Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57628
Gene name Gene Name - the full gene name approved by the HGNC.
Dipeptidyl peptidase like 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DPP10
Synonyms (NCBI Gene) Gene synonyms aliases
DPL2, DPPY, DPRP-3, DPRP3
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q14.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a single-pass type II membrane protein that is a member of the S9B family in clan SC of the serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally prese
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT944148 hsa-miR-4668-3p CLIP-seq
MIRT944149 hsa-miR-4668-5p CLIP-seq
MIRT944150 hsa-miR-4705 CLIP-seq
MIRT944151 hsa-miR-105 CLIP-seq
MIRT944152 hsa-miR-192 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
GO:0006508 Process Proteolysis IEA
GO:0008076 Component Voltage-gated potassium channel complex IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608209 20823 ENSG00000175497
Protein
UniProt ID Q8N608
Protein name Inactive dipeptidyl peptidase 10 (Dipeptidyl peptidase IV-related protein 3) (DPRP-3) (Dipeptidyl peptidase X) (DPP X) (Dipeptidyl peptidase-like protein 2) (DPL2)
Protein function Promotes cell surface expression of the potassium channel KCND2 (PubMed:15454437). Modulates the activity and gating characteristics of the potassium channel KCND2 (PubMed:15454437). Has no dipeptidyl aminopeptidase activity (PubMed:12662155). {
PDB 4WJL
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00930 DPPIV_N 133 500 Dipeptidyl peptidase IV (DPP IV) N-terminal region Family
PF00326 Peptidase_S9 580 784 Prolyl oligopeptidase family Domain
Tissue specificity TISSUE SPECIFICITY: Found in serum, T-cells and brain (at protein level). Expressed in brain, pancreas, spinal cord and adrenal glands. {ECO:0000269|PubMed:12662155, ECO:0000269|PubMed:14566338}.
Sequence
Sequence length 796
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Astrocytoma Pilocytic astrocytoma N/A N/A GWAS
Attention Deficit Hyperactivity Disorder Attention deficit hyperactivity disorder N/A N/A GWAS
Bipolar Disorder Bipolar disorder N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
AA amyloidosis Associate 10468868
Adenoma Associate 34477243
Alzheimer Disease Associate 25025038, 25740212, 36982982
Asthma Associate 19672052, 19910030, 19951440, 21103062, 22325360, 24253534, 32119686
Astrocytoma Associate 32647207
Attention Deficit Disorder with Hyperactivity Associate 28630479
Autism Spectrum Disorder Associate 18252227, 24736721, 28670437, 32393163, 32807774
Autistic Disorder Associate 23375656
Carcinogenesis Associate 29049217
Colitis Ulcerative Associate 33323040