| Type | Description |
|---|---|
| Definition | retrotransposon Gaglike 1 |
| Date | Results | Publications |
|---|---|---|
| 2020-12-26 13:12:00 | Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes. | 32878913 |
| 2017-03-18 13:19:00 | Paternally expressed 11/Retrotransposon-like 1 (Peg11/Rtl1) knockout (KO) mice show mid- to late fetal lethality or late fetal growth retardation associated with frequent neonatal lethality | 28111885 |
| 2015-10-10 11:38:00 | miR-127 is an essential regulator of Rtl1, mediated by a trans-homologue interaction between reciprocally imprinted genes on the maternally and paternally inherited chromosomes | 26138477 |
| 2010-12-09 14:16:00 | Rtl1, an imprinted gene with preferential expression from the paternal allele, is essential for maintenance of the fetal capillaries. | 18176565 |
| 2010-01-21 00:00:00 | These data support a role for mir-127 and mir-136 in the epigenetic reprogramming of the Rtl1 imprinting process. | 19126398 |
| Type | IDs |
|---|---|
| Synonymous | 6430411K18Rik, Mar, Mart1, Mor1, Peg11 |
| Gene |
UniProtKB-ID:
RTL1_MOUSE,
B4YB44_MOUSE
UniprotKB:
Q7M732,
B4YB44
UniParc:
UPI00001D9712
EMBL:
BK001261,
AC152063,
EU434913,
EU434918
Ensembl:
ENSMUSG00000098639,
ENSMUSG00000085925
KO:
mmu:353326
|
| Nucleutide sequences |
EMBL-CDS:
DAA01153.1,
ACF20051.1,
ACF20046.1
Ensembl_TRS:
ENSMUST00000184423,
ENSMUST00000149046
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000115957,
ENSMUSP00000138988
RefSeq:
XP_030102657.1,
NP_908998.1
|
| Others |
UniRef100:
UniRef100_Q7M732
UniRef90:
UniRef90_Q7M732
UniRef50:
UniRef50_Q7M732
UniGene:
Mm.23062,
Mm.490311
CCDS:
CCDS26170.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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