VIPAS39

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Spermatogenesis-defective protein 39 homolog is a protein that in humans is encoded by the VIPAS39 gene. This protein is involved in the sorting of lysosomal proteins. Mutations in this gene are associated with ARCS2 (arthrogryposis, renal dysfunction, and cholestasis-2). Alternative splicing results in multiple transcript variants. [5]

AliasesVIPAS39, C14orf133, SPE-39, SPE39, VIPAR, VPS16B, hSPE-39, VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
End77,457,952 bp[1]
Quick facts Identifiers, Aliases ...
VIPAS39
Identifiers
AliasesVIPAS39, C14orf133, SPE-39, SPE39, VIPAR, VPS16B, hSPE-39, VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
External IDsOMIM: 613401; MGI: 2144805; HomoloGene: 41464; GeneCards: VIPAS39; OMA:VIPAS39 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001193314
NM_001193315
NM_001193316
NM_001193317
NM_022067

NM_001142580
NM_001142581
NM_134044

RefSeq (protein)

NP_001180243
NP_001180244
NP_001180245
NP_001180246
NP_071350

NP_001136052
NP_001136053
NP_598805

Location (UCSC)Chr 14: 77.43 – 77.46 MbChr 12: 87.29 – 87.31 Mb
PubMed search[3][4]
Wikidata
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