Homo sapiens Gene: CXorf27
Summary
InnateDB Gene IDBG-55987.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CXorf27
Gene Name chromosome X open reading frame 27
Synonyms CXorf27; HIP17
Species Homo sapiens
Ensembl Gene ENSG00000187516
Encoded Proteins
chromosome X open reading frame 27
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a protein shown to interact with huntingtin, which contains an expanded polyglutamine tract in individuals with Huntington's disease (PMID: 9700202). [provided by RefSeq, Aug 2011]
This gene encodes a protein shown to interact with huntingtin, which contains an expanded polyglutamine tract in individuals with Huntington\'s disease (PMID: 9700202). [provided by RefSeq, Aug 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome X:37990817-37991317
Strand Forward strand
Band p11.4
Transcripts
ENST00000341016 ENSP00000339511
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0046982 protein heterodimerization activity
Biological Process
Cellular Component
Orthologs
No orthologs found for this gene
Cross-References
SwissProt O75409
TrEMBL
UniProt Splice Variant
Entrez Gene 25763
UniGene Hs.122959
RefSeq NM_012274
HUGO HGNC:18417
OMIM
CCDS CCDS43929
HPRD
IMGT
EMBL AF049615 BC104428 BC104429 BC113024 BC113025 CH471141
GenPept AAC26851 AAI04429 AAI04430 AAI13025 AAI13026 EAW59451
RNA Seq Atlas 25763