======= IFITM5 ======= == Gene Information == * **Official Symbol**: IFITM5 * **Official Name**: interferon induced transmembrane protein 5 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=387733|387733]] * **UniProt**: [[https://www.uniprot.org/uniprot/A6NNB3|A6NNB3]] * **Interactions**: [[https://thebiogrid.org/search.php?search=IFITM5&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20IFITM5|Open PubMed]] * **OMIM**: [[https://omim.org/entry/614757|Open OMIM]] == Function Summary == * **Entrez 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]. * **UniProt Summary**: Required for normal bone mineralization. {ECO:0000269|PubMed:24519609}. |CD225| |bone mineralization| |regulation of bone mineralization| |regulation of biomineralization| |biomineralization| |regulation of biomineral tissue development| |biomineral tissue development| |bone morphogenesis| |regulation of ossification| |bone development| |skeletal system morphogenesis| |ossification| |in utero embryonic development| |skeletal system development| |chordate embryonic development| |embryo development ending in birth or egg hatching| |animal organ morphogenesis| |embryo development| |integral component of plasma membrane| |tissue development| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp529|Thimerosal 0.85μM R08 exp529]]|1.78| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 1/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 9238 * **Expression level (log2 read counts)**: -6.6 {{:chemogenomics:nalm6 dist.png?nolink |}}