Type | Description |
---|---|
Definition | calmodulin-lysine N-methyltransferase |
Date | Results | Publications |
---|---|---|
2013-10-19 14:33:00 | Deletion of CAMKMT is associated with Hypotonia-cystinuria syndrome. | 23794250 |
2013-06-15 11:00:00 | The CaM KMT is the major, possibly the single, methyltransferase of calmodulin in human cells with a wide tissue distribution and is a novel Hsp90 client protein. | 23285036 |
2011-07-02 10:03:00 | Calmodulin methyltransferase is an evolutionarily conserved enzyme that trimethylates Lys-115 in calmodulin. | 20975703 |
2010-06-30 22:06:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2010-04-07 21:40:00 | Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) | 20200953 |
Type | IDs |
---|---|
Synonymous | C2orf34, CLNMT, CaM KMT, Cam, KMT |
Gene |
UniProtKB-ID:
CMKMT_HUMAN,
D6W5A4_HUMAN
UniprotKB:
Q7Z624,
D6W5A4
UniParc:
UPI000006F302,
UPI0000E073BF,
UPI0000070B33
EMBL:
BC053733,
BC029359,
AC016703,
CH471053,
AK027104,
AC067957
Ensembl:
ENSG00000143919
KO:
hsa:79823
|
Nucleutide sequences |
EMBL-CDS:
AAH53733.1,
AAX88866.1,
AAH29359.1,
BAB15658.1,
AAX93163.1,
EAX00274.1,
EAX00272.1
Gene_ORFName:
hCG_1818337
Ensembl_TRS:
ENST00000378494,
ENST00000403853
|
Protein sequencees |
Ensembl_PRO:
ENSP00000385124,
ENSP00000367755
RefSeq:
XP_016860465.1,
XP_011531413.1,
XP_016860464.1,
XP_016860468.1,
XP_011531415.1,
XP_016860469.1,
XP_016860471.1,
XP_016860459.1,
XP_016860467.1,
XP_016860470.1,
XP_016860472.1,
XP_016860461.1,
XP_016860460.1,
XP_016860466.1,
XP_016860463.1,
NP_079042.1,
XP_016860462.1
|
Others |
UniRef100:
UniRef100_Q7Z624
UniRef90:
UniRef90_Q7Z624
UniRef50:
UniRef50_Q7Z624
UniGene:
Hs.468349
CCDS:
CCDS1820.1
|
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