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
N-myc downstream regulated gene 1
NDRG1 (8q24.3)

* Charcot-Marie-Tooth disease, type 4D - CMT4D (14.19, 14.61)
* Neuropathy, hereditary motor and sensory, lom type - HMSNL (14.19, 14.61)
NADH-ubiquinone oxidoreductase 1 alpha subcomplex
NDUFAF1 (15q15.1)

* patient with HCM and isolated respiratory complex I deficiency - (10.24)
* Hypertrophic mitochondrial cardiomyopathy with NDUFAF1 defect - (10.24)
natriuretic peptide precursor A
NPPA (1p36)

* atrial fibrillation, familial, 6 - ATFB6 (10.106)
nebulin
NEB (2q22)

* Nemaline myopathy 2, autosomal recessive - NEM2 (3.2, 4.10)
nerve growth factor (beta polypeptide)
NGFB (1p13.1)

* neuropathy, hereditary sensory and autonomic type v - HSAN5 (14.60)
neurofilament, light polypeptide 68kDa
NEFL (8p21)

* Charcot-Marie-Tooth disease, type 2E - CMT2E (14.7, 14.40)
* Charcot-Marie-Tooth disease, type 1F - CMT1F (14.7, 14.40)
Nexilin(F-actin binding protein)
NEXN (1p32-p31 )

* Hypertrophic cardiomyopathy with nexilin defect - (10.21, 10.63)
* Cardiomyopathy, familial hypertrophic 20 - CMH20 (10.21, 10.63)
* Cardiomyopathy, dilated, 1CC - CMD1CC (10.21, 10.63)
non-imprinted in Prader-Willi/Angelman syndrome 1
NIPA1 (15q11.2)

* Spastic paraplegia 6 uncomplicated,autosomal dominant,Strumpell-Lorrain type - SPG6 (15.3)