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HIG1 hypoxia inducible domain family member 1B

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(Redirected from HIGD1B)
HIGD1B
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesHIGD1B, CLST11240, CLST11240-15, HIG1 hypoxia inducible domain family member 1B
External IDsMGI: 1922939; HomoloGene: 9508; GeneCards: HIGD1B; OMA:HIGD1B - orthologs
Orthologs
SpeciesHumanMouse
Entrez

51751

75689

Ensembl

ENSG00000131097

ENSMUSG00000020928

UniProt

Q9P298

Q99JY6

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
View/Edit HumanView/Edit Mouse

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

Function

[edit]

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.

References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000131097 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020928 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: HIG1 hypoxia inducible domain family member 1B". Retrieved 2017-10-07.

Further reading

[edit]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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