Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
C |
11: 110,152,063 |
N387D |
probably benign |
Het |
Adgrg5 |
T |
A |
8: 94,934,157 |
|
probably null |
Het |
Ahi1 |
C |
A |
10: 20,979,461 |
H556Q |
probably damaging |
Het |
Amph |
A |
G |
13: 19,086,621 |
|
probably null |
Het |
Apol7a |
T |
C |
15: 77,389,855 |
|
probably benign |
Het |
Apoo-ps |
A |
T |
13: 107,414,410 |
|
noncoding transcript |
Het |
Arpc1b |
A |
G |
5: 145,126,860 |
D306G |
probably damaging |
Het |
Astn2 |
T |
C |
4: 65,794,558 |
D615G |
probably damaging |
Het |
Atm |
A |
G |
9: 53,486,014 |
V1673A |
probably damaging |
Het |
B3gnt3 |
A |
T |
8: 71,693,822 |
V21E |
probably benign |
Het |
Bco1 |
A |
G |
8: 117,105,696 |
D77G |
probably damaging |
Het |
Brinp2 |
A |
T |
1: 158,246,621 |
H643Q |
probably damaging |
Het |
Bsn |
A |
G |
9: 108,105,742 |
F3604S |
unknown |
Het |
Cacna1c |
A |
G |
6: 118,602,229 |
F1753L |
probably damaging |
Het |
Cd74 |
T |
C |
18: 60,811,885 |
S201P |
probably damaging |
Het |
Cep192 |
T |
A |
18: 67,807,265 |
L101Q |
probably benign |
Het |
Cfap161 |
T |
C |
7: 83,793,276 |
I110V |
probably null |
Het |
Cnksr3 |
T |
C |
10: 7,120,463 |
D257G |
probably damaging |
Het |
Col14a1 |
A |
C |
15: 55,344,882 |
E121A |
unknown |
Het |
Cpne3 |
T |
C |
4: 19,532,486 |
D309G |
probably benign |
Het |
Ctnnd1 |
A |
G |
2: 84,602,896 |
I609T |
probably benign |
Het |
Cyp2s1 |
A |
G |
7: 25,809,258 |
V253A |
probably damaging |
Het |
Dock7 |
T |
C |
4: 99,055,349 |
D552G |
possibly damaging |
Het |
Dpyd |
A |
G |
3: 119,427,275 |
D965G |
probably damaging |
Het |
Efcab2 |
T |
A |
1: 178,481,346 |
M138K |
probably damaging |
Het |
Eml3 |
T |
C |
19: 8,933,285 |
S204P |
probably damaging |
Het |
Fbxw16 |
T |
A |
9: 109,436,168 |
S432C |
possibly damaging |
Het |
Fbxw20 |
T |
G |
9: 109,232,332 |
Q116H |
probably damaging |
Het |
Fech |
A |
G |
18: 64,458,169 |
S395P |
probably damaging |
Het |
Fgf7 |
A |
G |
2: 126,035,955 |
K81E |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,781,340 |
Y3868N |
possibly damaging |
Het |
Ganab |
A |
T |
19: 8,915,402 |
|
probably null |
Het |
Gfra1 |
T |
C |
19: 58,300,554 |
N153S |
possibly damaging |
Het |
Gja4 |
T |
A |
4: 127,312,127 |
Y281F |
probably benign |
Het |
Gm15448 |
T |
A |
7: 3,822,763 |
Y369F |
probably benign |
Het |
Gm4763 |
T |
A |
7: 24,724,197 |
N14I |
possibly damaging |
Het |
Gm5141 |
T |
C |
13: 62,774,132 |
T407A |
probably damaging |
Het |
Gm5422 |
T |
C |
10: 31,249,281 |
|
noncoding transcript |
Het |
Greb1 |
T |
C |
12: 16,696,456 |
Y1271C |
probably damaging |
Het |
Hp1bp3 |
C |
A |
4: 138,228,769 |
N50K |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,514,722 |
F589S |
probably damaging |
Het |
Ido1 |
A |
G |
8: 24,585,244 |
F183S |
probably damaging |
Het |
Iqgap1 |
T |
A |
7: 80,736,395 |
K936I |
probably damaging |
Het |
Kdm4a |
T |
C |
4: 118,175,689 |
D60G |
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 68,774,291 |
C558Y |
probably damaging |
Het |
Lrrc28 |
T |
C |
7: 67,618,085 |
N98S |
probably damaging |
Het |
Map1a |
A |
G |
2: 121,302,783 |
D1360G |
probably benign |
Het |
Megf10 |
C |
T |
18: 57,277,724 |
P702S |
probably benign |
Het |
Met |
A |
G |
6: 17,491,710 |
E157G |
probably benign |
Het |
Mff |
A |
G |
1: 82,750,564 |
D187G |
possibly damaging |
Het |
Mlph |
A |
T |
1: 90,942,908 |
I514F |
possibly damaging |
Het |
Mroh2a |
C |
T |
1: 88,230,680 |
R150* |
probably null |
Het |
Myo15b |
T |
C |
11: 115,864,642 |
V976A |
probably benign |
Het |
Myo9a |
A |
G |
9: 59,871,926 |
D1655G |
probably benign |
Het |
Ncoa6 |
C |
T |
2: 155,391,211 |
G2059D |
probably benign |
Het |
Ndst4 |
A |
T |
3: 125,611,539 |
H481L |
possibly damaging |
Het |
Nipbl |
A |
G |
15: 8,303,480 |
S2220P |
probably benign |
Het |
Nom1 |
C |
A |
5: 29,435,311 |
P212T |
probably damaging |
Het |
Nsd1 |
A |
G |
13: 55,247,586 |
D1000G |
possibly damaging |
Het |
Nudt9 |
T |
C |
5: 104,050,601 |
F44S |
possibly damaging |
Het |
Numb |
C |
T |
12: 83,795,792 |
V537I |
probably damaging |
Het |
Olfr1404 |
T |
A |
1: 173,215,957 |
I102N |
possibly damaging |
Het |
Olfr1463 |
A |
T |
19: 13,234,535 |
Y95F |
possibly damaging |
Het |
Olfr183 |
A |
G |
16: 58,999,700 |
N5S |
probably damaging |
Het |
Olfr60 |
A |
T |
7: 140,345,632 |
M119K |
probably damaging |
Het |
Olfr638 |
A |
G |
7: 104,003,239 |
|
probably null |
Het |
Olfr801 |
T |
A |
10: 129,670,379 |
T47S |
probably benign |
Het |
Osgin1 |
A |
T |
8: 119,445,472 |
Y335F |
probably damaging |
Het |
Pcdh10 |
T |
A |
3: 45,379,764 |
V171E |
probably damaging |
Het |
Plxna4 |
T |
C |
6: 32,185,501 |
N1359S |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,690,799 |
|
probably benign |
Het |
Prr5l |
T |
C |
2: 101,772,290 |
T2A |
possibly damaging |
Het |
Rbp3 |
T |
A |
14: 33,958,648 |
I1069N |
possibly damaging |
Het |
Sbno2 |
A |
T |
10: 80,067,294 |
V396E |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 141,954,958 |
T494A |
probably benign |
Het |
Serac1 |
G |
T |
17: 6,051,756 |
D384E |
probably damaging |
Het |
Sgk1 |
A |
G |
10: 21,882,657 |
N7D |
probably damaging |
Het |
Sigirr |
A |
T |
7: 141,093,067 |
V69D |
possibly damaging |
Het |
Slc17a3 |
C |
T |
13: 23,855,858 |
S293F |
probably damaging |
Het |
St6gal2 |
T |
C |
17: 55,498,289 |
Y396H |
probably benign |
Het |
Ttn |
A |
T |
2: 76,768,612 |
F19319Y |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,401,326 |
I599N |
probably damaging |
Het |
Vmn1r213 |
A |
G |
13: 23,011,394 |
|
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,597,568 |
M469K |
probably benign |
Het |
Wasf1 |
T |
A |
10: 40,931,906 |
|
probably null |
Het |
Wdr20rt |
T |
C |
12: 65,225,915 |
S51P |
probably damaging |
Het |
|