ZNF365

ZNF365
Identifiers
Aliases ZNF365, Su48, UAN, ZNF365D, zinc finger protein 365
External IDs MGI: 2143676 HomoloGene: 8975 GeneCards: ZNF365
Genetically Related Diseases
narcolepsy, breast cancer, atopic dermatitis[1]
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

22891

216049

Ensembl

ENSG00000138311

ENSMUSG00000037855

UniProt

Q70YC4
Q70YC5

Q8BG89

RefSeq (mRNA)

NM_014951
NM_199450
NM_199451
NM_199452

NM_178679

RefSeq (protein)

NP_955524.3
NP_055766.2
NP_955522.1
NP_955523.1

NP_848794.1

Location (UCSC) Chr 10: 62.37 – 62.67 Mb Chr 10: 67.89 – 67.91 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

Protein ZNF365 is a protein that in humans is encoded by the ZNF365 gene.[4][5][6]

Model organisms

Model organisms have been used in the study of ZNF365 function. A conditional knockout mouse line called Zfp365tm1a(KOMP)Wtsi was generated at the Wellcome Trust Sanger Institute.[7] Male and female animals underwent a standardized phenotypic screen[8] to determine the effects of deletion.[9][10][11][12] Additional screens performed: - In-depth immunological phenotyping[13] - in-depth bone and cartilage phenotyping[14]

References

  1. "Diseases that are genetically associated with ZNF365 view/edit references on wikidata".
  2. "Human PubMed Reference:".
  3. "Mouse PubMed Reference:".
  4. Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Dec 1998). "Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 5 (6): 355–64. doi:10.1093/dnares/5.6.355. PMID 10048485.
  5. Gianfrancesco F, Esposito T, Ombra MN, Forabosco P, Maninchedda G, Fattorini M, Casula S, Vaccargiu S, Casu G, Cardia F, Deiana I, Melis P, Falchi M, Pirastu M (Jun 2003). "Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate". American Journal of Human Genetics. 72 (6): 1479–91. doi:10.1086/375628. PMC 1180308Freely accessible. PMID 12740763.
  6. "Entrez Gene: ZNF365 zinc finger protein 365".
  7. Gerdin AK (2010). "The Sanger Mouse Genetics Programme: high throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x.
  8. 1 2 "International Mouse Phenotyping Consortium".
  9. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (Jun 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410Freely accessible. PMID 21677750.
  10. Dolgin E (Jun 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  11. Collins FS, Rossant J, Wurst W (Jan 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
  12. White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, Salisbury J, Clare S, Ingham NJ, Podrini C, Houghton R, Estabel J, Bottomley JR, Melvin DG, Sunter D, Adams NC, Tannahill D, Logan DW, Macarthur DG, Flint J, Mahajan VB, Tsang SH, Smyth I, Watt FM, Skarnes WC, Dougan G, Adams DJ, Ramirez-Solis R, Bradley A, Steel KP (Jul 2013). "Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes". Cell. 154 (2): 452–64. doi:10.1016/j.cell.2013.06.022. PMC 3717207Freely accessible. PMID 23870131.
  13. 1 2 "Infection and Immunity Immunophenotyping (3i) Consortium".
  14. 1 2 "OBCD Consortium".

Further reading

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


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