ZMYM2

ZMYM2
Identifiers
Aliases	ZMYM2 , FIM, MYM, RAMP, SCLL, ZNF198, zinc finger MYM-type containing 2, NECRC
External IDs	OMIM: 602221 MGI: 1923257 HomoloGene: 12631 GeneCards: ZMYM2
Gene location (Human)
Chr.	Chromosome 13 (human)
End	20,091,829 bp
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	57,200,158 bp
RNA expression pattern
	Top expressed in
	sperm; ; oocyte; ; secondary oocyte; ; ganglionic eminence; ; Achilles tendon; ; tibia; ; thymus; ; endometrium; ; gastric mucosa; ; corpus callosum;
	Top expressed in
	hand; ; spermatocyte; ; ganglionic eminence; ; medial ganglionic eminence; ; abdominal wall; ; maxillary prominence; ; mirror; ; atrioventricular valve; ; thymus; ; spermatid;
	More reference expression data
	; ; ; ;
	More reference expression data
Gene ontology
Molecular function	zinc ion binding ; metal ion binding ; ubiquitin conjugating enzyme binding ; DNA-binding transcription factor activity, RNA polymerase II-specific ; DNA binding ; protein tyrosine kinase activity ; protein binding ;
Cellular component	cytosol ; nucleus ; PML body ; cytoplasm ; nucleoplasm ;
Biological process	regulation of transcription, DNA-templated ; transcription, DNA-templated ; cytoskeleton organization ; regulation of cell morphogenesis ; multicellular organism development ; peptidyl-tyrosine phosphorylation ; regulation of transcription by RNA polymerase II ; biological process ;
	Sources:Amigo / QuickGO
Orthologs
	7750
	76007
	ENSG00000121741
	ENSMUSG00000021945
	Q9UBW7
	Q9CU65
NM_001190964 ; NM_001190965 ; NM_003453 ; NM_197968 ; NM_001353157 ;
	NM_001353159 ; NM_001353161 ; NM_001353162 ; NM_001353163 ; NM_001353164 ; NM_001353165 Contents See also ; References ; Further reading ;
	NM_029498 ; NM_177627 ; NM_001360643
NP_001177893 ; NP_001177894 ; NP_003444 ; NP_932072 ; NP_001340086 ;
	NP_001340088 ; NP_001340090 ; NP_001340091 ; NP_001340092 ; NP_001340093 ; NP_001340094
	NP_083774 ; NP_001347572 ; NP_808295
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated August 19, 2023

Zinc finger MYM-type protein 2 is a protein that in humans is encoded by the ZMYM2 gene.^[5]^[6]^[7]

Related Research Articles

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References

1 2 3 GRCh38: Ensembl release 89: ENSG00000121741 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000021945 - 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, Clark J, Warren W, Abdul-Rauf M, Somers G, Venter D, Fagan K, Cooper C, Shipley J (April 1998). "The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP". Human Molecular Genetics. 7 (4): 637–42. doi: 10.1093/hmg/7.4.637 . PMID 9499416.
↑ Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA (January 1998). "FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome". Nature Genetics. 18 (1): 84–7. doi:10.1038/ng0198-84. PMID 9425908. S2CID 826758.
↑ "Entrez Gene: ZMYM2 zinc finger, MYM-type 2".

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Still IH, Cowell JK (August 1998). "The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13". Blood. 92 (4): 1456–8. doi:10.1182/blood.V92.4.1456.splL3_1456_1458. PMID 9694738.
Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Gonçalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC (September 1998). "Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome". Blood. 92 (5): 1735–42. doi:10.1182/blood.V92.5.1735. PMID 9716603.
Kulkarni S, Reiter A, Smedley D, Goldman JM, Cross NC (January 1999). "The genomic structure of ZNF198 and location of breakpoints in the t(8;13) myeloproliferative syndrome". Genomics. 55 (1): 118–21. doi:10.1006/geno.1998.5634. PMID 9889006.
Ollendorff V, Guasch G, Isnardon D, Galindo R, Birnbaum D, Pébusque MJ (September 1999). "Characterization of FIM-FGFR1, the fusion product of the myeloproliferative disorder-associated t(8;13) translocation". The Journal of Biological Chemistry. 274 (38): 26922–30. doi: 10.1074/jbc.274.38.26922 . PMID 10480903.
Matsumoto K, Morita K, Takada S, Sakura T, Shiozaki H, Murakami H, Miyawaki S (December 1999). "A chronic myelogenous leukemia-like myeloproliferative disorder accompanied by T-cell lymphoblastic lymphoma with chromosome translocation t(8;13)(p11;q12): a Japanese case". International Journal of Hematology. 70 (4): 278–82. PMID 10643154.
Hartley JL, Temple GF, Brasch MA (November 2000). "DNA cloning using in vitro site-specific recombination". Genome Research. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948 . PMID 11076863.
Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Böcher M, Blöcker H, Bauersachs S, Blum H, Lauber J, Düsterhöft A, Beyer A, Köhrer K, Strack N, Mewes HW, Ottenwälder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (March 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Research. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072 . PMID 11230166.
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Hakimi MA, Dong Y, Lane WS, Speicher DW, Shiekhattar R (February 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.
Baumann H, Kunapuli P, Tracy E, Cowell JK (May 2003). "The oncogenic fusion protein-tyrosine kinase ZNF198/fibroblast growth factor receptor-1 has signaling function comparable with interleukin-6 cytokine receptors". The Journal of Biological Chemistry. 278 (18): 16198–208. doi: 10.1074/jbc.M300018200 . PMID 12594223.
Kunapuli P, Somerville R, Still IH, Cowell JK (May 2003). "ZNF198 protein, involved in rearrangement in myeloproliferative disease, forms complexes with the DNA repair-associated HHR6A/6B and RAD18 proteins". Oncogene. 22 (22): 3417–23. doi:10.1038/sj.onc.1206408. PMID 12776193.
Warner DR, Roberts EA, Greene RM, Pisano MM (December 2003). "Identification of novel Smad binding proteins". Biochemical and Biophysical Research Communications. 312 (4): 1185–90. doi:10.1016/j.bbrc.2003.11.049. PMID 14651998.
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Beausoleil SA, Jedrychowski M, Schwartz D, Elias JE, Villén J, Li J, Cohn MA, Cantley LC, Gygi SP (August 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.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000121741 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000021945 - 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.

[pmid9499416-5] Smedley D, Hamoudi R, Clark J, Warren W, Abdul-Rauf M, Somers G, Venter D, Fagan K, Cooper C, Shipley J (April 1998). "The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP". Human Molecular Genetics. 7 (4): 637–42. doi: 10.1093/hmg/7.4.637 . PMID 9499416.

[pmid9425908-6] Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA (January 1998). "FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome". Nature Genetics. 18 (1): 84–7. doi:10.1038/ng0198-84. PMID 9425908. S2CID 826758.

[entrez-7] "Entrez Gene: ZMYM2 zinc finger, MYM-type 2".

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ZMYM2

Contents

See also

Related Research Articles

References

Further reading