DBNDD2 (dysbindin domain containing 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 55861 |
| Gene name | Dysbindin domain containing 2 |
| Gene symbol | DBNDD2 |
| Synonyms (NCBI Gene) |
C20orf35CK1BPHSMNP1
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| Chromosome | 20 |
| Chromosome location | 20q13.12 |
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miRNA
miRNA information provided by mirtarbase database.
66
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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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
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| Tissue specificity | TISSUE SPECIFICITY: Detected in brain. {ECO:0000269|PubMed:16618118}. | ||||||||||
| Sequence |
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| Sequence length | 259 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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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)
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