Homo sapiens Gene: DCAF12L2
Summary
InnateDB Gene IDBG-85435.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DCAF12L2
Gene Name DDB1 and CUL4 associated factor 12-like 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000198354
Encoded Proteins
DDB1 and CUL4 associated factor 12-like 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by Gly-His and Trp-Asp (GH-WD), which may facilitate formation of heterotrimeric or multi-protein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 9. However, the CDS of this intronless gene remains intact, it is conserved in other mammalian species, it is known to be transcribed, and it is therefore thought to encode a functional protein. [provided by RefSeq, May 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome X:126164531-126165951
Strand Reverse strand
Band q25
Transcripts
ENST00000360028 ENSP00000353128
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt Q5VW00
TrEMBL
UniProt Splice Variant
Entrez Gene 340578
UniGene Hs.181867
RefSeq NM_001013628
HUGO HGNC:32950
OMIM
CCDS CCDS43991
HPRD
IMGT
EMBL AL445072 BC136673 BC136674 CH471107
GenPept AAI36674 AAI36675 CAH70502 EAX11842
RNA Seq Atlas 340578