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
immunoglobulin mu binding protein 2
IGHMBP2 (11q13.2-q13.4)

* Spinal muscular atrophy with respiratory distress - SMARD1 (12.5)
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-as
IKBKAP (9q31-q33)

* Neuropathy, hereditary sensory and autonomic, type III - HSAN3 (14.59, 16.3)
* Familial dysautonomia (Riley-Day syndrome) - (14.59, 16.3)
Inositol 1,4,5-triphosphate receptor type 1
ITPR1 (3p26.1-p25.3)

* Spinocerebellar ataxia 15 - SCA15 (13.14)
integrin alpha 7 precursor
ITGA7 (12q13)

* Congenital muscular dystrophy with integrin defect - (2.24)
integrin-linked kinase
ILK (11p15.5-p15.4)

* Dilated cardiomyopathy due to integrin-linked kinase defect - ILK (10.57)
Interferon-related developmental regulator 1
IFRD1 (7q22-q32)

* Spinocerebellar ataxia 18 - SCA18 (13.16)
iron-sulfur cluster scaffold homolog (E. coli)
ICSU (12q24.1)

* myopathy with deficiency of succinate dehydrogenase and aconitase - (5.23)
* myopathy with lactic acidosis, hereditary - HML (5.23)
* myopathy with exercise intolerance, swedish type - (5.23)