Homo sapiens Gene: ZNF630
Summary
InnateDB Gene IDBG-281550.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF630
Gene Name zinc finger protein 630
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000221994
Encoded Proteins
zinc finger protein 630
zinc finger protein 630
zinc finger protein 630
zinc finger protein 630
zinc finger protein 630
zinc finger protein 630
zinc finger protein 630
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 13 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked mental retardation. [provided by RefSeq, Jul 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome X:47983356-48071658
Strand Reverse strand
Band p11.23
Transcripts
ENST00000276054 ENSP00000354683
ENST00000409324 ENSP00000386393
ENST00000428463 ENSP00000400030
ENST00000428686 ENSP00000407278
ENST00000442455 ENSP00000393163
ENST00000421903 ENSP00000408054
ENST00000616492 ENSP00000480858
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003676 nucleic acid binding
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0046872 metal ion binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
Cellular Component
GO:0005622 intracellular
GO:0005634 nucleus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.650883
RefSeq NM_001037735 NM_001190255 NM_001282201 NM_001282202
HUGO
OMIM
CCDS CCDS35237 CCDS75971
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas