1. Gene
  2. PRMT1 - protein arginine methyltransferase 1 Gene

PRMT1 - protein arginine methyltransferase 1 Gene

Homo sapiens

Also known as ANM1; HCP1; IR1B4; HRMT1L2

Gene ID: 3276 | Gene type: protein coding

About PRMT1

Cytogenetic location: 19q13.33 Genomic coordinates (GRCh38): 19:49,676,153-49,688,447 (from NCBI)

This gene has 21 transcripts (splice variants), 206 orthologues and 7 paralogues. Ubiquitous expression in ovary (RPKM 42.8), heart (RPKM 38.0) and 25 other tissues.

Summary

This gene encodes a member of the protein arginine N-methyltransferase (PRMT) family. 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 terminal guanidino nitrogen atoms. The encoded protein is a type I PRMT and is responsible for the majority of cellular arginine methylation activity. Increased expression of this gene may play a role in many types of Cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 5. [provided by RefSeq, Dec 2011]

PRMT1 Products(9)

mRNA Protein Name
XM_047438742.1 XP_047294698.1 protein arginine N-methyltransferase 1 isoform X1
NR_033397.5
NM_198319.2
XM_017026735.2 XP_016882224.1 protein arginine N-methyltransferase 1 isoform X2
XM_017026736.2 XP_016882225.1 protein arginine N-methyltransferase 1 isoform X3
NM_001207042.3 NP_001193971.1 protein arginine N-methyltransferase 1 isoform 4
NM_001536.6 NP_001527.3 protein arginine N-methyltransferase 1 isoform 1
XM_047438743.1 XP_047294699.1 protein arginine N-methyltransferase 1 isoform X1
NM_198318.5 NP_938074.2 protein arginine N-methyltransferase 1 isoform 3
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables N-methyltransferase activity IDA
IDA: Inferred from direct assay
18657504 GOA
enables N-methyltransferase activity IMP
IMP: Inferred from mutant phenotype
19124016 GOA
enables S-adenosyl-L-methionine binding IDA
IDA: Inferred from direct assay
26876602 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
19460357 GOA
enables histone H4R3 methyltransferase activity IDA
IDA: Inferred from direct assay
11448779 GOA
enables histone H4R3 methyltransferase activity IMP
IMP: Inferred from mutant phenotype
25284789 GOA
enables histone methyltransferase activity IDA
IDA: Inferred from direct assay
19405910 GOA
enables identical protein binding IDA
IDA: Inferred from direct assay
26876602 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16169070 GOA
enables methyl-CpG binding IDA
IDA: Inferred from direct assay
25284789 GOA
enables mitogen-activated protein kinase p38 binding IPI
IPI: Inferred from physical interaction
23483889 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
8663146 GOA
enables protein methyltransferase activity IDA
IDA: Inferred from direct assay
19460357 GOA
enables protein methyltransferase activity IMP
IMP: Inferred from mutant phenotype
28040436 GOA
enables protein-arginine N-methyltransferase activity EXP
EXP: Inferred from Experiment
18316480 GOA
enables protein-arginine N-methyltransferase activity IDA
IDA: Inferred from direct assay
18495660 GOA
enables protein-arginine omega-N asymmetric methyltransferase activity IDA
IDA: Inferred from direct assay
15741314 GOA
enables protein-arginine omega-N asymmetric methyltransferase activity IMP
IMP: Inferred from mutant phenotype
25284789 GOA
enables protein-arginine omega-N monomethyltransferase activity IDA
IDA: Inferred from direct assay
26575292 GOA
Biological Process GO Annotation Evidence Reference Source
involved in DNA damage response IDA
IDA: Inferred from direct assay
15741314 GOA
involved in cellular response to methionine IDA
IDA: Inferred from direct assay
38006878 GOA
involved in negative regulation of JNK cascade IMP
IMP: Inferred from mutant phenotype
22095282 GOA
involved in negative regulation of megakaryocyte differentiation IDA
IDA: Inferred from direct assay
20442406 GOA
involved in neuron projection development IMP
IMP: Inferred from mutant phenotype
18773938 GOA
involved in peptidyl-arginine methylation IDA
IDA: Inferred from direct assay
18657504 GOA
involved in positive regulation of TORC1 signaling IDA
IDA: Inferred from direct assay
38006878 GOA
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
28040436 GOA
involved in positive regulation of double-strand break repair via homologous recombination IDA
IDA: Inferred from direct assay
15741314 GOA
involved in positive regulation of erythrocyte differentiation IMP
IMP: Inferred from mutant phenotype
23483889 GOA
involved in positive regulation of translation IDA
IDA: Inferred from direct assay
30765518 GOA
involved in protein homooligomerization IDA
IDA: Inferred from direct assay
26876602 GOA
involved in protein methylation IMP
IMP: Inferred from mutant phenotype
26876602 GOA
involved in regulation of BMP signaling pathway IDA
IDA: Inferred from direct assay
33667543 GOA
involved in regulation of megakaryocyte differentiation IDA
IDA: Inferred from direct assay
26575292 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
26876602 GOA
is active in lysosomal membrane IDA
IDA: Inferred from direct assay
38006878 GOA
part of methylosome IDA
IDA: Inferred from direct assay
25284789 GOA
located in nucleus IDA
IDA: Inferred from direct assay
10749851 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PRMT1 Protein Structure

Methyltransf_31

Methyltransf_31: Methyltransferase domain (88 - 162)

  • 0
  • 100
  • 200
  • 300
  • 371 a.a.
Protein Preferred Names Protein Names

protein arginine N-methyltransferase 1

HMT1 (hnRNP methyltransferase, S. cerevisiae)-like 2

heterogeneous nuclear ribonucleoprotein methyltransferase 1-like 2

highly conserved protein 1

histone-arginine N-methyltransferase PRMT1

interferon receptor 1-bound protein 4

PRMT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
PRMT1 Q99873 PRMT8 Homo sapiens Q9NR22-2
Y2H Array
25416956
Intra
PRMT1 Q99873 PRMT8 Homo sapiens Q9NR22-2
Y2H Prey Pooling
25416956
Intra
PRMT1 Q99873 SPEG Homo sapiens Q15772
Y2H Array
25416956
Intra
PRMT1 Q99873 SPSB2 Homo sapiens Q99619
Anti Tag CoIP
23455924
Cross
PRMT1 Q99873 N SARS-CoV-2 P0DTC9
Radiolabeled Methyl
34029587
Intra
PRMT1 Q99873 SPSB1 Homo sapiens Q96BD6
Y2H
23455924
Intra
PRMT1 Q99873 VHL Homo sapiens P40337
Y2H
23455924
Intra
PRMT1 Q99873 H4C16 Homo sapiens P62805
Methyltransferase Ass
21085121
Intra
PRMT1 Q99873 HNRNPK Homo sapiens P61978
Methyltransferase Ass
19101556
Intra
PRMT1 Q99873 CHTOP Homo sapiens Q9Y3Y2
Anti Bait CoIP
19858291
Intra
PRMT1 Q99873 HNRNPR Homo sapiens O43390
Y2H Array
31515488
Intra
PRMT1 Q99873 HNRNPR Homo sapiens O43390
Validated Y2H
25416956
Intra
PRMT1 Q99873 HNRNPR Homo sapiens O43390
Y2H Array
25416956
Intra
PRMT1 Q99873 NR4A1 Homo sapiens P22736
Pull Down
19095693
Intra
PRMT1 Q99873 EWSR1 Homo sapiens Q01844
Y2H
23455924
Intra
PRMT1 Q99873 DCAF8 Homo sapiens Q5TAQ9
Y2H
23455924
Intra
PRMT1 Q99873 NTAQ1 Homo sapiens Q96HA8
Validated Y2H
25416956
Intra
PRMT1 Q99873 PRMT8 Homo sapiens Q9NR22
Anti Tag CoIP
23455924
Intra
PRMT1 Q99873 NRIP1 Homo sapiens P48552
Anti Tag CoIP
17053781
Intra
PRMT1 Q99873 NRIP1 Homo sapiens P48552
Enzymatic Study
17053781
Intra
PRMT1 Q99873 ILF3 Homo sapiens Q12906
Pull Down
10749851
Intra
PRMT1 Q99873 PRMT1 Homo sapiens Q99873
Y2H Array
25416956
Intra
PRMT1 Q99873 PRMT1 Homo sapiens Q99873
Y2H
23455924
Intra
PRMT1 Q99873 PRMT1 Homo sapiens Q99873
Y2H Pooling
16169070
Intra
PRMT1 Q99873 PRMT1 Homo sapiens Q99873
Anti Tag CoIP
23455924
Intra
PRMT1 Q99873 FAM9A Homo sapiens Q8IZU1
Anti Tag CoIP
23455924
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Ewing Sarcoma

Neuroepithelioma

Ewing'S Tumor

Ewings Sarcoma

Ewing'S Sarcoma

Peripheral Neuroepithelioma

Primitive Neuroectodermal Tumor

ES

Ewings Sarcoma-Primitive Neuroectodermal Tumor

Localized Peripheral Primitive Neuroectodermal Tumor

Peripheral Primitive Neuroectodermal Tumor

Ewing Tumor

Sarcoma, Ewing'S

Extraosseous Ewing Tumor

Askin Tumor

Ewing'S Family Localized Tumor

Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor

Localized Ewing Sarcoma

Localized Ewing'S Sarcoma

Localized Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor

Localized Ewing'S Tumor

Pnet Of Thoracopulmonary Region

Ewing Family Of Tumors

Tumor Of The Ewing Family

Skeletal Ewing Sarcoma

Osseous Ewing Sarcoma

Ppnet

Peripheral Pnet

Extraskeletal Ewing Sarcoma

Eoe

Extraosseous Ewing Sarcoma

Extraskeletal Ewing Tumor

Esft

Ewing Sarcoma Family Of Tumors

Pne

Pnet

Pnet Of The Chest Wall

Sarcoma, Ewing

Neuroectodermal Tumors, Primitive, Peripheral

Neuroectodermal Tumor, Primitive

Disorder Of Eye

Askin'S Tumor

Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor

Neuroepithelioma, Peripheral

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Spinal Cord Primitive Neuroectodermal Neoplasm

Spinal Cord Pnet

Spinal Cord Primitive Neuroectodermal Tumor

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations

Severe Congenital Encephalopathy Due To Mecp2 Mutation

Severe Neonatal-Onset Encephalopathy With Microcephaly

Encephalopathy, Neonatal Severe

Neonatal Severe Encephalopathy Due To Mecp2 Mutations

Mecp2-Related Severe Neonatal Encephalopathy

Methyl-Cytosine Phosphate Guanine Binding Protein 2 Related Severe Neonatal Encephalopathy

Severe Neonatal Encephalopathy Due To Mecp2 Mutations

ENS-MECP2

Encephalopathy, Neonatal, Severe

Spinal Cord Neuroblastoma

Neuroblastoma Of The Spinal Cord

Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Felis catus PRMT1 VGNC VGNC:103742
Macaca mulatta PRMT1 VGNC VGNC:97809
Canis familiaris PRMT1 VGNC VGNC:44995
Mus musculus PRMT1 MGD MGI:107846
Bos taurus PRMT1 VGNC VGNC:52239
Rattus norvegicus PRMT1 RGD RGD:62020