1. Gene
  2. DPP3 - dipeptidyl peptidase 3 Gene

DPP3 - dipeptidyl peptidase 3 Gene

Homo sapiens

Also known as DPPIII

Gene ID: 10072 | Gene type: protein coding

About DPP3

Cytogenetic location: 11q13.2 Genomic coordinates (GRCh38): 11:66,480,434-66,509,657 (from NCBI)

This gene has 16 transcripts (splice variants) and 193 orthologues. Ubiquitous expression in colon (RPKM 13.2), appendix (RPKM 10.5) and 25 other tissues.

Summary

This gene encodes a protein that is a member of the M49 family of metallopeptidases. This cytoplasmic protein binds a single zinc ion with its zinc-binding motif (HELLGH) and has post-proline dipeptidyl Aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. Increased activity of this protein is associated with endometrial and ovarian cancers. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2012]

DPP3 Products(3)

mRNA Protein Name
NM_001256670.2 NP_001243599.1 dipeptidyl peptidase 3 isoform 2
NM_005700.5 NP_005691.2 dipeptidyl peptidase 3 isoform 1
NM_130443.4 NP_569710.2 dipeptidyl peptidase 3 isoform 1

DPP3 Protein Structure

Peptidase_M49

Peptidase_M49: Peptidase family M49 (143 - 704)

  • 0
  • 200
  • 400
  • 600
  • 737 a.a.
Protein Preferred Names Protein Names

dipeptidyl peptidase 3

DPP III

Recombinant DPP3 Proteins

Cat. No. Product Name Accession Purity
HY-P70112 Dipeptidyl peptidase 3/DPP3 Protein, Human (His) Q9NY33 (M1-A737) ≥95%

Related Diseases

Diseases Alias
Cardiac Arrest

Cardiopulmonary Arrest

Circulatory Arrest

Heart Arrest

Myasthenic Syndrome, Congenital, 10

Congenital Myasthenic Syndrome 10

CMS10

Lgm

Myasthenia, Limb-Girdle, Familial

Myasthenia, Limb-Girdle, Familial, Formerly

Lgm, Formerly

Congenital Myasthenic Syndrome Type Ib, Formerly

Cms1b, Formerly

Cms Ib, Formerly

Myasthenic Myopathy, Formerly

Familial Limb-Girdle Myasthenia

Cms1b

Cms Ib

Congenital Myasthenic Syndrome Type 1b

Congenital Myasthenic Syndrome Type Ib

Myasthenic Myopathy

Myasthenic Syndrome, Congenital, Type 10

Congenital Myasthenic Syndrome Ib

Myopathy In Myasthenia Gravis

Wilms Tumor 1

Nephroblastoma

Wilms Tumor

WT1

Wilms' Tumor

Bilateral Wilms Tumor

Wilms Tumor, Type 1

Wilms Tumor, Somatic

Adult Nephroblastoma

Wt1 Disorder

Renal Embryonic Tumor

Adult Kidney Wilms Tumor

Childhood Kidney Wilms Tumor

Nonanaplastic Kidney Wilms Tumor

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus DPP3 VGNC VGNC:61603
Rattus norvegicus DPP3 RGD RGD:621127
Mus musculus DPP3 MGD MGI:1922471
Canis familiaris DPP3 VGNC VGNC:40073
Bos taurus DPP3 VGNC VGNC:28187
Others DPP3 NCBI