Homo sapiens Gene: VCX2
Summary
InnateDB Gene IDBG-42201.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol VCX2
Gene Name variable charge, X-linked 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000177504
Encoded Proteins
variable charge, X-linked 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. The X-linked members are clustered on chromosome Xp22 and Y-linked members are two identical copies of the gene within a palindromic region on Yq11. The family members share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. VCX/Y genes encode small and highly charged proteins of unknown function. The presence of a putative bipartite nuclear localization signal suggests that VCX/Y members are nuclear proteins. This gene contains 2 repeats of the 30-bp unit. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome X:8169944-8171267
Strand Reverse strand
Band p22.31
Transcripts
ENST00000317103 ENSP00000321309
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:0003674 molecular_function
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
Orthologs
No orthologs found for this gene
Cross-References
SwissProt Q9H322
TrEMBL
UniProt Splice Variant
Entrez Gene 51480
UniGene Hs.279737
RefSeq NM_016378
HUGO HGNC:18158
OMIM 300532
CCDS CCDS35200
HPRD
IMGT
EMBL AC097626 AF159127 AF167079 BC096715 BC098113 BC098163 BC134350
GenPept AAF28172 AAG41765 AAH96715 AAH98113 AAH98163 AAI34351
RNA Seq Atlas 51480