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
kelch repeat and BTB (POZ) domain containing 13
KBTBD13 (15q22.31)

* Nemaline myopathy 6 - NEM6 (3.7)
kelch-like homologue 9
KLHL9 (9p21.2-p22.3)

* Early onset distal myopathy with KLHL9 mutations - (4.14)
KIAA1985 protein
SH3TC2 (5q32)

* Charcot-Marie-Tooth neuropathy Type 4F - CMT4C (14.18)
kinesin family member 1A
KIF1A (2q37.3)

* Spastic paraplegia 30 - SPG30 (14.57, 15.33)
* Neuropathy, hereditary sensory, type IIC - HSN2C (14.57, 15.33)
kinesin family member 1B
KIF1B (1p36.2)

* Charcot-Marie-Tooth disease, type 2A1 - CMT2A1 (14.35)
kinesin family member 21A
KIF21A (12q12)

* Fibrosis of extraocular muscles, congenital, 1 - CFEOM1 (16.5)
kinesin family member 5A
KIF5A (12q13.13)

* Spastic paraplegia 10 - SPG10 (15.6)
Kir2.6 (inwardly rectifying potassium channel 2.6)
KCNJ18 (17p11.2)

* Thyrotoxic periodic paralysis, susceptibility to, 2 - TTPP2 (7.13)