KRIT1

KRIT1
Available structures PDB Ortholog search: C9JD81 PDBe C9JD81 RCSB List of PDB id codes 3U7D, 4DX8, 4DXA, 4HDO, 4HDQ, 4JIF, 4TKN, 5D68
Identifiers
Aliases	KRIT1, ankyrin repeat containing, CAM, CCM1
External IDs	OMIM: 604214 MGI: 1930618 HomoloGene: 12746 GeneCards: KRIT1
Gene location (Mouse) Chr. Chromosome 5 (mouse) Band 5 A1|5 2.26 cM Start 3,853,184 bp End 3,895,564 bp
RNA expression pattern Bgee Human Mouse (ortholog) n/a Top expressed in interventricular septum mammillary body dorsomedial hypothalamic nucleus spermatocyte lateral hypothalamus pontine nuclei ventromedial nucleus habenula ventral tegmental area cerebellar vermis BioGPS More reference expression data
Gene ontology Molecular function microtubule binding protein binding phosphatidylinositol-4,5-bisphosphate binding protein-containing complex binding GTPase regulator activity Cellular component cytoskeleton membrane microtubule plasma membrane cytoplasm cell-cell junction cell junction extracellular space Biological process regulation of establishment of cell polarity negative regulation of angiogenesis small GTPase mediated signal transduction angiogenesis negative regulation of endothelial cell proliferation negative regulation of endothelial cell apoptotic process negative regulation of endothelial cell migration positive regulation of protein binding cell redox homeostasis regulation of catalytic activity Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 889 79264 Ensembl ENSG00000001631 ENSMUSG00000000600 UniProt O00522 Q6S5J6 RefSeq (mRNA) NM_001013406 NM_004912 NM_194454 NM_194455 NM_194456 NM_001170552 NM_030675 RefSeq (protein) NP_001013424 NP_004903 NP_919436 NP_919437 NP_919438 NP_001337598 NP_001337599 NP_001337600 NP_001337601 NP_001337602 NP_001337603 NP_001337604 NP_001337605 NP_001337606 NP_001337607 NP_001337608 NP_001337609 NP_001337610 NP_001337611 NP_001337612 NP_001337613 NP_001337614 NP_001337615 NP_001337616 NP_001337617 NP_001337618 NP_001337619 NP_001337620 NP_001337621 NP_001337622 NP_001337623 NP_001337624 NP_001337625 NP_001337626 NP_001164023 NP_109600 Location (UCSC) n/a Chr 5: 3.85 – 3.9 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Krev interaction trapped protein 1 or Cerebral cavernous malformations 1 protein is a protein that in humans is encoded by the KRIT1 gene. This gene contains 16 coding exons and is located on chromosome 7q21.2. Loss of function mutations in KRIT1 result in the onset of cerebral cavernous malformation. Cerebral cavernous malformations (CCMs) are vascular malformations in the brain and spinal cord made of dilated capillary vessels.

Interactions

The KRIT1 protein, is 736 amino acids in length and has a variety of functions. KRIT1 has been shown to interact with multiple signaling pathways including; ITGB1BP1., reactive oxygen species, cell death, and angiogenesis. Related to cerebral cavernous malformations, this protein is required for maintaining the structural integrity of the vasculature.

Further reading

• Verlaan DJ, Davenport WJ, Stefan H, Sure U, Siegel AM, Rouleau GA (Mar 2002). "Cerebral cavernous malformations: mutations in Krit1". Neurology. 58 (6): 853–7. doi:10.1212/wnl.58.6.853. PMID 11914398. S2CID 12113924.
• Marchuk DA, Gallione CJ, Morrison LA, Clericuzio CL, Hart BL, Kosofsky BE, Louis DN, Gusella JF, Davis LE, Prenger VL (Jul 1995). "A locus for cerebral cavernous malformations maps to chromosome 7q in two families". Genomics. 28 (2): 311–4. doi:10.1006/geno.1995.1147. PMID 8530042.
• Serebriiskii I, Estojak J, Sonoda G, Testa JR, Golemis EA (Aug 1997). "Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22". Oncogene. 15 (9): 1043–9. doi:10.1038/sj.onc.1201268. PMID 9285558.
• Deloulme JC, Prichard L, Delattre O, Storm DR (Oct 1997). "The prooncoprotein EWS binds calmodulin and is phosphorylated by protein kinase C through an IQ domain". The Journal of Biological Chemistry. 272 (43): 27369–77. doi:10.1074/jbc.272.43.27369. PMID 9341188.
• Laberge-le Couteulx S, Jung HH, Labauge P, Houtteville JP, Lescoat C, Cecillon M, Marechal E, Joutel A, Bach JF, Tournier-Lasserve E (Oct 1999). "Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas". Nature Genetics. 23 (2): 189–93. doi:10.1038/13815. PMID 10508515. S2CID 22297740.
• Sahoo T, Johnson EW, Thomas JW, Kuehl PM, Jones TL, Dokken CG, Touchman JW, Gallione CJ, Lee-Lin SQ, Kosofsky B, Kurth JH, Louis DN, Mettler G, Morrison L, Gil-Nagel A, Rich SS, Zabramski JM, Boguski MS, Green ED, Marchuk DA (Nov 1999). "Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)". Human Molecular Genetics. 8 (12): 2325–33. doi:10.1093/hmg/8.12.2325. PMID 10545614.
• Eerola I, Plate KH, Spiegel R, Boon LM, Mulliken JB, Vikkula M (May 2000). "KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation". Human Molecular Genetics. 9 (9): 1351–5. doi:10.1093/hmg/9.9.1351. PMID 10814716.
• Zhang J, Clatterbuck RE, Rigamonti D, Dietz HC (Dec 2000). "Cloning of the murine Krit1 cDNA reveals novel mammalian 5' coding exons". Genomics. 70 (3): 392–5. doi:10.1006/geno.2000.6410. PMID 11161791.
• Sahoo T, Goenaga-Diaz E, Serebriiskii IG, Thomas JW, Kotova E, Cuellar JG, Peloquin JM, Golemis E, Beitinjaneh F, Green ED, Johnson EW, Marchuk DA (Jan 2001). "Computational and experimental analyses reveal previously undetected coding exons of the KRIT1 (CCM1) gene". Genomics. 71 (1): 123–6. doi:10.1006/geno.2000.6426. PMID 11161805.
• Zhang J, Clatterbuck RE, Rigamonti D, Chang DD, Dietz HC (Dec 2001). "Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation". Human Molecular Genetics. 10 (25): 2953–60. doi:10.1093/hmg/10.25.2953. PMID 11741838.
• Couteulx SL, Brézin AP, Fontaine B, Tournier-Lasserve E, Labauge P (Feb 2002). "A novel KRIT1/CCM1 truncating mutation in a patient with cerebral and retinal cavernous angiomas". Archives of Ophthalmology. 120 (2): 217–8. PMID 11831930.
• Zawistowski JS, Serebriiskii IG, Lee MF, Golemis EA, Marchuk DA (Feb 2002). "KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesis". Human Molecular Genetics. 11 (4): 389–96. doi:10.1093/hmg/11.4.389. PMID 11854171.
• Verlaan DJ, Siegel AM, Rouleau GA (Jun 2002). "Krit1 missense mutations lead to splicing errors in cerebral cavernous malformation". American Journal of Human Genetics. 70 (6): 1564–7. doi:10.1086/340604. PMC 379143. PMID 11941540.
• Gunel M, Laurans MS, Shin D, DiLuna ML, Voorhees J, Choate K, Nelson-Williams C, Lifton RP (Aug 2002). "KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein". Proceedings of the National Academy of Sciences of the United States of America. 99 (16): 10677–82. Bibcode:2002PNAS...9910677G. doi:10.1073/pnas.122354499. PMC 125011. PMID 12140362.
• Kehrer-Sawatzki H, Wilda M, Braun VM, Richter HP, Hameister H (Sep 2002). "Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1)". Acta Neuropathologica. 104 (3): 231–40. doi:10.1007/s00401-002-0552-6. PMID 12172908. S2CID 1909964.
• Denier C, Gasc JM, Chapon F, Domenga V, Lescoat C, Joutel A, Tournier-Lasserve E (Sep 2002). "Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult". Mechanisms of Development. 117 (1–2): 363–7. doi:10.1016/S0925-4773(02)00209-5. PMID 12204286. S2CID 12682438.