ICMT - isoprenylcysteine carboxyl methyltransferase Gene
Also Known as PCMT; PPMT; PCCMT; HSTE14; MST098; MSTP098
Species: Homo sapiens
About ICMT
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.
Summary
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 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_012405.4 | NP_036537.1 | protein-S-isoprenylcysteine O-methyltransferase |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein C-terminal S-isoprenylcysteine carboxyl O-methyltransferase activity |
IDA
IDA: Inferred from direct assay
|
9614111 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in endoplasmic reticulum |
IDA
IDA: Inferred from direct assay
|
9614111 | GOA |
ICMT Protein Structure
ICMT: Isoprenylcysteine carboxyl methyltransferase (ICMT) family (164 - 257)
- 0
- 100
- 200
- 284 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
protein-S-isoprenylcysteine O-methyltransferase |
|
ICMT Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
ICMT | O60725 | JAGN1 | Homo sapiens | Q8N5M9 | 32296183 | |
|
Intra
|
ICMT | O60725 | JAGN1 | Homo sapiens | Q8N5M9 | 32296183 | |
|
Intra
|
ICMT | O60725 | JAGN1 | Homo sapiens | Q8N5M9 | 32296183 | |
|
Intra
|
ICMT | O60725 | ARL13B | Homo sapiens | Q3SXY8 | 32296183 | |
|
Intra
|
ICMT | O60725 | ARL13B | Homo sapiens | Q3SXY8 | 32296183 | |
|
Intra
|
ICMT | O60725 | ARL13B | Homo sapiens | Q3SXY8 | 32296183 | |
|
Intra
|
ICMT | O60725 | KCNJ6 | Homo sapiens | P48051 | 32296183 | |
|
Intra
|
ICMT | O60725 | KCNJ6 | Homo sapiens | P48051 | 32296183 | |
|
Intra
|
ICMT | O60725 | KCNJ6 | Homo sapiens | P48051 | 32296183 | |
|
Intra
|
ICMT | O60725 | AQP6 | Homo sapiens | Q13520 | 32296183 | |
|
Intra
|
ICMT | O60725 | AQP6 | Homo sapiens | Q13520 | 32296183 | |
|
Intra
|
ICMT | O60725 | AQP6 | Homo sapiens | Q13520 | 32296183 | |
|
Intra
|
ICMT | O60725 | MUC1 | Homo sapiens | P15941-11 | 32296183 | |
|
Intra
|
ICMT | O60725 | MUC1 | Homo sapiens | P15941-11 | 32296183 | |
|
Intra
|
ICMT | O60725 | MUC1 | Homo sapiens | P15941-11 | 32296183 | |
|
Intra
|
ICMT | O60725 | RNF19B | Homo sapiens | Q6ZMZ0 | 32296183 | |
|
Intra
|
ICMT | O60725 | RNF19B | Homo sapiens | Q6ZMZ0 | 32296183 | |
|
Intra
|
ICMT | O60725 | RNF19B | Homo sapiens | Q6ZMZ0 | 32296183 | |
|
Intra
|
ICMT | O60725 | PDZK1IP1 | Homo sapiens | Q13113 | 32296183 | |
|
Intra
|
ICMT | O60725 | PDZK1IP1 | Homo sapiens | Q13113 | 32296183 | |
|
Intra
|
ICMT | O60725 | PDZK1IP1 | Homo sapiens | Q13113 | 32296183 | |
|
Intra
|
ICMT | O60725 | TRIM32 | Homo sapiens | Q13049 | 32296183 | |
|
Intra
|
ICMT | O60725 | TRIM32 | Homo sapiens | Q13049 | 32296183 | |
|
Intra
|
ICMT | O60725 | TRIM32 | Homo sapiens | Q13049 | 32296183 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Hyperhomocysteinemia |
|
|
| Familial Partial Lipodystrophy |
|
|
| Hallermann-Streiff Syndrome |
|
|
| Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant |
|
|
| Hutchinson-Gilford Progeria Syndrome |
|
|
| Cardiomyopathy, Dilated, 1a |
|
|
Orthologs Information
| Species | Symbol | Source | 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 |
| Others | ICMT | NCBI |