Homo sapiens Gene: RNF112
Summary
InnateDB Gene IDBG-34776.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RNF112
Gene Name ring finger protein 112
Synonyms BFP; ZNF179
Species Homo sapiens
Ensembl Gene ENSG00000128482
Encoded Proteins
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:19411125-19417276
Strand Forward strand
Band p11.2
Transcripts
ENST00000461366 ENSP00000454919
ENST00000574149
ENST00000575165 ENSP00000464134
ENST00000574782
ENST00000580109
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003924 GTPase activity
GO:0005515 protein binding
GO:0005525 GTP binding
GO:0008270 zinc ion binding
Biological Process
GO:0006184 GTP catabolic process
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL J3QRB8
UniProt Splice Variant
Entrez Gene 7732
UniGene Hs.189482
RefSeq NM_007148
HUGO HGNC:12968
OMIM 601237
CCDS CCDS58529
HPRD 03140
IMGT
EMBL AC004448
GenPept
RNA Seq Atlas 7732