×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Roussy-Levy Syndrome (disorder)
0.900
Biomarker
MGD
A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
30239779
2019
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Roussy-Levy Syndrome (disorder)
0.900
Biomarker
MGD
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
1384988
1992
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Roussy-Levy Syndrome (disorder)
0.900
Biomarker
MGD
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
22689911
2012
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Roussy-Levy Syndrome (disorder)
0.900
Biomarker
MGD
Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
18326085
2008
×
Entrez Id:
4359
Gene Symbol:
MPZ
MPZ
Roussy-Levy Syndrome (disorder)
0.900
Biomarker
MGD
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
7581451
1995
×
Entrez Id:
5376
Gene Symbol:
PMP22
PMP22
Roussy-Levy Syndrome (disorder)
0.800
Biomarker
MGD
The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones.
17174099
2007
×
Entrez Id:
5376
Gene Symbol:
PMP22
PMP22
Roussy-Levy Syndrome (disorder)
0.800
Biomarker
MGD
Abnormal Schwann cell/axon interactions in the Trembler-J mouse.
9147228
1997
×
Entrez Id:
5376
Gene Symbol:
PMP22
PMP22
Roussy-Levy Syndrome (disorder)
0.800
Biomarker
MGD
Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model.
15748170
2005
×
Entrez Id:
5376
Gene Symbol:
PMP22
PMP22
Roussy-Levy Syndrome (disorder)
0.800
Biomarker
MGD
Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA.
15703401
2005
×
Entrez Id:
5376
Gene Symbol:
PMP22
PMP22
Roussy-Levy Syndrome (disorder)
0.800
Biomarker
MGD
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy.
17701891
2007
×
Entrez Id:
5376
Gene Symbol:
PMP22
PMP22
Roussy-Levy Syndrome (disorder)
0.800
Biomarker
MGD
Nerve conduction abnormalities in the trembler-j mouse: a model for Charcot-Marie-Tooth disease type 1A?
15363066
2004
×
Entrez Id:
9896
Gene Symbol:
FIG4
FIG4
Roussy-Levy Syndrome (disorder)
0.500
Biomarker
MGD
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
17572665
2007
×
Entrez Id:
9896
Gene Symbol:
FIG4
FIG4
Roussy-Levy Syndrome (disorder)
0.500
Biomarker
MGD
Neuronal expression of Fig4 is both necessary and sufficient to prevent spongiform neurodegeneration.
22581779
2012
×
Entrez Id:
90678
Gene Symbol:
LRSAM1
LRSAM1
Roussy-Levy Syndrome (disorder)
0.500
Biomarker
MGD
Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease.
23519028
2013
×
Entrez Id:
81846
Gene Symbol:
SBF2
SBF2
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2.
17855448
2007
×
Entrez Id:
1959
Gene Symbol:
EGR2
EGR2
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Congenital hypomyelinating neuropathy with lethal conduction failure in mice carrying the Egr2 I268N mutation.
19244508
2009
×
Entrez Id:
23095
Gene Symbol:
KIF1B
KIF1B
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta.
11389829
2001
×
Entrez Id:
121512
Gene Symbol:
FGD4
FGD4
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells.
23171661
2012
×
Entrez Id:
4747
Gene Symbol:
NEFL
NEFL
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype.
25552649
2015
×
Entrez Id:
79628
Gene Symbol:
SH3TC2
SH3TC2
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system.
19805030
2009
×
Entrez Id:
1959
Gene Symbol:
EGR2
EGR2
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Nab proteins are essential for peripheral nervous system myelination.
16136673
2005
×
Entrez Id:
9990
Gene Symbol:
SLC12A6
SLC12A6
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold.
14532115
2003
×
Entrez Id:
55526
Gene Symbol:
DHTKD1
DHTKD1
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice.
29661920
2018
×
Entrez Id:
2705
Gene Symbol:
GJB1
GJB1
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32.
9169515
1997
×
Entrez Id:
2617
Gene Symbol:
GARS1
GARS1
Roussy-Levy Syndrome (disorder)
0.200
Biomarker
MGD
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.
19470612
2009