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Gene : DCAF8L1 Homo sapiens

Name  ? DDB1 and CUL4 associated factor 8 like 1 Cytological Location  Xp21.3
Brief Description  DDB1 and CUL4 associated factor 8 like 1
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 the 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 1. However, the CDS of this intronless gene remains intact, it is conserved in other primate species, it is known to be transcribed, and it is therefore thought to encode a functional protein. [provided by RefSeq, May 2010]
  • synonyms:
  • WD repeat domain 42B,
  • WDR42B,
  • OTTHUMG00000021312,
  • uc004dbx.2,
  • HGNC:31810,
  • WDR42B,
  • NM_001017930,
  • DCAF8L1
  • identifiers:
  • 139425,
  • ENSG00000226372,
  • DCAF8L1

Genome feature

Region: gene ? Length: 3458  
Location: X:27977992-27981449 reverse strand Cyto location: Xp21.3


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Expression

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

Gene Ontology

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Other

0 Pathways

0 SN Ps

4 Cross References

13 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results