CAMKMT gene

calmodulin-lysine N-methyltransferase

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

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]

From UniProt:

Catalyzes the trimethylation of 'Lys-116' in calmodulin.

From UniProt:

Hypotonia-cystinuria syndrome (HCS): Characterized generalized hypotonia at birth, nephrolithiasis, growth hormone deficiency, minor facial dysmorphism, failure to thrive, followed by hyperphagia and rapid weight gain in late childhood. [MIM:606407]

Cytogenetic Location: 2p21, which is the short (p) arm of chromosome 2 at position 21

Molecular Location: base pairs 44,361,714 to 44,772,592 on chromosome 2 (Homo sapiens Updated Annotation Release 109.20200522, GRCh38.p13) (NCBI)

Cytogenetic Location: 2p21, which is the short (p) arm of chromosome 2 at position 21
  • C2orf34
  • Cam
  • CaM KMT
  • CLNMT
  • KMT