ZMYM3

From Wikipedia, the free encyclopedia

Zinc finger, MYM-type 3

Identifiers

ZMYM3; MYM; DXS6673E; KIAA0385; XFIM; ZNF198L2; ZNF261

External IDs

OMIM: 300061 MGI: 1927231 HomoloGene: 3736

Gene ontology
Molecular Function:	• DNA binding • zinc ion binding • metal ion binding
Cellular Component:	• nucleus
Biological Process:	• multicellular organismal development

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_005096 (mRNA)
NP_005087 (protein)

NM_019831 (mRNA)
NP_062805 (protein)

Location

Chr X: 70.38 - 70.39 Mb

Chr X: 97.61 - 97.62 Mb

Pubmed search

[1]

[2]

Zinc finger, MYM-type 3, also known as ZMYM3, is a human gene.^[1]

[edit] References

^ Entrez Gene: ZMYM3 zinc finger, MYM-type 3.

[edit] Further reading

van der Maarel SM, Scholten IH, Huber I, et al. (1997). "Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1.". Hum. Mol. Genet. 5 (7): 887-97. PMID 8817323.
Nagase T, Ishikawa K, Nakajima D, et al. (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 Res. 4 (2): 141-50. PMID 9205841.
Smedley D, Hamoudi R, Lu YJ, et al. (1999). "Cloning and mapping of members of the MYM family.". Genomics 60 (2): 244-7. doi:10.1006/geno.1999.5918. PMID 10486218.
Scheer MP, van der Maarel S, Kübart S, et al. (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.
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:10.1073/pnas.242603899. PMID 12477932.
Hakimi MA, Dong Y, Lane WS, et al. (2003). "A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexes.". J. Biol. Chem. 278 (9): 7234-9. doi:10.1074/jbc.M208992200. PMID 12493763.
Beever C, Lai BP, Baldry SE, et al. (2004). "Methylation of ZNF261 as an assay for determining X chromosome inactivation patterns.". Am. J. Med. Genet. A 120 (3): 439-41. doi:10.1002/ajmg.a.20045. PMID 12838571.
Beausoleil SA, Jedrychowski M, Schwartz D, et al. (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins.". Proc. Natl. Acad. Sci. U.S.A. 101 (33): 12130-5. doi:10.1073/pnas.0404720101. PMID 15302935.
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:10.1101/gr.2596504. PMID 15489334.
Cheng J, Kapranov P, Drenkow J, et al. (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, et al. (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.