Gene product table

A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

Protein
Gene Symbol
All allelic disease phenotypes - locus/disease symbols
gamma sarcoglycan
SGCG (13q12)

Muscular dystrophy, limb-girdle, type 2C -LGMD2C
ganglioside-induced differentiation-associated protein 1
GDAP1 (8q21.11)

Charcot-Marie-Tooth disease, mixed axonal and demyelinating type -CMT4A
Charcot-Marie-Tooth disease, type 4A -CMT4A
Charcot-Marie-Tooth disease, type 2G -CMT2G
Charcot-Marie-Tooth disease, type 2K -CMT2K
gap junction protein, beta 1, 32kDa (connexin 32)
GJB1 (Xq13.1)

Dejerine-Sottas hypertrophic neuropathy, recessive -
Charcot-Marie-Tooth neuropathy, X-linked -CMTX1
gelsolin
GSN (9q33)

Amyloidosis, Finnish type -GSN
gigaxonin
GAN (16q24.1)

Giant axonal neuropathy-1 -GAN1
GLE1 RNA export mediator homolog (yeast)
GLE1 (9q34.11)

lethal congenital contracture syndrome 1 -LCCS1
glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen dis
GBE1 (3p12)

Glycogen branching enzyme deficiency -GSD IV
glycerol-3-phosphate dehydrogenase 1-like
GPD1L (3p22.3)

brugada syndrome 2 -
glycogen phosphorylase
PYGM (11q12-q13.2)

McArdle disease -PYGM
glycogen synthase 3 glycogen synthase 1 (muscle) glycogen synthase 1 (muscle)
GYS1 (19q13.3)

glycogen storage disease type 0 -GSD0b
glycyl-tRNA synthetase
GARS (7p15)

Spinal muscular atrophy, distal, type V -DSMAV
Neuropathy, distal hereditary motor type V -HMN V
Charcot-Marie-Tooth disease, axonal, type 2D -CMT2D