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438 ASMT

438

ASMT

acetylserotonin O-methyltransferase

protein-coding

Homo sapiens

基因描述

Type Description
Definition acetylserotonin O-methyltransferase

研究结论

Date Results Publications
2020-04-06 08:39:00 The pseudoautosomal region of human X and Y chromosome encoded ASMT protein was predicted to interact with many small molecules than that of interacting proteins. 26279084
2019-02-16 10:34:00 Low HIOMT expression is associated with lung cancer. 29794137
2016-12-17 10:19:00 Even when considering only high-grade glioma patients, a low ASMT:CYP1B1 value, which suggests decreased melatonin and enhanced aggressiveness, was strongly associated with poor survival. Overall, our data reveal the prognostic value of the melatonergic system of gliomas and provide insights into the therapeutic role of melatonin. 26510398
2016-06-11 10:05:00 two single nucleotide polymorphisms (rs4446909 and rs5989681)in the promoter of ASMT do not contribute to the pathogenesis of schizophrenia in Chinese-Han subjects 26154813
2015-08-15 11:24:00 results indicate that expression of sleep onset delay relates to melatonin pathway genes. 25059483

名称对应

Type IDs
Synonymous ASMTY, HIOMT, HIOMTY
Gene
UniProtKB-ID: ASMT_HUMAN, A0A024RBT9_HUMAN, X5D784_HUMAN
UniprotKB: P46597, A0A024RBT9, X5D784
UniParc: UPI00001AEDD0, UPI0000000C2E, UPI000012C726
EMBL: AL683807, BC001620, U11097, U11094, KJ534775, U11098, CH471074, AK314922, U11089, M83779, U11093, U11091, U11096, U11090, U11095, U11092
Ensembl: ENSG00000196433
KO: hsa:438
Nucleutide sequences
EMBL-CDS: AAA75291.1, AAA75290.1, AAA75289.1, AAA58583.1, BAG37430.1, AAH01620.1, AAA58582.1, AAA17020.1, EAW98686.1, EAW98685.1, AHW56415.1
Gene_ORFName: hCG_1981394
Ensembl_TRS: ENST00000381241, ENST00000381233, ENST00000381229
Protein sequencees
Ensembl_PRO: ENSP00000370639, ENSP00000370627, ENSP00000370631
RefSeq: NP_001164510.1, NP_001164509.1, NP_004034.2
Others
UniRef100: UniRef100_P46597-2, UniRef100_A0A024RBT9, UniRef100_P46597
UniRef90: UniRef90_P46597, UniRef90_P46597-2
UniRef50: UniRef50_P46597, UniRef50_P46597-2
UniGene: Hs.522572
CCDS: CCDS55364.1, CCDS14117.1

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