Type | Description |
---|---|
Definition | CUGBP, Elav-like family member 4 |
Date | Results | Publications |
---|---|---|
2014-06-14 12:25:00 | Celf4 might be regulating alternative early in retinal development. | 23932931 |
2013-05-18 11:05:00 | we suggest that CELF4 deficiency leads to abnormal neuronal function by combining a specific effect on neuronal excitation with a general impairment of synaptic transmission. | 23209433 |
2012-02-25 10:07:00 | Data point strongly to the conclusion that Celf4 deletion primarily from excitatory neurons promotes convulsive seizure phenotypes. | 21745337 |
2010-01-21 00:00:00 | cloning and characterization | 12438720 |
2010-01-21 00:00:00 | Brunol4 deficiency in mice results in a complex seizure phenotype, likely due to the coordinate dysregulation of several molecules, providing a unique new animal model of epilepsy | 17677002 |
Type | IDs |
---|---|
Synonymous | A230070D14Rik, BRUNOL-4, Brul4, Brunol4, C130060B05Rik |
Gene |
UniProtKB-ID:
CELF4_MOUSE
UniprotKB:
Q7TSY6
UniParc:
UPI00000038AD,
UPI0000607EB7,
UPI000019B09F,
UPI0000171B92,
UPI00000EB569,
UPI000024DC4C,
UPI00001C60C5
EMBL:
AK048427,
AC121094,
AF314173,
AK044072,
BC052744,
AK051458,
AF515450,
AC144938,
AC153142,
BC048405
Ensembl:
ENSMUSG00000024268
KO:
mmu:108013
|
Nucleutide sequences |
EMBL-CDS:
AAO22167.1,
AAH48405.1,
BAC31762.1,
AAK00298.1,
BAC34649.1,
AAH52744.1,
BAC33334.1
Ensembl_TRS:
ENSMUST00000223704,
ENSMUST00000225477,
ENSMUST00000025117,
ENSMUST00000224553,
ENSMUST00000115816
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000153326,
ENSMUSP00000025117,
ENSMUSP00000153258,
ENSMUSP00000153226,
ENSMUSP00000111483
RefSeq:
NP_001349254.1,
NP_001349205.1,
NP_001349253.1,
XP_006525576.1,
NP_001139765.1,
NP_001349258.1,
NP_001349257.1,
NP_001349252.1,
NP_001349214.1,
NP_001349238.1,
NP_001349240.1,
NP_001139766.1,
XP_036016832.1,
NP_001349256.1,
NP_001349265.1,
XP_030106129.1,
NP_001349230.1,
NP_001349228.1,
NP_001349251.1,
NP_001139764.1,
NP_001349259.1,
NP_001349245.1,
NP_001349217.1,
NP_001349207.1,
XP_006525574.1,
NP_001349219.1,
NP_001349232.1,
NP_001349210.1,
NP_001349229.1,
NP_001349218.1,
NP_001167545.1,
NP_001349212.1,
NP_001349226.1,
NP_001349211.1,
XP_030106130.1,
NP_001349264.1,
NP_001349266.1,
NP_001349222.1,
NP_001349208.1,
NP_001349255.1,
NP_001349237.1,
NP_001349215.1,
NP_001349260.1,
NP_001349223.1,
NP_001349231.1,
XP_006525578.1,
NP_573458.2,
NP_001349242.1,
NP_001349239.1,
NP_001349244.1,
XP_036016833.1,
XP_006525581.1,
NP_001349221.1,
NP_001349261.1,
XP_006525580.1,
NP_001349263.1,
XP_036016831.1,
NP_001349213.1,
NP_001349209.1,
NP_001349206.1,
NP_001349224.1,
XP_030106128.1,
NP_001349233.1,
NP_001349220.1,
NP_001349204.1
|
Others |
UniRef100:
UniRef100_Q7TSY6
UniRef90:
UniRef90_Q9BZC1
UniRef50:
UniRef50_Q9BZC1
UniGene:
Mm.266435
CCDS:
CCDS89205.1,
CCDS89206.1,
CCDS29106.1,
CCDS89204.1,
CCDS50241.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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