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79823 CAMKMT

79823

CAMKMT

calmodulin-lysine N-methyltransferase

protein-coding

Homo sapiens

基因描述

Type Description
Definition calmodulin-lysine N-methyltransferase

研究结论

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

名称对应

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

全选

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