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Gene : DCAF12L2 Homo sapiens

Name  ? DDB1 and CUL4 associated factor 12 like 2 Cytological Location  Xq25
Brief Description  DDB1 and CUL4 associated factor 12 like 2
Description  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]
  • synonyms:
  • OTTHUMG00000022348,
  • WDR40C,
  • DCAF12L2,
  • WDR40C,
  • AL445072,
  • NM_001013628,
  • WD repeat domain 40C,
  • HGNC:32950,
  • uc004euk.3
  • identifiers:
  • 340578,
  • ENSG00000198354,
  • DCAF12L2

Genome feature

Region: gene ? Length: 2791  
Location: X:126163499-126166289 reverse strand Cyto location: Xq25

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

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Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3740 SN Ps

4 Cross References

14 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results