IFITM5
Sign in to saveAlso 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
Show 5 more facts
- HomoloGene ID
- 14210
- exact match
- identifiers.org/ncbigene/387733
- genomic end
- 299526
- genomic start
- 298200
- cytogenetic location
- 11p15.5
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