Gene Gene information from NCBI Gene database.
Entrez ID 55861
Gene name Dysbindin domain containing 2
Gene symbol DBNDD2
Synonyms (NCBI Gene)
C20orf35CK1BPHSMNP1
Chromosome 20
Chromosome location 20q13.12
miRNA miRNA information provided by mirtarbase database.
66
miRTarBase ID miRNA Experiments Reference
MIRT052207 hsa-let-7b-5p CLASH 23622248
MIRT573854 hsa-miR-4785 PAR-CLIP 20371350
MIRT573853 hsa-miR-766-5p PAR-CLIP 20371350
MIRT573851 hsa-miR-7154-3p PAR-CLIP 20371350
MIRT573852 hsa-miR-765 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16618118
GO:0005737 Component Cytoplasm IEA
GO:0005764 Component Lysosome IEA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0006469 Process Negative regulation of protein kinase activity IDA 16618118
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611453 15881 ENSG00000244274
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BQY9
Protein name Dysbindin domain-containing protein 2 (Casein kinase-1 binding protein) (CK1BP) (HSMNP1)
Protein function May modulate the activity of casein kinase-1. Inhibits CSNK1D autophosphorylation (in vitro).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04440 Dysbindin 101 241 Dysbindin (Dystrobrevin binding protein 1) Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain. {ECO:0000269|PubMed:16618118}.
Sequence
MGAGNFLTALEVPVAALAGAASDRRASCERVSPPPPLPHFRLPPLPRSRLPGPVSRPEPG
APLLGCWLQWGAPSPGPLCLLFRLCSCTCFAPLPAGADMDPNPRAALERQQLRLRERQKF
FEDILQPETEFVFPLSHLHLESQRPPIGSISSMEVNVDTLEQVELIDLGDPDAADVFLPC
EDPPPTPQSSGMDNHLEELSLPVPTSDRTTSRTSSSSSSDSSTNLHSPNPSDDGADTPLA
Q
SDEEEERGDGGAEPGACS
Sequence length 259
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
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations