DCAF8

DDB1 and CUL4 associated factor 8

Gene Function

May function as a substrate receptor for CUL4-DDB1 E3 ubiquitin-protein ligase complex Source: UniProt

Relationship to CMT

GAN AD
1 subtype
1q23.2
First described 2014

Subtype Inheritance Class OMIM Sentinel Publication
SubtypeGAN-2 Inheritanceautosomal dominant ClassGAN OMIM610100 Sentinel Publication

2014 · 10.1212/WNL.0000000000000206

Stored Identifiers

HGNC Aliases: WDR42A
hgnc_idHGNC:24891
ensembl_gene_idENSG00000132716
coords_grch38chr1:160214840-160263388
coords_grch37chr1:160185505-160254920
entrez_id50717
omim_gene615820
uniprot_idsQ5TAQ9
refseq_accessionNM_015726
mane_refseqNM_015726.4
mane_ensemblENST00000368074.6

ClinVar Variants

Pathogenic and likely pathogenic variants in DCAF8, as classified in ClinVar, are read live from NCBI. Only aggregate germline records are shown. Uncertain and conflicting classifications are not. Experts in CMT makes no claim to the accuracy of ClinVar data. This index is provided for informational purposes only.

Review stars are ClinVar’s measure of how well a classification is supported: four for a practice guideline, three for an expert panel review, two for agreement among multiple submitters, one for a single submitter with criteria provided, and none where no criteria were provided.

Reported in CMT
Reported in Other Diseases

Reported in a disease other than CMT. Listed apart rather than counted as CMT variants.

Variants w/o a Recorded Disease

Pathogenic or likely pathogenic in ClinVar, submitted without a disease recorded.

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