Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
C |
T |
11: 58,771,012 (GRCm39) |
L165F |
probably damaging |
Het |
Adamts18 |
A |
G |
8: 114,465,450 (GRCm39) |
V714A |
possibly damaging |
Het |
Adamtsl1 |
G |
T |
4: 86,171,055 (GRCm39) |
A518S |
probably benign |
Het |
Adcy2 |
C |
T |
13: 68,880,231 (GRCm39) |
V363M |
probably damaging |
Het |
Ago4 |
G |
T |
4: 126,419,870 (GRCm39) |
Q36K |
probably benign |
Het |
Akr1a1 |
A |
G |
4: 116,497,044 (GRCm39) |
V172A |
possibly damaging |
Het |
Alkbh2 |
T |
A |
5: 114,263,596 (GRCm39) |
N137I |
probably damaging |
Het |
Ank3 |
T |
A |
10: 69,715,756 (GRCm39) |
S470T |
probably damaging |
Het |
Ankrd12 |
T |
C |
17: 66,356,823 (GRCm39) |
T65A |
possibly damaging |
Het |
Aox1 |
A |
T |
1: 58,082,810 (GRCm39) |
|
probably benign |
Het |
Arhgap11a |
A |
T |
2: 113,670,163 (GRCm39) |
I320N |
probably benign |
Het |
Arhgap17 |
G |
A |
7: 122,893,867 (GRCm39) |
H518Y |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,611,348 (GRCm39) |
V1563A |
probably damaging |
Het |
Atf2 |
G |
A |
2: 73,649,500 (GRCm39) |
|
probably benign |
Het |
Bmpr2 |
C |
T |
1: 59,884,818 (GRCm39) |
T268I |
probably damaging |
Het |
Bpifb9a |
A |
G |
2: 154,106,608 (GRCm39) |
I380V |
probably benign |
Het |
C2cd2 |
G |
A |
16: 97,678,348 (GRCm39) |
T363I |
probably benign |
Het |
Catsperg2 |
T |
G |
7: 29,420,723 (GRCm39) |
N190H |
probably damaging |
Het |
Ccdc138 |
T |
C |
10: 58,397,789 (GRCm39) |
L543S |
probably damaging |
Het |
Ccdc170 |
A |
T |
10: 4,468,939 (GRCm39) |
K162N |
probably benign |
Het |
Cdca5 |
G |
T |
19: 6,140,328 (GRCm39) |
R163L |
probably damaging |
Het |
Cdh24 |
A |
G |
14: 54,870,054 (GRCm39) |
F239S |
probably benign |
Het |
Cdkl3 |
T |
C |
11: 51,895,882 (GRCm39) |
V43A |
probably damaging |
Het |
Cep152 |
G |
T |
2: 125,423,639 (GRCm39) |
Q921K |
possibly damaging |
Het |
Cftr |
G |
A |
6: 18,274,517 (GRCm39) |
|
probably benign |
Het |
Chmp5 |
T |
C |
4: 40,948,690 (GRCm39) |
|
probably benign |
Het |
Cit |
T |
A |
5: 116,071,452 (GRCm39) |
|
probably benign |
Het |
Cngb3 |
T |
A |
4: 19,309,517 (GRCm39) |
|
probably benign |
Het |
Cnr2 |
A |
G |
4: 135,644,912 (GRCm39) |
E330G |
probably benign |
Het |
Cyp21a1 |
A |
T |
17: 35,020,800 (GRCm39) |
L473Q |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,420,696 (GRCm39) |
T575A |
probably benign |
Het |
Dedd2 |
A |
G |
7: 24,903,050 (GRCm39) |
V303A |
probably damaging |
Het |
Dmd |
G |
T |
X: 83,469,344 (GRCm39) |
A2370S |
probably benign |
Het |
Dnah10 |
T |
A |
5: 124,885,915 (GRCm39) |
N3009K |
probably damaging |
Het |
Dnajc13 |
G |
T |
9: 104,077,708 (GRCm39) |
N934K |
probably damaging |
Het |
Dock1 |
C |
T |
7: 134,339,447 (GRCm39) |
L106F |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,909,025 (GRCm39) |
Y2326H |
probably benign |
Het |
Fhl5 |
A |
T |
4: 25,207,101 (GRCm39) |
C222* |
probably null |
Het |
Gnmt |
T |
C |
17: 47,036,854 (GRCm39) |
T252A |
probably benign |
Het |
Gpi-ps |
A |
G |
8: 5,689,888 (GRCm39) |
|
noncoding transcript |
Het |
Gsta5 |
C |
T |
9: 78,210,099 (GRCm39) |
A135V |
probably benign |
Het |
Gtf2f1 |
A |
G |
17: 57,311,307 (GRCm39) |
|
probably null |
Het |
Gtf3a |
T |
C |
5: 146,890,039 (GRCm39) |
Y187H |
probably damaging |
Het |
Hdac2 |
A |
G |
10: 36,850,788 (GRCm39) |
Y14C |
probably damaging |
Het |
Hnrnph1 |
T |
G |
11: 50,276,589 (GRCm39) |
|
probably benign |
Het |
Homer2 |
T |
C |
7: 81,268,351 (GRCm39) |
D92G |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,277,335 (GRCm39) |
S2885P |
probably damaging |
Het |
Insr |
A |
G |
8: 3,211,770 (GRCm39) |
S1084P |
probably damaging |
Het |
Ints11 |
T |
A |
4: 155,972,081 (GRCm39) |
V362E |
probably damaging |
Het |
Kank2 |
T |
C |
9: 21,691,195 (GRCm39) |
N513S |
probably damaging |
Het |
Kl |
T |
G |
5: 150,876,753 (GRCm39) |
V191G |
probably damaging |
Het |
Krt23 |
A |
G |
11: 99,377,524 (GRCm39) |
|
probably null |
Het |
Lama3 |
A |
C |
18: 12,583,481 (GRCm39) |
T690P |
possibly damaging |
Het |
Lamb1 |
G |
A |
12: 31,332,720 (GRCm39) |
A281T |
possibly damaging |
Het |
Lck |
T |
C |
4: 129,449,433 (GRCm39) |
E299G |
probably damaging |
Het |
Lonrf1 |
A |
G |
8: 36,689,864 (GRCm39) |
V703A |
probably damaging |
Het |
Ly6f |
T |
C |
15: 75,143,526 (GRCm39) |
C78R |
probably damaging |
Het |
Mapkap1 |
C |
T |
2: 34,423,793 (GRCm39) |
|
probably benign |
Het |
Mast1 |
T |
A |
8: 85,639,718 (GRCm39) |
I1204F |
probably damaging |
Het |
Mbd6 |
C |
T |
10: 127,121,742 (GRCm39) |
|
probably benign |
Het |
Mef2c |
A |
T |
13: 83,741,020 (GRCm39) |
T60S |
probably damaging |
Het |
Mgat4c |
C |
T |
10: 102,224,980 (GRCm39) |
T398I |
probably damaging |
Het |
Mmp12 |
C |
A |
9: 7,350,016 (GRCm39) |
H102Q |
probably damaging |
Het |
Mmp20 |
G |
A |
9: 7,645,374 (GRCm39) |
G308E |
probably damaging |
Het |
Mms19 |
A |
T |
19: 41,943,285 (GRCm39) |
L395Q |
probably damaging |
Het |
Mus81 |
A |
G |
19: 5,537,959 (GRCm39) |
|
probably benign |
Het |
Mypn |
C |
T |
10: 63,028,982 (GRCm39) |
R27H |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,689,161 (GRCm39) |
E372G |
probably damaging |
Het |
Ncoa1 |
T |
A |
12: 4,389,105 (GRCm39) |
I57F |
probably damaging |
Het |
Ncstn |
T |
C |
1: 171,910,159 (GRCm39) |
|
probably benign |
Het |
Nefm |
C |
T |
14: 68,361,608 (GRCm39) |
D219N |
probably damaging |
Het |
Notch2 |
C |
T |
3: 98,053,853 (GRCm39) |
T2172I |
possibly damaging |
Het |
Obscn |
T |
A |
11: 59,024,772 (GRCm39) |
K423* |
probably null |
Het |
Or51l14 |
A |
G |
7: 103,100,835 (GRCm39) |
N97S |
probably benign |
Het |
Or5d37 |
A |
C |
2: 87,923,972 (GRCm39) |
S103A |
probably benign |
Het |
Or5k1 |
T |
C |
16: 58,617,684 (GRCm39) |
N175S |
probably benign |
Het |
Or9a2 |
A |
T |
6: 41,749,198 (GRCm39) |
C12S |
probably benign |
Het |
Ostm1 |
T |
A |
10: 42,572,343 (GRCm39) |
M242K |
probably damaging |
Het |
Oxnad1 |
T |
A |
14: 31,821,437 (GRCm39) |
I154N |
probably damaging |
Het |
Pcdhb10 |
T |
A |
18: 37,546,152 (GRCm39) |
D409E |
probably damaging |
Het |
Pdcd11 |
T |
C |
19: 47,113,476 (GRCm39) |
|
probably benign |
Het |
Pex1 |
G |
A |
5: 3,656,444 (GRCm39) |
|
probably null |
Het |
Plk4 |
T |
A |
3: 40,760,075 (GRCm39) |
F324I |
probably benign |
Het |
Poglut2 |
C |
T |
1: 44,149,917 (GRCm39) |
W424* |
probably null |
Het |
Ppfibp1 |
C |
A |
6: 146,920,529 (GRCm39) |
|
probably null |
Het |
Prcp |
T |
A |
7: 92,568,290 (GRCm39) |
W276R |
probably damaging |
Het |
Prr14l |
T |
C |
5: 32,987,224 (GRCm39) |
E757G |
probably benign |
Het |
Prss52 |
T |
A |
14: 64,351,093 (GRCm39) |
Y293N |
probably damaging |
Het |
Prune2 |
A |
G |
19: 16,984,156 (GRCm39) |
|
probably benign |
Het |
Ptprk |
G |
C |
10: 28,461,943 (GRCm39) |
A84P |
probably damaging |
Het |
Ptprk |
C |
T |
10: 28,461,944 (GRCm39) |
A84V |
probably damaging |
Het |
Rock1 |
A |
G |
18: 10,079,120 (GRCm39) |
L1116P |
possibly damaging |
Het |
Sdha |
A |
T |
13: 74,475,452 (GRCm39) |
F526Y |
probably benign |
Het |
Sema4b |
T |
C |
7: 79,869,954 (GRCm39) |
F414S |
probably damaging |
Het |
Serpina12 |
T |
C |
12: 104,001,960 (GRCm39) |
D252G |
probably damaging |
Het |
Siglecg |
C |
T |
7: 43,060,550 (GRCm39) |
A310V |
probably benign |
Het |
Slc30a8 |
A |
G |
15: 52,188,966 (GRCm39) |
I194V |
probably benign |
Het |
Spred3 |
A |
G |
7: 28,862,400 (GRCm39) |
S148P |
probably damaging |
Het |
Taf9b |
A |
G |
X: 105,262,014 (GRCm39) |
S58P |
probably damaging |
Het |
Tgm4 |
A |
T |
9: 122,891,484 (GRCm39) |
Y109F |
probably benign |
Het |
Tmprss11c |
T |
G |
5: 86,385,468 (GRCm39) |
|
probably benign |
Het |
Tmtc3 |
A |
T |
10: 100,307,266 (GRCm39) |
V246D |
probably damaging |
Het |
Tnip1 |
C |
T |
11: 54,828,820 (GRCm39) |
G116R |
probably damaging |
Het |
Tpr |
A |
G |
1: 150,303,992 (GRCm39) |
E1455G |
possibly damaging |
Het |
Ttc3 |
T |
A |
16: 94,232,863 (GRCm39) |
L986* |
probably null |
Het |
Txndc15 |
A |
G |
13: 55,872,436 (GRCm39) |
I275V |
possibly damaging |
Het |
Ugt2b1 |
T |
A |
5: 87,074,315 (GRCm39) |
I15L |
probably benign |
Het |
Upf2 |
T |
C |
2: 5,962,445 (GRCm39) |
V49A |
possibly damaging |
Het |
Vmn1r117 |
G |
A |
7: 20,617,371 (GRCm39) |
P226S |
probably benign |
Het |
Vmn2r28 |
A |
T |
7: 5,493,456 (GRCm39) |
H163Q |
probably benign |
Het |
Vstm2a |
T |
A |
11: 16,213,240 (GRCm39) |
S208R |
probably damaging |
Het |
Zfp346 |
T |
A |
13: 55,260,910 (GRCm39) |
C79* |
probably null |
Het |
Zfp628 |
A |
T |
7: 4,924,615 (GRCm39) |
T946S |
probably benign |
Het |
|
Other mutations in Peak1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Peak1
|
APN |
9 |
56,134,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00544:Peak1
|
APN |
9 |
56,167,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01141:Peak1
|
APN |
9 |
56,165,811 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01743:Peak1
|
APN |
9 |
56,166,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Peak1
|
APN |
9 |
56,167,349 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01885:Peak1
|
APN |
9 |
56,167,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Peak1
|
APN |
9 |
56,166,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Peak1
|
APN |
9 |
56,134,757 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02719:Peak1
|
APN |
9 |
56,134,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03247:Peak1
|
APN |
9 |
56,165,214 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03259:Peak1
|
APN |
9 |
56,167,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Peak1
|
UTSW |
9 |
56,135,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Peak1
|
UTSW |
9 |
56,165,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R0569:Peak1
|
UTSW |
9 |
56,167,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:Peak1
|
UTSW |
9 |
56,134,382 (GRCm39) |
splice site |
probably benign |
|
R0865:Peak1
|
UTSW |
9 |
56,165,116 (GRCm39) |
missense |
probably benign |
0.02 |
R1117:Peak1
|
UTSW |
9 |
56,165,702 (GRCm39) |
missense |
probably benign |
0.05 |
R1922:Peak1
|
UTSW |
9 |
56,113,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Peak1
|
UTSW |
9 |
56,114,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Peak1
|
UTSW |
9 |
56,166,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Peak1
|
UTSW |
9 |
56,166,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Peak1
|
UTSW |
9 |
56,114,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Peak1
|
UTSW |
9 |
56,166,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R3832:Peak1
|
UTSW |
9 |
56,165,667 (GRCm39) |
missense |
probably benign |
|
R3938:Peak1
|
UTSW |
9 |
56,167,649 (GRCm39) |
missense |
probably benign |
0.01 |
R3964:Peak1
|
UTSW |
9 |
56,167,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R4192:Peak1
|
UTSW |
9 |
56,166,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4381:Peak1
|
UTSW |
9 |
56,165,711 (GRCm39) |
missense |
probably benign |
0.34 |
R4869:Peak1
|
UTSW |
9 |
56,134,876 (GRCm39) |
missense |
probably benign |
0.06 |
R4994:Peak1
|
UTSW |
9 |
56,148,560 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5062:Peak1
|
UTSW |
9 |
56,167,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Peak1
|
UTSW |
9 |
56,113,770 (GRCm39) |
missense |
probably damaging |
0.98 |
R5632:Peak1
|
UTSW |
9 |
56,165,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Peak1
|
UTSW |
9 |
56,166,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R5880:Peak1
|
UTSW |
9 |
56,114,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Peak1
|
UTSW |
9 |
56,114,622 (GRCm39) |
missense |
probably benign |
0.19 |
R5986:Peak1
|
UTSW |
9 |
56,166,726 (GRCm39) |
missense |
probably benign |
0.00 |
R6109:Peak1
|
UTSW |
9 |
56,166,567 (GRCm39) |
missense |
probably benign |
0.01 |
R6284:Peak1
|
UTSW |
9 |
56,167,580 (GRCm39) |
missense |
probably benign |
0.10 |
R6347:Peak1
|
UTSW |
9 |
56,165,495 (GRCm39) |
missense |
probably benign |
0.00 |
R6374:Peak1
|
UTSW |
9 |
56,164,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6471:Peak1
|
UTSW |
9 |
56,165,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R6717:Peak1
|
UTSW |
9 |
56,114,523 (GRCm39) |
missense |
probably benign |
0.00 |
R7033:Peak1
|
UTSW |
9 |
56,166,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Peak1
|
UTSW |
9 |
56,165,093 (GRCm39) |
missense |
probably benign |
0.01 |
R7100:Peak1
|
UTSW |
9 |
56,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R7604:Peak1
|
UTSW |
9 |
56,148,491 (GRCm39) |
nonsense |
probably null |
|
R7868:Peak1
|
UTSW |
9 |
56,167,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R7979:Peak1
|
UTSW |
9 |
56,114,676 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8258:Peak1
|
UTSW |
9 |
56,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8259:Peak1
|
UTSW |
9 |
56,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Peak1
|
UTSW |
9 |
56,166,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Peak1
|
UTSW |
9 |
56,114,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R8516:Peak1
|
UTSW |
9 |
56,167,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R8847:Peak1
|
UTSW |
9 |
56,114,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R8895:Peak1
|
UTSW |
9 |
56,113,938 (GRCm39) |
missense |
probably benign |
|
R9082:Peak1
|
UTSW |
9 |
56,165,504 (GRCm39) |
missense |
probably benign |
0.07 |
R9138:Peak1
|
UTSW |
9 |
56,164,925 (GRCm39) |
missense |
probably benign |
0.34 |
R9355:Peak1
|
UTSW |
9 |
56,167,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R9548:Peak1
|
UTSW |
9 |
56,113,917 (GRCm39) |
missense |
probably benign |
0.19 |
R9591:Peak1
|
UTSW |
9 |
56,166,834 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9642:Peak1
|
UTSW |
9 |
56,167,205 (GRCm39) |
missense |
probably benign |
|
|