Homo sapiens Gene: IFITM5
Summary
InnateDB Gene IDBG-16179.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol IFITM5
Gene Name interferon induced transmembrane protein 5
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000206013
Encoded Proteins
interferon induced transmembrane protein 5
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary 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]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:298200-299526
Strand Reverse strand
Band p15.5
Transcripts
ENST00000382614 ENSP00000372059
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0009607 response to biotic stimulus
GO:0030282 bone mineralization
GO:0030500 regulation of bone mineralization
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt A6NNB3
TrEMBL
UniProt Splice Variant
Entrez Gene 387733
UniGene Hs.443469
RefSeq NM_001025295
HUGO HGNC:16644
OMIM 614757
CCDS CCDS31323
HPRD
IMGT
EMBL BC150562 BC150563 CH471278
GenPept AAI50563 AAI50564 EAW61222
RNA Seq Atlas 387733