GNMT - glycine N-methyltransferase Gene

Also Known as HEL-S-182mP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 27232

About GNMT

Cytogenetic location: 6p21.1 Genomic coordinates (GRCh38): 6:42,960,754-42,963,880 (from NCBI)

This gene has 1 transcript (splice variant), 201 orthologues and is associated with 2 phenotypes. Biased expression in liver (RPKM 73.9), pancreas (RPKM 27.4) and 1 other tissue.

Summary

The protein encoded by this gene is an enzyme that catalyzes the conversion of S-adenosyl-L-methionine (along with glycine) to S-adenosyl-L-homocysteine and sarcosine. This protein is found in the cytoplasm and acts as a homotetramer. Defects in this gene are a cause of GNMT deficiency (hypermethioninemia). Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between the upstream CNPY3 (canopy FGF signaling regulator 3) gene and this gene and is represented with GeneID:107080644. [provided by RefSeq, Jan 2016]

GNMT Products (2)

mRNA Protein Name
NM_001318865.2 NP_001305794.1 glycine N-methyltransferase isoform 2
NM_018960.6 NP_061833.1 glycine N-methyltransferase isoform 1
Molecular Function GO Annotation Evidence Références Source
enables glycine N-methyltransferase activity IDA
IDA: Inferred from direct assay
15340920 GOA
enables glycine binding IDA
IDA: Inferred from direct assay
15340920 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence Références Source
involved in S-adenosylmethionine metabolic process IDA
IDA: Inferred from direct assay
15340920 GOA
involved in protein homotetramerization IPI
IPI: Inferred from physical interaction
15340920 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

GNMT Protein Structure

Methyltransf_18

Methyltransf_18: Methyltransferase domain (59 - 176)

  • 0
  • 100
  • 200
  • 295 a.a.
Protein Preferred Names Protein Names

glycine N-methyltransferase

  • epididymis secretory sperm binding protein Li 182mP

GNMT Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
GNMT Q14749 SNRNP200 Homo sapiens O75643 32296183
Intra
GNMT Q14749 SNRNP200 Homo sapiens O75643 32296183
Intra
GNMT Q14749 DRC12 Homo sapiens Q494R4-2 32296183
Intra
GNMT Q14749 DRC12 Homo sapiens Q494R4-2 32296183
Intra
GNMT Q14749 DRC12 Homo sapiens Q494R4-2 32296183
Intra
GNMT Q14749 GAGE2B Homo sapiens Q13066 32296183
Intra
GNMT Q14749 GAGE2B Homo sapiens Q13066 32296183
Intra
GNMT Q14749 GABRQ Homo sapiens Q9UN88 32296183
Intra
GNMT Q14749 GABRQ Homo sapiens Q9UN88 32296183
Intra
GNMT Q14749 GABRQ Homo sapiens Q9UN88 32296183
Intra
GNMT Q14749 SRD5A2 Homo sapiens P31213 32296183
Intra
GNMT Q14749 SRD5A2 Homo sapiens P31213 32296183
Intra
GNMT Q14749 TRIM35 Homo sapiens Q9UPQ4-2 32296183
Intra
GNMT Q14749 TRIM35 Homo sapiens Q9UPQ4-2 32296183
Intra
GNMT Q14749 TRIM35 Homo sapiens Q9UPQ4-2 32296183
Intra
GNMT Q14749 CTNS Homo sapiens O60931-2 32296183
Intra
GNMT Q14749 CTNS Homo sapiens O60931-2 32296183
Intra
GNMT Q14749 FRG1 Homo sapiens Q14331 32296183
Intra
GNMT Q14749 FRG1 Homo sapiens Q14331 32296183
Intra
GNMT Q14749 COX7B Homo sapiens P24311 32296183
Intra
GNMT Q14749 COX7B Homo sapiens P24311 32296183
Intra
GNMT Q14749 ZNF337 Homo sapiens Q9Y3M9 32296183
Intra
GNMT Q14749 ZNF337 Homo sapiens Q9Y3M9 32296183
Intra
GNMT Q14749 ZNF337 Homo sapiens Q9Y3M9 32296183
Intra
GNMT Q14749 NTAQ1 Homo sapiens Q96HA8 31515488
Intra
GNMT Q14749 NTAQ1 Homo sapiens Q96HA8 32296183
Intra
GNMT Q14749 ARRB1 Homo sapiens P49407 26871637
Intra
GNMT Q14749 ARRB1 Homo sapiens P49407 26871637
Intra
GNMT Q14749 ARRB1 Homo sapiens P49407 21988832
Intra
GNMT Q14749 ARRB1 Homo sapiens P49407 21988832
Intra
GNMT Q14749 ARRB1 Homo sapiens P49407 26871637
Intra
GNMT Q14749 ARRB1 Homo sapiens P49407
Y2H
21988832
Intra
GNMT Q14749 GNMT Homo sapiens Q14749 16189514
Intra
GNMT Q14749 GNMT Homo sapiens Q14749 31515488
Intra
GNMT Q14749 GNMT Homo sapiens Q14749 26871637
Intra
GNMT Q14749 GNMT Homo sapiens Q14749 26871637
Intra
GNMT Q14749 GNMT Homo sapiens Q14749 25502805
Intra
GNMT Q14749 GNMT Homo sapiens Q14749 26871637
Intra
GNMT Q14749 HPRT1 Homo sapiens P00492 32296183
Intra
GNMT Q14749 HPRT1 Homo sapiens P00492 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant GNMT Proteins

Cat. No. Nom du produit Accession Pureté
HY-P70835 GNMT Protein, Human (His) Q14749 (M1-D295) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Glycine N-Methyltransferase Deficiency
  • GNMT DEFICIENCY

  • Hypermethioninemia Due To Glycine N-Methyltransferase Deficiency

  • Hypermethioninemia Due To Gnmt Deficiency

  • Hypermethioninemia

  • Hepatic Methionine Adenosyltransferase Deficiency

Hypermethioninemia
  • Hepatic Methionine Adenosyltransferase Deficiency

  • Deficiency Of Methionine Adenosyltransferase

  • Glycine N-Methyltransferase Deficiency

  • Met

  • S-Adenosylhomocysteine Hydrolase Deficiency

  • Gnmt Deficiency

  • Mat Deficiency

  • Methionine Adenosyltransferase Deficiency

  • Methioninemia

  • Deficiency Of Acetyl-Coa Acetyltransferase

Liver Disease
  • Liver Failure

  • Liver Diseases

  • Abnormality Of The Liver

  • Liver Dysfunction

  • Disorder Of Liver

  • Hepatic Disorder

  • Hepatic Disease

  • Disease Of Bilirubin Metabolism

  • Disorder Of Bilirubin Metabolism

  • Liver Decompensation

  • Liver Function Failure

  • Hepatic Failure Nos

  • Liver Failure Nos

  • End Stage Liver Disease

  • Decompensated Liver Failure

  • Decompensation Of Liver Function

  • Hepatic Decompensation

  • Hepatic Insufficiency

  • Liver Cell Necrosis With Hepatic Failure

  • Liver Insufficiency

  • Decompensated Liver Disease

  • End Stage Liver Failure

  • Liver Necrosis With Hepatic Failure

Glycogen Storage Disease
  • Glycogenosis

  • Glycogenoses

  • Gsd

  • Storage Disease, Glycogen

  • Gsd - [Glycogen Storage Disease]

  • Glycogen Thesaurismosis

  • Diffuse Glycogenosis

  • Generalised Glycogen Storage Disease

  • Generalised Glycogenosis

  • Generalised Glycogen Storage Disease Of Infants

  • Glycogen Synthase Deficiency

Renal Pelvis Transitional Cell Carcinoma
  • Urothelial Cell Carcinoma Of Renal Pelvis

  • Renal Pelvis Urothelial Carcinoma

  • Transitional Cell Carcinoma Of Renal Pelvis

Hepatocellular Carcinoma
  • Liver Cancer

  • Primary Liver Cancer

  • HCC

  • Hepatoma

  • Malignant Neoplasm Of Liver

  • Liver Neoplasms

  • Cancer, Hepatocellular

  • Liver Cell Carcinoma

  • Lcc

  • Hepatoblastoma, Somatic

  • Hepatic Cancer

  • Primary Malignant Neoplasm Of Liver

  • Rare Tumor Of Liver And Intrahepatic Biliary Tract

  • Hepatocellular Carcinoma, Somatic

  • Hepatocellular Carcinoma, Childhood Type, Somatic

  • Hepatocellular Cancer, Somatic

  • Ca Liver - Primary

  • Hepatic Neoplasm

  • Malignant Hepato-Biliary Neoplasm

  • Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

  • Malignant Neoplasm Of Liver, Primary

  • Malignant Tumor Of Liver

  • Neoplasm Of Liver

  • Non-Resectable Primary Hepatic Malignant Neoplasm

  • Resectable Malignant Neoplasm Of Liver

  • Resectable Malignant Neoplasm Of The Liver

  • Primary Liver Carcinoma

  • Primary Malignant Liver Neoplasm

  • Primary Cancer Of Liver

  • Primary Tumor Of The Liver

  • Rare Tumor Of Liver And Ibt

  • Hepatocellular Cancer

  • Neoplasm Of The Liver

  • Carcinoma, Hepatocellular

  • Hepatomas

  • Liver Neoplasm

  • Liver Carcinoma

  • Liver And Intrahepatic Biliary Tract Carcinoma

  • Malignant Hepatobiliary Neoplasm

  • Adult Primary Hepatocellular Carcinoma

  • Hepatoblastoma

  • Carcinoma Of Liver

  • Malignant Liver Tumour

  • Malignant Hepatic Tumour

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 GNMT VGNC VGNC:62628
Rattus norvegicus GNMT RGD RGD:2719
Canis familiaris GNMT VGNC VGNC:41329
Mus musculus GNMT MGD MGI:1202304
Macaca mulatta GNMT VGNC VGNC:73099
Bos taurus GNMT VGNC VGNC:29475
Others GNMT NCBI