DBNDD2
Sign in to saveAlso known as C20orf35, CK1BP, HSMNP1, dysbindin domain containing 2
Dysbindin domain-containing protein 2 is a protein that in humans is encoded by the DBNDD2 gene.
In the Vinony graph
Within Vinony's link graph, DBNDD2 is referenced by 2 other articles, and connects out to PubMed, human chromosome 20 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 20.
Its subject is documented across 7 Wikipedia language editions.
Gene data
DBNDD2- Name
- dysbindin domain containing 2
- Type
- protein-coding
- Position
- 45,405,616–45,410,870 (+)
- Aliases
- C20orf35, CK1BP, HSMNP1
- Ensembl
- ENSG00000244274
- RefSeq RNA
- NM_001048221.3, NM_001048222.3, NM_001048223.3, NM_001048224.3, NM_001048225.4
- RefSeq protein
- NP_001041686.1, NP_001041687.1, NP_001041688.1, NP_001041689.1, NP_001041690.3
Involved in negative regulation of protein kinase activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]
Gene Ontology
Molecular function
Cellular component
via MyGene.info
Gene · Ensembl
dysbindin domain containing 2
- Symbol
- DBNDD2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 20:45,405,616-45,410,870
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 12276
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/55861
- genomic end
- 44039250
- genomic start
- 44034697
- chromosome
- human chromosome 20
- cytogenetic location
- 20q13.12
- expressed in
- left ventricle
Sources (3)
via Wikidata · CC0
Connections
PubMed
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human chromosome 20
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Ensembl genome database project
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human
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protein
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Wikidata
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gene
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chromosome
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digital object identifier
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bibcode
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human genome
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PubMed Central
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base pair
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locus
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gene expression
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Online Mendelian Inheritance in Man
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Semantic Scholar
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Entrez
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UniProt
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Gene Ontology
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