Type | Description |
---|---|
Definition | protein arginine methyltransferase 8 |
Date | Results | Publications |
---|---|---|
2018-05-05 10:17:00 | PRMT8 in human embryonic stem cells plays an important role not only in maintaining pluripotency but also in controlling mesodermal differentiation. | 28543863 |
2016-08-20 11:43:00 | Biochemical, biophysical and mutagenesis experiments demonstrated that hPRMT8 forms an octamer in solution. | 26876602 |
2014-01-18 10:44:00 | Mutational defects in PRMT8 is not the cause of frontotemporal lobar degeneration. | 23635657 |
2013-12-28 10:44:00 | automethylation of the N terminus likely regulates PRMT8 activity by decreasing the affinity of the enzyme for AdoMet | 23946480 |
2013-11-16 11:15:00 | wild type FUS (FUS-WT) specifically interacts with protein arginine methyltransferases 1 and 8 (PRMT1 and PRMT8) and undergoes asymmetric dimethylation | 23620769 |
Type | IDs |
---|---|
Synonymous | HRMT1L3, HRMT1L4 |
Gene |
UniProtKB-ID:
ANM8_HUMAN,
Q59GT2_HUMAN
UniprotKB:
Q9NR22,
Q59GT2
UniParc:
UPI0000E22F84,
UPI00004F6B3D,
UPI00005B2E00
EMBL:
AC005908,
AC005831,
AF263539,
AC005925,
BC022458,
AB209027,
AK315619
Ensembl:
ENSG00000111218
KO:
hsa:56341
|
Nucleutide sequences |
EMBL-CDS:
AAF91390.1,
AAH22458.2,
BAG37987.1,
BAD92264.1
Ensembl_TRS:
ENST00000452611,
ENST00000382622
|
Protein sequencees |
Ensembl_PRO:
ENSP00000414507,
ENSP00000372067
RefSeq:
XP_016875133.1,
XP_016875134.1,
NP_001243465.1,
NP_062828.3,
XP_024304827.1
|
Others |
UniRef100:
UniRef100_Q59GT2,
UniRef100_Q9NR22
UniRef90:
UniRef90_Q9NR22,
UniRef90_Q59GT2
UniRef50:
UniRef50_A0A287BTE0,
UniRef50_Q9NR22
UniGene:
Hs.504530
CCDS:
CCDS8521.2,
CCDS58200.1
|
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