P4HTM: Difference between revisions

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{{cite web
{{cite web
| title = Entrez Gene: Prolyl 4-hydroxylase, transmembrane
| title = Entrez Gene: Prolyl 4-hydroxylase, transmembrane
| url = http://www.ncbi.nlm.nih.gov/gene/54681
| url = https://www.ncbi.nlm.nih.gov/gene/54681
| accessdate = 2017-10-03
| accessdate = 2017-10-03
}}</ref>
}}</ref>

Latest revision as of 11:31, 20 December 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Prolyl 4-hydroxylase, transmembrane is a protein that in humans is encoded by the P4HTM gene. [1]

Function

The product of this gene belongs to the family of prolyl 4-hydroxylases. This protein is a prolyl hydroxylase that may be involved in the degradation of hypoxia-inducible transcription factors under normoxia. It plays a role in adaptation to hypoxia and may be related to cellular oxygen sensing. Alternatively spliced variants encoding different isoforms have been identified.

References

  1. "Entrez Gene: Prolyl 4-hydroxylase, transmembrane". Retrieved 2017-10-03.

Further reading


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