INMT indolethylamine N-methyltransferase

Information
Symbol
INMT
Type
protein-coding
Description
indolethylamine N-methyltransferase
Entrez Gene ID
11185
Genome
hg19
Position
chr7:30,791,751-30,797,218
Genome
hg38
Position
chr7:30,752,135-30,757,602
MIM
604854 OMIM
HGNC
HGNC:6069 HGNC
Ensembl
ENSG00000241644 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 14
Likely benign 0 4
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
62
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM TEMT
MIM 604854 OMIM
HGNC HGNC:6069 HGNC
Ensembl ENSG00000241644 Ensembl
AllianceGenome HGNC:6069
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409539.1 hg38 chr7 30,752,137 30,755,851 3,715
ENST00000013222.5 hg38 chr7 30,752,135 30,757,602 5,468
ENST00000013222.5 hg19 chr7 30,791,751 30,797,218 5,468
ENST00000409539.1 hg19 chr7 30,791,753 30,795,467 3,715
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