DCAF8L1 (DDB1 and CUL4 associated factor 8 like 1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 139425 |
| Gene name | DDB1 and CUL4 associated factor 8 like 1 |
| Gene symbol | DCAF8L1 |
| Synonyms (NCBI Gene) |
WDR42B
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| 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 |
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miRNA
miRNA information provided by mirtarbase database.
26
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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A6NGE4 | ||||||||||||||||||||
| Protein name | DDB1- and CUL4-associated factor 8-like protein 1 (WD repeat-containing protein 42B) | ||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 600 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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