DBNDD2 (dysbindin domain containing 2)
|
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
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
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
|
||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Detected in brain. {ECO:0000269|PubMed:16618118}. | ||||||||||
| Sequence |
MGAGNFLTALEVPVAALAGAASDRRASCERVSPPPPLPHFRLPPLPRSRLPGPVSRPEPG |
||||||||||
| Sequence length | 259 | ||||||||||
| Interactions | View interactions | ||||||||||
|
Related Genes
Genes most often co-reported with DBNDD2 across shared curated disease and pathway associations.
0
|
|
|
Diseases Linked via Similar Genes
Diseases curated for genes most similar to DBNDD2 (see Related Genes above), that are NOT already directly curated for DBNDD2 itself -- a lead worth checking, not a confirmed association.
0
|
|