Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamp |
A |
G |
1: 74,322,370 (GRCm39) |
S95P |
probably damaging |
Het |
Ankmy1 |
T |
C |
1: 92,816,397 (GRCm39) |
Y239C |
probably damaging |
Het |
Atp12a |
T |
C |
14: 56,617,512 (GRCm39) |
S601P |
probably damaging |
Het |
Atp1b3 |
T |
C |
9: 96,225,402 (GRCm39) |
T89A |
probably benign |
Het |
B3galt4 |
G |
A |
17: 34,169,813 (GRCm39) |
R142C |
probably damaging |
Het |
Brme1 |
A |
T |
8: 84,893,715 (GRCm39) |
Q294L |
probably benign |
Het |
Btnl2 |
A |
T |
17: 34,580,114 (GRCm39) |
I216F |
possibly damaging |
Het |
Ccdc68 |
T |
A |
18: 70,073,251 (GRCm39) |
D66E |
probably benign |
Het |
Cdc42ep4 |
T |
C |
11: 113,619,392 (GRCm39) |
D333G |
possibly damaging |
Het |
Ckmt1 |
G |
A |
2: 121,194,003 (GRCm39) |
D389N |
possibly damaging |
Het |
Dact1 |
G |
T |
12: 71,364,349 (GRCm39) |
V340F |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,412,024 (GRCm39) |
T246A |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,313,580 (GRCm39) |
|
probably null |
Het |
Ecm1 |
G |
A |
3: 95,643,275 (GRCm39) |
R342C |
probably damaging |
Het |
Efcab14 |
A |
G |
4: 115,613,746 (GRCm39) |
|
probably benign |
Het |
Eprs1 |
A |
G |
1: 185,133,707 (GRCm39) |
T795A |
probably damaging |
Het |
Esp36 |
T |
A |
17: 38,728,202 (GRCm39) |
E26D |
possibly damaging |
Het |
Fpr-rs7 |
T |
C |
17: 20,333,678 (GRCm39) |
T271A |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,813,131 (GRCm39) |
H3150L |
probably benign |
Het |
Gimap7 |
G |
A |
6: 48,700,953 (GRCm39) |
V180M |
probably damaging |
Het |
Gtf3c1 |
T |
C |
7: 125,275,833 (GRCm39) |
H531R |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,399,235 (GRCm39) |
|
probably benign |
Het |
Hip1r |
A |
G |
5: 124,140,203 (GRCm39) |
Y1061C |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,023,225 (GRCm39) |
Y420C |
probably damaging |
Het |
Ipo8 |
T |
C |
6: 148,712,163 (GRCm39) |
|
probably null |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Klhl1 |
A |
T |
14: 96,606,072 (GRCm39) |
M243K |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,297,107 (GRCm39) |
|
probably null |
Het |
Mag |
T |
C |
7: 30,601,277 (GRCm39) |
E439G |
probably damaging |
Het |
Mcm3ap |
T |
A |
10: 76,332,375 (GRCm39) |
F1231I |
probably benign |
Het |
Mcmdc2 |
C |
T |
1: 9,986,780 (GRCm39) |
Q204* |
probably null |
Het |
Mpl |
A |
C |
4: 118,301,221 (GRCm39) |
L548R |
probably damaging |
Het |
Mrps2 |
C |
T |
2: 28,359,500 (GRCm39) |
A119V |
probably benign |
Het |
Myo18b |
G |
A |
5: 113,023,132 (GRCm39) |
Q87* |
probably null |
Het |
Nfat5 |
A |
G |
8: 108,020,522 (GRCm39) |
Y22C |
probably damaging |
Het |
Nnt |
T |
A |
13: 119,523,197 (GRCm39) |
I232L |
possibly damaging |
Het |
Or2a52 |
A |
G |
6: 43,144,846 (GRCm39) |
N285D |
probably damaging |
Het |
Or8g17 |
T |
C |
9: 38,930,253 (GRCm39) |
N195D |
probably benign |
Het |
Or9s13 |
G |
A |
1: 92,548,467 (GRCm39) |
V280M |
possibly damaging |
Het |
Parp2 |
C |
T |
14: 51,048,001 (GRCm39) |
P76S |
probably benign |
Het |
Pick1 |
C |
T |
15: 79,129,501 (GRCm39) |
H169Y |
probably benign |
Het |
Prtg |
T |
A |
9: 72,750,089 (GRCm39) |
F164L |
probably benign |
Het |
Pygb |
A |
G |
2: 150,659,583 (GRCm39) |
D422G |
possibly damaging |
Het |
Samd9l |
C |
A |
6: 3,375,761 (GRCm39) |
C500F |
probably benign |
Het |
Sbno1 |
A |
C |
5: 124,522,567 (GRCm39) |
N1083K |
possibly damaging |
Het |
Septin7 |
C |
T |
9: 25,188,900 (GRCm39) |
S77F |
probably damaging |
Het |
Slc25a44 |
A |
G |
3: 88,323,314 (GRCm39) |
V264A |
possibly damaging |
Het |
Slco1a8 |
C |
T |
6: 141,926,598 (GRCm39) |
S576N |
probably benign |
Het |
Slf2 |
G |
T |
19: 44,930,512 (GRCm39) |
E530* |
probably null |
Het |
Svs5 |
A |
G |
2: 164,079,578 (GRCm39) |
S110P |
possibly damaging |
Het |
Tmbim7 |
G |
T |
5: 3,715,338 (GRCm39) |
|
probably null |
Het |
Tpgs2 |
T |
C |
18: 25,273,630 (GRCm39) |
D177G |
probably damaging |
Het |
Uba1y |
T |
A |
Y: 826,893 (GRCm39) |
F516L |
probably damaging |
Het |
Ulk1 |
A |
G |
5: 110,943,632 (GRCm39) |
V211A |
probably damaging |
Het |
Vmn1r237 |
T |
A |
17: 21,534,301 (GRCm39) |
I8N |
probably damaging |
Het |
Vmn2r103 |
G |
T |
17: 20,014,496 (GRCm39) |
M429I |
probably benign |
Het |
Vmn2r112 |
T |
C |
17: 22,833,989 (GRCm39) |
|
probably null |
Het |
Vmn2r84 |
T |
C |
10: 130,227,349 (GRCm39) |
|
probably null |
Het |
Vwa8 |
C |
T |
14: 79,145,670 (GRCm39) |
R116C |
probably damaging |
Het |
|
Other mutations in Cabs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01670:Cabs1
|
APN |
5 |
88,127,869 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01999:Cabs1
|
APN |
5 |
88,127,787 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02174:Cabs1
|
APN |
5 |
88,128,339 (GRCm39) |
missense |
probably benign |
|
IGL02930:Cabs1
|
APN |
5 |
88,127,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R0126:Cabs1
|
UTSW |
5 |
88,128,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Cabs1
|
UTSW |
5 |
88,127,894 (GRCm39) |
missense |
probably benign |
0.00 |
R2257:Cabs1
|
UTSW |
5 |
88,128,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R2364:Cabs1
|
UTSW |
5 |
88,128,092 (GRCm39) |
missense |
probably benign |
0.00 |
R4078:Cabs1
|
UTSW |
5 |
88,128,161 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Cabs1
|
UTSW |
5 |
88,128,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Cabs1
|
UTSW |
5 |
88,128,425 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5356:Cabs1
|
UTSW |
5 |
88,127,492 (GRCm39) |
missense |
probably benign |
|
R6152:Cabs1
|
UTSW |
5 |
88,127,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6154:Cabs1
|
UTSW |
5 |
88,127,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6159:Cabs1
|
UTSW |
5 |
88,127,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6169:Cabs1
|
UTSW |
5 |
88,127,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6177:Cabs1
|
UTSW |
5 |
88,127,613 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6505:Cabs1
|
UTSW |
5 |
88,128,522 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7726:Cabs1
|
UTSW |
5 |
88,128,145 (GRCm39) |
missense |
probably damaging |
0.98 |
R9035:Cabs1
|
UTSW |
5 |
88,128,309 (GRCm39) |
missense |
probably damaging |
0.98 |
R9239:Cabs1
|
UTSW |
5 |
88,127,385 (GRCm39) |
missense |
probably benign |
0.12 |
R9351:Cabs1
|
UTSW |
5 |
88,128,300 (GRCm39) |
missense |
probably damaging |
0.99 |
|