Homo sapiens Gene: ZNF513
Summary
InnateDB Gene IDBG-39020.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF513
Gene Name zinc finger protein 513
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000163795
Encoded Proteins
zinc finger protein 513
zinc finger protein 513
zinc finger protein 513
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:27377231-27380790
Strand Reverse strand
Band p23.3
Transcripts
ENST00000323703 ENSP00000318373
ENST00000407879 ENSP00000384874
ENST00000436006 ENSP00000394226
ENST00000491924
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Experimentally validated
Total 4 [view]
Protein-Protein 4 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 5 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0044212 transcription regulatory region DNA binding
GO:0046872 metal ion binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007601 visual perception
GO:0050896 response to stimulus
GO:0060041 retina development in camera-type eye
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.515872
RefSeq NM_001201459 NM_144631 XM_005264142 XM_005264143
HUGO
OMIM
CCDS CCDS1751 CCDS56114
HPRD 15813
IMGT
EMBL
GenPept
RNA Seq Atlas