Homo sapiens Gene: ASMT | |||||||||||||||
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Summary | |||||||||||||||
InnateDB Gene | IDBG-40457.5 | ||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||
Gene Symbol | ASMT | ||||||||||||||
Gene Name | acetylserotonin O-methyltransferase | ||||||||||||||
Synonyms | ASMTY; HIOMT; HIOMTY | ||||||||||||||
Species | Homo sapiens | ||||||||||||||
Ensembl Gene | ENSG00000196433 | ||||||||||||||
Encoded Proteins |
acetylserotonin O-methyltransferase
acetylserotonin O-methyltransferase
acetylserotonin O-methyltransferase
acetylserotonin O-methyltransferase
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Protein Structure | |||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||
Entrez Gene | |||||||||||||||
Summary |
This gene belongs to the methyltransferase superfamily, and is located in the pseudoautosomal region (PAR) at the end of the short arms of the X and Y chromosomes. The encoded enzyme catalyzes the final reaction in the synthesis of melatonin, and is abundant in the pineal gland. Alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Jan 2010] |
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Gene Information | |||||||||||||||
Type | Protein coding | ||||||||||||||
Genomic Location | Chromosome X:1615001-1643081 | ||||||||||||||
Strand | Forward strand | ||||||||||||||
Band | p22.33 | ||||||||||||||
Transcripts |
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Interactions | |||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||
No orthologs found for this gene | |||||||||||||||
Pathways | |||||||||||||||
NETPATH | |||||||||||||||
REACTOME |
Serotonin and melatonin biosynthesis pathway
Amine-derived hormones pathway
Metabolism of amino acids and derivatives pathway
Metabolism pathway
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KEGG |
Tryptophan metabolism pathway
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INOH |
Tryptophan degradation pathway
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PID NCI | |||||||||||||||
Cross-References | |||||||||||||||
SwissProt | P46597 | ||||||||||||||
TrEMBL | A0A024RBT9 I7HFW6 X5D2A4 X5D784 | ||||||||||||||
UniProt Splice Variant | |||||||||||||||
Entrez Gene | 438 | ||||||||||||||
UniGene | |||||||||||||||
RefSeq | NM_001171038 NM_001171039 NM_004043 | ||||||||||||||
HUGO | HGNC:750 | ||||||||||||||
OMIM | 300015 402500 | ||||||||||||||
CCDS | CCDS14117 CCDS55364 | ||||||||||||||
HPRD | |||||||||||||||
IMGT | |||||||||||||||
EMBL | AK314922 AL683807 BC001620 CH471074 KJ534774 KJ534775 KJ534776 M83779 U11089 U11090 U11091 U11092 U11093 U11094 U11095 U11096 U11097 U11098 | ||||||||||||||
GenPept | AAA17020 AAA58582 AAA58583 AAA75289 AAA75290 AAA75291 AAH01620 AHW56414 AHW56415 AHW56416 BAG37430 EAW98685 EAW98686 | ||||||||||||||
RNA Seq Atlas | 438 | ||||||||||||||