Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930442H23Rik |
T |
A |
10: 81,018,813 (GRCm39) |
|
probably benign |
Het |
Adam5 |
A |
T |
8: 25,296,542 (GRCm39) |
Y302N |
probably damaging |
Het |
Ankrd34c |
A |
T |
9: 89,612,132 (GRCm39) |
Y70N |
probably damaging |
Het |
Asph |
G |
A |
4: 9,601,349 (GRCm39) |
P190S |
possibly damaging |
Het |
Atp6v1h |
T |
C |
1: 5,194,525 (GRCm39) |
C235R |
probably damaging |
Het |
Brwd1 |
A |
G |
16: 95,804,023 (GRCm39) |
L2049P |
probably benign |
Het |
Capn2 |
T |
A |
1: 182,300,149 (GRCm39) |
I614F |
probably benign |
Het |
Ccdc126 |
T |
A |
6: 49,310,995 (GRCm39) |
M1K |
probably null |
Het |
Cdh9 |
T |
C |
15: 16,832,316 (GRCm39) |
I401T |
probably damaging |
Het |
Cep57l1 |
T |
C |
10: 41,605,382 (GRCm39) |
E121G |
probably damaging |
Het |
Cfap46 |
A |
G |
7: 139,194,386 (GRCm39) |
I2276T |
probably damaging |
Het |
Cnnm3 |
T |
C |
1: 36,559,239 (GRCm39) |
S490P |
probably benign |
Het |
D430041D05Rik |
C |
T |
2: 104,060,650 (GRCm39) |
V731I |
possibly damaging |
Het |
Dynlt2b |
T |
C |
16: 32,244,125 (GRCm39) |
V107A |
possibly damaging |
Het |
Fgf3 |
C |
A |
7: 144,394,487 (GRCm39) |
N100K |
probably damaging |
Het |
Gas7 |
G |
A |
11: 67,566,553 (GRCm39) |
|
probably null |
Het |
Gfm1 |
C |
T |
3: 67,382,100 (GRCm39) |
P725S |
possibly damaging |
Het |
Gimap4 |
T |
A |
6: 48,667,429 (GRCm39) |
C61* |
probably null |
Het |
Greb1 |
C |
T |
12: 16,758,724 (GRCm39) |
R664Q |
probably damaging |
Het |
Kpnb1 |
T |
A |
11: 97,068,086 (GRCm39) |
I295F |
possibly damaging |
Het |
Lamc3 |
A |
G |
2: 31,835,410 (GRCm39) |
E1577G |
probably benign |
Het |
Lrrk1 |
C |
T |
7: 65,924,620 (GRCm39) |
V235M |
probably damaging |
Het |
Meak7 |
A |
T |
8: 120,499,149 (GRCm39) |
D114E |
probably benign |
Het |
Mipol1 |
T |
A |
12: 57,352,829 (GRCm39) |
V56E |
possibly damaging |
Het |
Mycbp2 |
T |
C |
14: 103,442,621 (GRCm39) |
I1927V |
probably benign |
Het |
Ncaph |
A |
T |
2: 126,966,784 (GRCm39) |
N223K |
possibly damaging |
Het |
Nipbl |
A |
G |
15: 8,325,037 (GRCm39) |
M2542T |
probably benign |
Het |
Nolc1 |
C |
A |
19: 46,071,468 (GRCm39) |
|
probably benign |
Het |
Or10j5 |
G |
A |
1: 172,784,743 (GRCm39) |
C127Y |
probably damaging |
Het |
Or51h1 |
A |
G |
7: 102,308,384 (GRCm39) |
M119V |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,393,441 (GRCm39) |
|
probably null |
Het |
Ptpn13 |
A |
T |
5: 103,717,320 (GRCm39) |
M1821L |
possibly damaging |
Het |
Rabl3 |
C |
T |
16: 37,362,287 (GRCm39) |
S42L |
probably damaging |
Het |
Rbm12 |
C |
T |
2: 155,937,480 (GRCm39) |
|
probably benign |
Het |
Rfx3 |
G |
A |
19: 27,827,137 (GRCm39) |
H150Y |
possibly damaging |
Het |
Rngtt |
A |
G |
4: 33,356,098 (GRCm39) |
M312V |
possibly damaging |
Het |
Slc10a2 |
T |
A |
8: 5,148,499 (GRCm39) |
T149S |
probably damaging |
Het |
Spata21 |
T |
C |
4: 140,838,576 (GRCm39) |
|
probably benign |
Het |
Stx8 |
G |
T |
11: 67,860,598 (GRCm39) |
W6C |
probably damaging |
Het |
Tcn2 |
T |
C |
11: 3,877,504 (GRCm39) |
E48G |
possibly damaging |
Het |
Tecpr1 |
A |
T |
5: 144,143,364 (GRCm39) |
N670K |
probably benign |
Het |
Tmem255b |
G |
A |
8: 13,507,055 (GRCm39) |
M240I |
probably benign |
Het |
Ubr4 |
G |
A |
4: 139,186,445 (GRCm39) |
E651K |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 38,002,558 (GRCm39) |
T1498A |
probably benign |
Het |
Vmn2r95 |
G |
A |
17: 18,664,116 (GRCm39) |
C445Y |
probably damaging |
Het |
Zfp429 |
T |
A |
13: 67,547,855 (GRCm39) |
|
probably benign |
Het |
Zfp804b |
T |
G |
5: 6,821,392 (GRCm39) |
D557A |
possibly damaging |
Het |
|
Other mutations in Ppat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02545:Ppat
|
APN |
5 |
77,063,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Ppat
|
UTSW |
5 |
77,070,348 (GRCm39) |
missense |
probably benign |
0.09 |
R2327:Ppat
|
UTSW |
5 |
77,070,314 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2850:Ppat
|
UTSW |
5 |
77,067,222 (GRCm39) |
missense |
probably benign |
|
R3434:Ppat
|
UTSW |
5 |
77,065,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R4301:Ppat
|
UTSW |
5 |
77,076,348 (GRCm39) |
intron |
probably benign |
|
R4422:Ppat
|
UTSW |
5 |
77,063,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4423:Ppat
|
UTSW |
5 |
77,063,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Ppat
|
UTSW |
5 |
77,063,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Ppat
|
UTSW |
5 |
77,098,811 (GRCm39) |
nonsense |
probably null |
|
R4872:Ppat
|
UTSW |
5 |
77,074,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R5007:Ppat
|
UTSW |
5 |
77,076,525 (GRCm39) |
intron |
probably benign |
|
R5010:Ppat
|
UTSW |
5 |
77,076,525 (GRCm39) |
intron |
probably benign |
|
R5325:Ppat
|
UTSW |
5 |
77,076,269 (GRCm39) |
intron |
probably benign |
|
R5982:Ppat
|
UTSW |
5 |
77,063,112 (GRCm39) |
missense |
probably benign |
|
R6209:Ppat
|
UTSW |
5 |
77,065,993 (GRCm39) |
missense |
probably benign |
0.00 |
R6225:Ppat
|
UTSW |
5 |
77,070,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R6287:Ppat
|
UTSW |
5 |
77,066,061 (GRCm39) |
nonsense |
probably null |
|
R7367:Ppat
|
UTSW |
5 |
77,067,711 (GRCm39) |
nonsense |
probably null |
|
R7426:Ppat
|
UTSW |
5 |
77,063,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R7945:Ppat
|
UTSW |
5 |
77,063,238 (GRCm39) |
missense |
probably benign |
0.01 |
R8047:Ppat
|
UTSW |
5 |
77,073,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R9343:Ppat
|
UTSW |
5 |
77,063,884 (GRCm39) |
missense |
probably benign |
0.32 |
|