| Gene Symbol |
CAMKMT
|
| Entrez Gene |
79823
|
| Alt Symbol |
C2orf34, CLNMT, CaM KMT, Cam, KMT
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
calmodulin-lysine N-methyltransferase
|
| Other Description |
-
|
| Swissprots |
Q9H5G8 Q8N6P5 Q4ZG15 Q7Z624 Q53SS6
|
| Accessions |
AAX88866 AAX93163 EAX00272 EAX00273 EAX00274 Q7Z624 AI933944 AK027104 BAB15658 BC022192 BC029359 AAH29359 BC053733 AAH53733 DA760277 DB461740 HQ447588 ADQ32074 XM_005264567 XP_005264624 XM_011533111 XP_011531413 XM_011533112 XP_011531414 XM_011533113 XP_011531415 XR_939721 XR_939722 XR_939723 NM_024766 NP_079042
|
| Function |
Catalyzes the trimethylation of 'Lys-116' in calmodulin. {ECO:0000269|PubMed:20975703}.
|
| Subcellular Location |
Isoform 1: Cytoplasm. Nucleus.
|
| Tissue Specificity |
Isoform 1 is expressed in brain,liver, muscle colon and lung. Isoform 2 is expressed in colon, testis, kidney and brain. Isoform 1 and isoform 2 are expressed in normal lymphoblastoid cells but not in lymphoblastoid cells from patients with hypotonia-cystinuria syndrome. {ECO:0000269|PubMed:15913950}.
|
| Top Pathways |
Lysine degradation
|