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
Gene location (Human) Chr. X chromosome (human) Band Xq13.1 Start 71,239,624 bp End 71,255,146 bp
Gene location (Mouse) Chr. X chromosome (mouse) Band X D|X 44.1 cM Start 101,404,384 bp End 101,420,849 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right adrenal gland endothelial cell left adrenal gland right uterine tube embryo secondary oocyte Region I of hippocampus proper pancreatic ductal cell ganglionic eminence Brodmann area 46 Top expressed in superior frontal gyrus cerebellar cortex dorsomedial hypothalamic nucleus subiculum median eminence arcuate nucleus paraventricular nucleus of hypothalamus olfactory tubercle cumulus cell superior colliculus More reference expression data BioGPS 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 Species Human Mouse 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 Mb Chr X: 101.4 – 101.42 Mb PubMed search
Wikidata
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Zinc finger MYM-type protein 3 is a protein that in humans is encoded by the ZMYM3 gene.

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. 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.