2. Gene
  3. ERP29 - endoplasmic reticulum protein 29 Gene

ERP29 - endoplasmic reticulum protein 29 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as ERp28; ERp31; PDIA9; PDI-DB; C12orf8; HEL-S-107

Gene ID: 10961 | Gene type: protein coding

About ERP29

Cytogenetic location: 12q24.13 Genomic coordinates (GRCh38): 12:112,013,426-112,023,449 (from NCBI)

This gene has 5 transcripts (splice variants) and 136 orthologues. Ubiquitous expression in bone marrow (RPKM 73.5), prostate (RPKM 67.8) and 25 other tissues.

Summary

This gene encodes a protein which localizes to the lumen of the endoplasmic reticulum (ER). It is a member of the protein disulfide isomerase (PDI) protein family but lacks an active thioredoxin motif, suggesting that this protein does not function as a disulfide isomerase. The canonical protein dimerizes and is thought to play a role in the processing of secretory proteins within the ER. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016]

ERP29 Products(2)

mRNA Protein Name
NM_001034025.2 NP_001029197.1 endoplasmic reticulum resident protein 29 isoform 2 precursor
NM_006817.4 NP_006808.1 endoplasmic reticulum resident protein 29 isoform 1 precursor

ERP29 Protein Structure

ERp29_N

ERp29_N: ERp29, N-terminal domain (33 - 155)

ERp29

ERp29: Endoplasmic reticulum protein ERp29, C-terminal domain (156 - 252)

  • 0
  • 100
  • 200
  • 261 a.a.
Protein Preferred Names Protein Names

endoplasmic reticulum resident protein 29

endoplasmic reticulum lumenal protein ERp28

Recombinant ERP29 Proteins

Cat. No. Product Name Accession Purity
HY-P71686 ERP29 Protein, Human (GST) P30040 (40P-251F) ≥95%

Related Diseases

Diseases Alias
Pharynx Squamous Cell Carcinoma
Gallbladder Adenocarcinoma

Adenocarcinoma Of The Gallbladder

Carcinoma Of The Gallbladder
Congenital Hypothyroidism

Cretinism

Neonatal Hypothyroidism

Ch

Cht

Congenital Myxedema

Myxedema, Congenital

Endemic Cretinism

Congenital Iodine-Deficiency Syndrome

Fetal Iodine Deficiency Syndrome

Congenital Iodine-Deficiency Hypothyroidism Nos
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS04514 ERP29 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris ERP29 VGNC VGNC:40468
Felis catus ERP29 VGNC VGNC:80440
Bos taurus ERP29 VGNC VGNC:28596
Rattus norvegicus ERP29 RGD RGD:619781
Mus musculus ERP29 MGD MGI:1914647
Others ERP29 NCBI