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Gene : INMT Homo sapiens

Name  ? indolethylamine N-methyltransferase Cytological Location  7p14.3
Brief Description  indolethylamine N-methyltransferase
Description  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 transcription also exists between this gene and the downstream MINDY4 (aka FAM188B) gene. In rodents and other mammals such as cetartiodactyla this gene is in the opposite orientation compared to its orientation in human and other primates and this gene appears to have been lost in carnivora and chiroptera. [provided by RefSeq, Jul 2019]
  • synonyms:
  • uc003tbs.1,
  • NM_006774,
  • OTTHUMG00000167163,
  • HGNC:6069,
  • INMT,
  • TEMT
  • identifiers:
  • 11185,
  • ENSG00000241644,
  • INMT

Genome feature

Region: gene ? Length: 5468  
Location: 7:30752135-30757602 Cyto location: 7p14.3


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Function

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

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SNPs

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Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

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Other

987 SN Ps

5 Cross References

16 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results