Homo sapiens Protein: ZMYM3
Summary
InnateDB Protein IDBP-75387.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZMYM3
Protein Name zinc finger, MYM-type 3
Synonyms DXS6673E; MYM; XFIM; ZNF198L2; ZNF261;
Species Homo sapiens
Ensembl Protein ENSP00000363110
InnateDB Gene IDBG-75385 (ZMYM3)
Protein Structure
UniProt Annotation
Function Plays a role in the regulation of cell morphology and cytoskeletal organization. {ECO:0000269PubMed:21834987}.
Subcellular Localization Nucleus {ECO:0000250}.
Disease Associations Note=A chromosomal aberration involving ZMYM3 may be a cause of X-linked mental retardation in Xq13.1. Translocation t(X;13)(q13.1;?).
Tissue Specificity Most abundant in brain, moderate in muscle and heart, low in other tissues except placenta.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 21 experimentally validated interaction(s) in this database.
Experimentally validated
Total 21 [view]
Protein-Protein 21 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0008270 zinc ion binding
Biological Process
GO:0007010 cytoskeleton organization
GO:0007275 multicellular organismal development
GO:0022604 regulation of cell morphogenesis
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR010507 Zinc finger, MYM-type
IPR011017 TRASH domain
IPR021893 Protein of unknown function DUF3504
PFAM PF06467
PF12012
PRINTS
PIRSF
SMART SM00746
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q14202
PhosphoSite PhosphoSite-Q14202
TrEMBL
UniProt Splice Variant
Entrez Gene 9203
UniGene Hs.522684
RefSeq NP_001164633
HUGO HGNC:13054
OMIM 300061
CCDS CCDS55444
HPRD 02088
IMGT
EMBL AB002383 AL590762 BC013009 BC069057 BT007095 CH471132 X95808
GenPept AAH13009 AAH69057 AAP35759 BAA20839 CAA65075 EAX05302 EAX05303