ZNF41
From Wikipedia, the free encyclopedia
Zinc finger protein 41
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Identifiers | ||||||||||||||
Symbol(s) | ZNF41; MGC8941; MRX89 | |||||||||||||
External IDs | OMIM: 314995 HomoloGene: 56023 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 7592 | n/a | ||||||||||||
Ensembl | ENSG00000147124 | n/a | ||||||||||||
Uniprot | P51814 | n/a | ||||||||||||
Refseq | NM_007130 (mRNA) NP_009061 (protein) |
n/a (mRNA) n/a (protein) |
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Location | Chr X: 47.19 - 47.23 Mb | n/a | ||||||||||||
Pubmed search | [1] | n/a |
Zinc finger protein 41, also known as ZNF41, is a human gene.[1]
This gene product is a likely zinc finger family transcription factor. It contains KRAB-A and KRAB-B domains that act as transcriptional repressors in related proteins, and multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. This gene is part of a gene cluster on chromosome Xp11.23. Several alternatively spliced transcript variants have been described, however, the full-length nature of only some of them is known.[1]
[edit] References
[edit] Further reading
- Rosati M, Marino M, Franzè A, et al. (1991). "Members of the zinc finger protein gene family sharing a conserved N-terminal module.". Nucleic Acids Res. 19 (20): 5661–7. PMID 1945843.
- Franzè A, Archidiacono N, Rocchi M, et al. (1991). "Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome.". Genomics 9 (4): 728–36. PMID 2037297.
- Knight JC, Grimaldi G, Thiesen HJ, et al. (1994). "Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1.". Genomics 21 (1): 180–7. doi: . PMID 8088786.
- Rosati M, Franzé A, Matarazzo MR, Grimaldi G (1999). "Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41.". Cytogenet. Cell Genet. 85 (3-4): 291–6. PMID 10449920.
- 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.
- Shoichet SA, Hoffmann K, Menzel C, et al. (2004). "Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.". Am. J. Hum. Genet. 73 (6): 1341–54. PMID 14628291.
- Colland F, Jacq X, Trouplin V, et al. (2004). "Functional proteomics mapping of a human signaling pathway.". Genome Res. 14 (7): 1324–32. doi: . PMID 15231748.
- 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.
- Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325–37. doi: . PMID 15772651.
[edit] External links
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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