ZMYM3

ZMYM3
Identifiers
Aliases	ZMYM3, DXS6673E, MYM, XFIM, ZNF198L2, ZNF261, zinc finger MYM-type containing 3
External IDs	OMIM: 300061; MGI: 1927231; HomoloGene: 3736; GeneCards: ZMYM3; OMA:ZMYM3 - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	71,255,146 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	101,420,849 bp
RNA expression pattern
	Top expressed in
	right adrenal gland; ; right adrenal cortex; ; endothelial cell; ; right ovary; ; left ovary; ; left adrenal gland; ; left adrenal cortex; ; right uterine tube; ; embryo; ; secondary oocyte;
	Top expressed in
	neural layer of retina; ; superior frontal gyrus; ; primary visual cortex; ; genital tubercle; ; dentate gyrus of hippocampal formation granule cell; ; cerebellar cortex; ; dorsomedial hypothalamic nucleus; ; subiculum; ; tail of embryo; ; median eminence;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	DNA binding; zinc ion binding; metal ion binding; DNA-binding transcription factor activity, RNA polymerase II-specific;
Cellular component	nucleus; cytoplasm; nucleoplasm;
Biological process	multicellular organism development; regulation of cell morphogenesis; cytoskeleton organization; regulation of transcription by RNA polymerase II;
	Sources:Amigo / QuickGO
Orthologs
	9203
	56364
	ENSG00000147130
	ENSMUSG00000031310
	Q14202
	Q9JLM4
	NM_001171162; NM_001171163; NM_005096; NM_201599
	NM_001177985; NM_001177986; NM_001177987; NM_001177988; NM_019831
	NP_001164633; NP_001164634; NP_005087; NP_963893
	NP_001171456; NP_001171457; NP_001171458; NP_001171459; NP_062805
	Wikidata
View/Edit Human	View/Edit Mouse

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

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000147130 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000031310 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ 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.
^ "Entrez Gene: ZMYM3 zinc finger, MYM-type 3".

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. CiteSeerX 10.1.1.322.3999. 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. S2CID 45505878.
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. Bibcode:2004PNAS..10112130B. 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. Bibcode:2005Sci...308.1149C. doi:10.1126/science.1108625. PMID 15790807. S2CID 13047538.
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.

This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000147130 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000031310 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid10486218-5] 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.

[entrez-6] "Entrez Gene: ZMYM3 zinc finger, MYM-type 3".

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References

Further reading