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Symbol report for AP1B1

Stable symbol

HGNC data for AP1B1

Approved symbol
AP1B1
Approved name

adaptor related protein complex 1 subunit beta 1

Locus type
gene with protein product
HGNC ID
HGNC:554
Symbol status
Approved
Previous symbols
ADTB1
CLAPB2
Previous names
ADTB1, CLAPB2
adaptor related protein complex 1 beta 1 subunit
Alias symbols
BAM22
AP105A
Chromosomal location
22q12.2
UCSC
Alliance of Genome Resources
Bos taurus
AP1B1 VGNC:25976 VGNC
Canis familiaris
AP1B1 VGNC:37951 VGNC
Equus caballus
AP1B1 VGNC:15372 VGNC
Felis catus
AP1B1 VGNC:67719 VGNC
Macaca mulatta
AP1B1 VGNC:69957 VGNC
Mus musculus
Ap1b1 MGI:1096368 Curated
Pan troglodytes
AP1B1 VGNC:5949 VGNC
Rattus norvegicus
Ap1b1 RGD:2064
Sus scrofa
AP1B1 VGNC:85377 VGNC
Structure of the promoter and genomic organization of the human beta'-adaptin gene (BAM22) from chromosome 22q12.
Peyrard M et al. Genomics 1996 Aug;36(1)112-117
Peyrard M, Pan HQ, Kedra D, Fransson I, Swahn S, Hartman K, Clifton SW, Roe BA, Dumanski JP.
Genomics 1996 Aug;36(1)112-117
Abstract: Adaptins are major structural components of heterotetrameric protein complexes called adaptors, which are essential in intracellular receptor transport via clathrin-coated vesicles. beta-adaptins constitute one of three known classes (alpha, beta, gamma) of adaptins, including beta and beta' subtypes. We previously cloned the human beta'-adaptin gene (BAM22) (GDB symbol, ADTB1) from chromosome 22q12 and proposed its involvement in the development of meningiomas. Here we describe the genomic organization of this gene, which consists of 22 exons spanning over approximately 100 kb. We also report results from point mutation screening of 7 randomly chosen exons analyzed in 110 sporadic meningiomas. As part of the genomic characterization of the BAM22 locus, we sequenced 40 kb covering exons 1-4 and 12 kb upstream from the start of gene transcription. Analysis of the sequence suggests that the BAM22 gene has a CG-rich promoter.
Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene.
Peyrard M et al. Hum Mol Genet 1994 Aug;3(8)1393-1399
Peyrard M, Fransson I, Xie YG, Han FY, Ruttledge MH, Swahn S, Collins JE, Dunham I, Collins VP, Dumanski JP.
Hum Mol Genet 1994 Aug;3(8)1393-1399
Abstract: A 140 kb homozygous deletion from 22q12 in one meningioma directed us towards the cloning and characterization of a new member of the human beta-adaptin gene family (named BAM22). Adaptins are essential for the formation of clathrin coated vesicles in the course of intracellular transport of receptor-ligand complexes. The BAM22 gene is totally inactivated in the tumor with homozygous deletion. Northern blot analysis of 70 sporadic meningiomas showed specific loss of expression in 8 tumors, suggesting inactivation of BAM22. Based on this, we propose BAM22 as a second chromosome 22 locus important in meningioma development, after the neurofibromatosis type 2 gene.