Homo sapiens Gene: C20orf194
Summary
InnateDB Gene IDBG-46683.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C20orf194
Gene Name chromosome 20 open reading frame 194
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000088854
Encoded Proteins
chromosome 20 open reading frame 194
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:3249305-3407625
Strand Reverse strand
Band p13
Transcripts
ENST00000252032 ENSP00000252032
ENST00000619760
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q5TEA3
TrEMBL Q3KQR5
UniProt Splice Variant
Entrez Gene 25943
UniGene Hs.516853 Hs.694560 Hs.713335 Hs.740989
RefSeq NM_001009984 XM_005260684 XM_005260686 XM_005260687 XM_006723557
HUGO HGNC:17721
OMIM 614146
CCDS CCDS42851
HPRD
IMGT
EMBL AL109976 AL110249 AL117334 BC064352 BC080528 BC106086
GenPept AAH64352 AAH80528 AAI06087 CAB53697 CAI22431 CAI22834
RNA Seq Atlas 25943