Zinc finger protein 165

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Zinc finger protein 165
Identifiers
Symbols ZNF165 ; CT53; LD65; ZSCAN7
External IDs OMIM600834 HomoloGene122143 GeneCards: ZNF165 Gene
RNA expression pattern
PBB GE ZNF165 206683 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 7718 n/a
Ensembl ENSG00000197279 n/a
UniProt P49910 n/a
RefSeq (mRNA) NM_003447 n/a
RefSeq (protein) NP_003438 n/a
Location (UCSC) Chr 6:
28.08 – 28.09 Mb
n/a
PubMed search [1] n/a

Zinc finger protein 165 is a protein that in humans is encoded by the ZNF165 gene.[1][2]

Function[edit]

This gene encodes a member of the Kruppel family of zinc finger proteins. Members of this DNA-binding protein family act as transcriptional regulators. This gene is located within a cluster of zinc finger family members. The encoded protein may play a role in spermatogenesis.[2]

Interactions[edit]

Zinc finger protein 165 has been shown to interact with Ewing sarcoma breakpoint region 1[3] and DVL2.[3]

See also[edit]

References[edit]

  1. ^ Tirosvoutis KN, Divane A, Jones M, Affara NA (Jan 1996). "Characterization of a novel zinc finger gene (ZNF165) mapping to 6p21 that is expressed specifically in testis". Genomics 28 (3): 485–90. doi:10.1006/geno.1995.1178. PMID 7490084. 
  2. ^ a b "Entrez Gene: ZNF165 zinc finger protein 165". 
  3. ^ a b Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514. 

Further reading[edit]

  • Lee PL, Gelbart T, West C, Adams M, Blackstone R, Beutler E (1997). "Three genes encoding zinc finger proteins on human chromosome 6p21.3: members of a new subclass of the Kruppel gene family containing the conserved SCAN box domain.". Genomics 43 (2): 191–201. doi:10.1006/geno.1997.4806. PMID 9244436. 
  • Paoloni-Giacobino A, Kern I, Rumpler Y, Djlelati R, Morris MA, Dahoun SP (2001). "Familial t(6;21)(p21.1;p13) translocation associated with male-only sterility.". Clin. Genet. 58 (4): 324–8. doi:10.1034/j.1399-0004.2000.580411.x. PMID 11076058. 
  • Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514. 

External links[edit]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.