Type | Description |
---|---|
Definition | MGAT4 family member C |
Date | Results | Publications |
---|---|---|
2021-03-27 14:40:00 | Association of MGAT4C with major neurocognitive disorder in the Mexican population. | 33581268 |
2010-06-30 22:06:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2009-04-01 21:31:00 | Observational study of gene-disease association. (HuGE Navigator) | 19240061 |
Type | IDs |
---|---|
Synonymous | GNTIVH, HGNT-IV-H |
Gene |
UniProtKB-ID:
MGT4C_HUMAN
UniprotKB:
Q9UBM8
UniParc:
UPI00001B002C,
UPI00017A7C09
EMBL:
AB024729,
AB024911,
AB024730,
AC025157,
AC079596,
BC064141,
AC079865,
AC139663,
AC016993,
AC010196,
AC093122,
BC026068,
AC087887,
AK299253,
AC128681,
AC139697
Ensembl:
ENSG00000283530,
ENSG00000182050,
ENSG00000285137
KO:
hsa:25834
|
Nucleutide sequences |
EMBL-CDS:
BAA83074.1,
BAA83087.1,
BAA83075.1,
AAH26068.1,
BAG61284.1,
AAH64141.1
Ensembl_TRS:
ENST00000644829,
ENST00000643295,
ENST00000637362,
ENST00000636211,
ENST00000621808,
ENST00000646655,
ENST00000645144,
ENST00000552808,
ENST00000611864,
ENST00000638103,
ENST00000637661,
ENST00000548651,
ENST00000636626,
ENST00000620241,
ENST00000646486
|
Protein sequencees |
Ensembl_PRO:
ENSP00000478300,
ENSP00000447253,
ENSP00000490547,
ENSP00000494369,
ENSP00000477650,
ENSP00000489751,
ENSP00000481096,
ENSP00000494764,
ENSP00000495724,
ENSP00000489618,
ENSP00000496716,
ENSP00000446647,
ENSP00000490784,
ENSP00000495039,
ENSP00000490416
RefSeq:
NP_001338213.1,
NP_001338212.1,
XP_024304699.1,
XP_016874635.1,
NP_001338216.1,
NP_001338217.1,
XP_024304700.1,
XP_016874632.1,
NP_001338211.1,
NP_001338215.1,
NP_001338220.1,
NP_001338214.1,
XP_011536453.1,
XP_016874633.1,
NP_001338218.1,
NP_037376.2
|
Others |
UniRef100:
UniRef100_Q9UBM8
UniRef90:
UniRef90_Q9UBM8
UniRef50:
UniRef50_Q9UBM8
UniGene:
Hs.589093
CCDS:
CCDS9030.1
|
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Refseq |
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