Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afg1l |
C |
T |
10: 42,291,544 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
A |
T |
12: 112,780,802 (GRCm38) |
V70E |
|
Het |
Alpk3 |
A |
G |
7: 80,728,202 (GRCm39) |
E444G |
possibly damaging |
Het |
Amer2 |
T |
A |
14: 60,617,123 (GRCm39) |
D439E |
possibly damaging |
Het |
Ano6 |
A |
G |
15: 95,811,781 (GRCm39) |
Y222C |
probably damaging |
Het |
Atp4a |
A |
C |
7: 30,421,944 (GRCm39) |
K827Q |
probably benign |
Het |
Atp9a |
G |
A |
2: 168,576,047 (GRCm39) |
|
|
Het |
Casp7 |
T |
A |
19: 56,424,793 (GRCm39) |
C171S |
probably damaging |
Het |
Ccdc9b |
T |
A |
2: 118,591,164 (GRCm39) |
|
probably null |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cdkl1 |
A |
G |
12: 69,795,585 (GRCm39) |
L315S |
probably benign |
Het |
Cfap91 |
A |
G |
16: 38,148,708 (GRCm39) |
I240T |
probably damaging |
Het |
Crybg1 |
G |
T |
10: 43,873,619 (GRCm39) |
S1163* |
probably null |
Het |
Csmd1 |
A |
T |
8: 17,077,295 (GRCm39) |
W121R |
probably damaging |
Het |
Cyyr1 |
A |
T |
16: 85,262,493 (GRCm39) |
M88K |
possibly damaging |
Het |
Dlc1 |
T |
C |
8: 37,049,954 (GRCm39) |
Q587R |
probably damaging |
Het |
Dock2 |
T |
C |
11: 34,223,750 (GRCm39) |
E1128G |
possibly damaging |
Het |
Dynap |
T |
A |
18: 70,374,320 (GRCm39) |
T69S |
possibly damaging |
Het |
Esr1 |
T |
C |
10: 4,733,874 (GRCm39) |
C225R |
probably damaging |
Het |
Fbxo31 |
C |
T |
8: 122,305,503 (GRCm39) |
|
probably benign |
Het |
Fndc11 |
G |
A |
2: 180,863,893 (GRCm39) |
V233I |
possibly damaging |
Het |
Fto |
T |
C |
8: 92,211,818 (GRCm39) |
F381S |
probably damaging |
Het |
Gtf2ird1 |
A |
G |
5: 134,433,758 (GRCm39) |
L223P |
probably benign |
Het |
Ifi214 |
A |
T |
1: 173,357,042 (GRCm39) |
H20Q |
probably damaging |
Het |
Impa2 |
T |
A |
18: 67,439,806 (GRCm39) |
I101N |
probably damaging |
Het |
Kidins220 |
A |
T |
12: 25,061,570 (GRCm39) |
T854S |
probably benign |
Het |
Lamb1 |
T |
A |
12: 31,337,423 (GRCm39) |
C385S |
probably damaging |
Het |
Lrrc8c |
A |
G |
5: 105,755,853 (GRCm39) |
S543G |
probably benign |
Het |
Manba |
A |
T |
3: 135,248,137 (GRCm39) |
Y342F |
probably damaging |
Het |
Map3k1 |
T |
C |
13: 111,893,231 (GRCm39) |
D758G |
probably benign |
Het |
Mtor |
G |
T |
4: 148,630,942 (GRCm39) |
A2300S |
possibly damaging |
Het |
Musk |
T |
A |
4: 58,373,409 (GRCm39) |
M793K |
probably damaging |
Het |
Nup133 |
A |
C |
8: 124,649,153 (GRCm39) |
I563S |
probably benign |
Het |
Or10ab4 |
G |
A |
7: 107,654,423 (GRCm39) |
R78Q |
probably damaging |
Het |
Or10ag55-ps1 |
T |
A |
2: 87,114,725 (GRCm39) |
N30K |
probably benign |
Het |
Or4k77 |
A |
G |
2: 111,199,693 (GRCm39) |
T239A |
probably damaging |
Het |
Or8g21 |
A |
T |
9: 38,905,953 (GRCm39) |
Y259* |
probably null |
Het |
Pcdh12 |
C |
A |
18: 38,416,100 (GRCm39) |
V342F |
probably damaging |
Het |
Pcdhb4 |
T |
A |
18: 37,441,222 (GRCm39) |
H177Q |
possibly damaging |
Het |
Pcnx2 |
G |
A |
8: 126,613,690 (GRCm39) |
A587V |
probably benign |
Het |
Phkb |
C |
T |
8: 86,770,418 (GRCm39) |
P896S |
probably damaging |
Het |
Prss36 |
A |
G |
7: 127,543,877 (GRCm39) |
S165P |
probably benign |
Het |
Psmd14 |
T |
C |
2: 61,591,356 (GRCm39) |
V53A |
probably damaging |
Het |
Sel1l3 |
T |
G |
5: 53,273,704 (GRCm39) |
H1054P |
probably damaging |
Het |
Selenoh |
T |
C |
2: 84,500,631 (GRCm39) |
R70G |
probably damaging |
Het |
Serpinb9d |
A |
G |
13: 33,378,617 (GRCm39) |
Q21R |
probably benign |
Het |
Slc29a1 |
T |
C |
17: 45,899,288 (GRCm39) |
E262G |
probably benign |
Het |
Slc7a14 |
A |
G |
3: 31,278,384 (GRCm39) |
L407P |
probably damaging |
Het |
Smyd4 |
T |
C |
11: 75,281,325 (GRCm39) |
V266A |
possibly damaging |
Het |
Spata31d1a |
T |
A |
13: 59,849,913 (GRCm39) |
R738S |
probably benign |
Het |
Speer4a2 |
G |
A |
5: 26,292,993 (GRCm39) |
T67I |
probably benign |
Het |
Srcin1 |
C |
T |
11: 97,442,715 (GRCm39) |
G38S |
probably damaging |
Het |
Stab2 |
A |
T |
10: 86,838,972 (GRCm39) |
|
probably null |
Het |
Syde2 |
A |
G |
3: 145,726,031 (GRCm39) |
N1308D |
possibly damaging |
Het |
Trip11 |
A |
T |
12: 101,850,611 (GRCm39) |
M1151K |
probably damaging |
Het |
Ttll4 |
A |
T |
1: 74,727,820 (GRCm39) |
I861F |
possibly damaging |
Het |
Zfp319 |
G |
A |
8: 96,058,471 (GRCm39) |
|
probably benign |
Het |
Zfp518b |
T |
C |
5: 38,831,907 (GRCm39) |
N33D |
probably benign |
Het |
Zfp874a |
T |
A |
13: 67,591,415 (GRCm39) |
I90F |
probably benign |
Het |
Zmiz2 |
G |
T |
11: 6,349,593 (GRCm39) |
V412L |
probably damaging |
Het |
|
Other mutations in Prss43 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Prss43
|
APN |
9 |
110,658,538 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01636:Prss43
|
APN |
9 |
110,656,505 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03046:Prss43
|
UTSW |
9 |
110,660,049 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4576001:Prss43
|
UTSW |
9 |
110,656,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0020:Prss43
|
UTSW |
9 |
110,657,580 (GRCm39) |
unclassified |
probably benign |
|
R0278:Prss43
|
UTSW |
9 |
110,656,430 (GRCm39) |
missense |
probably benign |
0.07 |
R0883:Prss43
|
UTSW |
9 |
110,658,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Prss43
|
UTSW |
9 |
110,656,510 (GRCm39) |
missense |
probably benign |
0.10 |
R2212:Prss43
|
UTSW |
9 |
110,658,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R3412:Prss43
|
UTSW |
9 |
110,658,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R3808:Prss43
|
UTSW |
9 |
110,656,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R4202:Prss43
|
UTSW |
9 |
110,656,529 (GRCm39) |
missense |
probably benign |
0.08 |
R4530:Prss43
|
UTSW |
9 |
110,658,572 (GRCm39) |
missense |
probably benign |
0.38 |
R4752:Prss43
|
UTSW |
9 |
110,656,836 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5009:Prss43
|
UTSW |
9 |
110,656,489 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6920:Prss43
|
UTSW |
9 |
110,657,680 (GRCm39) |
missense |
probably benign |
0.04 |
R7406:Prss43
|
UTSW |
9 |
110,657,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7758:Prss43
|
UTSW |
9 |
110,658,459 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8257:Prss43
|
UTSW |
9 |
110,659,880 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8686:Prss43
|
UTSW |
9 |
110,658,494 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8885:Prss43
|
UTSW |
9 |
110,660,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R9217:Prss43
|
UTSW |
9 |
110,656,564 (GRCm39) |
missense |
possibly damaging |
0.75 |
|