2. Gene
  3. MPV17L - MPV17 mitochondrial inner membrane protein like Gene

MPV17L - MPV17 mitochondrial inner membrane protein like Gene

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

中文名称：MPV17 线粒体内膜蛋白样

种属: Homo sapiens

同用名: M-LPH; MLPH1; MLPH2; MPV17L1

基因 ID: 255027 | 基因类型: protein coding

关于 MPV17L

Cytogenetic location: 16p13.11 Genomic coordinates (GRCh38): 16:15,395,754-15,413,271 (from NCBI)

This gene has 3 transcripts (splice variants), 1 gene allele, 256 orthologues and 3 paralogues. Broad expression in kidney (RPKM 1.8), duodenum (RPKM 1.5) and 20 other tissues.

功能概要

参与过氧化氢生物合成过程的负调控；参与细胞凋亡信号通路的线粒体外膜透化的负调控；和活性氧代谢过程。位于过氧化物酶体中。 [由基因组资源联盟提供，2022 年 4 月]

Involved in negative regulation of hydrogen peroxide biosynthetic process; negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway; and Reactive Oxygen Species metabolic process. Located in peroxisome. [provided by Alliance of Genome Resources, Apr 2022]

MPV17L 基因产物(2)

mRNA Protein Name
NM_001128423.2 NP_001121895.1 mpv17-like protein isoform 1
NM_173803.4 NP_776164.2 mpv17-like protein isoform 2
基因本体论
  • 生物过程
  • 细胞组分
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of hydrogen peroxide biosynthetic process IDA
IDA: 通过直接分析推断
22306510 GOA
involved in negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway IDA
IDA: 通过直接分析推断
22306510 GOA
involved in reactive oxygen species metabolic process IDA
IDA: 通过直接分析推断
16631601 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
16631601 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

MPV17L 蛋白结构

Mpv17_PMP22

Mpv17_PMP22: Mpv17 / PMP22 family (105 - 168)

  • 0
  • 100
  • 196 a.a.
蛋白主名 其他名称

mpv17-like protein

M-LP homolog

关联疾病

疾病名称 别名
Ross River Fever

Ross River Virus Disease

Ross River Virus Infection
Autosomal Dominant Nonsyndromic Deafness 77

Dfna77
Autosomal Dominant Alport Syndrome

Alport Syndrome, Autosomal Dominant

Alport Syndrome Dominant Type

Renal Failure And Sensorineural Hearing Loss

Alport Syndrome, Dominant Type
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-RS08632 MPV17L Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus MPV17L RGD RGD:2324483
Mus musculus MPV17L MGD MGI:2135951
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