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
heat shock 27kDa protein 1
HSPB1 (7q11.23)

* Charcot-Marie-Tooth neuropathy Type 2F - CMT2F (12.11, 14.41)
* Neuropathy, distal hereditary motor, type IIB - HMN2B (12.11, 14.41)
heat shock 27kDa protein 8
HSPB8 (12q24.23)

* Neuropathy, distal hereditary motor, type II - HMN2A (12.10, 14.47)
* Charcot-Marie-Tooth neuropathy Type 2L - CMT2L (12.10, 14.47)
heat shock 60kDa protein 1 (chaperonin)
HSPD1 (2q33.1)

* Spastic paraplegia 13 - SPG13 (15.8)
homeobox D10
HOXD10 (2q31.1)

* Charcot-Marie-Tooth disease, congenital, vertical talus - (14.8)
HSP-40 homologue, subfamily B, number 6
DNAJB6 (7q36)

* Limb girdle muscular dystrophy 1D (autosomal dominant) - LGMD1D (1.14)
hyperpolarization activated cyclic nucleotide-gated potassium channel 4
HCN4 (15q24.1)

* Sick Sinus Syndrome 2, autosomal dominant - SSS2 (10.115)
* familial sinusal bradycardia - FSBD (10.115)
hypothetical protein LOC9907 ?
KIAA0415 (7p22.2)

* Spastic paraplegia 48, autosomal recessive - SPG48 (15.40)