Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd5 |
T |
A |
9: 122,351,815 |
V10E |
probably benign |
Het |
AI467606 |
A |
T |
7: 127,092,501 |
I83F |
probably damaging |
Het |
Atn1 |
A |
T |
6: 124,746,960 |
W437R |
unknown |
Het |
Atxn7l2 |
T |
C |
3: 108,208,974 |
|
probably benign |
Het |
AU040320 |
T |
C |
4: 126,841,143 |
F750S |
possibly damaging |
Het |
B3gnt6 |
A |
G |
7: 98,193,614 |
S380P |
probably benign |
Het |
Bod1l |
T |
C |
5: 41,788,872 |
Q3020R |
probably damaging |
Het |
Borcs6 |
A |
T |
11: 69,060,002 |
I69F |
probably benign |
Het |
Brd7 |
T |
A |
8: 88,354,712 |
M170L |
probably benign |
Het |
Cit |
C |
T |
5: 115,926,475 |
T472I |
possibly damaging |
Het |
Ddx25 |
G |
T |
9: 35,557,389 |
D57E |
probably benign |
Het |
Epb41l3 |
A |
G |
17: 69,247,646 |
D247G |
probably damaging |
Het |
Epha8 |
G |
T |
4: 136,938,586 |
L420M |
probably damaging |
Het |
Etaa1 |
A |
T |
11: 17,940,254 |
V869E |
probably damaging |
Het |
Exoc8 |
T |
A |
8: 124,896,030 |
I533F |
probably benign |
Het |
Fam117a |
A |
G |
11: 95,363,997 |
|
probably null |
Het |
Fam222a |
C |
T |
5: 114,611,031 |
T96I |
possibly damaging |
Het |
Fam71b |
C |
A |
11: 46,404,868 |
Y22* |
probably null |
Het |
Farsa |
C |
T |
8: 84,867,599 |
T326I |
probably damaging |
Het |
Fkbp1b |
T |
A |
12: 4,841,401 |
D12V |
probably damaging |
Het |
Gc |
C |
T |
5: 89,441,562 |
|
probably null |
Het |
Git2 |
T |
C |
5: 114,730,195 |
E705G |
probably damaging |
Het |
Gm10318 |
G |
A |
10: 77,853,244 |
C128Y |
unknown |
Het |
Hcar2 |
G |
A |
5: 123,864,508 |
R311* |
probably null |
Het |
Hira |
A |
G |
16: 18,927,511 |
Q468R |
possibly damaging |
Het |
Hist1h3c |
C |
A |
13: 23,745,410 |
A30S |
probably benign |
Het |
Hspa1l |
T |
C |
17: 34,978,116 |
V377A |
probably damaging |
Het |
Igkv2-137 |
T |
A |
6: 67,555,675 |
W14R |
probably damaging |
Het |
Itga3 |
A |
T |
11: 95,062,565 |
L317Q |
probably damaging |
Het |
Jade2 |
A |
C |
11: 51,825,079 |
L433W |
probably damaging |
Het |
Kif21a |
T |
C |
15: 90,956,356 |
T1186A |
probably benign |
Het |
Krtap28-10 |
C |
A |
1: 83,042,173 |
C82F |
unknown |
Het |
Ksr1 |
G |
A |
11: 79,040,883 |
T333M |
probably damaging |
Het |
Msi1 |
T |
C |
5: 115,435,539 |
F132S |
probably damaging |
Het |
Myo7b |
C |
A |
18: 31,966,349 |
K1673N |
probably null |
Het |
Myom3 |
T |
A |
4: 135,787,944 |
N716K |
|
Het |
Ndst4 |
G |
A |
3: 125,722,161 |
G312R |
probably damaging |
Het |
Ndufaf2 |
A |
G |
13: 108,052,782 |
V144A |
probably benign |
Het |
Olfr135 |
A |
G |
17: 38,208,413 |
H56R |
probably damaging |
Het |
Olfr328 |
G |
C |
11: 58,551,383 |
N285K |
probably damaging |
Het |
Olfr558 |
T |
A |
7: 102,710,012 |
I251N |
possibly damaging |
Het |
Olfr594 |
T |
C |
7: 103,220,186 |
L156P |
possibly damaging |
Het |
Olfr628 |
T |
C |
7: 103,732,013 |
I29T |
probably damaging |
Het |
Olfr64 |
G |
A |
7: 103,893,609 |
T42I |
probably benign |
Het |
Omd |
T |
C |
13: 49,590,100 |
S209P |
possibly damaging |
Het |
Patl1 |
T |
A |
19: 11,921,396 |
Y152N |
probably damaging |
Het |
Plaur |
T |
A |
7: 24,465,152 |
M27K |
probably benign |
Het |
Ppfia3 |
A |
G |
7: 45,340,676 |
V1142A |
probably damaging |
Het |
Psg28 |
T |
A |
7: 18,423,056 |
N418I |
probably damaging |
Het |
Ptprd |
A |
T |
4: 75,945,014 |
F1237I |
probably damaging |
Het |
Ptprj |
G |
A |
2: 90,440,643 |
P1247L |
probably damaging |
Het |
Rbms3 |
A |
T |
9: 116,695,818 |
|
probably null |
Het |
Rgs18 |
A |
G |
1: 144,753,828 |
V231A |
probably benign |
Het |
Rnf112 |
T |
C |
11: 61,452,451 |
R156G |
possibly damaging |
Het |
Rsad1 |
A |
C |
11: 94,548,184 |
V150G |
probably damaging |
Het |
Rxrg |
G |
A |
1: 167,634,436 |
V350I |
possibly damaging |
Het |
Sash1 |
A |
G |
10: 8,751,044 |
I192T |
possibly damaging |
Het |
Slc25a36 |
G |
A |
9: 97,079,206 |
T259I |
probably benign |
Het |
Smarcd3 |
T |
A |
5: 24,593,988 |
E324V |
probably null |
Het |
St3gal4 |
A |
G |
9: 35,055,648 |
V2A |
possibly damaging |
Het |
Stk17b |
A |
C |
1: 53,757,625 |
S328A |
probably benign |
Het |
Tbrg1 |
A |
G |
9: 37,652,653 |
Y229H |
probably damaging |
Het |
Tdg |
A |
G |
10: 82,648,680 |
N409S |
probably benign |
Het |
Terb1 |
T |
C |
8: 104,485,404 |
E315G |
possibly damaging |
Het |
Tmem131 |
A |
G |
1: 36,828,147 |
F402L |
probably benign |
Het |
Trav4-2 |
T |
C |
14: 53,418,733 |
I64T |
probably benign |
Het |
Trav4-4-dv10 |
A |
G |
14: 53,684,117 |
T91A |
probably benign |
Het |
Xdh |
C |
T |
17: 73,921,351 |
G352R |
probably damaging |
Het |
Zfp551 |
C |
A |
7: 12,422,632 |
|
probably benign |
Het |
|