Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
138009
Gene name Gene Name - the full gene name approved by the HGNC.
DDB1 and CUL4 associated factor 4 like 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DCAF4L2
Synonyms (NCBI Gene) Gene synonyms aliases
WDR21C
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q21.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017989 hsa-miR-335-5p Microarray 18185580
MIRT569839 hsa-miR-494-3p PAR-CLIP 20371350
MIRT569839 hsa-miR-494-3p PAR-CLIP 20371350
MIRT925057 hsa-miR-1233 CLIP-seq
MIRT925058 hsa-miR-1245b-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0080008 Component Cul4-RING E3 ubiquitin ligase complex IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620421 26657 ENSG00000176566
Protein
UniProt ID Q8NA75
Protein name DDB1- and CUL4-associated factor 4-like protein 2 (WD repeat-containing protein 21C)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00400 WD40 262 298 WD domain, G-beta repeat Repeat
Sequence
MESKRPRLLEEADKQKKTVRVGLNAPSMLRKNQLGFLRFANYCRIARELRVSCMQRKKVQ
IHSWDPSSLASDRFNRILANTNTDQLFTVNQVEAGGSKYGIITMRGLTTPELRVYPHKTL
YVPNRKVNSMCWASLNHLDSHLLLCFVGLADTPSCAVLLPASLFIGSFPGMRRPGMLCSF
QIPDAWSCAWSLSIHAYHSFSTGLSQQVLLTNVVTGHQQSFGTSSDVLAQQFAIMTPLLF
NGCRSGEIFGIDLRCGNQGSGWKAICLSHDSAVTSLQILQDGQFLVSSDMTGTIKLWDLR
ATKCVTQYEGHVNNSAYLPVHVNEEEGVVAAVGQDCYTRIWSLRHGHLLTTIPSPYPASE
NDIPSVAFSSRLGGFRGAPGLLMAVREDLYCFSYG
Sequence length 395
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Cleft Lip With Or Without Cleft Palate Cleft lip with or without cleft palate N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 32685988
Cleft Lip Associate 35191549
Cleft Palate Associate 23512105, 35191549
Fatty Liver Alcoholic Associate 32685988
Neoplasms Associate 32685988
Orofacial Cleft 1 Associate 35191549
Otofaciocervical Syndrome Associate 35191549
Virus Diseases Associate 32685988