======= 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 |}}