Type | Description |
---|---|
Definition | fragile X mental retardation 1 |
Date | Results | Publications |
---|---|---|
2021-04-17 13:14:00 | Depletion of Mitochondrial Components from Extracellular Vesicles Secreted from Astrocytes in a Mouse Model of Fragile X Syndrome. | 33401721 |
2021-04-13 10:14:00 | Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice. | 33692361 |
2021-04-03 13:35:00 | Effects of clonidine on progressive ratio schedule performance in Fmr1 knockout mice. | 33449137 |
2021-03-27 14:41:00 | Single-Cell and Neuronal Network Alterations in an In Vitro Model of Fragile X Syndrome. | 30958540 |
2021-03-27 14:40:00 | FMRP Control of Ribosome Translocation Promotes Chromatin Modifications and of Neuronal Genes Linked to Autism. | 32234480 |
Type | IDs |
---|---|
Synonymous | FMRP, Fmr-1 |
Gene |
UniProtKB-ID:
Q547R0_MOUSE,
Q6AXB7_MOUSE,
Q8BPK8_MOUSE,
E9QAT0_MOUSE,
E9QNF5_MOUSE
UniprotKB:
Q547R0,
Q6AXB7,
Q8BPK8,
E9QAT0,
E9QNF5
UniParc:
UPI00001F8482,
UPI0000000F20,
UPI00000EB079,
UPI0000564F53,
UPI00001C6490
EMBL:
BC079671,
AF461114,
AC055766,
AK053829
Ensembl:
ENSMUSG00000000838
KO:
mmu:14265
|
Nucleutide sequences |
EMBL-CDS:
AAL66364.1,
AAH79671.1,
BAC35545.1
Ensembl_TRS:
ENSMUST00000088546,
ENSMUST00000114653,
ENSMUST00000114657
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000085906,
ENSMUSP00000110301,
ENSMUSP00000110305
RefSeq:
NP_001361648.1,
XP_006527873.1,
NP_001277353.1,
XP_006527877.1,
NP_032057.2,
XP_006527876.1
|
Others |
UniRef100:
UniRef100_E9QNF5,
UniRef100_Q6AXB7,
UniRef100_E9QAT0,
UniRef100_E9QAS8,
UniRef100_Q547R0
UniRef90:
UniRef90_Q06787,
UniRef90_G1NTN1,
UniRef90_P35922-2
UniRef50:
UniRef50_Q06787-6,
UniRef50_Q06787-9,
UniRef50_Q06787
UniGene:
Mm.3451
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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