Gene Gene information from NCBI Gene database.
Entrez ID 122525
Gene name Dopamine receptor interacting protein 1
Gene symbol DORIP1
Synonyms (NCBI Gene)
C14orf28DRIP-1DRIP1c14_5270
Chromosome 14
Chromosome location 14q21.2
miRNA miRNA information provided by mirtarbase database.
394
miRTarBase ID miRNA Experiments Reference
MIRT017339 hsa-miR-335-5p Microarray 18185580
MIRT441083 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT441082 hsa-miR-20a-5p HITS-CLIP 22473208
MIRT441083 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT728145 hsa-miR-17-5p HITS-CLIP 22473208
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:0007212 Process G protein-coupled dopamine receptor signaling pathway IBA
GO:0007212 Process G protein-coupled dopamine receptor signaling pathway IEA
GO:0007613 Process Memory IEA
GO:0010467 Process Gene expression IEA
GO:0019933 Process CAMP-mediated signaling 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.
Q4W4Y0
Protein name Dopamine receptor-interacting protein 1
Protein function Could be a regulator of the dopamine receptor signaling pathway.
Family and domains
Sequence
MKTLFEEIKASIKNNYNQDRSFCRPVLPWGGVFTIKAGRKAVSCTPLYVEIRLKNTCTID
GFLMLLYVILNENENFPRELSLHFGREFVDCFLYLMDTYSFTTVKLLWIWDKMEKQQYKS
EVHKASLIIDLFGNEHDNFTKNLENLMSTIQESYCSNWRCPTRVQEDQQRTININPPQEI
PHGNLIRLAVNELFCSKIELCEEHGCGGLREFSQRIFCHGAPPFVVLNMQHWKSEDLAYV
PYYLDLSDHKYLLEGATLFNKEEHHYSAAFQIGGHWMHYDGLRNVNLILLNKPPEFLLLS
SLVYIRATEK
Sequence length 310
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
BIPOLAR DISORDER Disgenet
★★☆☆☆
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
Bipolar Disorder Bipolar Disorder PSYGENET_DG 20874815
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Colorectal Carcinoma Colorectal Cancer BEFREE 28455792
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 28455792
★☆☆☆☆
Found in Text Mining only