Gene table



Gene symbol and protein
Gene Location
All allelic disease phenotypes - locus/disease symbols

GAA
Acid alpha-glucosidase preproprotein



17q25.2-q25.3
* Limb-Girdle, Muscular dystrophy, type 2V - LGMD2V (1.42, 9.1, 10.74)
* Glycogen storage disease II - GSDII (1.42, 9.1, 10.74)

GAN
Gigaxonin



16q24.1
* Giant axonal neuropathy-1 - GAN1 (14.96)

GARS
Glycyl-tRNA synthetase



7p15
* Neuropathy, distal hereditary motor type V - HMN V (12.14, 14.44)
* Spinal muscular atrophy, distal, type V - DSMAV (12.14, 14.44)
* Charcot-Marie-Tooth disease, axonal, type 2D - CMT2D (12.14, 14.44)

GATAD1
GATA zinc finger domain containing 1



7q21-q22
* Cardiomyopathy, dilated, 2B - CMD2B (10.70)
* Dilated cardiomyopathy realted to GATAD1 - (10.70)

GBA2
glucosidase, beta (bile acid) 2



9p13.3
* Spastic paraplegia 46, autosomal recessive - SPG46 (15.41)

GBE1
Glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen disease, glycogen storage disease type IV)



3p12
* Glycogen branching enzyme deficiency - GSD IV (9.3)

GDAP1
Ganglioside-induced differentiation-associated protein 1



8q13-q21
* Charcot-Marie-Tooth disease, type 4A - CMT4A (14.17, 14.51)
* Charcot-Marie-Tooth disease, mixed axonal and demyelinating type - CMT4A (14.17, 14.51)
* Charcot-Marie-Tooth disease, type 2K - CMT2K (14.17, 14.51)

GFPT1
Glutamine-fructose-6-phosphate transaminase 1



2p12-p15
* Familial limb girdle myasthenia with tubular aggregates related to GFPT1 - CMSTA1 (11.17)

GJA5
Connexin 40



1q21.1
* atrial fibrillation, familial, 1 - ATFB1 (10.129, 10.130)

GJB1
Gap junction protein, beta 1, 32kDa (connexin 32)



Xq13.1
* Charcot-Marie-Tooth neuropathy, X-linked - CMTX1 (14.30, 14.38)

GJB3
Gap junction protein, beta 3, 31kDa (=connexin 31)



1p34.3
* Peripheral neuropathy and deafness, autosomal dominant - (14.94)

GJC2
gap junction protein, gamma 2, 47kDa



1q42.13
* Spastic paraplegia 44, autosomal recessive - SPG44 (15.39)

GLE1
GLE1 RNA export mediator homolog (yeast)



9q34.11
* Lethal congenital contracture syndrome 1 - LCCS1 (12.66)

GMPPB
GDP-mannose pyrophosphorylase B



3p21.31
* Muscle-eye-brain disease - MDDGA14 (1.40, 2.31, 2.38, 11.32)
* Limb-Girdle, Muscular dystrophy, type 2T - MDDGC14 (1.40, 2.31, 2.38, 11.32)
* Congenital Myasthenic syndrome related to GMPPB - (1.40, 2.31, 2.38, 11.32)

GNB4
Guanine nucleotidebinding protein, beta-4



3q28-q29
* Charcot-Marie-Tooth neuropathy Type F - CMTD1F (14.16)

GNE
UDP-N-acetylglucosamine-2- epimerase/N-acetylmannosamine kinase



9p13.3
* Nonaka myopathy - NM (4.3)
* Inclusion body myopathy, autosomal recessive - IBM2 (4.3)

GOLGA2
golgin A2



9q34.113
* GOLGA2-related congenital muscle dystrophy with brain involvement - (2.46)

GPD1L
Glycerol-3-phosphate dehydrogenase 1-like



3p22.3
* brugada syndrome 2 - (10.135)

GYG1
Glycogenin 1



3q24
* Glycogen storage disease XV - GSD15 (9.8)

GYS1
Glycogen synthase 3 glycogen synthase 1 (muscle) glycogen synthase 1 (muscle)



19q13.3
* glycogen storage disease type 0 - GSD0b (9.9)