Type | Description |
---|---|
Definition | UDP galactosyltransferase 8A |
Date | Results | Publications |
---|---|---|
2011-06-25 14:21:00 | Our study showed that the additional deletion of Fa2h does not obviously affect the phenotype of Cgt-/- mice. This suggests that HFA-GlcCer and HFA-sphingomyelin do not functionally compensate the loss of HFA-GalCer in Cgt-/- mice. | 21366909 |
2010-03-15 11:10:00 | Ugcg and Ugt8a deficient oligodendroglial did not exhibit any phenotypic or myelin structural abnormalities; abundant and structurally intact myelin can form in their absence | 19705459 |
2010-02-22 12:26:00 | This study provides new insights into the changes that occur in the composition/distribution of myelin proteins in mice lacking ceramide galactosyltransferase. | 19878436 |
2010-01-21 00:00:00 | Our results indicate that loss of CGT in oligodendrocytes is exclusively responsible for the myelin structural deficits, demyelination, and behavioral abnormalities in CGT-deficient mice. | 15968630 |
Type | IDs |
---|---|
Synonymous | AI850488, AW455908, Cgt, Ugt8, mCerGT |
Gene |
UniProtKB-ID:
CGT_MOUSE
UniprotKB:
Q64676
UniParc:
UPI0000026020
EMBL:
U48892,
X92122,
X92124,
AK137364,
U48896,
X92126,
U48894,
BC016885,
U48893,
X92177,
X92123,
X92125
Ensembl:
ENSMUSG00000032854
KO:
mmu:22239
|
Nucleutide sequences |
EMBL-CDS:
AAH16885.1,
CAA63091.1,
CAA63090.1,
BAE23325.1,
AAC53576.1
Ensembl_TRS:
ENSMUST00000198610,
ENSMUST00000057944
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000050852,
ENSMUSP00000143605
RefSeq:
XP_006501373.1,
NP_035804.2
|
Others |
UniRef100:
UniRef100_Q64676
UniRef90:
UniRef90_Q16880
UniRef50:
UniRef50_Q16880
UniGene:
Mm.306021
CCDS:
CCDS17821.1
|
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Refseq |
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