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Ask your administrator if you think this is wrong. ======= KRIT1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: KRIT1 * **<color #00a2e8>Official Name</color>**: KRIT1 ankyrin repeat containing * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=889|889]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/O00522|O00522]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=KRIT1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20KRIT1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/604214|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene encodes a protein containing four ankyrin repeats, a band 4.1/ezrin/radixin/moesin (FERM) domain, and multiple NPXY sequences. The encoded protein is localized in the nucleus and cytoplasm. It binds to integrin cytoplasmic domain-associated protein-1 alpha (ICAP1alpha), and plays a critical role in beta1-integrin-mediated cell proliferation. It associates with junction proteins and RAS-related protein 1A (Rap1A), which requires the encoded protein for maintaining the integrity of endothelial junctions. It is also a microtubule-associated protein and may play a role in microtubule targeting. Mutations in this gene result in cerebral cavernous malformations. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]. * **<color #00a2e8>UniProt Summary</color>**: N/A <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |Ank 2| |FERM M| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |GTPase regulator activity| |regulation of establishment of cell polarity| |regulation of establishment or maintenance of cell polarity| |negative regulation of endothelial cell apoptotic process| |negative regulation of endothelial cell proliferation| |negative regulation of epithelial cell apoptotic process| |negative regulation of endothelial cell migration| |regulation of endothelial cell apoptotic process| |negative regulation of epithelial cell migration| |cell redox homeostasis| |phosphatidylinositol-4,5-bisphosphate binding| |regulation of epithelial cell apoptotic process| |negative regulation of angiogenesis| |negative regulation of blood vessel morphogenesis| |negative regulation of vasculature development| |negative regulation of epithelial cell proliferation| |regulation of endothelial cell proliferation| |regulation of endothelial cell migration| |cell-cell junction| |regulation of epithelial cell migration| |microtubule binding| |negative regulation of cell migration| |negative regulation of cell motility| |regulation of angiogenesis| |negative regulation of cellular component movement| |angiogenesis| |small GTPase mediated signal transduction| |regulation of vasculature development| |negative regulation of locomotion| |regulation of epithelial cell proliferation| |cytoskeleton| |blood vessel morphogenesis| |blood vessel development| |vasculature development| |cardiovascular system development| |tube morphogenesis| |negative regulation of cell population proliferation| |tube development| |regulation of cell migration| |circulatory system development| |negative regulation of apoptotic process| |anatomical structure formation involved in morphogenesis| |cellular homeostasis| |negative regulation of programmed cell death| |regulation of cell motility| |negative regulation of developmental process| |regulation of locomotion| |negative regulation of cell death| |regulation of cellular component movement| |regulation of anatomical structure morphogenesis| |negative regulation of multicellular organismal process| |regulation of apoptotic process| |regulation of programmed cell death| |extracellular space| |regulation of cell population proliferation| |homeostatic process| |regulation of cell death| |intracellular signal transduction| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='primary' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp455|Benzoate 10000μM R08 exp455]]|-1.81| |[[:results:exp214|2-Deoxy-D-glucose 800μM R05 exp214]]|-1.79| |[[:results:exp210|LB-100 2μM R05 exp210]]|1.75| |[[:results:exp442|Ibrutinib 10μM R08 exp442]]|2.17| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> ^Gene^Correlation^ |[[:human genes:c:ccm2|CCM2]]|0.467| </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> 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| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 7032 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 6.05 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='KRIT1 Expression in NALM6 Cells: 6.05'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1