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9801 MRPL19

9801

MRPL19

mitochondrial ribosomal protein L19

protein-coding

Homo sapiens

基因描述

Type Description
Definition mitochondrial ribosomal protein L19

研究结论

Date Results Publications
2019-02-16 10:37:00 Candidate gene MRPL19 is involved in the development of Reading disorder. 29566979
2016-01-30 10:33:00 MRPL19 was initially implicated in dyslexia through family-based studies. 25448322
2013-11-16 11:54:00 study failed to show any association of MRPL19 SNPs with developmental dyslexia in an Indian population. 23954868
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20877624
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20846247

名称对应

Type IDs
Synonymous L19mt, MRP-L15, MRP-L19, MRPL15, RLX1, RPML15
Gene
UniProtKB-ID: RM19_HUMAN
UniprotKB: P49406
UniParc: UPI00002087A4
EMBL: AB051621, BC030144, D14660, AC005034
Ensembl: ENSG00000115364
KO: hsa:9801
Nucleutide sequences
EMBL-CDS: BAA03494.1, AAH30144.2, AAY14972.1, BAB54949.1
Ensembl_TRS: ENST00000409374, ENST00000393909
Protein sequencees
Ensembl_PRO: ENSP00000387284, ENSP00000377486
RefSeq: NP_055578.2
Others
UniRef100: UniRef100_P49406
UniRef90: UniRef90_P49406
UniRef50: UniRef50_P49406
UniGene: Hs.44024
CCDS: CCDS1960.2

全选

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研究热度

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