1. Gene
  2. MTFP1 - mitochondrial fission process 1 Gene

MTFP1 - mitochondrial fission process 1 Gene

中文名称:线粒体裂变过程 1

种属: Homo sapiens

同用名: MTP18; HSPC242

基因 ID: 51537 | 基因类型: protein coding

关于 MTFP1

Cytogenetic location: 22q12.2 Genomic coordinates (GRCh38): 22:30,425,768-30,429,054 (from NCBI)

This gene has 6 transcripts (splice variants) and 192 orthologues. Ubiquitous expression in duodenum (RPKM 6.4), placenta (RPKM 6.0) and 25 other tissues.

功能概要

MTP18 是一种线粒体蛋白和磷脂酰肌醇 3 激酶 (参见 PIK3CA,MIM 171834) 信号通路的下游靶标,在细胞活力和线粒体动力学中发挥作用 (Tondera 等人,2004 [PubMed 15155745]) 。[OMIM 提供, 2008 年 3 月]

MTP18 is a mitochondrial protein and downstream target of the phosphatidylinositol 3-kinase (see PIK3CA, MIM 171834) signaling pathway that plays a role in cell viability and mitochondrial dynamics (Tondera et al., 2004 [PubMed 15155745]).[supplied by OMIM, Mar 2008]

MTFP1 基因产物(2)

mRNA Protein Name
NM_001003704.3 NP_001003704.1 mitochondrial fission process protein 1 isoform b
NM_016498.5 NP_057582.2 mitochondrial fission process protein 1 isoform a
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
enables protein binding IPI
IPI: 通过物理相互作用推断
32814053 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in mitochondrial fission IMP
IMP: 通过突变表型推断
15985469 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in mitochondrial inner membrane IDA
IDA: 通过直接分析推断
15985469 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

MTFP1 蛋白结构

MTP18

MTP18: Mitochondrial 18 KDa protein (MTP18) (19 - 147)

  • 0
  • 100
  • 166 a.a.
蛋白主名 其他名称

mitochondrial fission process protein 1

mitochondrial 18 kDa protein

MTFP1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
MTFP1 Q9UDX5 OPTN Homo sapiens Q96CV9 32814053
种属内
MTFP1 Q9UDX5 OPTN Homo sapiens Q96CV9 32814053
种属内
MTFP1 Q9UDX5 OPTN Homo sapiens Q96CV9 32814053
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
3-Methylglutaconic Aciduria, Type Iii

Optic Atrophy

3-Methylglutaconic Aciduria Type 3

Costeff Syndrome

Mga3

Costeff Optic Atrophy Syndrome

Optic Atrophy Plus Syndrome

Infantile Optic Atrophy With Chorea And Spastic Paraplegia

3-Methylglutaconic Aciduria Type Iii

Autosomal Recessive Optic Atrophy Plus Syndrome

Autosomal Recessive Optic Atrophy Type 3

Opa3 Defect

MGCA3

Mga, Type Iii

Iraqi Jewish Optic Atrophy Plus

Mga Type Iii

Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia

Iraqi-Jewish 'Optic Atrophy Plus'

Optic Atrophy 3, Autosomal Recessive

Opa3, Autosomal Recessive

Opa3-Related 3-Methylglutaconic Aciduria

Iraqi-Jewish Optic Atrophy Plus

Atrophy Of Optic Disc

3-Alpha Methylglutaconic Aciduria Type Iii

Optic Atrophy 3

Optic Atrophy Infantile With Chorea And Spastic Paraplegia

Autosomal Recessive Opa3

Autosomal Recessive Optic Atrophy 3

3-Methylglutaconic Aciduria 3

3-Alpha-Methylglutaconic Aciduria Type 3

Optic Atrophy 3 Autosomal Recessive

Atrophy, Optic

Atrophy, Optic, Plus Syndrome

Optic Nerve Atrophy

Primary Optic Atrophy

Oa - [Optic Atrophy]

Second Cranial Nerve Atrophy

Second Cranium Nerve Atrophy

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
Canis familiaris MTFP1 VGNC VGNC:52952
Mus musculus MTFP1 MGD MGI:1916686
Bos taurus MTFP1 VGNC VGNC:31725
Rattus norvegicus MTFP1 RGD RGD:1359705
Felis catus MTFP1 VGNC VGNC:80455
Others MTFP1 NCBI