| Type | Description |
|---|---|
| Definition | mitochondrial ribosomal protein S7 |
| Date | Results | Publications |
|---|---|---|
| 2016-02-06 11:46:00 | Study identified MRPS7 mutation as a novel cause of congenital sensorineural deafness and progressive hepatic and renal failure. | 25556185 |
| 2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
| Type | IDs |
|---|---|
| Synonymous | COXPD34, MRP-S, MRP-S7, RP-S7, RPMS7, S7mt, bMRP27a |
| Gene |
UniProtKB-ID:
RT07_HUMAN,
A0A024R8L0_HUMAN
UniprotKB:
Q9Y2R9,
A0A024R8L0
UniParc:
UPI000013CBA7
EMBL:
BC000241,
AK222995,
AF077042,
AC022211,
CH471099,
AK313854
Ensembl:
ENSG00000125445
KO:
hsa:51081
|
| Nucleutide sequences |
EMBL-CDS:
AAH00241.1,
BAG36582.1,
AAD27775.1,
BAD96715.1,
EAW89261.1,
EAW89262.1
Gene_ORFName:
hCG_27458
Ensembl_TRS:
ENST00000245539
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000245539
RefSeq:
NP_057055.2
|
| Others |
UniRef100:
UniRef100_Q9Y2R9
UniRef90:
UniRef90_Q9Y2R9
UniRef50:
UniRef50_Q9Y2R9
UniGene:
Hs.71787
CCDS:
CCDS11718.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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