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Gene : CAMKMT Homo sapiens

Name  ? calmodulin-lysine N-methyltransferase Cytological Location  2p21
Brief Description  calmodulin-lysine N-methyltransferase
Description  This gene encodes a class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin. The protein contains a AdoMet-binding motif and may play a role in calcium-dependent signaling. [provided by RefSeq, Sep 2012]
  • synonyms:
  • CLNMT,
  • C2orf34,
  • Cam,
  • uc002rum.4,
  • OTTHUMG00000128761,
  • KMT,
  • CAMKMT,
  • CaM KMT,
  • C2orf34,
  • HGNC:26276,
  • CLNMT,
  • CaM KMT,
  • chromosome 2 open reading frame 34,
  • NM_024766
  • identifiers:
  • 79823,
  • ENSG00000143919,
  • CAMKMT

Genome feature

Region: gene ? Length: 410879  
Location: 2:44361714-44772592 Cyto location: 2p21


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

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Other

3753 SN Ps

5 Cross References

16 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results