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.
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
Show 5 more facts
- HomoloGene ID
- 12276
- exact match
- identifiers.org/ncbigene/55861
- genomic end
- 44039250
- genomic start
- 44034697
- cytogenetic location
- 20q13.12
Sources (3)
via Wikidata · CC0
~1 min read
Article
2 sectionsContents
- References
- Further reading
Dysbindin domain-containing protein 2 is a protein that in humans is encoded by the DBNDD2 gene.
==References==
Connections
Q180686
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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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Q229883
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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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Q22908627
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Entrez
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Q905695
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Gene Ontology
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