Gene Gene information from NCBI Gene database.
Entrez ID 404093
Gene name CUE domain containing 1
Gene symbol CUEDC1
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17q22
miRNA miRNA information provided by mirtarbase database.
64
miRTarBase ID miRNA Experiments Reference
MIRT018044 hsa-miR-335-5p Microarray 18185580
MIRT021437 hsa-miR-9-5p Microarray 17612493
MIRT1971776 hsa-miR-1269 CLIP-seq
MIRT1971777 hsa-miR-1269b CLIP-seq
MIRT1971778 hsa-miR-1273g CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 15231748, 24510904, 29513927, 32296183, 33961781
GO:0043130 Function Ubiquitin binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620552 31350 ENSG00000180891
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NWM3
Protein name CUE domain-containing protein 1
PDB 2DHY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02845 CUE 47 88 CUE domain Domain
Sequence
MTSLFRRSSSGSGGGGTAGARGGGGGTAAPQELNNSRPARQVRRLEFNQAMDDFKTMFPN
MDYDIIECVLRANSGAVDATIDQLLQMN
LEGGGSSGGVYEDSSDSEDSIPPEILERTLEP
DSSDEEPPPVYSPPAYHMHVFDRPYPLAPPTPPPRIDALGSGAPTSQRRYRNWNPPLLGN
LPDDFLRILPQQLDSIQGNAGGPKPGSGEGCPPAMAGPGPGDQESRWKQYLEDERIALFL
QNEEFMKELQRNRDFLLALERDRLKYESQKSKSSSVAVGNDFGFSSPVPGTGDANPAVSE
DALFRDKLKHMGKSTRRKLFELARAFSEKTKMRKSKRKHLLKHQSLGAAASTANLLDDVE
GHACDEDFRGRRQEAPKVEEGLREGQ
Sequence length 386
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ATRIAL FIBRILLATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MULTIPLE SCLEROSIS 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 30145202
★☆☆☆☆
Found in Text Mining only