PRMT9 - protein arginine methyltransferase 9 Gene
Also Known as PRMT10
Species: Homo sapiens
About PRMT9
This gene has 4 transcripts (splice variants), 204 orthologues, 7 paralogues and is associated with 1 phenotype. Ubiquitous expression in adrenal (RPKM 9.7), thyroid (RPKM 7.6) and 25 other tissues.
Summary
This gene encodes a type II methyltransferase. Post-translational modification of target proteins by PRMTs plays an important regulatory role in many biological processes, whereby PRMTs methylate arginine residues by transferring methyl groups from S-adenosyl-L-methionine to the guanidino nitrogen atoms of arginine. The protein encoded by this gene methylates spliceosome associated protein 145 to regulate alternative splicing and acts as a modulator of small nuclear ribonucleoprotein maturation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2017]
PRMT9 Products (6)
| mRNA | Protein | Name |
|---|---|---|
| NM_001304458.2 | NP_001291387.1 | protein arginine N-methyltransferase 9 isoform 2 |
| NM_001350141.2 | NP_001337070.1 | protein arginine N-methyltransferase 9 isoform 3 |
| NM_001350142.2 | NP_001337071.1 | protein arginine N-methyltransferase 9 isoform 2 |
| NM_001350143.2 | NP_001337072.1 | protein arginine N-methyltransferase 9 isoform 5 |
| NM_001350144.2 | NP_001337073.1 | protein arginine N-methyltransferase 9 isoform 6 |
| NM_138364.4 | NP_612373.2 | protein arginine N-methyltransferase 9 isoform 1 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
25737013 | GOA |
| enables protein-arginine N-methyltransferase activity |
IDA
IDA: Inferred from direct assay
|
25979344 | GOA |
| enables protein-arginine N-methyltransferase activity |
IMP
IMP: Inferred from mutant phenotype
|
25737013 | GOA |
| enables protein-arginine omega-N symmetric methyltransferase activity |
IMP
IMP: Inferred from mutant phenotype
|
25737013 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in mRNA processing |
IMP
IMP: Inferred from mutant phenotype
|
25737013 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in cytoplasm |
IDA
IDA: Inferred from direct assay
|
25737013 | GOA |
PRMT9 Protein Structure
TPR_2: Tetratricopeptide repeat (104 - 133)
PrmA: Ribosomal protein L11 methyltransferase (PrmA) (175 - 235)
- 0
- 200
- 400
- 600
- 800
- 845 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
protein arginine N-methyltransferase 9 |
|
PRMT9 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
PRMT9 | Q6P2P2 | SF3B4 | Homo sapiens | Q15427 | 25737013 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B4 | Homo sapiens | Q15427 | 35271311 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B4 | Homo sapiens | Q15427 | 25737013 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B2 | Homo sapiens | Q13435 | 25737013 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B2 | Homo sapiens | Q13435 | 25737013 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B2 | Homo sapiens | Q13435 | 25737013 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B2 | Homo sapiens | Q13435 | 25737013 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B2 | Homo sapiens | Q13435 | 35271311 | |
|
Intra
|
PRMT9 | Q6P2P2 | SF3B2 | Homo sapiens | Q13435 | 25737013 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Mandibulofacial Dysostosis With Alopecia |
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Mus musculus | PRMT9 | MGD | MGI:2142651 |
| Rattus norvegicus | PRMT9 | RGD | RGD:1306157 |
| Macaca mulatta | PRMT9 | VGNC | VGNC:76313 |
| Bos taurus | PRMT9 | VGNC | VGNC:33354 |
| Canis familiaris | PRMT9 | VGNC | VGNC:45002 |
| Felis catus | PRMT9 | VGNC | VGNC:64363 |
| Others | PRMT9 | NCBI |