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CANT1 gene

Known as: SCAN-1, Calcium Activated Nucleotidase 1 Gene, Soluble Ca-Activated Nucleotidase, isozyme 1 
This gene plays a role in both nucleotide hydrolysis and signal transduction.
National Institutes of Health

Related topics

Related topics

6 relations

Narrower (1)

CANT1 wt Allele

Broader (1)

Genes
HydrolysisNucleotide MetabolismSignal TransductionSoluble Calcium-Activated Nucleotidase 1

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
LncRNA CANT1 suppresses retinoblastoma progression by repellinghistone methyltransferase in PI3Kγ promoter
Retinoblastoma (RB) is the most common malignant intraocular tumor of childhood. Recent studies have shown that long noncoding… 
2019
2019
Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification
2017
2017
CANT1 lncRNA Triggers Efficient Therapeutic Efficacy by Correcting Aberrant lncing Cascade in Malignant Uveal Melanoma.
Highly Cited
2014
Highly Cited
2014
XYLT1 mutations in Desbuquois dysplasia type 2.
2012
2012
Further Delineation of CANT1 Phenotypic Spectrum and Demonstration of Its Role in Proteoglycan Synthesis
Desbuquois dysplasia (DD) is characterized by antenatal and postnatal short stature, multiple dislocations, and advanced carpal… 
2011
2011
Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene
We report on three hydropic fetuses of 17, 22 and 25 gestational weeks from three distinct families presenting with Desbuquois… 
2010
2010
CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant
Background Desbuquois dysplasia (DD) is a recessively inherited condition characterised by short stature, generalised skeletal… 
2010
2010
Mutation of CANT1 causes Desbuquois dysplasia
Desbuquois dysplasia is an autosomal recessive dysplasia characterized by severe growth restriction and distinct hand and… 
Highly Cited
2009
Highly Cited
2009
Identification of CANT1 mutations in Desbuquois dysplasia.
Highly Cited
2008
Highly Cited
2008
Two unique novel prostate-specific and androgen-regulated fusion partners of ETV4 in prostate cancer.
Recently, fusion of ERG to the androgen-regulated, prostate-specific TMPRSS2 gene has been identified as the most frequent… 
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