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23026 MYO16

23026

MYO16

myosin XVI

protein-coding

Homo sapiens

基因描述

Type Description
Definition myosin XVI

研究结论

Date Results Publications
2016-04-16 11:47:00 KIRREL3 interacting proteins MAP1B and MYO16 are potential candidates for intellectual disability and autism spectrum disorder. 25902260
2014-10-11 10:07:00 This study suggest that common variation within MYO16 may contribute to the genetic liability to schizophrenia. 24141571
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 19913121
2010-09-15 22:06:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086
2010-06-30 22:07:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614

名称对应

Type IDs
Synonymous MYAP3, MYR8, Myo16b, NYAP3, PPP1R107
Gene
UniProtKB-ID: MYO16_HUMAN, F8W883_HUMAN
UniprotKB: Q9Y6X6, F8W883
UniParc: UPI0001526370, UPI0000458817, UPI0001526371, UPI0000160FF2, UPI00002375AE
EMBL: BC146791, AL834447, AL161431, AK095691, AB290159, KF455825, AL390918, AL136132, AL512648, AL353143, AB020672, AK127806, AL157771
Ensembl: ENSG00000041515
KO: hsa:23026
Nucleutide sequences
EMBL-CDS: BAG06713.1, BAA74888.2, BAC87143.1, CAD39107.2, AAI46792.1, BAC04608.1
Ensembl_TRS: ENST00000356711, ENST00000251041, ENST00000457511
Protein sequencees
Ensembl_PRO: ENSP00000251041, ENSP00000349145, ENSP00000401633
RefSeq: NP_001185879.1, NP_055826.1, XP_011519364.1
Others
UniRef100: UniRef100_Q9Y6X6
UniRef90: UniRef90_Q9Y6X6
UniRef50: UniRef50_Q9ERC1
UniGene: Hs.656587
CCDS: CCDS32008.1

全选

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研究热度

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