1. Gene
  2. PECR - peroxisomal trans-2-enoyl-CoA reductase Gene

PECR - peroxisomal trans-2-enoyl-CoA reductase Gene

中文名称:过氧化物酶体反式-2-烯酰辅酶 A 还原酶

种属: Homo sapiens

同用名: TERP; DCRRP; PVIARL; HPDHASE; SDR29C1; HSA250303

基因 ID: 55825 | 基因类型: protein coding

关于 PECR

Cytogenetic location: 2q35 Genomic coordinates (GRCh38): 2:216,029,088-216,081,809 (from NCBI)

This gene has 8 transcripts (splice variants), 205 orthologues and is associated with 1 phenotype. Broad expression in liver (RPKM 14.1), fat (RPKM 7.2) and 15 other tissues.

功能概要

启用信号受体结合活性和反式 2-烯酰辅酶 A 还原酶 (NADPH) 活性。参与叶绿醇代谢过程。位于过氧化物酶体中。 [由基因组资源联盟提供,2022 年 4 月]

Enables signaling receptor binding activity and trans-2-enoyl-CoA reductase (NADPH) activity. Involved in phytol metabolic process. Located in peroxisome. [provided by Alliance of Genome Resources, Apr 2022]

PECR 基因产物(1)

mRNA Protein Name
NM_018441.6 NP_060911.2 peroxisomal trans-2-enoyl-CoA reductase
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
NOT enables 2,4-dienoyl-CoA reductase (NADPH) activity IDA
IDA: 通过直接分析推断
11669066 GOA
enables signaling receptor binding IPI
IPI: 通过物理相互作用推断
11669066 GOA
enables trans-2-enoyl-CoA reductase (NADPH) activity IDA
IDA: 通过直接分析推断
16546181 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in phytol metabolic process IDA
IDA: 通过直接分析推断
16546181 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in peroxisome IDA
IDA: 通过直接分析推断
11669066 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

PECR 蛋白结构

adh_short_C2

adh_short_C2: Enoyl-(Acyl carrier protein) reductase (28 - 264)

  • 0
  • 100
  • 200
  • 303 a.a.
蛋白主名 其他名称

peroxisomal trans-2-enoyl-CoA reductase

2,4-dienoyl-CoA reductase-related protein

关联疾病

疾病名称 别名
Hemopneumothorax

Haemopneumothorax

Ehlers-Danlos Syndrome, Hypermobility Type

Ehlers-Danlos Syndrome, Type 3

Ehlers-Danlos Syndrome, Type Iii

EDSHMB

Eds Iii

Benign Hypermobility Syndrome

Ehlers-Danlos Syndrome Hypermobility Type

Eds3

Type Iii Ehlers-Danlos Syndrome

Ehlers-Danlos Syndrome Type 3

Es-D3

Brugada Syndrome 2

BRGDA2

Brugada Syndrome, Type 2

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

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus PECR RGD RGD:70925
Mus musculus PECR MGD MGI:2148199
Canis familiaris PECR VGNC VGNC:44411
Felis catus PECR VGNC VGNC:64109
Macaca mulatta PECR VGNC VGNC:75827
Bos taurus PECR VGNC VGNC:32738