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FLASH GENE
Symbol CAMTA1 contributors: mct - updated : 01-03-2017
HGNC name calmodulin binding transcription activator 1
HGNC id 18806
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
4 - 743 - 80 - 2004 15138581
4 - 997 - 101 - 2004 15138581
23 - 8444 - 1673 - 2004 15138581
- - 8374 - 1643 - 2004 15138581
- - 8095 - 1567 - 2004 15138581
- - 8120 - 1565 - 2004 15138581
- - 8056 - 1537 - 2004 15138581
- - 5420 - 716 - 2004 15138581
- - 5701 - 704 - 2004 15138581
- - 5363 - 704 - 2004 15138581
- - 5381 - 704 - 2004 15138581
- - 5676 - 697 - 2004 15138581
- - 5413 - 697 - 2004 15138581
- - 5047 - 591 - 2004 15138581
- - 5393 - 591 - 2004 15138581
- - 5362 - 591 - 2004 15138581
- - 5005 - 591 - 2004 15138581
- - 5341 - 584 - 2004 15138581
- - 5043 - 584 - 2004 15138581
- - 5358 - 584 - 2004 15138581
- - 5041 - 584 - 2004 15138581
- - 770 - 92 - 2004 15138581
EXPRESSION
Type restricted
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Nervousbrain     Homo sapiens
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period
cell cycle     cell cycle, S, M
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • CG-1 domain
  • TIG domain
  • ankyrin repeats
  • and IQ motifs
  • HOMOLOGY
    Homologene
    FAMILY Calmodulin-binding transcription activator (CAMTA) family protein
    CATEGORY transcription factor , tumor suppressor
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,cytosolic
    intracellular,nucleus,nucleolus
    text
  • nuclear CAMTA1 expression is identified in the majority of Epithelioid hemangioendothelioma (EHE) cases
  • basic FUNCTION
  • play important roles in oncogenesis
  • may participate in induction of cell differentiation and cell cycle regulation
  • transcription factor that interfaces with the calcium-calmodulin system of the cell to alter gene expression patterns
  • potential role in human episodic memory
  • induced neurite-like processes and markers of neuronal differentiation in neuroblastoma cells
  • inhibits growth and activates differentiation programs in neuroblastoma cells
  • has a role in brain and cerebellar function
  • is a putative tumor suppressive transcription factor
  • is a regulator of long-term memory formation
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • putative transcription factor, which induces the expression of the anti-proliferative cardiac hormone natriuretic peptide A (NPPA)
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) CANPMR
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    tumoral fusion      
    WWTR1-CAMTA1 fusion in all epithelioid hemangioendothelioma tested from bone, soft tissue, and visceral location (liver, lung) in keeping with a unique and specific pathological entity
    tumoral     --low  
    independent predictor of poor outcome in neuroblastoma patients
    tumoral   translocation    
    with TFE3 in Epithelioid hemangioendotheliomas
    Susceptibility
  • to coronary artery disease (CAD) and periodontitis
  • to Sporadic Amyotrophic Lateral Sclerosis
  • Variant & Polymorphism other
  • risk alleles in the genes CDKN2B-AS1, CAMTA1 and PLG that are shared between coronary artery disease (CAD) and periodontitis
  • rs2412208 associated with longer survival
  • Candidate gene
    Marker
  • presence of WWTR1-CAMTA1 fusion may serve as a useful molecular diagnostic tool in challenging diagnoses
  • nuclear CAMTA1 expression is sensitive and highly specific for epithelioid haemangioendothelioma (EHE) and can be applied to diagnostic immunohistochemistry in epithelioid tumours
  • Therapy target
    ANIMAL & CELL MODELS
  • global or nervous system deletion of Camta1 in mice causes severe ataxia with Purkinje cell degeneration and cerebellar atrophy, partially resembling the consequences of haploinsufficiency of the human Camta1 locus