Gene Gene information from NCBI Gene database.
Entrez ID 11062
Gene name Dihydrouridine synthase 4 like
Gene symbol DUS4L
Synonyms (NCBI Gene)
DUS4PP35
Chromosome 7
Chromosome location 7q22.3
miRNA miRNA information provided by mirtarbase database.
31
miRTarBase ID miRNA Experiments Reference
MIRT023098 hsa-miR-124-3p Microarray 18668037
MIRT947323 hsa-miR-1260 CLIP-seq
MIRT947324 hsa-miR-1260b CLIP-seq
MIRT947325 hsa-miR-1283 CLIP-seq
MIRT947326 hsa-miR-1293 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0002943 Process TRNA dihydrouridine synthesis IDA 34798057
GO:0002943 Process TRNA dihydrouridine synthesis IEA
GO:0008033 Process TRNA processing IEA
GO:0016491 Function Oxidoreductase activity IEA
GO:0017150 Function TRNA dihydrouridine synthase activity IBA
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.
O95620
Protein name tRNA-dihydrouridine(20a/20b) synthase [NAD(P)+]-like (EC 1.3.1.90) (pp35) (tRNA-dihydrouridine synthase 4-like)
Protein function Catalyzes the synthesis of dihydrouridine, a modified base found in the D-loop of most tRNAs.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01207 Dus 30 310 Dihydrouridine synthase (Dus) Family
Sequence
Sequence length 317
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
COG5 CONGENITAL DISORDER OF GLYCOSYLATION Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL DISORDERS OF GLYCOSYLATION Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Degenerative polyarthritis Arthritis GWASDB_DG 21068099
★☆☆☆☆
Found in Text Mining only
Degenerative polyarthritis Arthritis GWASCAT_DG 21068099
★☆☆☆☆
Found in Text Mining only
Degenerative polyarthritis Arthritis BEFREE 22586168
★☆☆☆☆
Found in Text Mining only
Osteoarthritis Osteoarthritis Pubtator 24825461 Associate
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Osteoarthritis Knee Osteoarthritis Pubtator 36089590 Associate
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 28415823 Associate
★☆☆☆☆
Found in Text Mining only