Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
G |
5: 8,986,873 (GRCm39) |
F764C |
probably damaging |
Het |
Aff1 |
A |
G |
5: 103,982,078 (GRCm39) |
D739G |
possibly damaging |
Het |
Atosb |
A |
G |
4: 43,034,531 (GRCm39) |
S355P |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,677,980 (GRCm39) |
Y1012C |
probably damaging |
Het |
Btbd10 |
T |
C |
7: 112,929,133 (GRCm39) |
T206A |
probably benign |
Het |
Capn8 |
G |
T |
1: 182,456,199 (GRCm39) |
A650S |
possibly damaging |
Het |
Catsper1 |
A |
C |
19: 5,386,070 (GRCm39) |
N101T |
probably damaging |
Het |
Cdh23 |
A |
C |
10: 60,160,755 (GRCm39) |
S2070R |
probably benign |
Het |
Cep350 |
A |
G |
1: 155,737,518 (GRCm39) |
V2775A |
probably benign |
Het |
Clybl |
G |
A |
14: 122,419,194 (GRCm39) |
|
probably null |
Het |
Cog4 |
T |
A |
8: 111,579,004 (GRCm39) |
N148K |
probably benign |
Het |
Dbnl |
G |
A |
11: 5,741,839 (GRCm39) |
G44D |
possibly damaging |
Het |
Dgcr2 |
A |
T |
16: 17,667,630 (GRCm39) |
N276K |
possibly damaging |
Het |
Dnah9 |
T |
A |
11: 65,746,060 (GRCm39) |
T4018S |
possibly damaging |
Het |
Dock3 |
A |
G |
9: 106,774,539 (GRCm39) |
L72P |
probably benign |
Het |
Dync2i2 |
T |
C |
2: 29,928,374 (GRCm39) |
D84G |
probably benign |
Het |
Fabp4 |
T |
C |
3: 10,271,105 (GRCm39) |
T51A |
probably benign |
Het |
Fars2 |
T |
A |
13: 36,430,409 (GRCm39) |
I279N |
probably damaging |
Het |
Fas |
A |
T |
19: 34,296,049 (GRCm39) |
Q164L |
probably benign |
Het |
Focad |
A |
G |
4: 88,072,905 (GRCm39) |
K107E |
probably damaging |
Het |
Gga3 |
G |
A |
11: 115,479,305 (GRCm39) |
S338L |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,765,940 (GRCm39) |
R91G |
probably damaging |
Het |
Igkv3-7 |
A |
G |
6: 70,584,942 (GRCm39) |
D94G |
possibly damaging |
Het |
Kank3 |
G |
C |
17: 34,036,627 (GRCm39) |
R165P |
probably damaging |
Het |
Kmt2d |
A |
T |
15: 98,762,048 (GRCm39) |
L434Q |
unknown |
Het |
Krt18 |
A |
G |
15: 101,938,265 (GRCm39) |
T163A |
possibly damaging |
Het |
Lcn10 |
T |
A |
2: 25,575,298 (GRCm39) |
|
probably benign |
Het |
Lrrc37a |
G |
T |
11: 103,394,795 (GRCm39) |
P210Q |
probably benign |
Het |
Lyst |
T |
A |
13: 13,852,548 (GRCm39) |
S2183T |
probably benign |
Het |
Mga |
G |
A |
2: 119,769,272 (GRCm39) |
|
probably benign |
Het |
Myh9 |
G |
A |
15: 77,661,137 (GRCm39) |
A818V |
possibly damaging |
Het |
Or1j15 |
T |
C |
2: 36,458,703 (GRCm39) |
I31T |
probably benign |
Het |
Or1o3 |
G |
T |
17: 37,573,807 (GRCm39) |
Y249* |
probably null |
Het |
Or8b1 |
A |
T |
9: 38,399,597 (GRCm39) |
I91F |
probably benign |
Het |
Pde7b |
A |
G |
10: 20,314,469 (GRCm39) |
|
probably null |
Het |
Pik3cb |
A |
T |
9: 98,936,117 (GRCm39) |
Y772N |
possibly damaging |
Het |
Prl3d2 |
A |
T |
13: 27,307,926 (GRCm39) |
D69V |
probably benign |
Het |
Psd3 |
A |
G |
8: 68,172,596 (GRCm39) |
F871L |
probably damaging |
Het |
Rlf |
G |
A |
4: 121,045,432 (GRCm39) |
P152S |
probably benign |
Het |
Rpa1 |
T |
C |
11: 75,204,167 (GRCm39) |
E270G |
possibly damaging |
Het |
Scfd2 |
T |
C |
5: 74,691,656 (GRCm39) |
T209A |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,621,410 (GRCm39) |
L669P |
probably damaging |
Het |
Sec31b |
A |
T |
19: 44,506,106 (GRCm39) |
C933* |
probably null |
Het |
Serpina3k |
G |
T |
12: 104,309,292 (GRCm39) |
M245I |
probably benign |
Het |
Slc9a3 |
T |
A |
13: 74,305,823 (GRCm39) |
I280N |
probably damaging |
Het |
Soat1 |
A |
G |
1: 156,261,772 (GRCm39) |
V412A |
probably damaging |
Het |
Spata31d1a |
A |
T |
13: 59,850,596 (GRCm39) |
S511T |
possibly damaging |
Het |
Sphkap |
A |
T |
1: 83,253,384 (GRCm39) |
V1455E |
possibly damaging |
Het |
Spns1 |
G |
A |
7: 125,971,593 (GRCm39) |
S319F |
possibly damaging |
Het |
Tbxas1 |
G |
T |
6: 39,048,364 (GRCm39) |
M403I |
|
Het |
Tln2 |
A |
T |
9: 67,157,866 (GRCm39) |
C1158S |
probably damaging |
Het |
Tnrc18 |
T |
C |
5: 142,778,811 (GRCm39) |
T98A |
possibly damaging |
Het |
Ttc23 |
T |
C |
7: 67,319,494 (GRCm39) |
L118P |
probably damaging |
Het |
Tyr |
T |
A |
7: 87,087,223 (GRCm39) |
I430L |
probably damaging |
Het |
Uck2 |
A |
G |
1: 167,070,715 (GRCm39) |
F5L |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,485,847 (GRCm39) |
V2986I |
probably benign |
Het |
Vmn2r96 |
A |
G |
17: 18,802,888 (GRCm39) |
D266G |
probably benign |
Het |
Yrdc |
A |
G |
4: 124,747,677 (GRCm39) |
D213G |
probably benign |
Het |
Zfp612 |
C |
A |
8: 110,815,603 (GRCm39) |
T270K |
probably damaging |
Het |
|
Other mutations in Ppl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ppl
|
APN |
16 |
4,907,409 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00484:Ppl
|
APN |
16 |
4,905,816 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00654:Ppl
|
APN |
16 |
4,905,172 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00832:Ppl
|
APN |
16 |
4,906,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01104:Ppl
|
APN |
16 |
4,912,355 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01327:Ppl
|
APN |
16 |
4,905,508 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01644:Ppl
|
APN |
16 |
4,909,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01824:Ppl
|
APN |
16 |
4,905,753 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02071:Ppl
|
APN |
16 |
4,930,936 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02085:Ppl
|
APN |
16 |
4,907,680 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02282:Ppl
|
APN |
16 |
4,919,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02635:Ppl
|
APN |
16 |
4,907,631 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02649:Ppl
|
APN |
16 |
4,905,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02888:Ppl
|
APN |
16 |
4,918,271 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03305:Ppl
|
APN |
16 |
4,911,097 (GRCm39) |
missense |
possibly damaging |
0.62 |
G4846:Ppl
|
UTSW |
16 |
4,905,070 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03097:Ppl
|
UTSW |
16 |
4,914,590 (GRCm39) |
missense |
probably damaging |
0.98 |
R0759:Ppl
|
UTSW |
16 |
4,907,641 (GRCm39) |
missense |
probably benign |
0.00 |
R0786:Ppl
|
UTSW |
16 |
4,906,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Ppl
|
UTSW |
16 |
4,917,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R1498:Ppl
|
UTSW |
16 |
4,922,629 (GRCm39) |
missense |
probably benign |
0.05 |
R1544:Ppl
|
UTSW |
16 |
4,920,461 (GRCm39) |
nonsense |
probably null |
|
R1597:Ppl
|
UTSW |
16 |
4,925,438 (GRCm39) |
missense |
probably benign |
0.20 |
R1863:Ppl
|
UTSW |
16 |
4,905,844 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1921:Ppl
|
UTSW |
16 |
4,923,988 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2230:Ppl
|
UTSW |
16 |
4,906,845 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2275:Ppl
|
UTSW |
16 |
4,912,416 (GRCm39) |
missense |
probably benign |
0.00 |
R2355:Ppl
|
UTSW |
16 |
4,912,361 (GRCm39) |
missense |
probably benign |
0.00 |
R3410:Ppl
|
UTSW |
16 |
4,925,381 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3737:Ppl
|
UTSW |
16 |
4,924,721 (GRCm39) |
missense |
probably benign |
|
R3797:Ppl
|
UTSW |
16 |
4,922,414 (GRCm39) |
splice site |
probably benign |
|
R3968:Ppl
|
UTSW |
16 |
4,918,196 (GRCm39) |
splice site |
probably null |
|
R3970:Ppl
|
UTSW |
16 |
4,918,196 (GRCm39) |
splice site |
probably null |
|
R4034:Ppl
|
UTSW |
16 |
4,924,721 (GRCm39) |
missense |
probably benign |
|
R4583:Ppl
|
UTSW |
16 |
4,922,400 (GRCm39) |
missense |
probably benign |
0.02 |
R4639:Ppl
|
UTSW |
16 |
4,907,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R4762:Ppl
|
UTSW |
16 |
4,906,846 (GRCm39) |
missense |
probably benign |
0.00 |
R4828:Ppl
|
UTSW |
16 |
4,922,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R4869:Ppl
|
UTSW |
16 |
4,922,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R4925:Ppl
|
UTSW |
16 |
4,922,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Ppl
|
UTSW |
16 |
4,906,582 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4984:Ppl
|
UTSW |
16 |
4,905,505 (GRCm39) |
missense |
probably benign |
|
R4997:Ppl
|
UTSW |
16 |
4,907,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Ppl
|
UTSW |
16 |
4,906,742 (GRCm39) |
missense |
probably benign |
0.01 |
R5073:Ppl
|
UTSW |
16 |
4,906,742 (GRCm39) |
missense |
probably benign |
0.01 |
R5074:Ppl
|
UTSW |
16 |
4,906,742 (GRCm39) |
missense |
probably benign |
0.01 |
R5286:Ppl
|
UTSW |
16 |
4,906,987 (GRCm39) |
nonsense |
probably null |
|
R5398:Ppl
|
UTSW |
16 |
4,922,786 (GRCm39) |
missense |
probably benign |
0.00 |
R5448:Ppl
|
UTSW |
16 |
4,925,430 (GRCm39) |
missense |
probably benign |
|
R5664:Ppl
|
UTSW |
16 |
4,923,919 (GRCm39) |
missense |
probably benign |
0.00 |
R5873:Ppl
|
UTSW |
16 |
4,923,913 (GRCm39) |
critical splice donor site |
probably null |
|
R5918:Ppl
|
UTSW |
16 |
4,922,765 (GRCm39) |
missense |
probably benign |
0.00 |
R5951:Ppl
|
UTSW |
16 |
4,906,492 (GRCm39) |
missense |
probably benign |
0.25 |
R6038:Ppl
|
UTSW |
16 |
4,920,445 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6038:Ppl
|
UTSW |
16 |
4,920,445 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6088:Ppl
|
UTSW |
16 |
4,922,852 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6149:Ppl
|
UTSW |
16 |
4,925,460 (GRCm39) |
nonsense |
probably null |
|
R6358:Ppl
|
UTSW |
16 |
4,905,793 (GRCm39) |
nonsense |
probably null |
|
R6379:Ppl
|
UTSW |
16 |
4,915,555 (GRCm39) |
missense |
probably benign |
0.02 |
R6468:Ppl
|
UTSW |
16 |
4,910,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R6514:Ppl
|
UTSW |
16 |
4,905,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6528:Ppl
|
UTSW |
16 |
4,905,480 (GRCm39) |
missense |
probably benign |
0.00 |
R6703:Ppl
|
UTSW |
16 |
4,907,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R6721:Ppl
|
UTSW |
16 |
4,925,333 (GRCm39) |
missense |
probably damaging |
0.97 |
R6811:Ppl
|
UTSW |
16 |
4,907,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R6934:Ppl
|
UTSW |
16 |
4,912,373 (GRCm39) |
missense |
probably benign |
0.00 |
R7034:Ppl
|
UTSW |
16 |
4,905,366 (GRCm39) |
missense |
probably benign |
0.29 |
R7076:Ppl
|
UTSW |
16 |
4,917,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7300:Ppl
|
UTSW |
16 |
4,920,235 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7349:Ppl
|
UTSW |
16 |
4,922,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R7359:Ppl
|
UTSW |
16 |
4,907,205 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7378:Ppl
|
UTSW |
16 |
4,930,860 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7383:Ppl
|
UTSW |
16 |
4,915,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Ppl
|
UTSW |
16 |
4,924,577 (GRCm39) |
splice site |
probably null |
|
R7445:Ppl
|
UTSW |
16 |
4,906,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7687:Ppl
|
UTSW |
16 |
4,915,806 (GRCm39) |
missense |
probably benign |
0.00 |
R7752:Ppl
|
UTSW |
16 |
4,920,166 (GRCm39) |
missense |
probably benign |
0.09 |
R7827:Ppl
|
UTSW |
16 |
4,905,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7836:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7898:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7943:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R8126:Ppl
|
UTSW |
16 |
4,906,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R8284:Ppl
|
UTSW |
16 |
4,950,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Ppl
|
UTSW |
16 |
4,905,300 (GRCm39) |
missense |
probably benign |
0.01 |
R8781:Ppl
|
UTSW |
16 |
4,915,800 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8835:Ppl
|
UTSW |
16 |
4,906,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R8836:Ppl
|
UTSW |
16 |
4,906,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R8866:Ppl
|
UTSW |
16 |
4,920,211 (GRCm39) |
missense |
probably benign |
0.12 |
R8894:Ppl
|
UTSW |
16 |
4,925,206 (GRCm39) |
intron |
probably benign |
|
R8922:Ppl
|
UTSW |
16 |
4,923,815 (GRCm39) |
missense |
probably benign |
|
R8927:Ppl
|
UTSW |
16 |
4,905,474 (GRCm39) |
missense |
probably benign |
0.19 |
R8928:Ppl
|
UTSW |
16 |
4,905,474 (GRCm39) |
missense |
probably benign |
0.19 |
R9070:Ppl
|
UTSW |
16 |
4,907,208 (GRCm39) |
missense |
probably benign |
0.00 |
R9314:Ppl
|
UTSW |
16 |
4,922,367 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9642:Ppl
|
UTSW |
16 |
4,915,602 (GRCm39) |
missense |
probably benign |
0.01 |
RF009:Ppl
|
UTSW |
16 |
4,915,795 (GRCm39) |
missense |
probably benign |
0.00 |
X0054:Ppl
|
UTSW |
16 |
4,922,766 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Ppl
|
UTSW |
16 |
4,907,371 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Ppl
|
UTSW |
16 |
4,924,642 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Ppl
|
UTSW |
16 |
4,915,821 (GRCm39) |
missense |
probably benign |
0.00 |
|