Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cfap54 |
A |
G |
10: 92,672,374 (GRCm39) |
S2899P |
probably benign |
Het |
Chil5 |
A |
G |
3: 105,926,977 (GRCm39) |
W82R |
probably damaging |
Het |
Dennd3 |
A |
G |
15: 73,426,965 (GRCm39) |
T781A |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,048,824 (GRCm39) |
D597G |
probably damaging |
Het |
Gcn1 |
A |
G |
5: 115,744,597 (GRCm39) |
T1598A |
probably benign |
Het |
Glp2r |
A |
G |
11: 67,621,497 (GRCm39) |
F162S |
probably benign |
Het |
Gm17655 |
T |
A |
5: 110,195,039 (GRCm39) |
R248* |
probably null |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Hapln2 |
A |
G |
3: 87,931,135 (GRCm39) |
Y127H |
probably damaging |
Het |
Hdac4 |
G |
T |
1: 91,909,875 (GRCm39) |
T463K |
probably damaging |
Het |
Ift80 |
A |
C |
3: 68,835,068 (GRCm39) |
S458A |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,098,459 (GRCm39) |
D1846G |
possibly damaging |
Het |
Map3k8 |
A |
G |
18: 4,340,801 (GRCm39) |
I171T |
probably benign |
Het |
Micu1 |
A |
G |
10: 59,576,489 (GRCm39) |
E115G |
probably damaging |
Het |
Mrpl39 |
A |
G |
16: 84,532,080 (GRCm39) |
V9A |
unknown |
Het |
Ncoa7 |
T |
G |
10: 30,570,117 (GRCm39) |
I281L |
possibly damaging |
Het |
Nms |
A |
G |
1: 38,980,976 (GRCm39) |
E54G |
probably benign |
Het |
Nrip1 |
G |
A |
16: 76,091,305 (GRCm39) |
A84V |
probably damaging |
Het |
Or10ak9 |
T |
A |
4: 118,726,335 (GRCm39) |
M119K |
probably damaging |
Het |
Or11g27 |
G |
A |
14: 50,771,330 (GRCm39) |
V154M |
probably benign |
Het |
Pcdhga10 |
T |
A |
18: 37,881,285 (GRCm39) |
S349T |
probably damaging |
Het |
R3hcc1 |
G |
A |
14: 69,935,024 (GRCm39) |
P454L |
probably damaging |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Ryr3 |
T |
C |
2: 112,788,520 (GRCm39) |
D170G |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,570,447 (GRCm39) |
V151A |
probably damaging |
Het |
Scp2 |
C |
A |
4: 107,962,283 (GRCm39) |
G81C |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,844,695 (GRCm39) |
T173A |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 4,998,887 (GRCm39) |
H8142R |
probably benign |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,772,272 (GRCm39) |
T520A |
probably damaging |
Het |
Tpm1 |
A |
G |
9: 66,939,256 (GRCm39) |
S170P |
probably damaging |
Het |
Try5 |
T |
C |
6: 41,288,733 (GRCm39) |
D54G |
possibly damaging |
Het |
Vmn2r-ps158 |
T |
C |
7: 42,673,475 (GRCm39) |
F178L |
probably benign |
Het |
Zan |
T |
C |
5: 137,417,342 (GRCm39) |
E3041G |
unknown |
Het |
Zfp1001 |
A |
T |
2: 150,165,987 (GRCm39) |
Q56L |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,975,828 (GRCm39) |
H699L |
probably damaging |
Het |
|
Other mutations in Gnptab |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01326:Gnptab
|
APN |
10 |
88,268,927 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01346:Gnptab
|
APN |
10 |
88,272,041 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01626:Gnptab
|
APN |
10 |
88,273,357 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01642:Gnptab
|
APN |
10 |
88,271,994 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02121:Gnptab
|
APN |
10 |
88,265,323 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03076:Gnptab
|
APN |
10 |
88,276,151 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03130:Gnptab
|
APN |
10 |
88,272,233 (GRCm39) |
missense |
possibly damaging |
0.95 |
maze
|
UTSW |
10 |
88,268,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Gnptab
|
UTSW |
10 |
88,265,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Gnptab
|
UTSW |
10 |
88,265,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R0114:Gnptab
|
UTSW |
10 |
88,269,262 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0206:Gnptab
|
UTSW |
10 |
88,275,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R0288:Gnptab
|
UTSW |
10 |
88,268,967 (GRCm39) |
missense |
probably benign |
0.00 |
R0329:Gnptab
|
UTSW |
10 |
88,276,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R0330:Gnptab
|
UTSW |
10 |
88,276,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Gnptab
|
UTSW |
10 |
88,269,456 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0385:Gnptab
|
UTSW |
10 |
88,272,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0522:Gnptab
|
UTSW |
10 |
88,267,328 (GRCm39) |
splice site |
probably benign |
|
R0569:Gnptab
|
UTSW |
10 |
88,264,419 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0671:Gnptab
|
UTSW |
10 |
88,279,166 (GRCm39) |
splice site |
probably benign |
|
R0834:Gnptab
|
UTSW |
10 |
88,265,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1375:Gnptab
|
UTSW |
10 |
88,268,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R1443:Gnptab
|
UTSW |
10 |
88,269,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Gnptab
|
UTSW |
10 |
88,281,616 (GRCm39) |
splice site |
probably benign |
|
R1471:Gnptab
|
UTSW |
10 |
88,281,625 (GRCm39) |
missense |
probably benign |
|
R1570:Gnptab
|
UTSW |
10 |
88,255,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R1612:Gnptab
|
UTSW |
10 |
88,264,344 (GRCm39) |
splice site |
probably null |
|
R1614:Gnptab
|
UTSW |
10 |
88,250,451 (GRCm39) |
missense |
probably benign |
|
R1638:Gnptab
|
UTSW |
10 |
88,272,029 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1739:Gnptab
|
UTSW |
10 |
88,271,957 (GRCm39) |
missense |
probably benign |
0.14 |
R1894:Gnptab
|
UTSW |
10 |
88,254,989 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2092:Gnptab
|
UTSW |
10 |
88,276,167 (GRCm39) |
nonsense |
probably null |
|
R2118:Gnptab
|
UTSW |
10 |
88,272,260 (GRCm39) |
missense |
probably benign |
0.13 |
R2144:Gnptab
|
UTSW |
10 |
88,264,368 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2174:Gnptab
|
UTSW |
10 |
88,269,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Gnptab
|
UTSW |
10 |
88,269,439 (GRCm39) |
nonsense |
probably null |
|
R3943:Gnptab
|
UTSW |
10 |
88,269,756 (GRCm39) |
missense |
probably benign |
|
R4434:Gnptab
|
UTSW |
10 |
88,248,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R4545:Gnptab
|
UTSW |
10 |
88,250,457 (GRCm39) |
missense |
probably benign |
0.00 |
R4776:Gnptab
|
UTSW |
10 |
88,272,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Gnptab
|
UTSW |
10 |
88,272,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Gnptab
|
UTSW |
10 |
88,268,413 (GRCm39) |
nonsense |
probably null |
|
R4889:Gnptab
|
UTSW |
10 |
88,269,775 (GRCm39) |
missense |
probably benign |
0.00 |
R4923:Gnptab
|
UTSW |
10 |
88,265,485 (GRCm39) |
missense |
probably benign |
0.17 |
R5694:Gnptab
|
UTSW |
10 |
88,250,348 (GRCm39) |
missense |
probably benign |
0.01 |
R5943:Gnptab
|
UTSW |
10 |
88,269,376 (GRCm39) |
missense |
probably benign |
0.00 |
R6027:Gnptab
|
UTSW |
10 |
88,269,087 (GRCm39) |
missense |
probably damaging |
0.98 |
R6074:Gnptab
|
UTSW |
10 |
88,268,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6119:Gnptab
|
UTSW |
10 |
88,267,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Gnptab
|
UTSW |
10 |
88,265,342 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6757:Gnptab
|
UTSW |
10 |
88,273,364 (GRCm39) |
missense |
probably damaging |
0.98 |
R6911:Gnptab
|
UTSW |
10 |
88,267,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7094:Gnptab
|
UTSW |
10 |
88,215,366 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7101:Gnptab
|
UTSW |
10 |
88,276,174 (GRCm39) |
missense |
probably benign |
0.19 |
R7164:Gnptab
|
UTSW |
10 |
88,269,932 (GRCm39) |
nonsense |
probably null |
|
R7214:Gnptab
|
UTSW |
10 |
88,215,019 (GRCm39) |
unclassified |
probably benign |
|
R7316:Gnptab
|
UTSW |
10 |
88,236,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R7463:Gnptab
|
UTSW |
10 |
88,267,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R7596:Gnptab
|
UTSW |
10 |
88,279,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R7654:Gnptab
|
UTSW |
10 |
88,281,681 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7722:Gnptab
|
UTSW |
10 |
88,215,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R7770:Gnptab
|
UTSW |
10 |
88,247,782 (GRCm39) |
missense |
probably benign |
0.41 |
R7791:Gnptab
|
UTSW |
10 |
88,276,084 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7838:Gnptab
|
UTSW |
10 |
88,276,254 (GRCm39) |
critical splice donor site |
probably null |
|
R8002:Gnptab
|
UTSW |
10 |
88,276,130 (GRCm39) |
missense |
probably benign |
0.14 |
R8168:Gnptab
|
UTSW |
10 |
88,254,995 (GRCm39) |
missense |
probably benign |
0.41 |
R8219:Gnptab
|
UTSW |
10 |
88,269,654 (GRCm39) |
missense |
probably benign |
|
R8221:Gnptab
|
UTSW |
10 |
88,276,254 (GRCm39) |
critical splice donor site |
probably null |
|
R8313:Gnptab
|
UTSW |
10 |
88,275,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Gnptab
|
UTSW |
10 |
88,250,348 (GRCm39) |
missense |
probably benign |
0.01 |
R8487:Gnptab
|
UTSW |
10 |
88,268,508 (GRCm39) |
critical splice donor site |
probably null |
|
R9108:Gnptab
|
UTSW |
10 |
88,269,400 (GRCm39) |
missense |
|
|
R9352:Gnptab
|
UTSW |
10 |
88,268,350 (GRCm39) |
missense |
probably benign |
0.05 |
R9489:Gnptab
|
UTSW |
10 |
88,268,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R9598:Gnptab
|
UTSW |
10 |
88,247,876 (GRCm39) |
missense |
probably damaging |
0.97 |
R9760:Gnptab
|
UTSW |
10 |
88,267,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R9771:Gnptab
|
UTSW |
10 |
88,268,485 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Gnptab
|
UTSW |
10 |
88,272,392 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Gnptab
|
UTSW |
10 |
88,247,873 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Gnptab
|
UTSW |
10 |
88,267,230 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gnptab
|
UTSW |
10 |
88,276,132 (GRCm39) |
missense |
probably damaging |
1.00 |
|