PLEKHC1
From Wikipedia, the free encyclopedia
Pleckstrin homology domain containing, family C (with FERM domain) member 1
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Identifiers | ||||||||||||||
Symbol(s) | PLEKHC1; FLJ34213; FLJ44462; KIND2; MIG2; UNC112; mig-2 | |||||||||||||
External IDs | OMIM: 607746 MGI: 2385001 HomoloGene: 4976 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 10979 | 218952 | ||||||||||||
Ensembl | ENSG00000073712 | ENSMUSG00000037712 | ||||||||||||
Uniprot | Q96AC1 | Q3TLE2 | ||||||||||||
Refseq | NM_006832 (mRNA) NP_006823 (protein) |
NM_146054 (mRNA) NP_666166 (protein) |
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Location | Chr 14: 52.39 - 52.49 Mb | Chr 14: 44.38 - 44.45 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Pleckstrin homology domain containing, family C (with FERM domain) member 1, also known as PLEKHC1, is a human gene.[1]
[edit] References
[edit] Further reading
- Wick M, Bürger C, Brüsselbach S, et al. (1994). "Identification of serum-inducible genes: different patterns of gene regulation during G0-->S and G1-->S progression.". J. Cell. Sci. 107 ( Pt 1): 227–39. PMID 8175911.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi: . PMID 12477932.
- Heilig R, Eckenberg R, Petit JL, et al. (2003). "The DNA sequence and analysis of human chromosome 14.". Nature 421 (6923): 601–7. doi: . PMID 12508121.
- Tu Y, Wu S, Shi X, et al. (2003). "Migfilin and Mig-2 link focal adhesions to filamin and the actin cytoskeleton and function in cell shape modulation.". Cell 113 (1): 37–47. PMID 12679033.
- Weinstein EJ, Bourner M, Head R, et al. (2003). "URP1: a member of a novel family of PH and FERM domain-containing membrane-associated proteins is significantly over-expressed in lung and colon carcinomas.". Biochim. Biophys. Acta 1637 (3): 207–16. PMID 12697302.
- Siegel DH, Ashton GH, Penagos HG, et al. (2003). "Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.". Am. J. Hum. Genet. 73 (1): 174–87. PMID 12789646.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi: . PMID 14702039.
- Kato K, Shiozawa T, Mitsushita J, et al. (2004). "Expression of the mitogen-inducible gene-2 (mig-2) is elevated in human uterine leiomyomas but not in leiomyosarcomas.". Hum. Pathol. 35 (1): 55–60. PMID 14745725.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi: . PMID 15489334.
- Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi: . PMID 16189514.
- Olsen JV, Blagoev B, Gnad F, et al. (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.". Cell 127 (3): 635–48. doi: . PMID 17081983.