Homo sapiens Gene: CHURC1-FNTB
Summary
InnateDB Gene IDBG-9500.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CHURC1-FNTB
Gene Name CHURC1-FNTB readthrough
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000125954
Encoded Proteins
CHURC1-FNTB readthrough
CHURC1-FNTB readthrough
CHURC1-FNTB readthrough
CHURC1-FNTB readthrough
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 14:64914485-65061803
Strand Forward strand
Band q23.3
Transcripts
ENST00000552941 ENSP00000449668
ENST00000549987 ENSP00000447121
ENST00000553743 ENSP00000450692
ENST00000551823 ENSP00000449709
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:0003824 catalytic activity
GO:0008270 zinc ion binding
GO:0016740 transferase activity
Biological Process
GO:0007275 multicellular organismal development
GO:0018343 protein farnesylation
GO:0042127 regulation of cell proliferation
GO:0045893 positive regulation of transcription, DNA-templated
Cellular Component
GO:0005965 protein farnesyltransferase complex
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene 100529261
UniGene
RefSeq NM_001202559
HUGO HGNC:42960
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas 100529261