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HIG1 hypoxia inducible domain family member 1B

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

HIG1 hypoxia inducible domain family member 1B is a protein that in humans is encoded by the HIGD1B gene.[5]

AliasesHIGD1B, CLST11240, CLST11240-15, HIG1 hypoxia inducible domain family member 1B
External IDsMGI: 1922939; GeneCards: HIGD1B
PDBOrtholog search: PDBe RCSB
Quick facts HIGD1B, Identifiers ...
HIGD1B
Identifiers
AliasesHIGD1B, CLST11240, CLST11240-15, HIG1 hypoxia inducible domain family member 1B
External IDsMGI: 1922939; GeneCards: HIGD1B
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001271880
NM_016438

NM_080846
NM_001357580

RefSeq (protein)

NP_001258809
NP_057522

NP_543122
NP_001344509

Location (UCSC)Chr 17: 44.85 – 44.85 MbChr 11: 102.73 – 102.73 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of the hypoxia inducible gene 1 (HIG1) domain family. The encoded protein is localized to the cell membrane and has been linked to tumorigenesis and the progression of pituitary adenomas. Alternative splicing results in multiple transcript variants.

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