Entity Details

Primary name HNMT
Entity type gene
Source Source Link

Details

PrimaryID3176
RefseqGeneNG_012966
SymbolHNMT
Namehistamine N-methyltransferase
Chromosome2
Location2q22.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsHNMT_HUMAN

GO terms

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GOName
GO:0001692 histamine metabolic process
GO:0001695 histamine catabolic process
GO:0002347 response to tumor cell
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005829 cytosol
GO:0006548 histidine catabolic process
GO:0006972 hyperosmotic response
GO:0007420 brain development
GO:0007585 respiratory gaseous exchange by respiratory system
GO:0014075 response to amine
GO:0032259 methylation
GO:0035902 response to immobilization stress
GO:0042220 response to cocaine
GO:0043005 neuron projection
GO:0046539 histamine N-methyltransferase activity
GO:0051384 response to glucocorticoid
GO:0070062 extracellular exosome
GO:0070555 response to interleukin-1

Diseases

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Disease IDSourceNameDescription
616739 OMIMMental retardation, autosomal recessive 51 (MRT51)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting distinct genetic loci, including the gene represented in this entry.

Interactions

6 interactions

InteractorPartnerSourcesPublicationsLink
HNMTCAMK2DBioGRID, IntAct21988832 details
HNMTTERF1bhf-ucl, BioGRID21044950 details
HNMTTINF2bhf-ucl, BioGRID21044950 details
HNMTPOT1bhf-ucl, BioGRID21044950 details
HNMTCLK1BioGRID26167880 details
HNMTDSPBioGRID22939629 details