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 (1.21)
ganglioside-induced differentiation-associated protein 1
GDAP1 (8q13-q21)

* Charcot-Marie-Tooth disease, type 4A - CMT4A (14.15, 14.46)
* Charcot-Marie-Tooth disease, mixed axonal and demyelinating type - CMT4A (14.15, 14.46)
* Charcot-Marie-Tooth disease, type 2K - CMT2K (14.15, 14.46)
gap junction protein, beta 1, 32kDa (connexin 32)
GJB1 (Xq13.1)

* Charcot-Marie-Tooth neuropathy, X-linked - CMTX1 (14.26, 14.33)
gelsolin
gigaxonin
GAN (16q24.1)

* Giant axonal neuropathy-1 - GAN1 (14.65)
GLE1 RNA export mediator homolog (yeast)
GLE1 (9q34.11)

* Lethal congenital contracture syndrome 1 - LCCS1 (12.33)
glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen dis
GBE1 (3p12)

* Glycogen branching enzyme deficiency - GSD IV (9.3)
glutamine-fructose-6-phosphate transaminase 1
GFPT1 (2p12-p15)

* Myastenia, Limb-Girdle, With tubular aggregates - LGM (11.16)
glycerol-3-phosphate dehydrogenase 1-like
GPD1L (3p22.3)

* brugada syndrome 2 - (10.112)
glycogen phosphorylase
PYGM (11q12-q13.2)

* McArdle disease - PYGM (9.4)
glycogen synthase 3 glycogen synthase 1 (muscle) glycogen synthase 1 (muscle)
GYS1 (19q13.3)

* glycogen storage disease type 0 - GSD0b (9.9)
glycyl-tRNA synthetase
GARS (7p15)

* Neuropathy, distal hereditary motor type V - HMN V (12.14, 14.39)
* Spinal muscular atrophy, distal, type V - DSMAV (12.14, 14.39)
* Charcot-Marie-Tooth disease, axonal, type 2D - CMT2D (12.14, 14.39)