P4HTM

Protein-coding gene in the species Homo sapiens

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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.