Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamp |
C |
T |
1: 74,323,165 (GRCm39) |
E53K |
possibly damaging |
Het |
Amotl1 |
T |
C |
9: 14,469,780 (GRCm39) |
E651G |
probably damaging |
Het |
Ankrd11 |
A |
C |
8: 123,610,921 (GRCm39) |
V2655G |
probably damaging |
Het |
Apbb1ip |
G |
A |
2: 22,757,683 (GRCm39) |
V434M |
probably benign |
Het |
Atp5pd |
T |
C |
11: 115,306,611 (GRCm39) |
Y150C |
probably damaging |
Het |
Ccdc13 |
T |
A |
9: 121,637,254 (GRCm39) |
D75V |
probably damaging |
Het |
Col4a4 |
C |
T |
1: 82,471,312 (GRCm39) |
G681E |
unknown |
Het |
Crh |
T |
C |
3: 19,748,171 (GRCm39) |
H157R |
probably damaging |
Het |
Cstdc6 |
T |
C |
16: 36,142,205 (GRCm39) |
D57G |
probably damaging |
Het |
Dpp4 |
G |
A |
2: 62,190,680 (GRCm39) |
T392I |
probably damaging |
Het |
Ehd3 |
G |
T |
17: 74,127,498 (GRCm39) |
A144S |
probably benign |
Het |
Fnip2 |
A |
T |
3: 79,373,015 (GRCm39) |
I1021N |
probably damaging |
Het |
Fus |
T |
A |
7: 127,584,719 (GRCm39) |
|
probably benign |
Het |
Glo1 |
T |
C |
17: 30,819,047 (GRCm39) |
T92A |
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Gm15130 |
A |
C |
2: 110,965,754 (GRCm39) |
M165R |
unknown |
Het |
Gon4l |
T |
C |
3: 88,794,897 (GRCm39) |
L700P |
probably damaging |
Het |
Grm1 |
C |
A |
10: 10,608,936 (GRCm39) |
D566Y |
possibly damaging |
Het |
Guca1b |
T |
C |
17: 47,702,195 (GRCm39) |
|
probably benign |
Het |
Has3 |
A |
G |
8: 107,600,747 (GRCm39) |
M70V |
probably damaging |
Het |
Hydin |
G |
T |
8: 111,178,612 (GRCm39) |
C1069F |
possibly damaging |
Het |
Ints1 |
A |
C |
5: 139,750,137 (GRCm39) |
L920R |
probably damaging |
Het |
Kdm2a |
T |
C |
19: 4,381,297 (GRCm39) |
I54V |
probably benign |
Het |
Kpna2 |
G |
A |
11: 106,881,658 (GRCm39) |
T324I |
probably damaging |
Het |
Lrr1 |
T |
C |
12: 69,221,428 (GRCm39) |
L190S |
probably damaging |
Het |
Lrrc49 |
A |
T |
9: 60,594,461 (GRCm39) |
H16Q |
probably benign |
Het |
Mab21l4 |
C |
T |
1: 93,087,575 (GRCm39) |
D93N |
probably benign |
Het |
Mapkap1 |
A |
G |
2: 34,334,360 (GRCm39) |
E147G |
probably damaging |
Het |
Mrpl2 |
C |
T |
17: 46,959,992 (GRCm39) |
R219W |
possibly damaging |
Het |
Muc21 |
A |
G |
17: 35,932,224 (GRCm39) |
|
probably benign |
Het |
Ndc80 |
A |
G |
17: 71,828,130 (GRCm39) |
S66P |
probably benign |
Het |
Notch1 |
A |
G |
2: 26,358,638 (GRCm39) |
Y1398H |
probably damaging |
Het |
Olfml2b |
C |
T |
1: 170,508,758 (GRCm39) |
R539* |
probably null |
Het |
Or6b9 |
T |
A |
7: 106,555,955 (GRCm39) |
T63S |
probably benign |
Het |
Pde7a |
T |
C |
3: 19,314,420 (GRCm39) |
T59A |
probably damaging |
Het |
Plekhg1 |
G |
A |
10: 3,906,654 (GRCm39) |
V524I |
probably benign |
Het |
Plin4 |
T |
A |
17: 56,413,777 (GRCm39) |
M283L |
probably benign |
Het |
Prp2 |
C |
T |
6: 132,577,606 (GRCm39) |
P298S |
unknown |
Het |
Rap1gap2 |
G |
A |
11: 74,286,651 (GRCm39) |
R550C |
probably damaging |
Het |
Reln |
G |
A |
5: 22,216,161 (GRCm39) |
T1008I |
probably damaging |
Het |
Rffl |
T |
C |
11: 82,703,615 (GRCm39) |
K103E |
probably damaging |
Het |
Rmnd5b |
A |
T |
11: 51,517,887 (GRCm39) |
F156I |
probably damaging |
Het |
Rtn4ip1 |
T |
C |
10: 43,778,461 (GRCm39) |
I68T |
probably damaging |
Het |
Samhd1 |
T |
C |
2: 156,951,412 (GRCm39) |
I442V |
possibly damaging |
Het |
Slc12a4 |
A |
T |
8: 106,677,326 (GRCm39) |
|
probably null |
Het |
Slc35b1 |
G |
T |
11: 95,275,814 (GRCm39) |
|
probably benign |
Het |
Ssh1 |
A |
G |
5: 114,088,606 (GRCm39) |
V354A |
probably damaging |
Het |
Stk4 |
C |
T |
2: 163,952,199 (GRCm39) |
R19* |
probably null |
Het |
Tas2r136 |
A |
T |
6: 132,754,374 (GRCm39) |
I251N |
probably damaging |
Het |
Tbr1 |
A |
T |
2: 61,635,244 (GRCm39) |
T65S |
probably benign |
Het |
Tkt |
C |
T |
14: 30,282,575 (GRCm39) |
S124F |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,555,000 (GRCm39) |
I228V |
possibly damaging |
Het |
Tmem236 |
A |
G |
2: 14,179,644 (GRCm39) |
I82V |
probably benign |
Het |
Vmn2r110 |
T |
C |
17: 20,800,899 (GRCm39) |
Q511R |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,300,981 (GRCm39) |
M661T |
probably benign |
Het |
Vps13a |
T |
A |
19: 16,655,334 (GRCm39) |
K1898I |
probably damaging |
Het |
Zc3h12a |
T |
C |
4: 125,020,558 (GRCm39) |
E95G |
probably benign |
Het |
|
Other mutations in Stk33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01137:Stk33
|
APN |
7 |
108,928,775 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01467:Stk33
|
APN |
7 |
108,928,796 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01558:Stk33
|
APN |
7 |
108,940,491 (GRCm39) |
intron |
probably benign |
|
IGL01775:Stk33
|
APN |
7 |
108,911,574 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0052:Stk33
|
UTSW |
7 |
108,878,876 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0336:Stk33
|
UTSW |
7 |
108,930,681 (GRCm39) |
missense |
probably benign |
0.01 |
R0394:Stk33
|
UTSW |
7 |
108,940,696 (GRCm39) |
missense |
probably benign |
|
R0579:Stk33
|
UTSW |
7 |
108,924,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R0727:Stk33
|
UTSW |
7 |
108,920,725 (GRCm39) |
missense |
probably damaging |
0.96 |
R1363:Stk33
|
UTSW |
7 |
108,879,028 (GRCm39) |
missense |
probably benign |
0.06 |
R1574:Stk33
|
UTSW |
7 |
108,879,027 (GRCm39) |
missense |
probably benign |
0.01 |
R1574:Stk33
|
UTSW |
7 |
108,879,027 (GRCm39) |
missense |
probably benign |
0.01 |
R2153:Stk33
|
UTSW |
7 |
108,940,527 (GRCm39) |
missense |
probably benign |
0.01 |
R4366:Stk33
|
UTSW |
7 |
108,879,002 (GRCm39) |
missense |
probably benign |
0.06 |
R4896:Stk33
|
UTSW |
7 |
108,926,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4994:Stk33
|
UTSW |
7 |
108,939,605 (GRCm39) |
missense |
probably benign |
0.08 |
R6339:Stk33
|
UTSW |
7 |
108,920,672 (GRCm39) |
missense |
probably benign |
0.03 |
R6547:Stk33
|
UTSW |
7 |
108,920,042 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6717:Stk33
|
UTSW |
7 |
108,926,823 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6894:Stk33
|
UTSW |
7 |
108,935,269 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8975:Stk33
|
UTSW |
7 |
108,935,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Stk33
|
UTSW |
7 |
108,928,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R9175:Stk33
|
UTSW |
7 |
108,920,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:Stk33
|
UTSW |
7 |
108,940,686 (GRCm39) |
missense |
probably benign |
0.00 |
R9416:Stk33
|
UTSW |
7 |
108,940,689 (GRCm39) |
missense |
probably benign |
0.39 |
Z1176:Stk33
|
UTSW |
7 |
108,935,266 (GRCm39) |
missense |
possibly damaging |
0.51 |
|