| Type | Description |
|---|---|
| Definition | ribosomal protein L13 |
| Date | Results | Publications |
|---|---|---|
| 2020-06-06 13:25:00 | Using a combination of human genetics and cardiac model systems, RPL13 gene was identified as a new candidate for congenital heart pathogenesis. | 31625562 |
| 2020-04-04 10:45:00 | The identified RPL13 variants cause a human ribosomopathy defined by a rare skeletal dysplasia. | 31630789 |
| 2010-01-21 00:00:00 | Ribosomal protein L13 plays an essential role in the progression of some gastrointestinal malignancies. | 16786168 |
| 2008-12-15 15:41:00 | This protein has been found differentially expressed in the temporal lobe from patients with schizophrenia. | 19034380 |
| Type | IDs |
|---|---|
| Synonymous | BBC1, D16S444E, D16S44E, L13 |
| Gene |
UniProtKB-ID:
RL13_HUMAN,
A8K4C8_HUMAN
UniprotKB:
P26373,
A8K4C8
UniParc:
UPI0000001228,
UPI00020659F7
EMBL:
X64707,
BC007805,
AC092123,
BC007345,
BC020804,
BC013078,
CH471184,
AB062392,
AK127579,
BC007563,
BC027463,
BC093063,
BC004954,
BC010994,
BC106058,
AK290893,
AK297198,
BC063378,
BC014167
Ensembl:
ENSG00000167526
KO:
hsa:6137
|
| Nucleutide sequences |
EMBL-CDS:
AAI06059.1,
AAH14167.1,
AAH07805.1,
CAA45963.1,
AAH93063.1,
AAH13078.1,
AAH63378.1,
AAH07345.1,
BAG59685.1,
AAH20804.1,
AAH27463.1,
AAH07563.1,
AAH10994.1,
AAH04954.1,
BAB93479.1,
BAF83582.1,
BAG54527.1,
EAW66725.1,
EAW66724.1
Gene_ORFName:
OK/SW-cl.46,
hCG_1723872
Ensembl_TRS:
ENST00000567815,
ENST00000452368,
ENST00000311528,
ENST00000393099
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000376811,
ENSP00000307889,
ENSP00000455009,
ENSP00000438959
RefSeq:
NP_001230060.1,
NP_000968.2,
NP_150254.1
|
| Others |
UniRef100:
UniRef100_P26373
UniRef90:
UniRef90_P26373
UniRef50:
UniRef50_P26373
UniGene:
Hs.410817
CCDS:
CCDS58492.1,
CCDS10979.1
|