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CBLC gene

Known as: RNF57, Cbl proto-oncogene C, E3 ubiquitin protein ligase, CBL-SL 
This gene is involved in both ubiquitination and signaling.
National Institutes of Health

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CBLC wt Allele
Signal TransductionSignal Transduction InhibitionSignal Transduction Protein CBL-CUbiquitination

Papers overview

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2019
2019
Sp-CBL inhibits white spot syndrome virus replication by enhancing apoptosis in mud crab (Scylla paramamosain).
2015
2015
Co-occurrence of the Poland sequence in a patient with the cobalamin C defect: more than just a coincidence?
A newborn male born to a non-consanguineous Mexican couple was evaluated for lethargy and elevated C3 acylcarnitine (18 μmol/L… 
2015
2015
Prenatal diagnosis of methymalonic aciduria and homocystinuria cblC type using DNA analysis
Methylmalonic aciduria (MMA) and homocystinuria, cblC type is the most frequent inborn error of vitamin B12. CblC patients… 
2012
2012
CBL mutations in myeloproliferative neoplasms are also found in the gene’s proline-rich domain and in patients with the V617FJAK2
Background Despite the discovery of the p.V617F in JAK2, the molecular pathogenesis of some chronic myeloproliferative neoplasms… 
2010
2010
Gain of CBL-interacting protein, a possible alternative to CBL mutations in myeloid malignancies
Gain of CBL-interacting protein, a possible alternative to CBL mutations in myeloid malignancies 
2008
2008
The Arabidopsis Calcium Sensor Calcineurin B-Like 3 Inhibits the 5′-Methylthioadenosine Nucleosidase in a Calcium-Dependent Manner1[C][W][OA]
Calcineurin B-like (CBL) proteins represent a unique family of calcium sensors in plant cells. Sensing the calcium signals… 
2008
2008
CD2AP and Cbl-3/Cbl-c Constitute a Critical Checkpoint in the Regulation of Ret Signal Transduction
The glial cell line-derived neurotrophic factor (GDNF) family ligands (GFLs) are critical for nervous system development and… 
2007
2007
DNA-based diagnosis of methylmalonic aciduria and homocystinuria, cblC type in a Chinese patient presenting with mild developmental delay.
1998
1998
A third human CBL gene is on chromosome 19.
CBL genes encode cytoplasmic proteins involved in signal transduction downstream of a number of receptors including tyrosine… 
1992
1992
Clinical and biochemical observations in a patient with combined Pompe disease and cblC mutation
Metabolic studies are described in a patient who presented at 3 weeks of age with severe anaemia, hyperbilirubinaemia and… 
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