Entity Details

Primary name DPP10
Entity type gene
Source Source Link

Details

PrimaryID57628
RefseqGene
SymbolDPP10
Namedipeptidyl peptidase like 10
Chromosome2
Location2q14.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-09-18
ModificationDate2021-06-22

Ontological Relatives

UniProt IDsDPP10_HUMAN

GO terms

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GOName
GO:0005886 plasma membrane
GO:0008076 voltage-gated potassium channel complex
GO:0008236 serine-type peptidase activity
GO:0015459 potassium channel regulator activity
GO:0016020 membrane
GO:0044325 transmembrane transporter binding
GO:0072659 protein localization to plasma membrane
GO:1901379 regulation of potassium ion transmembrane transport
GO:1903078 positive regulation of protein localization to plasma membrane

Diseases

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Disease IDSourceNameDescription
600807 OMIMAsthma (ASTHMA)The most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment. It is characterized by recurrent attacks of paroxysmal dyspnea, with wheezing due to spasmodic contraction of the bronchi. Disease susceptibility is associated with variants affecting the gene represented in this entry.

Interactions

5 interactions

InteractorPartnerSourcesPublicationsLink
DPP10KCND2BioGRID15454437 details
DPP10SMAD2IntAct20195357 details
DPP10KCND3BioGRID22387313 details
DPP10DPP10BioGRID22387313 details
DPP10BAG3BioGRID23824909 details