ENSG00000143919


Homo sapiens

Features
Gene ID: ENSG00000143919
  
Biological name :CAMKMT
  
Synonyms : calmodulin-lysine N-methyltransferase / CAMKMT / Q7Z624
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: 1
Band: p21
Gene start: 44361950
Gene end: 44772592
  
Corresponding Affymetrix probe sets: 1554875_at (Human Genome U133 Plus 2.0 Array)   219617_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000406936
Ensembl peptide - ENSP00000385587
Ensembl peptide - ENSP00000407594
Ensembl peptide - ENSP00000482360
Ensembl peptide - ENSP00000410783
Ensembl peptide - ENSP00000367755
Ensembl peptide - ENSP00000384039
Ensembl peptide - ENSP00000385124
NCBI entrez gene - 79823     See in Manteia.
OMIM - 609559
RefSeq - XM_017004983
RefSeq - NM_024766
RefSeq - XM_011533111
RefSeq - XM_011533113
RefSeq - XM_017004972
RefSeq - XM_017004977
RefSeq - XM_017004978
RefSeq - XM_017004982
RefSeq Peptide - NP_079042
swissprot - B5MC79
swissprot - B5MC16
swissprot - H7C2N4
swissprot - Q7Z624
swissprot - H7C3B0
swissprot - A0A0C4DGY0
swissprot - H7C2T0
Ensembl - ENSG00000143919
  
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 camkmtENSDARG00000095224Danio rerio
 si:ch73-54n14.2ENSDARG00000091900Danio rerio
 CAMKMTENSGALG00000035800Gallus gallus
 CamkmtENSMUSG00000071037Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR019410  Lysine methyltransferase
 IPR025800  Calmodulin-lysine N-methyltransferase
 IPR029063  S-adenosyl-L-methionine-dependent methyltransferase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006479 protein methylation TAS
 biological_processGO:0007005 mitochondrion organization IEA
 biological_processGO:0018022 peptidyl-lysine methylation IEA
 biological_processGO:0022400 regulation of rhodopsin mediated signaling pathway TAS
 biological_processGO:0032259 methylation IEA
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0032991 protein-containing complex IDA
 molecular_functionGO:0008168 methyltransferase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0018025 calmodulin-lysine N-methyltransferase activity TAS
 molecular_functionGO:0031072 heat shock protein binding IPI


Pathways (from Reactome)
Pathway description
Inactivation, recovery and regulation of the phototransduction cascade
Protein methylation


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000135 Hypogonadism "Reduced function of the gonads (testes in males or ovaries in females)." [HPO:curators]
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 HP:0000368 Low-set, posteriorly rotated ears 
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 HP:0000527 Long eyelashes "Mid upper eyelash length >10 mm or increased length of the eyelashes (subjective)." [pmid:19125427]
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 HP:0000787 Kidney stones 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001508 Failure to thrive 
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 HP:0001510 Growth retardation 
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 HP:0001558 Decreased fetal movement "An abnormal reduction in quantity or strength of fetal movements." [HPO:curators]
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 HP:0001611 Nasal speech 
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 HP:0001943 Hypoglycemia "A lower than normal level of blood glucose." [HPO:curators]
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 HP:0002007 Frontal bossing "The presence of an unusually prominent forehead." [HPO:curators]
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 HP:0002342 Mental retardation, moderate "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 35-49." [HPO:curators]
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 HP:0002901 Hypocalcemia "A level of blood calcium that is lower than normal." [HPO:curators]
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 HP:0003128 Lactic acidemia "An abnormal buildup of `lactic acid` (CHEBI:28358) in the body, leading to `acidification` (GO:0045851) of the blood." [HPO:probinson]
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 HP:0003131 Cystinuria 
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 HP:0005280 Depressed nasal root and bridge 
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 HP:0200125 Mitochondrial respiratory chain defects 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000198668 CALM1 / P0DP23 / calmodulin 1  / reaction






 

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contact: otassy@igbmc.fr