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

ERP29 - endoplasmic reticulum protein 29 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：内质网蛋白 29

种属: Homo sapiens

同用名: ERp28; ERp31; PDIA9; PDI-DB; C12orf8; HEL-S-107

基因 ID: 10961 | 基因类型: protein coding

关于 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.

功能概要

该基因编码一种定位于内质网 (ER) 腔的蛋白质。它是蛋白质二硫化物异构酶 (PDI) 蛋白家族的成员，但缺乏活性硫氧还蛋白基序，表明该蛋白质不具有二硫化物异构酶的功能。典型蛋白二聚化，被认为在 ER 内分泌蛋白的加工过程中发挥作用。可变剪接导致编码不同异构体的多个转录变体。[RefSeq 提供，2016 年 12 月]

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 基因产物(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 蛋白结构

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.
蛋白主名 其他名称

endoplasmic reticulum resident protein 29

endoplasmic reticulum lumenal protein ERp28

重组 ERP29 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71686 ERP29 Protein, Human (GST) P30040 (40P-251F) ≥95%

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS04514 ERP29 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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
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