1. Gene
  2. ICMT - isoprenylcysteine carboxyl methyltransferase Gene

ICMT - isoprenylcysteine carboxyl methyltransferase Gene

中文名称:异戊二烯半胱氨酸羧甲基转移酶

种属: Homo sapiens

同用名: PCMT; PPMT; PCCMT; HSTE14; MST098; MSTP098

基因 ID: 23463 | 基因类型: protein coding

关于 ICMT

Cytogenetic location: 1p36.31 Genomic coordinates (GRCh38): 1:6,221,193-6,235,964 (from NCBI)

This gene has 4 transcripts (splice variants) and 207 orthologues. Ubiquitous expression in kidney (RPKM 21.7), placenta (RPKM 18.3) and 25 other tissues.

功能概要

该基因编码三种酶中的第三种,这些酶在翻译后修饰某些蛋白质中异戊二烯化的 C 末端半胱氨酸残基,并将这些蛋白质靶向细胞膜。该酶定位于内质网。选择性剪接可能会导致其他转录本变体,但这些转录本的生物学有效性尚未确定。[RefSeq 提供,2008 年 7 月]

This gene encodes the third of three Enzymes that posttranslationally modify isoprenylated C-terminal cysteine residues in certain proteins and target those proteins to the cell membrane. This Enzyme localizes to the endoplasmic reticulum. Alternative splicing may result in Other transcript variants, but the biological validity of those transcripts has not been determined. [provided by RefSeq, Jul 2008]

ICMT 基因产物(1)

mRNA Protein Name
NM_012405.4 NP_036537.1 protein-S-isoprenylcysteine O-methyltransferase
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein C-terminal S-isoprenylcysteine carboxyl O-methyltransferase activity IDA
IDA: 通过直接分析推断
9614111 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in endoplasmic reticulum IDA
IDA: 通过直接分析推断
9614111 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

ICMT 蛋白结构

ICMT

ICMT: Isoprenylcysteine carboxyl methyltransferase (ICMT) family (164 - 257)

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

protein-S-isoprenylcysteine O-methyltransferase

prenylated protein carboxyl methyltransferase

ICMT 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
ICMT O60725 JAGN1 Homo sapiens Q8N5M9 32296183
种属内
ICMT O60725 JAGN1 Homo sapiens Q8N5M9 32296183
种属内
ICMT O60725 JAGN1 Homo sapiens Q8N5M9 32296183
种属内
ICMT O60725 ARL13B Homo sapiens Q3SXY8 32296183
种属内
ICMT O60725 ARL13B Homo sapiens Q3SXY8 32296183
种属内
ICMT O60725 ARL13B Homo sapiens Q3SXY8 32296183
种属内
ICMT O60725 KCNJ6 Homo sapiens P48051 32296183
种属内
ICMT O60725 KCNJ6 Homo sapiens P48051 32296183
种属内
ICMT O60725 KCNJ6 Homo sapiens P48051 32296183
种属内
ICMT O60725 AQP6 Homo sapiens Q13520 32296183
种属内
ICMT O60725 AQP6 Homo sapiens Q13520 32296183
种属内
ICMT O60725 AQP6 Homo sapiens Q13520 32296183
种属内
ICMT O60725 MUC1 Homo sapiens P15941-11 32296183
种属内
ICMT O60725 MUC1 Homo sapiens P15941-11 32296183
种属内
ICMT O60725 MUC1 Homo sapiens P15941-11 32296183
种属内
ICMT O60725 RNF19B Homo sapiens Q6ZMZ0 32296183
种属内
ICMT O60725 RNF19B Homo sapiens Q6ZMZ0 32296183
种属内
ICMT O60725 RNF19B Homo sapiens Q6ZMZ0 32296183
种属内
ICMT O60725 PDZK1IP1 Homo sapiens Q13113 32296183
种属内
ICMT O60725 PDZK1IP1 Homo sapiens Q13113 32296183
种属内
ICMT O60725 PDZK1IP1 Homo sapiens Q13113 32296183
种属内
ICMT O60725 TRIM32 Homo sapiens Q13049 32296183
种属内
ICMT O60725 TRIM32 Homo sapiens Q13049 32296183
种属内
ICMT O60725 TRIM32 Homo sapiens Q13049 32296183
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
Hyperhomocysteinemia
Familial Partial Lipodystrophy

Lipodystrophy, Familial Partial

Fpld

Kobberling-Dunnigan Syndrome

Dunnigan Syndrome

Koberling-Dunnigan Syndrome

Dunnigan-Kobberling Syndrome

Fpl

Familial Partial Lipodystrophy, Type 2

Hallermann-Streiff Syndrome

Francois Dyscephalic Syndrome

HSS

Hallermann'S Syndrome

Oculomandibulofacial Syndrome

Hallerman - Streiff Syndrome

François Dyscephalic Syndrome

Hallermann Streiff Francois Syndrome

Hallermann Streiff Syndrome

Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant

EDMD2

Autosomal Dominant Emery-Dreifuss Muscular Dystrophy

Emd2

Emery-Dreifuss Muscular Dystrophy, Autosomal Dominant

Scapuloilioperoneal Atrophy With Cardiopathy

Muscular Dystrophy With Early Contractures And Cardiomyopathy, Autosomal Dominant

Hauptmann-Thannhauser Muscular Dystrophy

Cardiomyopathy, Dilated, With Quadriceps Myopathy

Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 2

Muscular Dystrophy, Limb-Girdle, Type 1b

Muscular Dystrophy, Limb-Girdle, Type 1b, Formerly

Lgmd1b, Formerly

Muscular Dystrophy, Proximal, Type 1b, Formerly

Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1b

Lgmd1b

Limb-Girdle Muscular Dystrophy 1b

Muscular Dystrophy, Proximal, Type 1b

Muscular Dystrophy With Early Contractures And Cardiomyopathy Autosomal Dominant

Hutchinson-Gilford Progeria Syndrome

Progeria

HGPS

Hutchinson-Gilford Syndrome

Hutchinson-Gilford Progeria

Hutchinson Gilford Syndrome

Hutchinson Gilford Progeria Syndrome

Hutchinson-Gilford Disease

Progeria Of Childhood

Hutchinson-Gilford-Progeria Syndrome

Cardiomyopathy, Dilated, 1a

Dilated Cardiomyopathy 1a

Cdcd1

CMD1A

Cardiomyopathy, Familial Idiopathic

Familial Dilated Cardiomyopathy With Conduction Defect Due To Lmna Mutation

Cardiomyopathy, Dilated, With Conduction Defect 1

Cardiomyopathy, Idiopathic Dilated

Cardiomyopathy, Congestive

Dilated Cardiomyopathy With Conduction Defect 1

Cardiomyopathy Dilated With Conduction Defect Type 1

Cardiomyopathy, Dilated 1a

Cardiomyopathy Dilated With Conduction Defect 1

Cardiomyopathy, Dilated, Type 1a

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
Felis catus ICMT VGNC VGNC:67690
Macaca mulatta ICMT VGNC VGNC:73554
Bos taurus ICMT VGNC VGNC:30029
Mus musculus ICMT MGD MGI:1888594
Rattus norvegicus ICMT RGD RGD:621618