Homo sapiens Gene: ZNF19
Summary
InnateDB Gene IDBG-40925.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ZNF19
Gene Name zinc finger protein 19
Synonyms KOX12
Species Homo sapiens
Ensembl Gene ENSG00000157429
Encoded Proteins
zinc finger protein 19
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene contains a zinc finger, a nucleic acid-binding domain present in many transcription factors. This gene is located in a region next to ZNF23, a gene also encoding a zinc finger protein, on chromosome 16. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:71464555-71565089
Strand Reverse strand
Band q22.2
Transcripts
ENST00000288177 ENSP00000288177
ENST00000568815 ENSP00000455796
ENST00000562210
ENST00000569072 ENSP00000457992
ENST00000565100 ENSP00000462810
ENST00000565637 ENSP00000454864
ENST00000565541 ENSP00000454549
ENST00000561469 ENSP00000462021
ENST00000568446
ENST00000569717 ENSP00000456143
ENST00000566202 ENSP00000454862
ENST00000567225 ENSP00000462566
ENST00000564225 ENSP00000455575
ENST00000564230 ENSP00000458105
ENST00000617615
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
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
Pathways
NETPATH
REACTOME
Generic Transcription Pathway pathway
Gene Expression pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL H3BNH9 H3BQ26
UniProt Splice Variant
Entrez Gene 7567
UniGene Hs.199739 Hs.660076
RefSeq NM_006961
HUGO HGNC:12981
OMIM 194525
CCDS CCDS10901
HPRD 01914
IMGT
EMBL AC010547
GenPept
RNA Seq Atlas 7567