Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
54165
Gene name Gene Name - the full gene name approved by the HGNC.
Defective in cullin neddylation 1 domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DCUN1D1
Synonyms (NCBI Gene) Gene synonyms aliases
DCNL1, DCUN1L1, RP42, SCCRO, SCRO, Tes3
Disease Acronyms (UniProt) Disease acronyms from UniProt database
RP42
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q26.33
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023689 hsa-miR-1-3p Proteomics 18668040
MIRT023689 hsa-miR-1-3p Proteomics;Microarray 18668037
MIRT044328 hsa-miR-106b-5p CLASH 23622248
MIRT558470 hsa-miR-6835-3p PAR-CLIP 21572407
MIRT558469 hsa-miR-30a-5p PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000151 Component Ubiquitin ligase complex IBA 21873635
GO:0000151 Component Ubiquitin ligase complex IDA 18826954
GO:0005515 Function Protein binding IPI 16189514, 18826954, 19617556, 21145461, 23401859, 25416956, 26906416, 27107012, 28514442, 28581483, 30587576, 32296183
GO:0005634 Component Nucleus IMP 26906416
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605905 18184 ENSG00000043093
Protein
UniProt ID Q96GG9
Protein name DCN1-like protein 1 (DCNL1) (DCUN1 domain-containing protein 1) (Defective in cullin neddylation protein 1-like protein 1) (Squamous cell carcinoma-related oncogene)
Protein function Part of an E3 ubiquitin ligase complex for neddylation (PubMed:18826954). Promotes neddylation of cullin components of E3 cullin-RING ubiquitin ligase complexes (PubMed:19617556, PubMed:23201271, PubMed:23401859, PubMed:26906416). Acts by bindin
PDB 3TDU , 3TDZ , 4P5O , 5UFI , 5V83 , 5V86 , 5V88 , 6B5Q , 6BG3 , 6BG5 , 6P5V , 6P5W , 6XOL , 6XOM , 6XON , 6XOO , 6XOP , 6XOQ , 7KWA , 8OR2 , 8OR3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14555 UBA_4 9 50 Domain
PF03556 Cullin_binding 136 246 Cullin binding Family
Tissue specificity TISSUE SPECIFICITY: Expressed in pancreas, kidney, placenta, brain and heart. Weakly or not expressed in liver, skeletal muscle and lung. Strongly overexpressed in thyroid tumors, bronchioloalveolar carcinomas, and malignant tissues of squamous cell carci
Sequence
MNKLKSSQKDKVRQFMIFTQSSEKTAVSCLSQNDWKLDVATDNFFQNPELYIRESVKGSL
DRKKLEQLYNRYKDPQDENKIGIDGIQQFCDDLALDPASISVLIIAWKFRAATQCEFSKQ
EFMDGMTELGCDSIEKLKAQIPKMEQELKEPGRFKDFYQFTFNFAKNPGQKGLDLEMAIA
YWNLVLNGRFKFLDLWNKFLLEHHKRSIPKDTWNLLLDFSTMIADDMSNYDEEGAWPVLI
DDFVEF
ARPQIAGTKSTTV
Sequence length 259
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Neddylation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Parkinson disease Parkinson Disease rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432
View all (84 more)
21738487
Associations from Text Mining
Disease Name Relationship Type References
Atypical Squamous Cells of the Cervix Associate 34436017
Carcinoma Squamous Cell Associate 24004673
Colorectal Neoplasms Associate 28470146
Laryngeal Neoplasms Associate 28791411
Neoplasms Associate 24874471, 34436017
Neoplasms Inhibit 25349211
Neoplasms Stimulate 29077169
Prostatic Neoplasms Associate 29077169
Squamous Cell Carcinoma of Head and Neck Associate 24278325, 28791411, 30548484
Uterine Cervical Neoplasms Associate 27285984, 29750306