Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11185
Gene name Gene Name - the full gene name approved by the HGNC.
Indolethylamine N-methyltransferase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
INMT
Synonyms (NCBI Gene) Gene synonyms aliases
TEMT
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p14.3
Summary Summary of gene provided in NCBI Entrez Gene.
N-methylation of endogenous and xenobiotic compounds is a major method by which they are degraded. This gene encodes an enzyme that N-methylates indoles such as tryptamine. Alternative splicing results in multiple transcript variants. Read-through transcr
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT697177 hsa-miR-4761-5p HITS-CLIP 23313552
MIRT697178 hsa-miR-1226-3p HITS-CLIP 23313552
MIRT697175 hsa-miR-4733-3p HITS-CLIP 23313552
MIRT697176 hsa-miR-4768-3p HITS-CLIP 23313552
MIRT697174 hsa-miR-4459 HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004790 Function Thioether S-methyltransferase activity IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005829 Component Cytosol IBA 21873635
GO:0005829 Component Cytosol IDA 10552930
GO:0008170 Function N-methyltransferase activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604854 6069 ENSG00000241644
Protein
UniProt ID O95050
Protein name Indolethylamine N-methyltransferase (Indolamine N-methyltransferase) (EC 2.1.1.49) (EC 2.1.1.96) (Aromatic alkylamine N-methyltransferase) (Amine N-methyltransferase) (Arylamine N-methyltransferase) (Thioether S-methyltransferase) (TEMT)
Protein function Functions as a thioether S-methyltransferase and is active with a variety of thioethers and the corresponding selenium and tellurium compounds, including 3-methylthiopropionaldehyde, dimethyl selenide, dimethyl telluride, 2-methylthioethylamine,
PDB 2A14
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01234 NNMT_PNMT_TEMT 1 259 NNMT/PNMT/TEMT family Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. The highest levels were in thyroid, adrenal gland, adult and fetal lung. Intermediate levels in heart, placenta, skeletal muscle, testis, small intestine, pancreas, stomach, spinal cord, lymph node and trachea. Very l
Sequence
Sequence length 263
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Tryptophan metabolism
Selenocompound metabolism
Metabolic pathways
 
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Urolithiasis Urolithiasis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Atrial Fibrillation Associate 33062700
Carcinoma Hepatocellular Inhibit 37202783
Lung Neoplasms Associate 30177858
Nephrolithiasis Associate 22396660
Obesity Associate 24696292
Pregnancy in Diabetics Associate 24696292
Prostatic Neoplasms Associate 22075945