Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
C |
11: 110,042,889 (GRCm39) |
N387D |
probably benign |
Het |
Adgrg5 |
T |
A |
8: 95,660,785 (GRCm39) |
|
probably null |
Het |
Ahi1 |
C |
A |
10: 20,855,360 (GRCm39) |
H556Q |
probably damaging |
Het |
Amph |
A |
G |
13: 19,270,791 (GRCm39) |
|
probably null |
Het |
Apol7a |
T |
C |
15: 77,274,055 (GRCm39) |
|
probably benign |
Het |
Arpc1b |
A |
G |
5: 145,063,670 (GRCm39) |
D306G |
probably damaging |
Het |
Astn2 |
T |
C |
4: 65,712,795 (GRCm39) |
D615G |
probably damaging |
Het |
Atm |
A |
G |
9: 53,397,314 (GRCm39) |
V1673A |
probably damaging |
Het |
B3gnt3 |
A |
T |
8: 72,146,466 (GRCm39) |
V21E |
probably benign |
Het |
Bco1 |
A |
G |
8: 117,832,435 (GRCm39) |
D77G |
probably damaging |
Het |
Brinp2 |
A |
T |
1: 158,074,191 (GRCm39) |
H643Q |
probably damaging |
Het |
Bsn |
A |
G |
9: 107,982,941 (GRCm39) |
F3604S |
unknown |
Het |
Cacna1c |
A |
G |
6: 118,579,190 (GRCm39) |
F1753L |
probably damaging |
Het |
Cd74 |
T |
C |
18: 60,944,957 (GRCm39) |
S201P |
probably damaging |
Het |
Cep192 |
T |
A |
18: 67,940,336 (GRCm39) |
L101Q |
probably benign |
Het |
Cfap161 |
T |
C |
7: 83,442,484 (GRCm39) |
I110V |
probably null |
Het |
Cnksr3 |
T |
C |
10: 7,070,463 (GRCm39) |
D257G |
probably damaging |
Het |
Col14a1 |
A |
C |
15: 55,208,278 (GRCm39) |
E121A |
unknown |
Het |
Cpne3 |
T |
C |
4: 19,532,486 (GRCm39) |
D309G |
probably benign |
Het |
Ctnnd1 |
A |
G |
2: 84,433,240 (GRCm39) |
I609T |
probably benign |
Het |
Cyp2s1 |
A |
G |
7: 25,508,683 (GRCm39) |
V253A |
probably damaging |
Het |
Dock7 |
T |
C |
4: 98,943,586 (GRCm39) |
D552G |
possibly damaging |
Het |
Dpyd |
A |
G |
3: 119,220,924 (GRCm39) |
D965G |
probably damaging |
Het |
Efcab2 |
T |
A |
1: 178,308,911 (GRCm39) |
M138K |
probably damaging |
Het |
Eml3 |
T |
C |
19: 8,910,649 (GRCm39) |
S204P |
probably damaging |
Het |
Fbxw16 |
T |
A |
9: 109,265,236 (GRCm39) |
S432C |
possibly damaging |
Het |
Fbxw20 |
T |
G |
9: 109,061,400 (GRCm39) |
Q116H |
probably damaging |
Het |
Fech |
A |
G |
18: 64,591,240 (GRCm39) |
S395P |
probably damaging |
Het |
Fgf7 |
A |
G |
2: 125,877,875 (GRCm39) |
K81E |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,929,199 (GRCm39) |
Y3868N |
possibly damaging |
Het |
Ganab |
A |
T |
19: 8,892,766 (GRCm39) |
|
probably null |
Het |
Gfra1 |
T |
C |
19: 58,288,986 (GRCm39) |
N153S |
possibly damaging |
Het |
Gja4 |
T |
A |
4: 127,205,920 (GRCm39) |
Y281F |
probably benign |
Het |
Gm5141 |
T |
C |
13: 62,921,946 (GRCm39) |
T407A |
probably damaging |
Het |
Gm5422 |
T |
C |
10: 31,125,277 (GRCm39) |
|
noncoding transcript |
Het |
Greb1 |
T |
C |
12: 16,746,457 (GRCm39) |
Y1271C |
probably damaging |
Het |
Hp1bp3 |
C |
A |
4: 137,956,080 (GRCm39) |
N50K |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,242,033 (GRCm39) |
F589S |
probably damaging |
Het |
Ido1 |
A |
G |
8: 25,075,260 (GRCm39) |
F183S |
probably damaging |
Het |
Iqgap1 |
T |
A |
7: 80,386,143 (GRCm39) |
K936I |
probably damaging |
Het |
Kdm4a |
T |
C |
4: 118,032,886 (GRCm39) |
D60G |
probably benign |
Het |
L3mbtl4 |
G |
A |
17: 69,081,286 (GRCm39) |
C558Y |
probably damaging |
Het |
Lrrc28 |
T |
C |
7: 67,267,833 (GRCm39) |
N98S |
probably damaging |
Het |
Lypd11 |
T |
A |
7: 24,423,622 (GRCm39) |
N14I |
possibly damaging |
Het |
Map1a |
A |
G |
2: 121,133,264 (GRCm39) |
D1360G |
probably benign |
Het |
Megf10 |
C |
T |
18: 57,410,796 (GRCm39) |
P702S |
probably benign |
Het |
Met |
A |
G |
6: 17,491,709 (GRCm39) |
E157G |
probably benign |
Het |
Mff |
A |
G |
1: 82,728,285 (GRCm39) |
D187G |
possibly damaging |
Het |
Mlph |
A |
T |
1: 90,870,630 (GRCm39) |
I514F |
possibly damaging |
Het |
Mroh2a |
C |
T |
1: 88,158,402 (GRCm39) |
R150* |
probably null |
Het |
Myo15b |
T |
C |
11: 115,755,468 (GRCm39) |
V976A |
probably benign |
Het |
Myo9a |
A |
G |
9: 59,779,209 (GRCm39) |
D1655G |
probably benign |
Het |
Ncoa6 |
C |
T |
2: 155,233,131 (GRCm39) |
G2059D |
probably benign |
Het |
Ndst4 |
A |
T |
3: 125,405,188 (GRCm39) |
H481L |
possibly damaging |
Het |
Nipbl |
A |
G |
15: 8,332,964 (GRCm39) |
S2220P |
probably benign |
Het |
Nom1 |
C |
A |
5: 29,640,309 (GRCm39) |
P212T |
probably damaging |
Het |
Nsd1 |
A |
G |
13: 55,395,399 (GRCm39) |
D1000G |
possibly damaging |
Het |
Nudt9 |
T |
C |
5: 104,198,467 (GRCm39) |
F44S |
possibly damaging |
Het |
Numb |
C |
T |
12: 83,842,566 (GRCm39) |
V537I |
probably damaging |
Het |
Or10j3b |
T |
A |
1: 173,043,524 (GRCm39) |
I102N |
possibly damaging |
Het |
Or13a27 |
A |
T |
7: 139,925,545 (GRCm39) |
M119K |
probably damaging |
Het |
Or51q1c |
A |
G |
7: 103,652,446 (GRCm39) |
|
probably null |
Het |
Or5b109 |
A |
T |
19: 13,211,899 (GRCm39) |
Y95F |
possibly damaging |
Het |
Or5h17 |
A |
G |
16: 58,820,063 (GRCm39) |
N5S |
probably damaging |
Het |
Or6c211 |
T |
A |
10: 129,506,248 (GRCm39) |
T47S |
probably benign |
Het |
Osgin1 |
A |
T |
8: 120,172,211 (GRCm39) |
Y335F |
probably damaging |
Het |
Pcdh10 |
T |
A |
3: 45,334,199 (GRCm39) |
V171E |
probably damaging |
Het |
Pira13 |
T |
A |
7: 3,825,762 (GRCm39) |
Y369F |
probably benign |
Het |
Plxna4 |
T |
C |
6: 32,162,436 (GRCm39) |
N1359S |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Prr5l |
T |
C |
2: 101,602,635 (GRCm39) |
T2A |
possibly damaging |
Het |
Rbp3 |
T |
A |
14: 33,680,605 (GRCm39) |
I1069N |
possibly damaging |
Het |
Rnf144b |
A |
G |
13: 47,373,983 (GRCm39) |
Y60C |
probably damaging |
Het |
Sbno2 |
A |
T |
10: 79,903,128 (GRCm39) |
V396E |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 141,940,713 (GRCm39) |
T494A |
probably benign |
Het |
Serac1 |
G |
T |
17: 6,102,031 (GRCm39) |
D384E |
probably damaging |
Het |
Sgk1 |
A |
G |
10: 21,758,556 (GRCm39) |
N7D |
probably damaging |
Het |
Sigirr |
A |
T |
7: 140,672,980 (GRCm39) |
V69D |
possibly damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
St6gal2 |
T |
C |
17: 55,805,290 (GRCm39) |
Y396H |
probably benign |
Het |
Ttn |
A |
T |
2: 76,598,956 (GRCm39) |
F19319Y |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,128,637 (GRCm39) |
I599N |
probably damaging |
Het |
Vmn1r213 |
A |
G |
13: 23,195,564 (GRCm39) |
|
probably benign |
Het |
Vmn2r96 |
T |
A |
17: 18,817,830 (GRCm39) |
M469K |
probably benign |
Het |
Wasf1 |
T |
A |
10: 40,807,902 (GRCm39) |
|
probably null |
Het |
Wdr20rt |
T |
C |
12: 65,272,689 (GRCm39) |
S51P |
probably damaging |
Het |
|