Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Surprisingly, Rab18 colocalizes, cofractionates, and coprecipitates with the lysosomal regulator Rab7, mutations of which cause Charcot-Marie-Tooth (CMT) neuropathy type 2B. 30721447 2019
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE (2019) show that the lysosomal GTPase Rab7 regulates inter-mitochondrial contacts to control mitochondrial motility and identify dysregulated inter-mitochondrial tethering as a common theme in Charcot-Marie-Tooth (CMT) type 2 disease. 31386859 2019
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Charcot-Marie-Tooth type 2B (CMT2B) disease is a dominant axonal peripheral neuropathy caused by 5 mutations in the RAB7A gene, a ubiquitously expressed GTPase controlling late endocytic trafficking. 29130394 2018
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE To evaluate, by skin biopsy, dermal nerve fibers in 31 patients with 3 common Charcot-Marie-Tooth (CMT) genotypes (CMT1A, late-onset CMT1B, and CMTX1), and rarer forms of CMT caused by mutations in RAB7 (CMT2B), TRPV4 (CMT2C), and GDAP1 (AR-CMT2K) genes. 26362287 2015
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE A novel RAB7 mutation in a Chinese family with Charcot-Marie-Tooth type 2B disease. 24498653 2014
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Rab7 mutants associated with Charcot-Marie-Tooth disease cause delayed growth factor receptor transport and altered endosomal and nuclear signaling. 23188822 2013
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE Charcot-Marie-Tooth type 2B (CMT2B) is a peripheral ulcero-mutilating neuropathy caused by four missense mutations in the rab7a gene. 23179371 2013
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE Charcot-Marie-Tooth type 2B (CMT2B) is one of the most common inherited peripheral neuropathies characterized by severe terminal axonal loss. 23616551 2013
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Missense mutations of the GTPase Rab7 cause a dominantly inherited axonal degeneration known as Charcot-Marie-Tooth type 2B through an unknown mechanism. 20028791 2010
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE The mood stabilizer valproic acid improves defective neurite formation caused by Charcot-Marie-Tooth disease-associated mutant Rab7 through the JNK signaling pathway. 20645406 2010
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE RAB7 mutations were only found in patients with a Charcot-Marie-Tooth type 2B (CMT2B) phenotype, an axonal sensory-motor neuropathy with pronounced ulcero-mutilations. 19651702 2009
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE The CMT2B (Charcot-Marie-Tooth type 2B) disease is an autosomal dominant axonal neuropathy. 19754445 2009
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE Four missense mutations, that target highly conserved amino acid residues in the small GTPase Rab7, have been associated with the Charcot-Marie-Tooth (CMT) type 2B phenotype. 18501189 2008
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Recently, four missense mutations in the small GTPase Rab7 associated with the Charcot-Marie Tooth type 2B phenotype have been identified. 18272684 2008
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene. 17060578 2006
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy. 12545426 2003
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE Genetically related are the Dunnigan-type of familial partial lipodystrophy (FPLD) and Charcot-Marie-Tooth neuropathy type 2 (CMT2B). 12138994 2002
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 Biomarker disease BEFREE CMT2B is a rare disorder belonging to the group of axonal CMT syndromes that is clinically characterized by marked distal muscle weakness and wasting as well as a high frequency of foot ulcers, infections, and amputations. 11094113 2000
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Results of linkage analysis excluded the Charcot-Marie-Tooth 2A (CMT2A) and CMT2B loci and suggested the possibility of a linkage to HSAN-I locus on 9q22.1-q22.3. 11003785 2000
Entrez Id: 7879
Gene Symbol: RAB7A
RAB7A
0.100 GeneticVariation disease BEFREE Three congenital disorders have been localised to this region: blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), Charcot-Marie-Tooth neuropathy type IIB (CMT2B) and Mobius syndrome type 2 (MBS2). 10830911 2000