Gene Gene information from NCBI Gene database.
Entrez ID 139425
Gene name DDB1 and CUL4 associated factor 8 like 1
Gene symbol DCAF8L1
Synonyms (NCBI Gene)
WDR42B
Chromosome X
Chromosome location Xp21.3
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 the formation of heterotrimeric or multi-protei
miRNA miRNA information provided by mirtarbase database.
26
miRTarBase ID miRNA Experiments Reference
MIRT925612 hsa-miR-1303 CLIP-seq
MIRT925613 hsa-miR-3156-3p CLIP-seq
MIRT925614 hsa-miR-4275 CLIP-seq
MIRT925615 hsa-miR-4301 CLIP-seq
MIRT925616 hsa-miR-508-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IBA
GO:0080008 Component Cul4-RING E3 ubiquitin ligase complex IBA
GO:0080008 Component Cul4-RING E3 ubiquitin ligase complex IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A6NGE4
Protein name DDB1- and CUL4-associated factor 8-like protein 1 (WD repeat-containing protein 42B)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00400 WD40 186 224 WD domain, G-beta repeat Repeat
PF00400 WD40 425 466 WD domain, G-beta repeat Repeat
PF00400 WD40 470 509 WD domain, G-beta repeat Repeat
Sequence
MSHQEGSTGGLPDLVTESLFSSPEEQSGVAAVTAASSDIEMAATEPSTGDGGDTRDGGFL
NDASTENQNTDSESSSEDVELESMGEGLFGYPLVGEETEREEEEEEMEEEGEEEEQPRMC
PRCGGTNHDQCLLDEDQALEEWISSETSALPRSRWQVLTALRQRQLGSSARFVYEACGAR
TFVQRFRLQYLLGSHAGSVSTIHFNQRGTRLASSGDDLRVIVWDWVRQKPVLNFESGHDI
NVIQAKFFPNCGDSTLAMCGHDGQVRVAELINASYCENTKRVAKHRGPAHELALEPDSPY
KFLTSGEDAVVFTIDLRQDRPASKVVVTRENDKKVGLYTISMNPANIYQFAVGGHDQFVR
IYDQRRIDKKENNGVLKKFTPHHLVYCDFPTNITCVVYSHDGTELLASYNDEDIYLFNSS
LSDGAQYVKRYKGHRNNDTIKCVNFYGPRSEFVVSGSDCGHVFFWEKSSSQIIQFMEGDR
GDIVNCLEPHPYLPVLATSGLDQHVRIWT
PTAKTATELTGLKDVIKKNKQERDEDNLNYT
DSFDNRMLRFFVRHLLQRAHQPGWRDHGAEFPDEEELDESSSTSDTSEEEGQDRVQCIPS
Sequence length 600
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ERECTILE DYSFUNCTION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 35280675
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 36714595
★☆☆☆☆
Found in Text Mining only
Hereditary Breast and Ovarian Cancer Syndrome Associate 35280675
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 35280675
★☆☆☆☆
Found in Text Mining only
Obesity Associate 36714595
★☆☆☆☆
Found in Text Mining only
Overweight Associate 36714595
★☆☆☆☆
Found in Text Mining only