======= ITGA7 =======
== Gene Information ==
* **Official Symbol**: ITGA7
* **Official Name**: integrin subunit alpha 7
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=3679|3679]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q13683|Q13683]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=ITGA7&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20ITGA7|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/600536|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2009].
* **UniProt Summary**: N/A
|Integrin alpha2|
|FG-GAP|
|integrin complex|
|heterotypic cell-cell adhesion|
|endodermal cell differentiation|
|endoderm formation|
|endoderm development|
|integrin-mediated signaling pathway|
|formation of primary germ layer|
|cell-matrix adhesion|
|regulation of cell shape|
|gastrulation|
|cell-substrate adhesion|
|muscle organ development|
|extracellular matrix organization|
|extracellular structure organization|
|muscle structure development|
|regulation of cell morphogenesis|
|cell-cell adhesion|
|embryonic morphogenesis|
|cell surface|
|anatomical structure formation involved in morphogenesis|
|cell adhesion|
|biological adhesion|
|embryo development|
|regulation of anatomical structure morphogenesis|
|tissue development|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp468|CB-5083 0.4μM R08 exp468]]|1.77|
|[[:results:exp271|CCT251545 0.2μM R06 exp271]]|1.77|
No correlation found to any other genes in chemogenomics.
Global Fraction of Cell Lines Where Essential: 0/739
^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**: 3901
* **Expression level (log2 read counts)**: -0.06
{{:chemogenomics:nalm6 dist.png?nolink |}}