ASMTL (GeneID: 8623) | Homo sapiens
Description: acetylserotonin O-methyltransferase like [Source:HGNC Symbol;Acc:HGNC:751]
Synonyms: ASMTLX, ASTML, ASMTLY
Other ID(s): ENSG00000169093, HGNC:751
Protein Accession Numbers: ENST00000381333, NP_004183, ENST00000534940, ENST00000381317, NP_001166945, ENST00000416733, NP_001166944
Statistics: gnomAD(813) COSMIC(278) PTM(40)
Post translational modifications (PTM) by Type

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000381317 You are here now! ENST00000381333 ENST00000416733 ENST00000534940 NP_001166944 NP_001166945 NP_004183 You are here now!


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00891 Methyltransf_2 O-methyltransferase domain 388-600 CL0063 NADP_Rossmann Homo sapiens
PF02545 Maf Maf-like protein 14-211 CL0269 Maf Homo sapiens
PF16864 Dimerisation2 Dimerisation domain 287-371 CL0123 HTH Homo sapiens

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Leukemia, Myelocytic, Acute Neoplasms ; 0.857 0.103
Acute Myeloid Leukemia, M1 Neoplasms ; 0.857 0.103
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.857 0.103
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.857 0.103
NO RESULT FOUND
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