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RAB7A wt Allele

Known as: PRO2706, RAB7, Member RAS Oncogene Family Gene, CMT2B 
Human RAB7A wild-type allele is located in the vicinity of 3q21 and is approximately 89 kb in length. This allele, which encodes ras-related protein… 
National Institutes of Health

Related topics

Related topics

6 relations
3q21Homo sapiensIntracellular TransportProtein Degradation, Regulatory

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
PREDOMINANTLY MOTOR CMT2B ASSOCIATED WITH A NOVEL PATHOGENIC RAB7 MUTATION
2017
2017
MP069OVEREXPRESSION OF RAB7 AMELIORATES ABNORMAL EXTRACELLULAR MATRIX METABOLISM BY REGULATING AUTOPHAGIC FLUX IN RENAL PROXIMAL TUBULAR CELLS OVERLOADED WITH ALBUMIN
2016
2016
A NOVEL PATHOGENIC RAB7 MUTATION CAUSING PREDOMINANTLY MOTOR CMT2B
2013
2013
A novel RAB 7 mutation in a Chinese family with Charcot – Marie – Tooth type 2 B disease
a Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology and Center for… 
2009
2009
[Molecular diagnosis of axonal forms of Charcot-Marie-Tooth disease].
Review
2006
Review
2006
[Molecular genetics of inherited neuropathies].
Inherited neuropathies are clinically and genetically heterogeneous. At least 28 genes and 12 loci have been associated with… 
2005
2005
SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies
Background: The variable clinical features of hereditary sensory and autonomic neuropathy (HSAN I) suggest heterogeneity. Some… 
2004
2004
Ulcero-mutilating neuropathy: Clinical, pathological and molecular genetic study of a family with a novel RAB7 mutation
2004
2004
Neuropathies périphériques et petites protéines de choc thermique
> Les neuropathies peripheriques hereditaires, dont la prevalence est d’environ 1/5000, sont les maladies monogeniques du systeme… 
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