Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apba1 |
A |
T |
19: 23,870,195 (GRCm39) |
E9V |
probably benign |
Het |
Armc8 |
T |
A |
9: 99,418,333 (GRCm39) |
T32S |
probably benign |
Het |
Atr |
T |
A |
9: 95,752,658 (GRCm39) |
|
probably null |
Het |
Blm |
A |
G |
7: 80,143,862 (GRCm39) |
L859P |
probably benign |
Het |
Cacna2d3 |
A |
T |
14: 28,691,171 (GRCm39) |
F51L |
probably damaging |
Het |
Cdcp2 |
A |
G |
4: 106,964,197 (GRCm39) |
N349S |
probably damaging |
Het |
Cfap57 |
G |
A |
4: 118,457,124 (GRCm39) |
H442Y |
possibly damaging |
Het |
Chrm3 |
A |
G |
13: 9,928,517 (GRCm39) |
L173P |
probably damaging |
Het |
Cpb1 |
C |
G |
3: 20,317,920 (GRCm39) |
M201I |
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,076,178 (GRCm39) |
N2K |
probably damaging |
Het |
Dnah3 |
A |
T |
7: 119,528,079 (GRCm39) |
|
probably null |
Het |
Dnah6 |
T |
A |
6: 73,077,071 (GRCm39) |
Q2398L |
probably benign |
Het |
Dpep2 |
A |
T |
8: 106,716,080 (GRCm39) |
|
probably null |
Het |
Eif2ak4 |
C |
A |
2: 118,303,142 (GRCm39) |
T1504K |
probably damaging |
Het |
Exoc6b |
A |
G |
6: 84,828,896 (GRCm39) |
V496A |
probably damaging |
Het |
Fam174a |
A |
C |
1: 95,241,620 (GRCm39) |
S27R |
probably benign |
Het |
Fat2 |
T |
A |
11: 55,182,840 (GRCm39) |
Q1339L |
probably benign |
Het |
Fkbpl |
T |
A |
17: 34,864,797 (GRCm39) |
D188E |
possibly damaging |
Het |
Focad |
A |
G |
4: 88,325,402 (GRCm39) |
D89G |
possibly damaging |
Het |
Fstl4 |
C |
A |
11: 53,077,225 (GRCm39) |
Q661K |
probably benign |
Het |
Gck |
T |
C |
11: 5,853,253 (GRCm39) |
Y289C |
probably benign |
Het |
Gm16181 |
T |
A |
17: 35,442,913 (GRCm39) |
|
probably benign |
Het |
Herc1 |
G |
A |
9: 66,358,073 (GRCm39) |
G2385S |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,902,606 (GRCm39) |
|
probably null |
Het |
Il12b |
T |
C |
11: 44,299,353 (GRCm39) |
W141R |
probably damaging |
Het |
Itga6 |
T |
A |
2: 71,664,414 (GRCm39) |
S517T |
probably benign |
Het |
Kank1 |
A |
G |
19: 25,388,813 (GRCm39) |
S801G |
probably benign |
Het |
Klrh1 |
A |
G |
6: 129,752,343 (GRCm39) |
|
probably null |
Het |
Lctl |
A |
G |
9: 64,039,003 (GRCm39) |
D205G |
probably damaging |
Het |
Lhx3 |
A |
C |
2: 26,093,986 (GRCm39) |
V79G |
probably damaging |
Het |
Lrrc9 |
T |
C |
12: 72,543,912 (GRCm39) |
I1127T |
probably damaging |
Het |
Ltbp3 |
A |
T |
19: 5,797,877 (GRCm39) |
E505D |
probably benign |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Map6 |
A |
G |
7: 98,965,083 (GRCm39) |
S291G |
probably damaging |
Het |
Mapk7 |
A |
G |
11: 61,380,239 (GRCm39) |
F671L |
probably benign |
Het |
Mau2 |
A |
G |
8: 70,484,142 (GRCm39) |
W149R |
probably damaging |
Het |
Mb21d2 |
C |
T |
16: 28,647,267 (GRCm39) |
V236I |
possibly damaging |
Het |
Mc5r |
C |
G |
18: 68,471,741 (GRCm39) |
|
probably null |
Het |
Mical1 |
C |
A |
10: 41,361,466 (GRCm39) |
P797Q |
probably benign |
Het |
Mnx1 |
G |
A |
5: 29,679,043 (GRCm39) |
R347C |
unknown |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Nlrp2 |
G |
T |
7: 5,330,715 (GRCm39) |
C560* |
probably null |
Het |
Npat |
T |
A |
9: 53,474,416 (GRCm39) |
L736H |
probably damaging |
Het |
Nup155 |
T |
A |
15: 8,145,010 (GRCm39) |
V147E |
probably damaging |
Het |
Nxpe2 |
A |
G |
9: 48,238,121 (GRCm39) |
F45L |
probably benign |
Het |
Obscn |
T |
C |
11: 58,951,741 (GRCm39) |
D4370G |
probably benign |
Het |
Or2d3b |
A |
G |
7: 106,514,273 (GRCm39) |
I289M |
probably damaging |
Het |
Or4a79 |
T |
C |
2: 89,551,550 (GRCm39) |
K302E |
probably benign |
Het |
Or4c35 |
T |
C |
2: 89,808,671 (GRCm39) |
L183S |
probably damaging |
Het |
Or4d10 |
A |
G |
19: 12,051,183 (GRCm39) |
V271A |
probably benign |
Het |
Or52n4 |
A |
G |
7: 104,294,004 (GRCm39) |
S190P |
probably benign |
Het |
Or5g23 |
T |
A |
2: 85,439,188 (GRCm39) |
H22L |
probably benign |
Het |
Or8k3 |
A |
C |
2: 86,059,072 (GRCm39) |
M81R |
probably damaging |
Het |
Pcx |
T |
C |
19: 4,671,249 (GRCm39) |
I1157T |
possibly damaging |
Het |
Pias2 |
T |
A |
18: 77,240,412 (GRCm39) |
S589R |
probably benign |
Het |
Plcb1 |
T |
C |
2: 135,186,093 (GRCm39) |
F687L |
probably benign |
Het |
Plk5 |
G |
T |
10: 80,196,403 (GRCm39) |
|
probably null |
Het |
Pnpla2 |
T |
A |
7: 141,035,329 (GRCm39) |
Y44N |
probably damaging |
Het |
Ppp1r12a |
T |
A |
10: 108,098,292 (GRCm39) |
D337E |
possibly damaging |
Het |
Prl2c5 |
G |
T |
13: 13,365,358 (GRCm39) |
|
probably null |
Het |
Prom2 |
T |
C |
2: 127,378,514 (GRCm39) |
D460G |
probably damaging |
Het |
Pros1 |
A |
G |
16: 62,748,498 (GRCm39) |
H657R |
possibly damaging |
Het |
Prune2 |
A |
G |
19: 17,100,856 (GRCm39) |
E2120G |
probably damaging |
Het |
Rap2a |
T |
A |
14: 120,716,347 (GRCm39) |
L70Q |
probably damaging |
Het |
Rbl2 |
A |
T |
8: 91,839,157 (GRCm39) |
E858D |
probably benign |
Het |
Rbm48 |
T |
C |
5: 3,645,997 (GRCm39) |
Y69C |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,123,018 (GRCm39) |
I267N |
probably damaging |
Het |
Rpusd2 |
G |
T |
2: 118,865,728 (GRCm39) |
A142S |
probably benign |
Het |
Rspo2 |
A |
T |
15: 42,939,332 (GRCm39) |
W153R |
probably damaging |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Serinc5 |
T |
A |
13: 92,842,771 (GRCm39) |
M407K |
probably damaging |
Het |
Slain2 |
T |
C |
5: 73,114,665 (GRCm39) |
S299P |
probably damaging |
Het |
Slc17a4 |
A |
G |
13: 24,084,528 (GRCm39) |
Y419H |
possibly damaging |
Het |
Slc22a19 |
A |
T |
19: 7,688,506 (GRCm39) |
I18N |
probably damaging |
Het |
Slc37a3 |
A |
T |
6: 39,336,902 (GRCm39) |
F91L |
probably damaging |
Het |
Spag5 |
C |
A |
11: 78,195,281 (GRCm39) |
T196K |
possibly damaging |
Het |
Susd2 |
G |
T |
10: 75,475,566 (GRCm39) |
A326D |
probably damaging |
Het |
Syna |
G |
T |
5: 134,588,769 (GRCm39) |
A60D |
probably damaging |
Het |
Tchh |
A |
T |
3: 93,355,067 (GRCm39) |
E1502D |
unknown |
Het |
Tecta |
T |
C |
9: 42,303,320 (GRCm39) |
H104R |
probably damaging |
Het |
Tmed1 |
T |
C |
9: 21,420,387 (GRCm39) |
D102G |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,722,781 (GRCm39) |
D128G |
probably damaging |
Het |
Uroc1 |
A |
G |
6: 90,338,506 (GRCm39) |
M656V |
probably benign |
Het |
Usp47 |
T |
A |
7: 111,701,077 (GRCm39) |
V1096D |
possibly damaging |
Het |
Utp20 |
T |
A |
10: 88,598,632 (GRCm39) |
K115* |
probably null |
Het |
Vmn2r19 |
G |
T |
6: 123,308,597 (GRCm39) |
|
probably null |
Het |
Vmn2r86 |
A |
T |
10: 130,282,255 (GRCm39) |
V787D |
probably damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,308,441 (GRCm39) |
I599N |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,644,492 (GRCm39) |
D2449G |
possibly damaging |
Het |
Zbtb7c |
T |
A |
18: 76,269,977 (GRCm39) |
C22S |
probably benign |
Het |
Zc3h7a |
A |
G |
16: 10,965,168 (GRCm39) |
I655T |
possibly damaging |
Het |
Zfp764l1 |
A |
G |
7: 126,992,503 (GRCm39) |
W36R |
probably damaging |
Het |
|
Other mutations in Slc1a6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Slc1a6
|
APN |
10 |
78,637,647 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00496:Slc1a6
|
APN |
10 |
78,629,142 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01099:Slc1a6
|
APN |
10 |
78,624,831 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02299:Slc1a6
|
APN |
10 |
78,629,137 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02677:Slc1a6
|
APN |
10 |
78,624,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02705:Slc1a6
|
APN |
10 |
78,637,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03024:Slc1a6
|
APN |
10 |
78,650,442 (GRCm39) |
missense |
probably benign |
|
IGL03185:Slc1a6
|
APN |
10 |
78,637,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03046:Slc1a6
|
UTSW |
10 |
78,636,008 (GRCm39) |
missense |
probably benign |
0.19 |
R0183:Slc1a6
|
UTSW |
10 |
78,627,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Slc1a6
|
UTSW |
10 |
78,637,756 (GRCm39) |
nonsense |
probably null |
|
R0730:Slc1a6
|
UTSW |
10 |
78,631,842 (GRCm39) |
missense |
probably benign |
0.13 |
R0774:Slc1a6
|
UTSW |
10 |
78,648,658 (GRCm39) |
missense |
probably benign |
0.03 |
R0838:Slc1a6
|
UTSW |
10 |
78,632,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R1449:Slc1a6
|
UTSW |
10 |
78,635,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R1822:Slc1a6
|
UTSW |
10 |
78,648,765 (GRCm39) |
nonsense |
probably null |
|
R1853:Slc1a6
|
UTSW |
10 |
78,648,758 (GRCm39) |
missense |
probably damaging |
0.97 |
R1854:Slc1a6
|
UTSW |
10 |
78,648,758 (GRCm39) |
missense |
probably damaging |
0.97 |
R1855:Slc1a6
|
UTSW |
10 |
78,648,758 (GRCm39) |
missense |
probably damaging |
0.97 |
R2073:Slc1a6
|
UTSW |
10 |
78,635,964 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2279:Slc1a6
|
UTSW |
10 |
78,624,882 (GRCm39) |
missense |
probably benign |
0.12 |
R2360:Slc1a6
|
UTSW |
10 |
78,648,718 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2939:Slc1a6
|
UTSW |
10 |
78,650,448 (GRCm39) |
makesense |
probably null |
|
R3111:Slc1a6
|
UTSW |
10 |
78,624,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R3926:Slc1a6
|
UTSW |
10 |
78,648,715 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4116:Slc1a6
|
UTSW |
10 |
78,623,723 (GRCm39) |
missense |
probably benign |
0.00 |
R4798:Slc1a6
|
UTSW |
10 |
78,635,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Slc1a6
|
UTSW |
10 |
78,632,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Slc1a6
|
UTSW |
10 |
78,650,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5166:Slc1a6
|
UTSW |
10 |
78,632,103 (GRCm39) |
critical splice donor site |
probably null |
|
R5304:Slc1a6
|
UTSW |
10 |
78,629,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Slc1a6
|
UTSW |
10 |
78,623,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Slc1a6
|
UTSW |
10 |
78,631,816 (GRCm39) |
missense |
probably benign |
0.00 |
R5635:Slc1a6
|
UTSW |
10 |
78,624,925 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5773:Slc1a6
|
UTSW |
10 |
78,629,111 (GRCm39) |
splice site |
probably null |
|
R6117:Slc1a6
|
UTSW |
10 |
78,624,822 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6167:Slc1a6
|
UTSW |
10 |
78,637,671 (GRCm39) |
missense |
probably benign |
0.40 |
R6174:Slc1a6
|
UTSW |
10 |
78,637,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Slc1a6
|
UTSW |
10 |
78,635,910 (GRCm39) |
missense |
probably damaging |
0.98 |
R6323:Slc1a6
|
UTSW |
10 |
78,648,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Slc1a6
|
UTSW |
10 |
78,635,919 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6670:Slc1a6
|
UTSW |
10 |
78,623,646 (GRCm39) |
missense |
probably benign |
0.00 |
R7166:Slc1a6
|
UTSW |
10 |
78,648,646 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7292:Slc1a6
|
UTSW |
10 |
78,650,438 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7548:Slc1a6
|
UTSW |
10 |
78,650,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Slc1a6
|
UTSW |
10 |
78,631,789 (GRCm39) |
missense |
probably damaging |
0.96 |
R7843:Slc1a6
|
UTSW |
10 |
78,632,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R8068:Slc1a6
|
UTSW |
10 |
78,648,706 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8190:Slc1a6
|
UTSW |
10 |
78,627,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Slc1a6
|
UTSW |
10 |
78,632,091 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8846:Slc1a6
|
UTSW |
10 |
78,637,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R9216:Slc1a6
|
UTSW |
10 |
78,637,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Slc1a6
|
UTSW |
10 |
78,648,698 (GRCm39) |
missense |
probably benign |
0.06 |
R9798:Slc1a6
|
UTSW |
10 |
78,629,167 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Slc1a6
|
UTSW |
10 |
78,631,909 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1177:Slc1a6
|
UTSW |
10 |
78,648,728 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Slc1a6
|
UTSW |
10 |
78,627,101 (GRCm39) |
missense |
possibly damaging |
0.79 |
|