Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd7 |
G |
T |
6: 18,868,100 (GRCm39) |
|
probably null |
Het |
Aoc1l2 |
A |
T |
6: 48,907,975 (GRCm39) |
Y325F |
probably damaging |
Het |
Aplnr |
A |
T |
2: 84,970,155 (GRCm39) |
|
probably benign |
Het |
Capns2 |
T |
C |
8: 93,628,605 (GRCm39) |
S165P |
probably damaging |
Het |
Col25a1 |
T |
C |
3: 130,378,377 (GRCm39) |
|
probably null |
Het |
Crocc2 |
T |
C |
1: 93,143,304 (GRCm39) |
V1302A |
probably benign |
Het |
Cul9 |
C |
A |
17: 46,821,952 (GRCm39) |
R1841M |
possibly damaging |
Het |
Dnhd1 |
T |
C |
7: 105,336,584 (GRCm39) |
L1213P |
probably damaging |
Het |
Dscam |
A |
T |
16: 96,631,100 (GRCm39) |
I305K |
probably benign |
Het |
Dsp |
A |
G |
13: 38,376,193 (GRCm39) |
E1326G |
possibly damaging |
Het |
Eif4a3l1 |
T |
A |
6: 136,305,617 (GRCm39) |
V26E |
probably benign |
Het |
Emc9 |
A |
G |
14: 55,822,367 (GRCm39) |
|
probably null |
Het |
Eppk1 |
A |
C |
15: 75,996,126 (GRCm39) |
S252A |
probably benign |
Het |
Fn1 |
T |
A |
1: 71,639,572 (GRCm39) |
T1830S |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,179,485 (GRCm39) |
M2974K |
probably damaging |
Het |
Gdpd3 |
C |
A |
7: 126,370,201 (GRCm39) |
S250* |
probably null |
Het |
Gnl3 |
A |
T |
14: 30,735,136 (GRCm39) |
S485R |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hsd17b3 |
T |
C |
13: 64,207,339 (GRCm39) |
Y234C |
probably benign |
Het |
Lima1 |
T |
C |
15: 99,679,148 (GRCm39) |
H271R |
possibly damaging |
Het |
Nfu1 |
G |
A |
6: 86,994,034 (GRCm39) |
|
probably null |
Het |
Noto |
A |
G |
6: 85,404,942 (GRCm39) |
E97G |
probably damaging |
Het |
Ntng1 |
T |
C |
3: 109,779,534 (GRCm39) |
K348E |
probably damaging |
Het |
Or2y13 |
G |
A |
11: 49,414,536 (GRCm39) |
|
probably benign |
Het |
Or4a70 |
C |
T |
2: 89,324,594 (GRCm39) |
G21R |
possibly damaging |
Het |
Osmr |
C |
A |
15: 6,845,364 (GRCm39) |
V801F |
probably damaging |
Het |
Papln |
A |
G |
12: 83,824,234 (GRCm39) |
E554G |
probably benign |
Het |
Pitrm1 |
T |
C |
13: 6,605,495 (GRCm39) |
L175P |
probably damaging |
Het |
Pramel22 |
A |
T |
4: 143,382,053 (GRCm39) |
N214K |
probably damaging |
Het |
Pramel7 |
T |
C |
2: 87,320,070 (GRCm39) |
T408A |
probably damaging |
Het |
Serinc2 |
A |
T |
4: 130,149,235 (GRCm39) |
D322E |
probably benign |
Het |
Setx |
T |
C |
2: 29,038,120 (GRCm39) |
V1535A |
probably benign |
Het |
Sgce |
A |
T |
6: 4,689,666 (GRCm39) |
V389E |
probably damaging |
Het |
Snx11 |
G |
A |
11: 96,659,888 (GRCm39) |
T267I |
probably benign |
Het |
Spata6l |
T |
G |
19: 28,921,688 (GRCm39) |
Q146P |
probably benign |
Het |
Specc1 |
G |
A |
11: 62,009,162 (GRCm39) |
S306N |
probably benign |
Het |
Spocd1 |
A |
G |
4: 129,850,305 (GRCm39) |
|
probably benign |
Het |
St7 |
T |
A |
6: 17,854,945 (GRCm39) |
V294D |
probably damaging |
Het |
Tcf21 |
T |
C |
10: 22,695,403 (GRCm39) |
I134V |
probably benign |
Het |
Tgfb2 |
T |
A |
1: 186,364,697 (GRCm39) |
I266F |
probably damaging |
Het |
Tgfbr3l |
A |
G |
8: 4,300,365 (GRCm39) |
I209M |
possibly damaging |
Het |
Tmcc3 |
A |
G |
10: 94,387,034 (GRCm39) |
|
probably null |
Het |
Toe1 |
A |
G |
4: 116,664,671 (GRCm39) |
S16P |
probably damaging |
Het |
Vps16 |
T |
C |
2: 130,279,601 (GRCm39) |
V38A |
possibly damaging |
Het |
Wnk2 |
G |
T |
13: 49,224,557 (GRCm39) |
D1001E |
probably damaging |
Het |
|
Other mutations in Stab1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Stab1
|
APN |
14 |
30,883,314 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00323:Stab1
|
APN |
14 |
30,861,263 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00515:Stab1
|
APN |
14 |
30,881,686 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00844:Stab1
|
APN |
14 |
30,869,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Stab1
|
APN |
14 |
30,869,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01384:Stab1
|
APN |
14 |
30,872,365 (GRCm39) |
missense |
probably benign |
|
IGL01431:Stab1
|
APN |
14 |
30,870,952 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01787:Stab1
|
APN |
14 |
30,861,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02128:Stab1
|
APN |
14 |
30,872,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Stab1
|
APN |
14 |
30,865,470 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02256:Stab1
|
APN |
14 |
30,863,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Stab1
|
APN |
14 |
30,862,367 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02507:Stab1
|
APN |
14 |
30,861,167 (GRCm39) |
unclassified |
probably benign |
|
IGL02695:Stab1
|
APN |
14 |
30,881,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Stab1
|
APN |
14 |
30,861,595 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02870:Stab1
|
APN |
14 |
30,861,354 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02884:Stab1
|
APN |
14 |
30,872,100 (GRCm39) |
splice site |
probably null |
|
IGL03035:Stab1
|
APN |
14 |
30,869,726 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03267:Stab1
|
APN |
14 |
30,864,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Stab1
|
APN |
14 |
30,881,283 (GRCm39) |
splice site |
probably benign |
|
IGL03366:Stab1
|
APN |
14 |
30,872,220 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03412:Stab1
|
APN |
14 |
30,876,364 (GRCm39) |
missense |
probably benign |
0.42 |
R0906_Stab1_335
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R5086_Stab1_467
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Stab1
|
UTSW |
14 |
30,867,981 (GRCm39) |
critical splice donor site |
probably null |
|
K7371:Stab1
|
UTSW |
14 |
30,872,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0363:Stab1
|
UTSW |
14 |
30,880,965 (GRCm39) |
splice site |
probably benign |
|
R0387:Stab1
|
UTSW |
14 |
30,870,058 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Stab1
|
UTSW |
14 |
30,865,375 (GRCm39) |
missense |
probably benign |
0.21 |
R0513:Stab1
|
UTSW |
14 |
30,870,902 (GRCm39) |
missense |
probably benign |
0.08 |
R0546:Stab1
|
UTSW |
14 |
30,861,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0825:Stab1
|
UTSW |
14 |
30,874,557 (GRCm39) |
missense |
probably benign |
0.16 |
R0906:Stab1
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R0963:Stab1
|
UTSW |
14 |
30,869,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R1219:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
splice site |
probably null |
|
R1234:Stab1
|
UTSW |
14 |
30,872,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Stab1
|
UTSW |
14 |
30,873,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Stab1
|
UTSW |
14 |
30,861,787 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1440:Stab1
|
UTSW |
14 |
30,873,647 (GRCm39) |
nonsense |
probably null |
|
R1472:Stab1
|
UTSW |
14 |
30,863,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Stab1
|
UTSW |
14 |
30,871,818 (GRCm39) |
missense |
probably benign |
0.45 |
R1475:Stab1
|
UTSW |
14 |
30,885,785 (GRCm39) |
missense |
probably benign |
|
R1509:Stab1
|
UTSW |
14 |
30,873,541 (GRCm39) |
splice site |
probably benign |
|
R1551:Stab1
|
UTSW |
14 |
30,882,456 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Stab1
|
UTSW |
14 |
30,872,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Stab1
|
UTSW |
14 |
30,872,337 (GRCm39) |
splice site |
probably null |
|
R1719:Stab1
|
UTSW |
14 |
30,867,985 (GRCm39) |
nonsense |
probably null |
|
R1733:Stab1
|
UTSW |
14 |
30,867,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Stab1
|
UTSW |
14 |
30,890,373 (GRCm39) |
missense |
probably benign |
0.04 |
R1808:Stab1
|
UTSW |
14 |
30,863,101 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1816:Stab1
|
UTSW |
14 |
30,879,422 (GRCm39) |
missense |
probably benign |
0.03 |
R1853:Stab1
|
UTSW |
14 |
30,862,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Stab1
|
UTSW |
14 |
30,863,287 (GRCm39) |
missense |
probably benign |
0.07 |
R1984:Stab1
|
UTSW |
14 |
30,872,605 (GRCm39) |
missense |
probably benign |
0.20 |
R1998:Stab1
|
UTSW |
14 |
30,884,110 (GRCm39) |
nonsense |
probably null |
|
R2165:Stab1
|
UTSW |
14 |
30,890,392 (GRCm39) |
missense |
probably benign |
0.20 |
R2191:Stab1
|
UTSW |
14 |
30,881,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Stab1
|
UTSW |
14 |
30,864,757 (GRCm39) |
missense |
probably benign |
0.03 |
R2233:Stab1
|
UTSW |
14 |
30,883,837 (GRCm39) |
missense |
probably benign |
0.08 |
R2303:Stab1
|
UTSW |
14 |
30,868,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2496:Stab1
|
UTSW |
14 |
30,883,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Stab1
|
UTSW |
14 |
30,884,997 (GRCm39) |
critical splice donor site |
probably null |
|
R2519:Stab1
|
UTSW |
14 |
30,876,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2926:Stab1
|
UTSW |
14 |
30,883,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4025:Stab1
|
UTSW |
14 |
30,876,909 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4113:Stab1
|
UTSW |
14 |
30,890,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R4258:Stab1
|
UTSW |
14 |
30,876,629 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4588:Stab1
|
UTSW |
14 |
30,879,402 (GRCm39) |
missense |
probably benign |
0.01 |
R4644:Stab1
|
UTSW |
14 |
30,862,444 (GRCm39) |
unclassified |
probably benign |
|
R4660:Stab1
|
UTSW |
14 |
30,876,872 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4801:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4802:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4870:Stab1
|
UTSW |
14 |
30,864,000 (GRCm39) |
missense |
probably benign |
0.13 |
R4872:Stab1
|
UTSW |
14 |
30,862,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Stab1
|
UTSW |
14 |
30,865,629 (GRCm39) |
missense |
probably benign |
0.32 |
R4941:Stab1
|
UTSW |
14 |
30,873,528 (GRCm39) |
missense |
probably benign |
0.00 |
R5061:Stab1
|
UTSW |
14 |
30,885,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,865,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5087:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.01 |
R5102:Stab1
|
UTSW |
14 |
30,869,974 (GRCm39) |
critical splice donor site |
probably null |
|
R5107:Stab1
|
UTSW |
14 |
30,885,752 (GRCm39) |
splice site |
probably null |
|
R5195:Stab1
|
UTSW |
14 |
30,862,478 (GRCm39) |
unclassified |
probably benign |
|
R5217:Stab1
|
UTSW |
14 |
30,881,476 (GRCm39) |
missense |
probably benign |
0.25 |
R5285:Stab1
|
UTSW |
14 |
30,865,433 (GRCm39) |
unclassified |
probably benign |
|
R5327:Stab1
|
UTSW |
14 |
30,883,793 (GRCm39) |
nonsense |
probably null |
|
R5647:Stab1
|
UTSW |
14 |
30,879,397 (GRCm39) |
nonsense |
probably null |
|
R5696:Stab1
|
UTSW |
14 |
30,882,178 (GRCm39) |
missense |
probably benign |
|
R5996:Stab1
|
UTSW |
14 |
30,861,508 (GRCm39) |
missense |
probably benign |
0.39 |
R6016:Stab1
|
UTSW |
14 |
30,880,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Stab1
|
UTSW |
14 |
30,863,501 (GRCm39) |
missense |
probably benign |
0.00 |
R6174:Stab1
|
UTSW |
14 |
30,884,476 (GRCm39) |
nonsense |
probably null |
|
R6366:Stab1
|
UTSW |
14 |
30,863,395 (GRCm39) |
missense |
probably benign |
0.10 |
R6754:Stab1
|
UTSW |
14 |
30,863,038 (GRCm39) |
missense |
probably benign |
|
R6788:Stab1
|
UTSW |
14 |
30,861,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Stab1
|
UTSW |
14 |
30,882,824 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7145:Stab1
|
UTSW |
14 |
30,867,030 (GRCm39) |
critical splice donor site |
probably null |
|
R7153:Stab1
|
UTSW |
14 |
30,882,541 (GRCm39) |
missense |
probably benign |
0.16 |
R7213:Stab1
|
UTSW |
14 |
30,865,630 (GRCm39) |
missense |
probably benign |
|
R7215:Stab1
|
UTSW |
14 |
30,882,754 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7319:Stab1
|
UTSW |
14 |
30,862,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Stab1
|
UTSW |
14 |
30,869,196 (GRCm39) |
missense |
probably benign |
0.00 |
R7400:Stab1
|
UTSW |
14 |
30,879,341 (GRCm39) |
missense |
probably null |
1.00 |
R7427:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7484:Stab1
|
UTSW |
14 |
30,882,274 (GRCm39) |
missense |
probably benign |
0.00 |
R7568:Stab1
|
UTSW |
14 |
30,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Stab1
|
UTSW |
14 |
30,876,622 (GRCm39) |
missense |
probably benign |
|
R7619:Stab1
|
UTSW |
14 |
30,867,194 (GRCm39) |
missense |
probably benign |
|
R7623:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
missense |
probably benign |
0.03 |
R7721:Stab1
|
UTSW |
14 |
30,863,413 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7869:Stab1
|
UTSW |
14 |
30,876,429 (GRCm39) |
missense |
probably benign |
0.01 |
R7936:Stab1
|
UTSW |
14 |
30,879,372 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7956:Stab1
|
UTSW |
14 |
30,881,981 (GRCm39) |
missense |
probably benign |
0.02 |
R7973:Stab1
|
UTSW |
14 |
30,881,590 (GRCm39) |
critical splice donor site |
probably null |
|
R8059:Stab1
|
UTSW |
14 |
30,882,198 (GRCm39) |
missense |
probably benign |
0.02 |
R8116:Stab1
|
UTSW |
14 |
30,880,910 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8304:Stab1
|
UTSW |
14 |
30,870,911 (GRCm39) |
missense |
probably benign |
0.14 |
R8368:Stab1
|
UTSW |
14 |
30,870,368 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8495:Stab1
|
UTSW |
14 |
30,877,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Stab1
|
UTSW |
14 |
30,871,747 (GRCm39) |
critical splice donor site |
probably null |
|
R8544:Stab1
|
UTSW |
14 |
30,885,008 (GRCm39) |
nonsense |
probably null |
|
R8671:Stab1
|
UTSW |
14 |
30,879,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Stab1
|
UTSW |
14 |
30,883,771 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8974:Stab1
|
UTSW |
14 |
30,882,779 (GRCm39) |
missense |
probably benign |
|
R9022:Stab1
|
UTSW |
14 |
30,882,226 (GRCm39) |
missense |
probably benign |
0.01 |
R9059:Stab1
|
UTSW |
14 |
30,876,805 (GRCm39) |
missense |
probably benign |
0.01 |
R9226:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.00 |
R9272:Stab1
|
UTSW |
14 |
30,867,298 (GRCm39) |
missense |
probably benign |
0.05 |
R9388:Stab1
|
UTSW |
14 |
30,876,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Stab1
|
UTSW |
14 |
30,883,069 (GRCm39) |
missense |
probably benign |
|
R9433:Stab1
|
UTSW |
14 |
30,865,531 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Stab1
|
UTSW |
14 |
30,884,896 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9505:Stab1
|
UTSW |
14 |
30,877,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Stab1
|
UTSW |
14 |
30,864,638 (GRCm39) |
missense |
probably benign |
0.01 |
R9624:Stab1
|
UTSW |
14 |
30,863,345 (GRCm39) |
missense |
|
|
R9694:Stab1
|
UTSW |
14 |
30,876,901 (GRCm39) |
missense |
probably benign |
0.06 |
R9723:Stab1
|
UTSW |
14 |
30,885,848 (GRCm39) |
missense |
probably benign |
0.10 |
X0026:Stab1
|
UTSW |
14 |
30,884,148 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:Stab1
|
UTSW |
14 |
30,872,617 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Stab1
|
UTSW |
14 |
30,863,995 (GRCm39) |
missense |
probably benign |
0.00 |
|