Source: MGD

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K
disease 0.910 None 1.000 1 0 1985 2017
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease
disease 0.700 moderate 0.987 1 0 1993 2019
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
Hereditary Motor and Sensory Neuropathies
group 0.220 None 1.000 1 0 2000 2015
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder)
disease 0.200 None 1.000 1 0 2015 2015
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder)
disease 0.200 None 1.000 1 0 2015 2015
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy
disease 0.200 None 1.000 1 0 2015 2015
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
Hereditary motor and sensory neuropathy, types I-IV
disease 0.200 None 1.000 1 0 2015 2015
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
disease 0.200 None 1.000 1 0 2015 2015
Entrez Id: 54332
Gene Symbol: GDAP1
GDAP1
ganglioside induced differentiation associated protein 1 0.612 0.538 3.2E-08
Peroneal muscular atrophy (axonal type) (hypertrophic type)
disease 0.200 None 1.000 1 0 2015 2015