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Gene : ASMT Homo sapiens

Name  ? acetylserotonin O-methyltransferase Cytological Location  Xp22.33 and Yp11.2
Brief Description  acetylserotonin O-methyltransferase
description  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]
  • synonyms:
  • HIOMT,
  • HIOMT,
  • HIOMTY,
  • NM_004043,
  • ASMT,
  • ASMTY,
  • HGNC:750,
  • HIOMTY,
  • uc065cod.1,
  • ASMTY,
  • M83779,
  • OTTHUMG00000021065
  • identifiers:
  • 438,
  • ENSG00000196433,
  • ASMT

Genome feature

Region: gene ? Length: 47627  
Location: X:1595455-1643081 Cyto location: Xp22.33 and Yp11.2


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

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

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

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Other

60 SN Ps

5 Cross References

15 Data Sets

4 Homologues

0 Located Features

90 Rna Seq Results