CAMKMT - calmodulin-lysine N-methyltransferase Gene

Homo sapiens

Also known as Cam; KMT; CLNMT; C2orf34; CaM KMT

Gene ID: 79823 | Gene type: protein coding

About CAMKMT

Cytogenetic location: 2p21 Genomic coordinates (GRCh38): 2:44,361,947-44,772,592 (from NCBI)

This gene has 10 transcripts (splice variants), 205 orthologues and is associated with 3 phenotypes. Low expression observed in reference dataset.

Summary

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]

CAMKMT Products(1)

mRNA	Protein	Name
NM_024766.5	NP_079042.1	calmodulin-lysine N-methyltransferase

CAMKMT Protein Structure

Methyltransf_16

0
100
200
300
323 a.a.

Protein Preferred Names

Protein Names

calmodulin-lysine N-methyltransferase

Related Diseases

Diseases

Alias

Hypotonia-Cystinuria Syndrome

Cystinuria With Mitochondrial Disease	2p21 Microdeletion Syndrome
HCS	Homozygous 2p16 Deletion Syndrome, Formerly
2p21 Deletion Syndrome	Del(2)(P21)
Monosomy 2p21	Atypical Hypotonia-Cystinuria Syndrome
Atypical Hcs

2p21 Microdeletion Syndrome Without Cystinuria

Del(2)(P21) Without Cystinuria

Cystinuria

CSNU	Cystinuria Type B
Cystinuria Type A	Cystinuria, Type I, Formerly
Csnu1, Formerly	Cystinuria, Type Ii, Formerly
Cystinuria, Type Iii, Formerly	Csnu3, Formerly
Cystinuria, Type Non-I, Formerly	Cystinuria-Lysinuria
Cystinuria-Lysinuria Syndrome	Csnu1
Csnu3	Cystinuria 1
Cystinuria Type A/B	Cystinuria Type I
Cystinuria Type Ii	Cystinuria Type Iii
Cystinuria Type Non-I	Cystinuria, Type A/B
Cystinuria Type 1	Cystinuria - Lysinuria
Csnu - [Cystinuria]	Cystine Disease

Hypotonia

Meier-Gorlin Syndrome 1

Meier-Gorlin Syndrome	Ear, Patella, Short Stature Syndrome
Microtia, Absent Patellae, Micrognathia Syndrome	MGORS1
Eps	Ear-Patella-Short Stature Syndrome
Ear Patella Short Stature Syndrome	Microtia Absent Patellae Micrognathia Syndrome
Meier-Gorlin Syndrome, Type 1

Kabuki Syndrome 1

Kabuki Syndrome	Niikawa-Kuroki Syndrome
Kabuki Make-Up Syndrome	Kms
KABUK1	Kabuki Make Up Syndrome
Nks	Kabuki Makeup Syndrome
Kabuki Syndrome, Type 1

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS01867	CAMKMT Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	CAMKMT	RGD	RGD:1310453
Macaca mulatta	CAMKMT	VGNC	VGNC:70637
Bos taurus	CAMKMT	VGNC	VGNC:26727
Felis catus	CAMKMT	VGNC	VGNC:99042
Mus musculus	CAMKMT	MGD	MGI:1920832
Canis familiaris	CAMKMT	VGNC	VGNC:38685

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