Homo sapiens Protein: ZNF644
Summary
InnateDB Protein IDBP-100217.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF644
Protein Name zinc finger protein 644
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000354659
InnateDB Gene IDBG-100213 (ZNF644)
Protein Structure
UniProt Annotation
Function May be involved in transcriptional regulation.
Subcellular Localization Nucleus.
Disease Associations Myopia 21, autosomal dominant (MYP21) [MIM:614167]: A refractive error of the eye, in which parallel rays from a distant object come to focus in front of the retina, vision being better for near objects than for far. {ECO:0000269PubMed:21695231}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in liver, placenta, retina and retinal pigment epithelium. {ECO:0000269PubMed:21695231}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated
Total 8 [view]
Protein-Protein 6 [view]
Protein-DNA 2 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0046872 metal ion binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9H582
PhosphoSite PhosphoSite-Q9H582
TrEMBL
UniProt Splice Variant
Entrez Gene 84146
UniGene Hs.743452
RefSeq NP_115562
HUGO HGNC:29222
OMIM 614159
CCDS CCDS732
HPRD 15885
IMGT
EMBL AB019255 AB033047 AK291520 AL136109 BC050656 BC063683 BC110841 BC132776 BC132778 CH471097
GenPept AAH50656 AAH63683 AAI10842 AAI32777 AAI32779 BAA86535 BAD32777 BAF84209 CAI23362 CAI23363 EAW73118