INMT Back

indolethylamine N-methyltransferase

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of INMT

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 FAM188B (family with sequence similarity 188, member B) gene.

Community Annotation of INMT Add / Edit INMT: Annotations

No community annotations yet for INMT.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

INMT is highly significantly mutated in
(none)
INMT is significantly mutated in
(none)
INMT is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for INMT