Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aard |
A |
T |
15: 51,908,316 (GRCm39) |
D157V |
probably damaging |
Het |
Abcg5 |
A |
G |
17: 84,977,803 (GRCm39) |
V151A |
probably damaging |
Het |
Acss3 |
A |
G |
10: 106,772,029 (GRCm39) |
V682A |
probably benign |
Het |
Adamts9 |
A |
T |
6: 92,836,830 (GRCm39) |
C641S |
probably damaging |
Het |
Adipor1 |
T |
C |
1: 134,350,771 (GRCm39) |
S7P |
probably benign |
Het |
Ankrd27 |
T |
A |
7: 35,303,264 (GRCm39) |
Y215N |
probably damaging |
Het |
Arhgef7 |
T |
A |
8: 11,855,266 (GRCm39) |
L182Q |
probably damaging |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Arrdc4 |
T |
C |
7: 68,391,547 (GRCm39) |
K240R |
probably benign |
Het |
Atg2b |
T |
C |
12: 105,635,677 (GRCm39) |
Y197C |
probably damaging |
Het |
Atp13a2 |
A |
G |
4: 140,731,572 (GRCm39) |
K907R |
possibly damaging |
Het |
Cadps2 |
A |
T |
6: 23,287,685 (GRCm39) |
M1160K |
probably damaging |
Het |
Cdk12 |
A |
G |
11: 98,110,042 (GRCm39) |
T688A |
probably benign |
Het |
Cfap43 |
T |
A |
19: 47,885,649 (GRCm39) |
Y322F |
probably benign |
Het |
Crabp2 |
T |
C |
3: 87,856,193 (GRCm39) |
F16L |
probably damaging |
Het |
Creb3 |
A |
G |
4: 43,563,279 (GRCm39) |
|
probably null |
Het |
Crk |
T |
C |
11: 75,583,496 (GRCm39) |
Y239H |
possibly damaging |
Het |
Cyp3a13 |
A |
G |
5: 137,908,204 (GRCm39) |
I215T |
probably benign |
Het |
D130043K22Rik |
A |
G |
13: 25,069,578 (GRCm39) |
Y879C |
probably damaging |
Het |
Depdc5 |
T |
C |
5: 33,061,175 (GRCm39) |
V334A |
probably damaging |
Het |
Dgkh |
T |
C |
14: 78,855,981 (GRCm39) |
N231S |
probably damaging |
Het |
Disp2 |
T |
A |
2: 118,622,704 (GRCm39) |
H1145Q |
probably benign |
Het |
Epb41l4b |
T |
C |
4: 57,038,553 (GRCm39) |
T563A |
possibly damaging |
Het |
Ephb3 |
G |
A |
16: 21,040,132 (GRCm39) |
R498H |
probably damaging |
Het |
F10 |
T |
C |
8: 13,105,422 (GRCm39) |
I329T |
probably damaging |
Het |
Fam13b |
G |
T |
18: 34,578,382 (GRCm39) |
Q760K |
possibly damaging |
Het |
Fmo4 |
G |
A |
1: 162,631,259 (GRCm39) |
T236I |
probably benign |
Het |
Foxp4 |
C |
T |
17: 48,186,796 (GRCm39) |
R378Q |
unknown |
Het |
Fpr-rs4 |
A |
G |
17: 18,242,518 (GRCm39) |
Y175C |
probably damaging |
Het |
Fzd8 |
T |
A |
18: 9,214,502 (GRCm39) |
M528K |
probably damaging |
Het |
Gcc2 |
A |
G |
10: 58,121,965 (GRCm39) |
H1134R |
possibly damaging |
Het |
Gdf10 |
G |
A |
14: 33,654,710 (GRCm39) |
A406T |
probably benign |
Het |
Ggn |
T |
A |
7: 28,871,341 (GRCm39) |
S240R |
probably damaging |
Het |
Git2 |
C |
T |
5: 114,887,398 (GRCm39) |
W299* |
probably null |
Het |
Gm42669 |
A |
T |
5: 107,656,738 (GRCm39) |
E355D |
possibly damaging |
Het |
Gm5134 |
T |
C |
10: 75,840,680 (GRCm39) |
F508S |
possibly damaging |
Het |
Gm9923 |
G |
T |
10: 72,145,490 (GRCm39) |
V114L |
probably benign |
Het |
Has3 |
A |
T |
8: 107,605,435 (GRCm39) |
Y547F |
probably benign |
Het |
Heatr5a |
A |
G |
12: 51,992,202 (GRCm39) |
|
probably null |
Het |
Hnrnpk |
A |
T |
13: 58,544,000 (GRCm39) |
|
probably null |
Het |
Ifna4 |
A |
T |
4: 88,760,311 (GRCm39) |
I72F |
probably damaging |
Het |
Ip6k3 |
A |
T |
17: 27,370,142 (GRCm39) |
L92Q |
probably benign |
Het |
Itpripl1 |
T |
C |
2: 126,983,927 (GRCm39) |
E65G |
probably damaging |
Het |
Kcnh5 |
G |
C |
12: 74,944,358 (GRCm39) |
Q964E |
probably benign |
Het |
Kmt2d |
A |
G |
15: 98,757,471 (GRCm39) |
|
probably benign |
Het |
Lrrc69 |
A |
G |
4: 14,665,986 (GRCm39) |
V324A |
possibly damaging |
Het |
Mefv |
T |
C |
16: 3,535,691 (GRCm39) |
Q79R |
probably damaging |
Het |
Mettl17 |
T |
C |
14: 52,126,254 (GRCm39) |
S168P |
probably damaging |
Het |
Mpp4 |
A |
T |
1: 59,197,811 (GRCm39) |
S23T |
probably benign |
Het |
Nabp1 |
A |
T |
1: 51,517,004 (GRCm39) |
V24D |
probably damaging |
Het |
Nod2 |
T |
A |
8: 89,390,836 (GRCm39) |
F359Y |
probably damaging |
Het |
Or10g1b |
C |
T |
14: 52,628,037 (GRCm39) |
M64I |
probably benign |
Het |
Or1p1c |
A |
T |
11: 74,160,670 (GRCm39) |
T152S |
probably damaging |
Het |
Or51b17 |
T |
G |
7: 103,542,925 (GRCm39) |
S6R |
probably benign |
Het |
Or52d3 |
C |
A |
7: 104,229,116 (GRCm39) |
L88M |
probably damaging |
Het |
Or5ak4 |
T |
C |
2: 85,161,444 (GRCm39) |
D266G |
probably benign |
Het |
Or5b107 |
T |
C |
19: 13,142,560 (GRCm39) |
Y61H |
probably damaging |
Het |
Or6a2 |
C |
T |
7: 106,600,342 (GRCm39) |
A242T |
probably damaging |
Het |
Or7a39 |
A |
G |
10: 78,715,267 (GRCm39) |
Q87R |
probably benign |
Het |
Phf1 |
T |
A |
17: 27,154,719 (GRCm39) |
|
probably null |
Het |
Pold3 |
T |
C |
7: 99,737,318 (GRCm39) |
K379R |
probably benign |
Het |
Polr1f |
T |
A |
12: 33,487,817 (GRCm39) |
V244D |
probably benign |
Het |
Pou2f3 |
T |
A |
9: 43,056,534 (GRCm39) |
T108S |
probably benign |
Het |
Prdm5 |
C |
A |
6: 65,913,060 (GRCm39) |
T203K |
probably damaging |
Het |
Psma5 |
A |
G |
3: 108,173,760 (GRCm39) |
S79G |
probably benign |
Het |
Psme4 |
T |
A |
11: 30,782,424 (GRCm39) |
S889T |
probably damaging |
Het |
Ptk2 |
A |
T |
15: 73,087,832 (GRCm39) |
V902D |
possibly damaging |
Het |
Rad54l |
T |
A |
4: 115,967,554 (GRCm39) |
I243F |
probably damaging |
Het |
Ralgapa2 |
A |
G |
2: 146,302,679 (GRCm39) |
F95L |
probably benign |
Het |
Rassf6 |
G |
A |
5: 90,763,730 (GRCm39) |
Q71* |
probably null |
Het |
Ryr2 |
A |
T |
13: 11,695,966 (GRCm39) |
L2967H |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,346,479 (GRCm39) |
T1058A |
possibly damaging |
Het |
Sdk1 |
T |
C |
5: 142,080,336 (GRCm39) |
L1276P |
probably damaging |
Het |
Serpina12 |
T |
G |
12: 104,002,048 (GRCm39) |
T223P |
probably damaging |
Het |
Sh3yl1 |
A |
G |
12: 30,992,787 (GRCm39) |
|
probably null |
Het |
Spata31g1 |
A |
T |
4: 42,970,105 (GRCm39) |
|
probably null |
Het |
St6galnac5 |
T |
A |
3: 152,552,120 (GRCm39) |
Q149L |
probably benign |
Het |
Stam2 |
T |
C |
2: 52,598,239 (GRCm39) |
|
probably null |
Het |
Tac2 |
A |
G |
10: 127,564,349 (GRCm39) |
|
probably null |
Het |
Tbata |
G |
A |
10: 61,019,256 (GRCm39) |
D271N |
probably damaging |
Het |
Tbx3 |
T |
C |
5: 119,819,018 (GRCm39) |
V531A |
probably benign |
Het |
Tektl1 |
A |
G |
10: 78,586,373 (GRCm39) |
|
probably null |
Het |
Thra |
T |
A |
11: 98,654,567 (GRCm39) |
D312E |
probably benign |
Het |
Tlr1 |
T |
A |
5: 65,082,520 (GRCm39) |
I686F |
probably damaging |
Het |
Tmem86b |
A |
T |
7: 4,631,706 (GRCm39) |
F115L |
probably benign |
Het |
Tmem94 |
A |
G |
11: 115,679,500 (GRCm39) |
D259G |
possibly damaging |
Het |
Trim69 |
G |
A |
2: 122,004,956 (GRCm39) |
|
probably null |
Het |
Usp43 |
T |
A |
11: 67,795,159 (GRCm39) |
Q243L |
probably damaging |
Het |
Vcam1 |
T |
C |
3: 115,919,606 (GRCm39) |
Y226C |
probably damaging |
Het |
Vmn2r104 |
A |
T |
17: 20,262,313 (GRCm39) |
N272K |
probably damaging |
Het |
Vmn2r26 |
G |
A |
6: 124,030,846 (GRCm39) |
C527Y |
probably damaging |
Het |
Vmn2r84 |
G |
A |
10: 130,226,677 (GRCm39) |
A387V |
probably benign |
Het |
Vps13b |
A |
T |
15: 35,869,553 (GRCm39) |
I2686F |
probably damaging |
Het |
Vps8 |
C |
T |
16: 21,279,892 (GRCm39) |
T281M |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,067,275 (GRCm39) |
V1219A |
probably benign |
Het |
Wnt9b |
A |
G |
11: 103,621,638 (GRCm39) |
C340R |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,520,774 (GRCm39) |
V632A |
probably benign |
Het |
Zfp1006 |
A |
T |
8: 129,948,309 (GRCm39) |
D41E |
possibly damaging |
Het |
Zfp341 |
A |
T |
2: 154,480,132 (GRCm39) |
T528S |
probably benign |
Het |
Zfp990 |
G |
A |
4: 145,261,452 (GRCm39) |
A33T |
probably damaging |
Het |
Zranb1 |
T |
G |
7: 132,584,458 (GRCm39) |
S601R |
probably damaging |
Het |
Zyx |
A |
T |
6: 42,328,289 (GRCm39) |
K166I |
probably damaging |
Het |
|
Other mutations in Pcdh18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00543:Pcdh18
|
APN |
3 |
49,707,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00639:Pcdh18
|
APN |
3 |
49,710,065 (GRCm39) |
missense |
probably benign |
0.34 |
IGL00954:Pcdh18
|
APN |
3 |
49,710,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01338:Pcdh18
|
APN |
3 |
49,710,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Pcdh18
|
APN |
3 |
49,710,247 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01687:Pcdh18
|
APN |
3 |
49,707,982 (GRCm39) |
splice site |
probably benign |
|
IGL01727:Pcdh18
|
APN |
3 |
49,710,149 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01788:Pcdh18
|
APN |
3 |
49,710,371 (GRCm39) |
nonsense |
probably null |
|
IGL01824:Pcdh18
|
APN |
3 |
49,709,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01834:Pcdh18
|
APN |
3 |
49,711,279 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01913:Pcdh18
|
APN |
3 |
49,709,698 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01915:Pcdh18
|
APN |
3 |
49,699,370 (GRCm39) |
missense |
probably benign |
|
IGL02095:Pcdh18
|
APN |
3 |
49,710,605 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02128:Pcdh18
|
APN |
3 |
49,711,135 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02302:Pcdh18
|
APN |
3 |
49,710,387 (GRCm39) |
missense |
probably benign |
|
IGL02342:Pcdh18
|
APN |
3 |
49,710,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:Pcdh18
|
APN |
3 |
49,699,052 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02499:Pcdh18
|
APN |
3 |
49,707,896 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02570:Pcdh18
|
APN |
3 |
49,711,074 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02745:Pcdh18
|
APN |
3 |
49,710,340 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03073:Pcdh18
|
APN |
3 |
49,707,816 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4469001:Pcdh18
|
UTSW |
3 |
49,709,518 (GRCm39) |
missense |
probably benign |
|
R0078:Pcdh18
|
UTSW |
3 |
49,710,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Pcdh18
|
UTSW |
3 |
49,711,147 (GRCm39) |
splice site |
probably null |
|
R0524:Pcdh18
|
UTSW |
3 |
49,710,091 (GRCm39) |
missense |
probably damaging |
0.98 |
R0661:Pcdh18
|
UTSW |
3 |
49,707,767 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0900:Pcdh18
|
UTSW |
3 |
49,711,252 (GRCm39) |
missense |
probably benign |
0.25 |
R1101:Pcdh18
|
UTSW |
3 |
49,707,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Pcdh18
|
UTSW |
3 |
49,709,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R1778:Pcdh18
|
UTSW |
3 |
49,710,083 (GRCm39) |
missense |
probably benign |
0.19 |
R1850:Pcdh18
|
UTSW |
3 |
49,710,854 (GRCm39) |
missense |
probably benign |
0.22 |
R1875:Pcdh18
|
UTSW |
3 |
49,709,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R1903:Pcdh18
|
UTSW |
3 |
49,709,896 (GRCm39) |
missense |
probably benign |
|
R2044:Pcdh18
|
UTSW |
3 |
49,709,389 (GRCm39) |
missense |
probably benign |
|
R2303:Pcdh18
|
UTSW |
3 |
49,709,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Pcdh18
|
UTSW |
3 |
49,709,240 (GRCm39) |
missense |
probably benign |
|
R3732:Pcdh18
|
UTSW |
3 |
49,709,240 (GRCm39) |
missense |
probably benign |
|
R3733:Pcdh18
|
UTSW |
3 |
49,709,240 (GRCm39) |
missense |
probably benign |
|
R3973:Pcdh18
|
UTSW |
3 |
49,709,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R4281:Pcdh18
|
UTSW |
3 |
49,710,982 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4601:Pcdh18
|
UTSW |
3 |
49,699,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Pcdh18
|
UTSW |
3 |
49,710,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R4752:Pcdh18
|
UTSW |
3 |
49,709,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R4840:Pcdh18
|
UTSW |
3 |
49,699,117 (GRCm39) |
missense |
probably damaging |
0.98 |
R4867:Pcdh18
|
UTSW |
3 |
49,709,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Pcdh18
|
UTSW |
3 |
49,708,906 (GRCm39) |
missense |
probably benign |
0.23 |
R5039:Pcdh18
|
UTSW |
3 |
49,709,305 (GRCm39) |
missense |
probably benign |
|
R5169:Pcdh18
|
UTSW |
3 |
49,710,415 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5438:Pcdh18
|
UTSW |
3 |
49,710,465 (GRCm39) |
nonsense |
probably null |
|
R5579:Pcdh18
|
UTSW |
3 |
49,699,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Pcdh18
|
UTSW |
3 |
49,708,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R6220:Pcdh18
|
UTSW |
3 |
49,699,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Pcdh18
|
UTSW |
3 |
49,710,344 (GRCm39) |
missense |
probably damaging |
0.98 |
R6789:Pcdh18
|
UTSW |
3 |
49,710,364 (GRCm39) |
missense |
probably benign |
0.00 |
R7011:Pcdh18
|
UTSW |
3 |
49,709,231 (GRCm39) |
missense |
probably benign |
|
R7146:Pcdh18
|
UTSW |
3 |
49,710,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7150:Pcdh18
|
UTSW |
3 |
49,709,143 (GRCm39) |
missense |
probably benign |
0.31 |
R7205:Pcdh18
|
UTSW |
3 |
49,709,923 (GRCm39) |
missense |
probably benign |
|
R7326:Pcdh18
|
UTSW |
3 |
49,711,309 (GRCm39) |
missense |
probably benign |
|
R7413:Pcdh18
|
UTSW |
3 |
49,699,232 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7755:Pcdh18
|
UTSW |
3 |
49,709,278 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7848:Pcdh18
|
UTSW |
3 |
49,710,446 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8169:Pcdh18
|
UTSW |
3 |
49,699,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Pcdh18
|
UTSW |
3 |
49,711,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Pcdh18
|
UTSW |
3 |
49,699,624 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8406:Pcdh18
|
UTSW |
3 |
49,710,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Pcdh18
|
UTSW |
3 |
49,699,624 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8489:Pcdh18
|
UTSW |
3 |
49,709,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8526:Pcdh18
|
UTSW |
3 |
49,710,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R9075:Pcdh18
|
UTSW |
3 |
49,699,339 (GRCm39) |
missense |
probably benign |
|
R9285:Pcdh18
|
UTSW |
3 |
49,707,786 (GRCm39) |
missense |
probably damaging |
0.97 |
R9316:Pcdh18
|
UTSW |
3 |
49,709,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Pcdh18
|
UTSW |
3 |
49,709,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R9410:Pcdh18
|
UTSW |
3 |
49,699,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R9425:Pcdh18
|
UTSW |
3 |
49,709,051 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9432:Pcdh18
|
UTSW |
3 |
49,699,667 (GRCm39) |
missense |
probably damaging |
0.96 |
R9547:Pcdh18
|
UTSW |
3 |
49,709,506 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9567:Pcdh18
|
UTSW |
3 |
49,710,884 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9622:Pcdh18
|
UTSW |
3 |
49,711,229 (GRCm39) |
missense |
probably benign |
0.20 |
R9687:Pcdh18
|
UTSW |
3 |
49,711,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|