NDDVD - Neurodegenerative Diseases Variation Database
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267 entries on 3 pages. Showing entries 1 - 100.
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ID
Chr
Gene ID
Name
NCBI ID
NCBI Protein ID
Variants
00000168
19
ABCA7
ATP-binding cassette, sub-family A (ABC1), member 7
NM_019112.3
NP_061985.2
5
00000248
3
ADCY5
transcript variant 1
NM_183357.2
NP_899200.1
1
00000276
1
ADORA1
transcript variant 1
NM_000674.2
NP_000665.1
1
00000267
18
AFG3L2
AFG3-like AAA ATPase 2
NM_006796.2
NP_006787.2
4
00000232
7
AGBL3
ATP/GTP binding protein-like 3
NM_178563.3
NP_848658.3
1
00000033
2
ALS2
transcript variant 1
NM_020919.3
NP_065970.2
25
00000011
14
ANG
transcript variant 1
NM_001145.4
NP_001136.1
32
00000315
10
ANXA11
transcript variant a
NM_001157.2
NP_001148.1
6
00000012
14
APEX1
transcript variant 1
NM_001641.3
NP_001632.2
1
00000053
11
APOA1
apolipoprotein A-I
NM_000039.1
NP_000030.1
1
00000204
19
APOE
transcript variant 2
NM_000041.3
NP_000032.1
2
00000008
21
APP
transcript variant 1
NM_000484.3
NP_000475.1
74
00000157
5
ARHGEF28
transcript variant 1
NM_001080479.2
NP_001073948.2
1
00000037
17
ASPA
transcript variant 1
NM_000049.2
NP_000040.1
86
00000249
11
ATM
ATM serine/threonine kinase
NM_000051.3
NP_000042.3
5
00000048
19
ATP1A3
transcript variant 1
NM_152296.4
NP_689509.1
11
00000110
X
ATP7A
transcript variant 1
NM_000052.6
NP_000043.4
163
00000058
13
ATP7B
transcript variant 1
NM_000053.3
NP_000044.2
164
00000213
19
ATP8B3
ATPase, aminophospholipid transporter, class I, type 8B, member 3, transcript variant 1
NM_138813.3
NP_620168.1
1
00000330
12
ATXN2
ataxin 2
NM_002973.3
NP_002964.3
1
00000133
10
C10orf2
transcript variant 1
NM_021830.4
NP_068602.2
8
00000228
16
C16orf96
chromosome 16 open reading frame 96
NM_001145011.1
NP_001138483.1
1
00000222
3
C3orf20
transcript variant 3
NM_001184957.1
NP_001171886.1
1
00000244
9
C9orf72
transcript variant 1
NM_145005.6
NP_659442.2
1
00000294
9
C9orf72
transcript variant 3
NM_001256054.2
NP_001242983.1
4
00000306
9
C9orf72
C9orf72-SMCR8 complex subunit, transcript variant 3
NM_001256054.3
NP_001242983.1
12
00000135
19
CACNA1A
transcript variant 1
NM_000068.3
NP_000059.3
5
00000290
17
CACNA1G
transcript variant 1
NM_018896.4
NP_061496.2
1
00000202
20
CASS4
transcript variant 2
NM_020356.3
NP_065089.2
1
00000239
16
CCNF
transcript variant 1
NM_001761.2
NP_001752.2
13
00000193
6
CD2AP
CD2-associated protein
NM_012120.2
NP_036252.1
1
00000167
19
CD33
transcript variant 1
NM_001772.3
NP_001763.3
2
00000129
X
CDKL5
transcript variant I
NM_003159.2
NP_003150.1
65
00000200
11
CELF1
CUGBP, Elav-like family member 1, transcript variant 1
NM_006560.3
NP_006551.1
1
00000230
13
CENPJ
transcript variant 1
NM_018451.4
NP_060921.3
1
00000231
10
CFAP70
cilia and flagella associated protein 70
NM_145170.3
NP_660153.3
1
00000152
22
CHCHD10
coiled-coil-helix-coiled-coil-helix domain containing 10
NM_213720.1
NP_998885.1
21
00000313
22
CHCHD10
coiled-coil-helix-coiled-coil-helix domain containing 10, transcript variant 1
NM_001301339.2
NP_001288268.1
3
00000218
20
CHGB
chromogranin B (secretogranin 1)
NM_001819.2
NP_001810.2
1
00000031
3
CHMP2B
transcript variant 1
NM_014043.3
NP_054762.2
11
00000103
7
CLCN1
transcript variant 1
NM_000083.2
NP_000074.2
110
00000119
1
CLCN6
transcript variant 1
NM_001286.3
NP_001277.1
3
00000114
16
CLN3
transcript variant 2
NM_000086.2
NP_000077.1
58
00000115
13
CLN5
ceroid-lipofuscinosis, neuronal 5
NM_006493.2
NP_006484.1
45
00000116
15
CLN6
ceroid-lipofuscinosis, neuronal 6, late infantile, variant
NM_017882.2
NP_060352.1
64
00000118
8
CLN8
ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
NM_018941.3
NP_061764.2
24
00000171
8
CLU
transcript variant 1
NM_001831.3
NP_001822.3
3
00000162
4
COQ2
coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
NM_015697.7
NP_056512.5
24
00000166
1
CR1
complement component (3b/4b) receptor 1 (Knops blood group), transcript variant F
NM_000573.3
NP_000564.2
3
00000175
20
CST3
transcript variant 1
NM_000099.3
NP_000090.1
2
00000138
21
CSTB
cystatin B (stefin B)
NM_000100.3
NP_000091.1
14
00000111
11
CTSD
cathepsin D
NM_001909.4
NP_001900.1
3
00000206
11
CTSF
cathepsin F
NM_003793.3
NP_003784.2
1
00000326
16
CYLD
cylindromatosis (turban tumor syndrome), transcript variant 1
NM_015247.2
NP_056062.1
1
00000098
22
CYP2D6
transcript variant 1
NM_000106.5
NP_000097.3
1
00000260
1
DCAF8
transcript variant 1
NM_015726.3
NP_056541.2
1
00000013
2
DCTN1
transcript variant 1
NM_004082.4
NP_004073.2
9
00000163
3
DNAJC13
DnaJ (Hsp40) homolog, subfamily C, member 13
NM_015268.3
NP_056083.3
19
00000328
17
DNAJC7
DnaJ (Hsp40) homolog, subfamily C, member 7, transcript variant 1
NM_003315.3
NP_003306.3
2
00000309
5
DPYSL3
dihydropyrimidinase-like 3, transcript variant 2
NM_001387.2
NP_001378.1
1
00000261
14
DYNC1H1
dynein, cytoplasmic 1, heavy chain 1
NM_001376.4
NP_001367.2
1
00000211
10
EBLN1
endogenous Bornavirus-like nucleoprotein 1
NM_001199938.1
NP_001186867.1
1
00000073
10
EGR2
transcript variant 1
NM_000399.3
NP_000390.2
4
00000287
6
ELOVL4
ELOVL fatty acid elongase 4
NM_022726.3
NP_073563.1
3
00000288
6
ELOVL5
transcript variant 1
NM_021814.4
NP_068586.1
3
00000088
6
EPM2A
transcript variant 1
NM_005670.3
NP_005661.1
63
00000324
2
ERBB4
v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4, transcript variant JM-a/CVT-2
NM_001042599.1
NP_001036064.1
1
00000158
13
ERCC5
excision repair cross-complementing rodent repair deficiency, complementation group 5
NM_000123.3
NP_000114.2
25
00000039
10
ERCC6
excision repair cross-complementing rodent repair deficiency, complementation group 6
NM_000124.3
NP_000115.1
73
00000038
5
ERCC8
excision repair cross-complementing rodent repair deficiency, complementation group 8
NM_000082.3
NP_000073.1
26
00000321
10
ERLIN1
ER lipid raft associated 1
NM_006459.3
NP_006450.2
1
00000065
5
FAM134B
transcript variant 1
NM_001034850.2
NP_001030022.1
4
00000224
4
FAM47E
family with sequence similarity 47, member E, transcript variant 2
NM_001242936.1
NP_001229865.1
1
00000272
22
FBXO7
transcript variant 1
NM_012179.3
NP_036311.3
1
00000201
14
FERMT2
transcript variant 1
NM_006832.2
NP_006823.1
1
00000085
12
FGD4
FYVE, RhoGEF and PH domain containing 4
NM_139241.2
NP_640334.2
7
00000082
6
FIG4
FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
NM_014845.5
NP_055660.1
5
00000298
X
FMR1
fragile X mental retardation 1, transcript variant ISO12
NM_001185081.1
NP_001172010.1
1
00000128
14
FOXG1
forkhead box G1
NM_005249.4
NP_005240.3
22
00000223
19
FPR1
transcript variant 1
NM_001193306.1
NP_001180235.1
1
00000216
4
FRAS1
transcript variant 1
NM_025074.6
NP_079350.5
1
00000015
16
FUS
fused in sarcoma, transcript variant 1
NM_004960.3
NP_004951.1
132
00000229
7
GAL3ST4
galactose-3-O-sulfotransferase 4
NM_024637.4
NP_078913.3
1
00000099
1
GBA
transcript variant 1
NM_000157.3
NP_000148.2
5
00000043
14
GCH1
transcript variant 1
NM_000161.2
NP_000152.1
74
00000080
8
GDAP1
transcript variant 1
NM_018972.2
NP_061845.2
16
00000001
17
GFAP
transcript variant 1
NM_002055.4
NP_002046.1
144
00000074
X
GJB1
transcript variant 1
NM_001097642.2
NP_001091111.1
34
00000156
9
GLE1
transcript variant 1
NM_001003722.1
NP_001003722.1
1
00000252
18
GNAL
transcript variant 3
NM_001142339.2
NP_001135811.1
5
00000319
9
GNE
transcript variant 1
NM_001128227.2
NP_001121699.1
1
00000207
2
GPR45
G protein-coupled receptor 45
NM_007227.3
NP_009158.3
1
00000055
17
GRN
granulin
NM_002087.2
NP_002078.1
99
00000164
3
GSK3B
transcript variant 1
NM_002093.3
NP_002084.2
1
00000052
9
GSN
transcript variant 1
NM_000177.4
NP_000168.1
1
00000137
15
HDC
histidine decarboxylase
NM_002112.3
NP_002103.2
1
00000215
4
HERC6
transcript variant 1
NM_017912.3
NP_060382.3
1
00000131
15
HEXA
hexosaminidase A (alpha polypeptide)
NM_000520.4
NP_000511.2
2
00000016
6
HFE
transcript variant 1
NM_000410.3
NP_000401.1
5
00000176
5
HMGCR
transcript variant 1
NM_000859.2
NP_000850.1
1
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