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GeneQ14566783· pop 5· linked from 6 articles

Also known as interferon induced transmembrane protein 5, BRIL, DSPA1, Hrmp1, OI5, fragilis4

protein-coding gene in the species Homo sapiens

Gene data

IFITM5
Name
interferon induced transmembrane protein 5
Type
protein-coding
Aliases
BRIL, DSPA1, Hrmp1, OI5, fragilis4

This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012].

via MyGene.info

Wikidata facts

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HomoloGene ID
14210
genomic end
299526
genomic start
298200
cytogenetic location
11p15.5
Sources (5)

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