ZMYM3

ZMYM3
Identifiers
AliasesZMYM3, DXS6673E, MYM, XFIM, ZNF198L2, ZNF261, zinc finger MYM-type containing 3
External IDsMGI: 1927231 HomoloGene: 3736 GeneCards: ZMYM3
Gene location (Human)
Chr.X chromosome (human)[1]
BandXq13.1Start71,239,624 bp[1]
End71,255,146 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

9203

56364

Ensembl

ENSG00000147130

ENSMUSG00000031310

UniProt

Q14202

Q9JLM4

RefSeq (mRNA)

NM_001171162
NM_001171163
NM_005096
NM_201599

NM_001177985
NM_001177986
NM_001177987
NM_001177988
NM_019831

RefSeq (protein)

NP_001164633
NP_001164634
NP_005087
NP_963893

NP_001171456
NP_001171457
NP_001171458
NP_001171459
NP_062805

Location (UCSC)Chr X: 71.24 – 71.26 MbChr X: 101.4 – 101.42 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Zinc finger MYM-type protein 3 is a protein that in humans is encoded by the ZMYM3 gene.[5][6]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000147130 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000031310 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ Smedley D, Hamoudi R, Lu YJ, Cooper C, Shipley J (Sep 1999). "Cloning and mapping of members of the MYM family". Genomics. 60 (2): 244–7. doi:10.1006/geno.1999.5918. PMID 10486218.
  6. ↑ "Entrez Gene: ZMYM3 zinc finger, MYM-type 3".

Further reading

  • van der Maarel SM, Scholten IH, Huber I, Philippe C, Suijkerbuijk RF, Gilgenkrantz S, Kere J, Cremers FP, Ropers HH (Jul 1996). "Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1". Human Molecular Genetics. 5 (7): 887–97. doi:10.1093/hmg/5.7.887. PMID 8817323.
  • Nagase T, Ishikawa K, Nakajima D, Ohira M, Seki N, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Apr 1997). "Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro". DNA Research. 4 (2): 141–50. doi:10.1093/dnares/4.2.141. PMID 9205841.
  • Scheer MP, van der Maarel S, Kübart S, Schulz A, Wirth J, Schweiger S, Ropers H, Nothwang HG (Jan 2000). "DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner". Genomics. 63 (1): 123–32. doi:10.1006/geno.1999.6027. PMID 10662551.
  • Hakimi MA, Dong Y, Lane WS, Speicher DW, Shiekhattar R (Feb 2003). "A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexes". The Journal of Biological Chemistry. 278 (9): 7234–9. doi:10.1074/jbc.M208992200. PMID 12493763.
  • Beever C, Lai BP, Baldry SE, Peñaherrera MS, Jiang R, Robinson WP, Brown CJ (Jul 2003). "Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns". American Journal of Medical Genetics Part A. 120A (3): 439–41. doi:10.1002/ajmg.a.20045. PMID 12838571.
  • Beausoleil SA, Jedrychowski M, Schwartz D, Elias JE, Villén J, Li J, Cohn MA, Cantley LC, Gygi SP (Aug 2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proceedings of the National Academy of Sciences of the United States of America. 101 (33): 12130–5. doi:10.1073/pnas.0404720101. PMC 514446. PMID 15302935.
  • Cheng J, Kapranov P, Drenkow J, Dike S, Brubaker S, Patel S, Long J, Stern D, Tammana H, Helt G, Sementchenko V, Piccolboni A, Bekiranov S, Bailey DK, Ganesh M, Ghosh S, Bell I, Gerhard DS, Gingeras TR (May 2005). "Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution". Science. 308 (5725): 1149–54. doi:10.1126/science.1108625. PMID 15790807.
  • Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M (Nov 2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983.


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