Type | Description |
---|---|
Definition | mitochondrial ribosomal protein L19 |
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 |
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
|
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