychiatria Polska 2551:10.1093/hmg/ddl174 2262:10.1093/hmg/ddm014 1405:missense mutations 1375:-aminobutyric acid 1324:signaling peptides 947:ENSMUSG00000033676 762:chloride transport 742:neuron development 710:Biological process 701:GABA-ergic synapse 634:Cellular component 583:Molecular function 476:olfactory tubercle 149:GABRB3 - orthologs 3913: 3912: 3909: 3908: 3837: 3836: 3668:Ligand-gated only 3650: 3649: 3048:Neuropharmacology 2831:(12): 2127–2133. 2586:(8789): 366–367. 2544:(16): 2533–2541. 2441:Epilepsy Research 2384:978-1-118-05981-4 2231:Protein Data Bank 2181:(7514): 270–275. 1895:10.1038/ng0194-41 1525:Angelman syndrome 1519:vestibular system 1514:knockout mutation 1424:crystal structure 1286:. The effects of 1272:Angelman syndrome 1198: 1197: 1194: 1193: 1167: 1166: 1132: 1131: 1107: 1106: 1065: 1064: 1040: 1039: 998: 997: 979: 978: 953: 952: 934: 933: 908: 907: 889: 888: 837: 836: 696:neuron projection 567: 566: 563: 562: 532: 531: 519: 518: 488:nucleus accumbens 457: 456: 450:prefrontal cortex 438:postcentral gyrus 422:entorhinal cortex 355: 354: 254: 253: 81: 80: 77: 76: 45:Ortholog search: 3943: 3936:Causes of autism 3852: 3851: 3664: 3663: 3208: 3207: 3180: 3173: 3166: 3157: 3156: 3100: 3079: 3042: 3032: 3007: 2989: 2959: 2949: 2924: 2879: 2850: 2840: 2815: 2786: 2776: 2767:(6): 1216–1229. 2751: 2741: 2732:(6): 4420–4428. 2716: 2706: 2681: 2671: 2646: 2636: 2611: 2564: 2563: 2553: 2529: 2523: 2522: 2512: 2495:(6): 1249–1261. 2479: 2473: 2472: 2447:(2–3): 123–132. 2436: 2430: 2429: 2419: 2395: 2389: 2388: 2370: 2364: 2363: 2334: 2328: 2327: 2290: 2284: 2283: 2273: 2241: 2235: 2234: 2223: 2217: 2216: 2206: 2166: 2157: 2156: 2154: 2153: 2139: 2133: 2132: 2096: 2090: 2089: 2079: 2047: 2028: 2027: 1990: 1979: 1978: 1968: 1958: 1941:(5): 2050–2054. 1926: 1915: 1914: 1878: 1872: 1871: 1864: 1858: 1857: 1840:(4): 1071–1078. 1828: 1819: 1818: 1808: 1776: 1770: 1769: 1759: 1742:(5): 1077–1083. 1727: 1714: 1713: 1685: 1674: 1673: 1662: 1656: 1655: 1644: 1638: 1628: 1617: 1607: 1379:neurotransmitter 1232:protein isoforms 1180: 1179: 1151: 1144: 1127: 1111: 1110: 1102: 1074: 1073: 1070:RefSeq (protein) 1060: 1044: 1043: 1035: 1007: 1006: 983: 982: 964: 963: 938: 937: 919: 918: 893: 892: 874: 873: 843: 842: 573: 572: 559: 550: 543: 542: 528: 468: 466:Top expressed in 461: 460: 426:endothelial cell 418:Brodmann area 23 406: 404:Top expressed in 399: 398: 378: 377: 361: 360: 351: 338: 327: 312: 305: 299: 288: 276: 260: 259: 250: 237: 226: 211: 204: 198: 187: 173: 157: 156: 151: 102: 95: 72: 59: 58: 53: 32: 31: 19: 18: 3951: 3950: 3946: 3945: 3944: 3942: 3941: 3940: 3916: 3915: 3914: 3905: 3833: 3827: 3819: 3797: 3732: 3646: 3628: 3623: 3615:- Ganglion type 3614: 3610: 3602: 3594: 3590: 3582: 3578: 3478: 3469: 3461: 3453: 3445: 3428: 3422: 3414: 3406: 3397: 3367: 3359: 3351: 3343: 3335: 3327: 3319: 3311: 3303: 3295: 3287: 3279: 3271: 3254: 3223: 3197: 3184: 3108: 3103: 2572: 2570:Further reading 2567: 2530: 2526: 2480: 2476: 2437: 2433: 2396: 2392: 2385: 2371: 2367: 2335: 2331: 2291: 2287: 2242: 2238: 2225: 2224: 2220: 2167: 2160: 2151: 2149: 2141: 2140: 2136: 2097: 2093: 2048: 2031: 1991: 1982: 1927: 1918: 1883:Nature Genetics 1879: 1875: 1866: 1865: 1861: 1829: 1822: 1777: 1773: 1728: 1717: 1686: 1677: 1664: 1663: 1659: 1646: 1645: 1641: 1629: 1620: 1608: 1599: 1595: 1578: 1569: 1553: 1536: 1527: 1503: 1488: 1483: 1470: 1442: 1437: 1430: 1420: 1388: 1384: 1364: 1357: 1304: 1264:piriform cortex 1244:cerebral cortex 1239: 1189:View/Edit Mouse 1184:View/Edit Human 1147: 1140: 1137:Location (UCSC) 1123: 1119: 1098: 1094: 1090: 1086: 1082: 1056: 1052: 1031: 1027: 1023: 1019: 1015: 928:ENSG00000166206 821: 705: 681:plasma membrane 629: 555: 524: 515: 512:globus pallidus 510: 506: 502: 500:mammillary body 498: 496:arcuate nucleus 494: 490: 486: 482: 478: 464: 453: 448: 444: 440: 436: 432: 428: 424: 420: 416: 402: 346: 333: 325: 315: 314: 313: 306: 286: 263:Gene location ( 245: 232: 224: 214: 213: 212: 205: 183: 160:Gene location ( 111: 98: 91: 68: 46: 17: 12: 11: 5: 3949: 3939: 3938: 3933: 3928: 3911: 3910: 3907: 3906: 3904: 3903: 3902: 3901: 3896: 3891: 3886: 3881: 3876: 3871: 3860: 3858: 3849: 3847:gated channels 3839: 3838: 3835: 3834: 3832: 3831: 3830: 3829: 3825: 3821: 3817: 3807: 3805: 3799: 3798: 3796: 3795: 3794: 3793: 3788: 3783: 3778: 3773: 3768: 3763: 3758: 3753: 3742: 3740: 3734: 3733: 3731: 3730: 3729: 3728: 3723: 3718: 3713: 3708: 3698: 3692: 3687: 3682: 3672: 3670: 3661: 3652: 3651: 3648: 3647: 3645: 3644: 3642:Zinc-activated 3638: 3636: 3630: 3629: 3627: 3626: 3621: 3617: 3612: 3608: 3604: 3600: 3596: 3592: 3588: 3584: 3580: 3576: 3568: 3567: 3562: 3557: 3552: 3547: 3542: 3537: 3532: 3527: 3522: 3517: 3512: 3507: 3502: 3497: 3488: 3486: 3480: 3479: 3477: 3476: 3471: 3467: 3463: 3459: 3455: 3451: 3447: 3443: 3438: 3436: 3430: 3429: 3427: 3426: 3425: 3424: 3420: 3416: 3412: 3408: 3404: 3395: 3391: 3390: 3389: 3384: 3379: 3374: 3369: 3365: 3361: 3357: 3353: 3349: 3345: 3341: 3337: 3333: 3329: 3325: 3321: 3317: 3313: 3309: 3305: 3301: 3297: 3293: 3289: 3285: 3281: 3277: 3269: 3264: 3262: 3256: 3255: 3253: 3252: 3251: 3250: 3245: 3240: 3235: 3230: 3221: 3216: 3214: 3212:5-HT/serotonin 3205: 3199: 3198: 3183: 3182: 3175: 3168: 3160: 3141: 3140: 3119: 3107: 3106:External links 3104: 3102: 3101: 3091:(5): 779–791. 3080: 3054:(4): 482–491. 3043: 3008: 2972:(2): 154–160. 2966:Human Genetics 2960: 2940:(3): 311–316. 2925: 2880: 2862:(2): 213–222. 2851: 2816: 2787: 2752: 2717: 2682: 2662:(3): 528–533. 2647: 2627:(2): 330–337. 2612: 2573: 2571: 2568: 2566: 2565: 2524: 2474: 2431: 2410:(3): 311–316. 2390: 2383: 2365: 2346:(7): 856–863. 2329: 2285: 2256:(6): 691–703. 2236: 2218: 2158: 2134: 2113:10.1038/nn1030 2107:(4): 362–369. 2091: 2062:(2): 207–220. 2029: 1996:Human Genetics 1980: 1916: 1873: 1859: 1820: 1791:(2): 401–420. 1771: 1748:10.1086/301832 1715: 1675: 1657: 1639: 1618: 1596: 1594: 1591: 1590: 1589: 1584: 1582:GABAA receptor 1577: 1574: 1568: 1565: 1552: 1549: 1535: 1532: 1526: 1523: 1502: 1499: 1486: 1482: 1479: 1469: 1466: 1440: 1436: 1433: 1428: 1419: 1416: 1386: 1382: 1363: 1360: 1355: 1303: 1300: 1237: 1196: 1195: 1192: 1191: 1186: 1176: 1175: 1169: 1168: 1165: 1164: 1162: 1160: 1153: 1152: 1145: 1138: 1134: 1133: 1130: 1129: 1115: 1114: 1108: 1105: 1104: 1078: 1077: 1071: 1067: 1066: 1063: 1062: 1048: 1047: 1041: 1038: 1037: 1011: 1010: 1004: 1000: 999: 996: 995: 987: 986: 980: 977: 976: 968: 967: 961: 955: 954: 951: 950: 942: 941: 935: 932: 931: 923: 922: 916: 910: 909: 906: 905: 897: 896: 890: 887: 886: 878: 877: 871: 865: 864: 859: 854: 850: 849: 839: 838: 835: 834: 823: 822: 820: 819: 814: 809: 804: 799: 794: 789: 784: 779: 774: 769: 764: 759: 754: 749: 744: 739: 734: 729: 724: 719: 713: 711: 707: 706: 704: 703: 698: 693: 688: 683: 678: 673: 668: 663: 658: 653: 648: 643: 637: 635: 631: 630: 628: 627: 622: 617: 612: 607: 602: 597: 592: 586: 584: 580: 579: 569: 568: 565: 564: 561: 560: 552: 551: 540: 534: 533: 530: 529: 521: 520: 517: 516: 514: 513: 509: 508:olfactory bulb 505: 501: 497: 493: 489: 485: 481: 477: 473: 470: 469: 458: 455: 454: 452: 451: 447: 443: 439: 435: 431: 427: 423: 419: 415: 411: 408: 407: 395: 394: 386: 375: 369: 368: 365:RNA expression 357: 356: 353: 352: 344: 340: 339: 331: 328: 323: 317: 316: 307: 300: 294: 290: 289: 284: 278: 277: 269: 268: 256: 255: 252: 251: 243: 239: 238: 230: 227: 222: 216: 215: 206: 199: 193: 189: 188: 181: 175: 174: 166: 165: 153: 152: 109: 105: 104: 96: 88: 87: 83: 82: 79: 78: 75: 74: 64: 63: 55: 54: 43: 37: 36: 28: 27: 24: 23: 15: 9: 6: 4: 3: 2: 3948: 3937: 3934: 3932: 3929: 3927: 3924: 3923: 3921: 3900: 3897: 3895: 3892: 3890: 3887: 3885: 3882: 3880: 3877: 3875: 3872: 3870: 3867: 3866: 3865: 3862: 3861: 3859: 3857: 3853: 3850: 3848: 3844: 3840: 3828: 3822: 3820: 3814: 3813: 3812: 3809: 3808: 3806: 3804: 3800: 3792: 3789: 3787: 3784: 3782: 3779: 3777: 3774: 3772: 3769: 3767: 3764: 3762: 3759: 3757: 3754: 3752: 3749: 3748: 3747: 3744: 3743: 3741: 3739: 3735: 3727: 3724: 3722: 3719: 3717: 3714: 3712: 3709: 3707: 3704: 3703: 3702: 3699: 3696: 3693: 3691: 3688: 3686: 3683: 3681: 3677: 3674: 3673: 3671: 3669: 3665: 3662: 3660: 3657: 3653: 3643: 3640: 3639: 3637: 3635: 3631: 3625: 3618: 3616: 3605: 3603: 3597: 3595: 3585: 3583: 3573: 3570: 3569: 3566: 3563: 3561: 3558: 3556: 3553: 3551: 3548: 3546: 3543: 3541: 3538: 3536: 3533: 3531: 3528: 3526: 3523: 3521: 3518: 3516: 3513: 3511: 3508: 3506: 3503: 3501: 3498: 3496: 3493: 3490: 3489: 3487: 3485: 3481: 3475: 3472: 3470: 3464: 3462: 3456: 3454: 3448: 3446: 3440: 3439: 3437: 3435: 3431: 3423: 3417: 3415: 3409: 3407: 3401: 3400: 3399: 3392: 3388: 3385: 3383: 3380: 3378: 3375: 3373: 3370: 3368: 3362: 3360: 3354: 3352: 3346: 3344: 3338: 3336: 3330: 3328: 3322: 3320: 3314: 3312: 3306: 3304: 3298: 3296: 3290: 3288: 3282: 3280: 3274: 3273: 3272: 3266: 3265: 3263: 3261: 3257: 3249: 3246: 3244: 3241: 3239: 3236: 3234: 3231: 3229: 3226: 3225: 3224: 3218: 3217: 3215: 3213: 3209: 3206: 3204: 3200: 3196: 3192: 3188: 3181: 3176: 3174: 3169: 3167: 3162: 3161: 3158: 3154: 3153: 3151: 3150:public domain 3147: 3138: 3134: 3133: 3128: 3124: 3120: 3117: 3113: 3110: 3109: 3098: 3094: 3090: 3086: 3081: 3077: 3073: 3069: 3065: 3061: 3057: 3053: 3049: 3044: 3040: 3036: 3031: 3026: 3022: 3018: 3014: 3009: 3005: 3001: 2997: 2993: 2988: 2987:2027.42/42268 2983: 2979: 2975: 2971: 2967: 2961: 2957: 2953: 2948: 2943: 2939: 2935: 2931: 2926: 2922: 2918: 2914: 2910: 2906: 2902: 2898: 2894: 2890: 2886: 2881: 2877: 2873: 2869: 2865: 2861: 2857: 2852: 2848: 2844: 2839: 2834: 2830: 2826: 2822: 2817: 2813: 2809: 2805: 2801: 2797: 2793: 2788: 2784: 2780: 2775: 2770: 2766: 2762: 2758: 2753: 2749: 2745: 2740: 2735: 2731: 2727: 2723: 2718: 2714: 2710: 2705: 2700: 2696: 2692: 2688: 2683: 2679: 2675: 2670: 2665: 2661: 2657: 2653: 2648: 2644: 2640: 2635: 2630: 2626: 2622: 2618: 2613: 2609: 2605: 2601: 2597: 2593: 2589: 2585: 2581: 2575: 2574: 2561: 2557: 2552: 2547: 2543: 2539: 2535: 2528: 2520: 2516: 2511: 2506: 2502: 2498: 2494: 2490: 2486: 2478: 2470: 2466: 2462: 2458: 2454: 2450: 2446: 2442: 2435: 2427: 2423: 2418: 2413: 2409: 2405: 2401: 2394: 2386: 2380: 2376: 2369: 2361: 2357: 2353: 2349: 2345: 2341: 2333: 2325: 2321: 2317: 2313: 2309: 2305: 2301: 2297: 2289: 2281: 2277: 2272: 2267: 2263: 2259: 2255: 2251: 2247: 2240: 2232: 2228: 2222: 2214: 2210: 2205: 2200: 2196: 2192: 2188: 2184: 2180: 2176: 2172: 2165: 2163: 2148: 2144: 2138: 2130: 2126: 2122: 2118: 2114: 2110: 2106: 2102: 2095: 2087: 2083: 2078: 2073: 2069: 2065: 2061: 2057: 2053: 2046: 2044: 2042: 2040: 2038: 2036: 2034: 2025: 2021: 2017: 2013: 2009: 2005: 2001: 1997: 1989: 1987: 1985: 1976: 1972: 1967: 1962: 1957: 1952: 1948: 1944: 1940: 1936: 1932: 1925: 1923: 1921: 1912: 1908: 1904: 1900: 1896: 1892: 1888: 1884: 1877: 1869: 1863: 1855: 1851: 1847: 1843: 1839: 1835: 1827: 1825: 1816: 1812: 1807: 1802: 1798: 1794: 1790: 1786: 1782: 1775: 1767: 1763: 1758: 1753: 1749: 1745: 1741: 1737: 1733: 1726: 1724: 1722: 1720: 1711: 1707: 1703: 1699: 1695: 1691: 1684: 1682: 1680: 1671: 1667: 1661: 1653: 1649: 1643: 1636: 1632: 1627: 1625: 1623: 1615: 1611: 1606: 1604: 1602: 1597: 1588: 1585: 1583: 1580: 1579: 1573: 1564: 1561: 1557: 1548: 1546: 1541: 1531: 1522: 1520: 1515: 1512:In mice, the 1510: 1508: 1498: 1496: 1491: 1478: 1476: 1465: 1461: 1459: 1456:occur in the 1455: 1450: 1446: 1432: 1425: 1415: 1412: 1410: 1406: 1403: 1400: 1399: 1394: 1392: 1380: 1376: 1374: 1369: 1359: 1352: 1347: 1345: 1341: 1337: 1333: 1329: 1325: 1321: 1317: 1313: 1309: 1299: 1297: 1293: 1289: 1285: 1281: 1277: 1273: 1269: 1265: 1261: 1257: 1253: 1249: 1245: 1241: 1233: 1229: 1225: 1224:coding region 1221: 1217: 1213: 1210: 1206: 1202: 1190: 1185: 1181: 1177: 1174: 1170: 1163: 1161: 1158: 1154: 1150: 1146: 1143: 1139: 1135: 1128: 1126: 1122: 1116: 1112: 1109: 1103: 1101: 1097: 1093: 1089: 1085: 1079: 1075: 1072: 1068: 1061: 1059: 1055: 1049: 1045: 1042: 1036: 1034: 1030: 1026: 1022: 1018: 1012: 1008: 1005: 1003:RefSeq (mRNA) 1001: 994: 993: 988: 984: 981: 975: 974: 969: 965: 962: 960: 956: 949: 948: 943: 939: 936: 930: 929: 924: 920: 917: 915: 911: 904: 903: 898: 894: 891: 885: 884: 879: 875: 872: 870: 866: 863: 860: 858: 855: 851: 848: 844: 840: 833: 829: 824: 818: 815: 813: 810: 808: 805: 803: 800: 798: 795: 793: 790: 788: 785: 783: 780: 778: 775: 773: 770: 768: 765: 763: 760: 758: 755: 753: 752:ion transport 750: 748: 745: 743: 740: 738: 735: 733: 730: 728: 725: 723: 720: 718: 715: 714: 712: 709: 708: 702: 699: 697: 694: 692: 689: 687: 684: 682: 679: 677: 674: 672: 671:cell junction 669: 667: 664: 662: 659: 657: 654: 652: 649: 647: 644: 642: 639: 638: 636: 633: 632: 626: 623: 621: 618: 616: 613: 611: 608: 606: 603: 601: 598: 596: 593: 591: 588: 587: 585: 582: 581: 578: 577:Gene ontology 574: 570: 558: 553: 549: 544: 541: 539: 535: 527: 522: 511: 507: 503: 499: 495: 491: 487: 483: 479: 475: 474: 471: 467: 462: 459: 449: 445: 441: 437: 433: 430:parietal lobe 429: 425: 421: 417: 413: 412: 409: 405: 400: 397: 396: 393: 391: 387: 385: 384: 380: 379: 376: 374: 370: 366: 362: 358: 350: 345: 341: 337: 332: 322: 318: 311: 304: 298: 291: 283: 279: 275: 270: 266: 261: 257: 249: 244: 240: 236: 231: 221: 217: 210: 203: 197: 190: 186: 180: 176: 172: 167: 163: 158: 154: 150: 146: 142: 138: 134: 130: 126: 122: 118: 114: 106: 101: 94: 89: 84: 73: 71: 65: 60: 57: 56: 52: 49: 42: 38: 33: 29: 25: 20: 3931:Ion channels 3846: 3810: 3802: 3737: 3667: 3633: 3571: 3491: 3339: 3143: 3142: 3130: 3088: 3084: 3051: 3047: 3023:(1): 91–96. 3020: 3016: 2969: 2965: 2937: 2933: 2891:(1): 58–64. 2888: 2884: 2859: 2855: 2828: 2824: 2798:(1): 63–69. 2795: 2791: 2764: 2760: 2729: 2725: 2694: 2690: 2659: 2655: 2624: 2620: 2583: 2579: 2541: 2537: 2527: 2492: 2488: 2477: 2444: 2440: 2434: 2407: 2403: 2393: 2374: 2368: 2343: 2339: 2332: 2302:(1): 87–97. 2299: 2295: 2288: 2253: 2249: 2239: 2230: 2221: 2178: 2174: 2150:. Retrieved 2146: 2137: 2104: 2100: 2094: 2059: 2055: 2002:(1): 15–20. 1999: 1995: 1938: 1934: 1889:(1): 41–46. 1886: 1882: 1876: 1862: 1837: 1833: 1788: 1784: 1774: 1739: 1735: 1696:(1): 63–69. 1693: 1689: 1669: 1660: 1651: 1642: 1570: 1562: 1558: 1554: 1537: 1528: 1511: 1504: 1492: 1484: 1471: 1462: 1438: 1421: 1413: 1402:heterozygous 1397: 1395: 1372: 1365: 1348: 1312:gene cluster 1305: 1288:methaqualone 1260:olivary body 1208: 1200: 1199: 1121:NP_001033790 1118: 1096:NP_001265560 1092:NP_001178250 1088:NP_001178249 1081: 1054:NM_001038701 1051: 1029:NM_001278631 1025:NM_001191321 1021:NM_001191320 1014: 990: 971: 945: 926: 900: 881: 861: 856: 388: 381: 108:External IDs 67: 3187:Ion channel 1454:mouse brain 1248:hippocampus 1222:within its 767:innervation 347:57,478,550 334:57,069,440 246:26,939,539 233:26,543,546 86:Identifiers 3920:Categories 3659:glutamates 3656:Ionotropic 3572:pentamers: 2152:2017-11-30 1637:, May 2017 1616:, May 2017 1593:References 1481:Regulation 1435:Expression 1358:receptor. 1351:vertebrate 1336:imprinting 1308:chromosome 1252:cerebellum 392:(ortholog) 129:HomoloGene 3492:monomers: 3076:140209788 1545:transgene 1418:Structure 1292:etomidate 1226:. Due to 1125:NP_032097 1100:NP_068712 1084:NP_000805 1058:NM_008071 1033:NM_021912 1017:NM_000814 847:Orthologs 504:subiculum 137:GeneCards 3803:‘Orphan’ 3097:12491987 3068:12367595 3039:12225856 3004:10982155 2996:12189488 2956:11920158 2921:13569188 2913:11085308 2876:10023064 2792:Genomics 2656:Genomics 2608:40634548 2560:16835263 2519:18514161 2469:13656488 2461:10515160 2426:11920158 2360:12819446 2316:12595241 2280:17339270 2213:24909990 2147:omim.org 2129:24096465 2121:12640458 2086:17983671 2024:23459069 2016:11810291 1911:35832564 1834:Genomics 1815:26056160 1690:Genomics 1633:– 1612:– 1576:See also 1458:Purkinje 1449:thalamus 1362:Function 1332:isoforms 1280:epilepsy 1256:thalamus 1240:receptor 1173:Wikidata 826:Sources: 651:membrane 3701:Kainate 3434:Glycine 3137:PDBe-KB 3127:UniProt 2893:Bibcode 2847:9328477 2812:9126483 2783:8389098 2774:1682269 2748:8382702 2713:8175718 2678:7851879 2643:1714232 2634:1683305 2600:1346439 2510:2427288 2324:6172436 2271:1934608 2204:4167603 2183:Bibcode 2077:2684890 1975:8095339 1943:Bibcode 1903:8136833 1854:1664410 1806:4518083 1766:9545402 1757:1377089 1710:9126483 1635:Ensembl 1614:Ensembl 1409:neurons 1398:De novo 1205:protein 959:UniProt 914:Ensembl 853:Species 832:QuickGO 747:hearing 656:synapse 367:pattern 93:Aliases 3132:P28472 3118:(MeSH) 3095:  3074:  3066:  3037:  3002:  2994:  2954:  2919:  2911:  2874:  2845:  2810:  2781:  2771:  2746:  2711:  2676:  2641:  2631:  2606:  2598:  2580:Lancet 2558:  2517:  2507:  2467:  2459:  2424:  2381:  2358:  2322:  2314:  2278:  2268:  2211:  2201:  2175:Nature 2127:  2119:  2084:  2074:  2022:  2014:  1973:  1963:  1909:  1901:  1852:  1813:  1803:  1764:  1754:  1708:  1540:palate 1507:savant 1344:allele 1340:intron 1320:GABRA5 1316:GABRG3 1284:autism 1216:genome 1209:GABRB3 1159:search 1157:PubMed 992:P63080 973:P28472 869:Entrez 538:BioGPS 141:GABRB3 117:137192 100:GABRB3 22:GABRB3 3072:S2CID 3000:S2CID 2917:S2CID 2604:S2CID 2465:S2CID 2320:S2CID 2125:S2CID 2020:S2CID 1966:46018 1907:S2CID 1495:MECP2 1475:mouse 1373:gamma 1220:exons 1203:is a 902:14402 862:Mouse 857:Human 828:Amigo 390:Mouse 383:Human 330:Start 265:Mouse 229:Start 225:15q12 162:Human 125:95621 3811:GluD 3746:NMDA 3676:AMPA 3634:Zinc 3620:(α1) 3611:(β4) 3607:(α1) 3599:(α7) 3591:(β2) 3587:(α4) 3579:(β4) 3575:(α3) 3394:GABA 3268:GABA 3260:GABA 3220:5-HT 3125:for 3093:PMID 3064:PMID 3035:PMID 3021:1565 2992:PMID 2952:PMID 2909:PMID 2872:PMID 2856:Gene 2843:PMID 2808:PMID 2779:PMID 2744:PMID 2709:PMID 2674:PMID 2639:PMID 2596:PMID 2556:PMID 2515:PMID 2457:PMID 2422:PMID 2379:ISBN 2356:PMID 2312:PMID 2276:PMID 2209:PMID 2117:PMID 2082:PMID 2012:PMID 1971:PMID 1899:PMID 1850:PMID 1811:PMID 1762:PMID 1706:PMID 1427:GABA 1422:The 1391:ions 1354:GABA 1318:and 1302:Gene 1290:and 1282:and 1262:and 1236:GABA 1212:gene 883:2562 373:Bgee 321:Band 282:Chr. 220:Band 179:Chr. 113:OMIM 70:4COF 51:RCSB 48:PDBe 3864:P2X 3843:ATP 3791:L1B 3786:L1A 3535:α10 3123:PDB 3056:doi 3025:doi 2982:hdl 2974:doi 2970:111 2942:doi 2901:doi 2889:914 2864:doi 2860:227 2833:doi 2800:doi 2769:PMC 2734:doi 2730:268 2699:doi 2695:269 2664:doi 2629:PMC 2588:doi 2584:339 2546:doi 2505:PMC 2497:doi 2449:doi 2412:doi 2348:doi 2304:doi 2266:PMC 2258:doi 2199:PMC 2191:doi 2179:512 2109:doi 2072:PMC 2064:doi 2060:187 2004:doi 2000:110 1961:PMC 1951:doi 1891:doi 1842:doi 1801:PMC 1793:doi 1752:PMC 1744:doi 1698:doi 343:End 242:End 145:OMA 133:633 121:MGI 41:PDB 3922:: 3781:3B 3776:3A 3771:2D 3766:2C 3761:2B 3756:2A 3555:β4 3550:β3 3545:β2 3540:β1 3530:α9 3525:α7 3520:α6 3515:α5 3510:α4 3505:α3 3500:α2 3495:α1 3398:-ρ 3193:: 3189:, 3129:: 3089:36 3087:. 3070:. 3062:. 3052:43 3050:. 3033:. 3019:. 3015:. 2998:. 2990:. 2980:. 2968:. 2950:. 2936:. 2932:. 2915:. 2907:. 2899:. 2887:. 2870:. 2858:. 2841:. 2827:. 2823:. 2806:. 2796:41 2794:. 2777:. 2765:52 2763:. 2759:. 2742:. 2728:. 2724:. 2707:. 2693:. 2689:. 2672:. 2660:23 2658:. 2654:. 2637:. 2625:49 2623:. 2619:. 2602:. 2594:. 2582:. 2554:. 2542:15 2540:. 2536:. 2513:. 2503:. 2493:82 2491:. 2487:. 2463:. 2455:. 2445:36 2443:. 2420:. 2406:. 2402:. 2354:. 2344:42 2342:. 2318:. 2310:. 2300:22 2298:. 2274:. 2264:. 2254:16 2252:. 2248:. 2229:. 2207:. 2197:. 2189:. 2177:. 2173:. 2161:^ 2145:. 2123:. 2115:. 2103:. 2080:. 2070:. 2058:. 2054:. 2032:^ 2018:. 2010:. 1998:. 1983:^ 1969:. 1959:. 1949:. 1939:90 1937:. 1933:. 1919:^ 1905:. 1897:. 1885:. 1848:. 1838:11 1836:. 1823:^ 1809:. 1799:. 1789:88 1787:. 1783:. 1760:. 1750:. 1740:62 1738:. 1734:. 1718:^ 1704:. 1694:41 1692:. 1678:^ 1668:. 1650:. 1621:^ 1600:^ 1326:. 1298:. 1274:, 1258:, 1254:, 1250:, 1246:, 830:/ 349:bp 336:bp 248:bp 235:bp 143:; 139:: 135:; 131:: 127:; 123:: 119:; 115:: 3899:7 3894:6 3889:5 3884:4 3879:3 3874:2 3869:1 3845:- 3826:2 3824:δ 3818:1 3816:δ 3751:1 3726:5 3721:4 3716:3 3711:2 3706:1 3697:) 3695:4 3690:3 3685:2 3680:1 3678:( 3622:2 3613:3 3609:2 3601:5 3593:3 3589:2 3581:3 3577:2 3565:ε 3560:δ 3474:β 3468:4 3466:α 3460:3 3458:α 3452:2 3450:α 3444:1 3442:α 3421:3 3419:ρ 3413:2 3411:ρ 3405:1 3403:ρ 3396:A 3387:θ 3382:π 3377:ε 3372:δ 3366:3 3364:γ 3358:2 3356:γ 3350:1 3348:γ 3342:3 3340:β 3334:2 3332:β 3326:1 3324:β 3318:6 3316:α 3310:5 3308:α 3302:4 3300:α 3294:3 3292:α 3286:2 3284:α 3278:1 3276:α 3270:A 3248:E 3243:D 3238:C 3233:B 3228:A 3222:3 3179:e 3172:t 3165:v 3152:. 3139:. 3099:. 3078:. 3058:: 3041:. 3027:: 3006:. 2984:: 2976:: 2958:. 2944:: 2938:7 2923:. 2903:: 2895:: 2878:. 2866:: 2849:. 2835:: 2829:6 2814:. 2802:: 2785:. 2750:. 2736:: 2715:. 2701:: 2680:. 2666:: 2645:. 2610:. 2590:: 2562:. 2548:: 2521:. 2499:: 2471:. 2451:: 2428:. 2414:: 2408:7 2387:. 2362:. 2350:: 2326:. 2306:: 2282:. 2260:: 2215:. 2193:: 2185:: 2155:. 2131:. 2111:: 2105:6 2088:. 2066:: 2026:. 2006:: 1977:. 1953:: 1945:: 1913:. 1893:: 1887:6 1870:. 1856:. 1844:: 1817:. 1795:: 1768:. 1746:: 1712:. 1700:: 1672:. 1654:. 1487:A 1441:A 1429:A 1387:A 1383:A 1356:A 1238:A 267:) 164:) 147::

Index

PDB
PDBe
RCSB
4COF
Aliases
GABRB3
OMIM
137192
MGI
95621
HomoloGene
633
GeneCards
GABRB3
OMA
GABRB3 - orthologs
Human
Chromosome 15 (human)
Chr.
Chromosome 15 (human)
Chromosome 15 (human)
Genomic location for GABRB3
Genomic location for GABRB3
Band
bp
bp
Mouse
Chromosome 7 (mouse)
Chr.
Chromosome 7 (mouse)

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