Identity
HGNC
LOCATION
2p21
LOCUSID
ALIAS
C2orf34,CLNMT,CaM KMT,Cam,KMT
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 79823
MIM: 609559
HGNC: 26276
Ensembl: ENSG00000143919
Variants:
dbSNP: 79823
ClinVar: 79823
TCGA: ENSG00000143919
COSMIC: CAMKMT
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 23794250 | 2013 | Further delineation of genotype-phenotype correlation in homozygous 2p21 deletion syndromes: first description of patients without cystinuria. | 11 |
| 23794250 | 2013 | Further delineation of genotype-phenotype correlation in homozygous 2p21 deletion syndromes: first description of patients without cystinuria. | 11 |
| 23285036 | 2012 | Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence. | 8 |
| 23285036 | 2012 | Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence. | 8 |
| 20200953 | 2010 | Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study. | 27 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20975703 | 2010 | Calmodulin methyltransferase is an evolutionarily conserved enzyme that trimethylates Lys-115 in calmodulin. | 52 |
| 20200953 | 2010 | Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study. | 27 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20975703 | 2010 | Calmodulin methyltransferase is an evolutionarily conserved enzyme that trimethylates Lys-115 in calmodulin. | 52 |
| 19575798 | 2009 | Cooperation between NRF-2 and YY-1 transcription factors is essential for triggering the expression of the PREPL-C2ORF34 bidirectional gene pair. | 8 |
| 19575798 | 2009 | Cooperation between NRF-2 and YY-1 transcription factors is essential for triggering the expression of the PREPL-C2ORF34 bidirectional gene pair. | 8 |
| 18234729 | 2008 | Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome. | 18 |
| 18234729 | 2008 | Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome. | 18 |
Citation
Dessen P
CAMKMT (calmodulin-lysine N-methyltransferase)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61396/camkmt-(calmodulin-lysine-n-methyltransferase)
