Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933434E20Rik |
C |
G |
3: 89,960,848 (GRCm39) |
Q34E |
probably damaging |
Het |
4933434E20Rik |
G |
T |
3: 89,960,890 (GRCm39) |
V48F |
probably damaging |
Het |
4933434E20Rik |
A |
T |
3: 89,960,849 (GRCm39) |
Q34L |
probably damaging |
Het |
Abra |
T |
C |
15: 41,729,302 (GRCm39) |
D366G |
probably damaging |
Het |
Acvr2a |
T |
C |
2: 48,760,447 (GRCm39) |
S68P |
probably damaging |
Het |
Adamts1 |
T |
A |
16: 85,599,393 (GRCm39) |
E69V |
probably benign |
Het |
Adgra1 |
A |
T |
7: 139,455,505 (GRCm39) |
M378L |
probably benign |
Het |
Adgra2 |
T |
A |
8: 27,588,850 (GRCm39) |
N101K |
possibly damaging |
Het |
Adhfe1 |
T |
A |
1: 9,646,475 (GRCm39) |
F449L |
probably damaging |
Het |
Akap6 |
T |
A |
12: 52,842,668 (GRCm39) |
S5R |
possibly damaging |
Het |
Akap9 |
G |
A |
5: 4,105,339 (GRCm39) |
R2883Q |
probably benign |
Het |
Ank3 |
T |
A |
10: 69,542,688 (GRCm39) |
I16N |
probably benign |
Het |
Api5 |
A |
T |
2: 94,253,816 (GRCm39) |
F296I |
possibly damaging |
Het |
Ceacam14 |
G |
T |
7: 17,547,975 (GRCm39) |
|
probably null |
Het |
Cep295 |
C |
T |
9: 15,242,128 (GRCm39) |
G1768S |
probably damaging |
Het |
Cldn12 |
A |
G |
5: 5,558,385 (GRCm39) |
F14S |
probably damaging |
Het |
Cp |
C |
A |
3: 20,026,811 (GRCm39) |
T413K |
probably benign |
Het |
Ctdsp2 |
T |
G |
10: 126,828,938 (GRCm39) |
V104G |
probably damaging |
Het |
Ctrc |
T |
A |
4: 141,573,607 (GRCm39) |
|
probably null |
Het |
Dbt |
T |
C |
3: 116,326,945 (GRCm39) |
I98T |
probably damaging |
Het |
Dcaf10 |
G |
A |
4: 45,372,769 (GRCm39) |
R394Q |
possibly damaging |
Het |
Dctn1 |
T |
A |
6: 83,166,920 (GRCm39) |
M257K |
possibly damaging |
Het |
Depp1 |
T |
A |
6: 116,629,096 (GRCm39) |
C146* |
probably null |
Het |
Dlgap5 |
C |
T |
14: 47,638,977 (GRCm39) |
|
probably null |
Het |
Drd3 |
G |
T |
16: 43,643,164 (GRCm39) |
E467* |
probably null |
Het |
Exoc8 |
A |
G |
8: 125,623,989 (GRCm39) |
V126A |
probably benign |
Het |
Fam185a |
T |
A |
5: 21,660,785 (GRCm39) |
S267T |
probably damaging |
Het |
Fhod1 |
T |
C |
8: 106,064,493 (GRCm39) |
|
probably benign |
Het |
Fn1 |
T |
C |
1: 71,687,307 (GRCm39) |
|
probably null |
Het |
Gadl1 |
A |
T |
9: 115,783,685 (GRCm39) |
T214S |
possibly damaging |
Het |
Gem |
G |
T |
4: 11,706,074 (GRCm39) |
R54L |
probably damaging |
Het |
Ghr |
A |
G |
15: 3,355,422 (GRCm39) |
V287A |
probably benign |
Het |
Gm3642 |
G |
A |
14: 18,212,879 (GRCm39) |
T215I |
probably benign |
Het |
Grip1 |
T |
A |
10: 119,874,588 (GRCm39) |
I732K |
probably benign |
Het |
Gtpbp2 |
A |
T |
17: 46,478,147 (GRCm39) |
|
probably null |
Het |
Heatr6 |
C |
T |
11: 83,670,374 (GRCm39) |
R976* |
probably null |
Het |
Hipk2 |
T |
A |
6: 38,675,327 (GRCm39) |
T1084S |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,570,584 (GRCm39) |
|
probably null |
Het |
Hspg2 |
T |
A |
4: 137,249,438 (GRCm39) |
M1328K |
probably damaging |
Het |
Ifna4 |
C |
A |
4: 88,760,519 (GRCm39) |
T141K |
probably benign |
Het |
Ighv1-64 |
A |
G |
12: 115,471,466 (GRCm39) |
V17A |
probably benign |
Het |
Iqgap2 |
G |
T |
13: 95,772,005 (GRCm39) |
N1391K |
possibly damaging |
Het |
Irf7 |
A |
T |
7: 140,844,648 (GRCm39) |
L148Q |
possibly damaging |
Het |
Kat6b |
G |
A |
14: 21,711,030 (GRCm39) |
R768K |
probably benign |
Het |
Lepr |
G |
A |
4: 101,622,562 (GRCm39) |
W447* |
probably null |
Het |
Letmd1 |
A |
G |
15: 100,367,619 (GRCm39) |
Y59C |
probably damaging |
Het |
Lingo4 |
A |
T |
3: 94,310,183 (GRCm39) |
K374* |
probably null |
Het |
Loxl4 |
G |
T |
19: 42,596,785 (GRCm39) |
D62E |
probably benign |
Het |
Lrfn2 |
A |
G |
17: 49,377,462 (GRCm39) |
D181G |
probably damaging |
Het |
Lrrc71 |
A |
T |
3: 87,646,481 (GRCm39) |
F526L |
probably damaging |
Het |
Ltbp1 |
A |
T |
17: 75,620,003 (GRCm39) |
M711L |
probably damaging |
Het |
Mcm7 |
A |
T |
5: 138,167,387 (GRCm39) |
D78E |
probably damaging |
Het |
Mdh1 |
T |
C |
11: 21,512,957 (GRCm39) |
N136D |
probably damaging |
Het |
Meltf |
T |
A |
16: 31,711,323 (GRCm39) |
N515K |
probably benign |
Het |
Mis18bp1 |
T |
A |
12: 65,205,513 (GRCm39) |
T220S |
probably benign |
Het |
Mtss1 |
C |
T |
15: 58,953,367 (GRCm39) |
V4M |
probably damaging |
Het |
Nacc2 |
A |
T |
2: 25,980,185 (GRCm39) |
F84I |
probably damaging |
Het |
Nedd9 |
A |
G |
13: 41,470,073 (GRCm39) |
V360A |
possibly damaging |
Het |
Nek11 |
T |
A |
9: 105,270,169 (GRCm39) |
I18F |
possibly damaging |
Het |
Nkd2 |
C |
T |
13: 73,995,124 (GRCm39) |
V13M |
probably damaging |
Het |
Nkx6-3 |
A |
G |
8: 23,646,285 (GRCm39) |
I152V |
probably damaging |
Het |
Npdc1 |
G |
A |
2: 25,298,957 (GRCm39) |
D284N |
probably damaging |
Het |
Oprm1 |
A |
T |
10: 6,708,656 (GRCm39) |
R16* |
probably null |
Het |
Or1e16 |
A |
T |
11: 73,285,981 (GRCm39) |
I289N |
probably damaging |
Het |
Or51b4 |
A |
G |
7: 103,530,856 (GRCm39) |
V198A |
probably benign |
Het |
Or5an1 |
T |
C |
19: 12,260,460 (GRCm39) |
L16P |
probably damaging |
Het |
Or5p69 |
T |
A |
7: 107,967,205 (GRCm39) |
F169L |
probably benign |
Het |
Or6d15 |
T |
C |
6: 116,559,898 (GRCm39) |
N3S |
probably damaging |
Het |
Or7a36 |
A |
G |
10: 78,820,356 (GRCm39) |
H244R |
probably damaging |
Het |
Ostf1 |
G |
A |
19: 18,571,231 (GRCm39) |
P62L |
probably damaging |
Het |
Pcdha2 |
A |
T |
18: 37,073,568 (GRCm39) |
T400S |
possibly damaging |
Het |
Pcdha5 |
A |
T |
18: 37,094,549 (GRCm39) |
T353S |
possibly damaging |
Het |
Pelo |
A |
G |
13: 115,225,271 (GRCm39) |
F318S |
probably damaging |
Het |
Polr2f |
T |
C |
15: 79,030,269 (GRCm39) |
V36A |
probably benign |
Het |
Ppan |
G |
A |
9: 20,799,806 (GRCm39) |
R41H |
probably benign |
Het |
Ppp1r21 |
C |
T |
17: 88,863,019 (GRCm39) |
R253* |
probably null |
Het |
Prf1 |
T |
A |
10: 61,139,487 (GRCm39) |
W482R |
probably damaging |
Het |
Ralgapa2 |
T |
C |
2: 146,187,453 (GRCm39) |
T1397A |
possibly damaging |
Het |
Rev3l |
T |
A |
10: 39,722,802 (GRCm39) |
Y2598* |
probably null |
Het |
Scaf11 |
G |
T |
15: 96,312,729 (GRCm39) |
D1437E |
probably benign |
Het |
Sec23a |
C |
T |
12: 59,025,292 (GRCm39) |
G510R |
probably damaging |
Het |
Sel1l2 |
A |
G |
2: 140,082,847 (GRCm39) |
M597T |
probably damaging |
Het |
Slc11a2 |
A |
T |
15: 100,304,219 (GRCm39) |
S160T |
possibly damaging |
Het |
Slc18a1 |
A |
T |
8: 69,526,301 (GRCm39) |
L129* |
probably null |
Het |
Smg8 |
A |
C |
11: 86,977,047 (GRCm39) |
L178R |
probably benign |
Het |
Sp4 |
T |
C |
12: 118,225,544 (GRCm39) |
T607A |
probably benign |
Het |
Ssbp2 |
A |
G |
13: 91,836,933 (GRCm39) |
D266G |
possibly damaging |
Het |
Sstr3 |
A |
T |
15: 78,423,897 (GRCm39) |
Y283* |
probably null |
Het |
Stk32b |
C |
T |
5: 37,612,278 (GRCm39) |
|
probably null |
Het |
Svep1 |
T |
C |
4: 58,070,752 (GRCm39) |
T2345A |
possibly damaging |
Het |
Synpo2 |
A |
G |
3: 122,907,940 (GRCm39) |
S459P |
probably damaging |
Het |
Sytl2 |
A |
G |
7: 89,998,000 (GRCm39) |
M1V |
probably null |
Het |
Tas2r102 |
T |
A |
6: 132,739,520 (GRCm39) |
W143R |
probably damaging |
Het |
Thy1 |
T |
C |
9: 43,958,645 (GRCm39) |
V129A |
probably damaging |
Het |
Tlr2 |
A |
T |
3: 83,745,492 (GRCm39) |
I197N |
probably damaging |
Het |
Tmem101 |
A |
G |
11: 102,044,269 (GRCm39) |
I206T |
probably benign |
Het |
Tmem108 |
A |
G |
9: 103,376,688 (GRCm39) |
S254P |
possibly damaging |
Het |
Tmem198b |
T |
C |
10: 128,637,350 (GRCm39) |
Q263R |
probably damaging |
Het |
Vangl1 |
T |
C |
3: 102,091,870 (GRCm39) |
D72G |
probably damaging |
Het |
Vmn1r4 |
T |
A |
6: 56,934,349 (GRCm39) |
D284E |
probably benign |
Het |
Vmn2r31 |
G |
A |
7: 7,387,757 (GRCm39) |
L605F |
possibly damaging |
Het |
Zfand4 |
T |
C |
6: 116,250,780 (GRCm39) |
V70A |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,653,665 (GRCm39) |
E53G |
probably damaging |
Het |
Zfp541 |
A |
T |
7: 15,815,612 (GRCm39) |
I805F |
probably damaging |
Het |
Zfp976 |
T |
C |
7: 42,262,457 (GRCm39) |
H460R |
possibly damaging |
Het |
|
Other mutations in Adam28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Adam28
|
APN |
14 |
68,859,569 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL00654:Adam28
|
APN |
14 |
68,886,877 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01021:Adam28
|
APN |
14 |
68,879,563 (GRCm39) |
missense |
probably benign |
|
IGL01099:Adam28
|
APN |
14 |
68,874,778 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01349:Adam28
|
APN |
14 |
68,848,455 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01744:Adam28
|
APN |
14 |
68,844,956 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01805:Adam28
|
APN |
14 |
68,879,540 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02007:Adam28
|
APN |
14 |
68,870,668 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02828:Adam28
|
APN |
14 |
68,884,319 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03180:Adam28
|
APN |
14 |
68,874,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Adam28
|
APN |
14 |
68,872,252 (GRCm39) |
splice site |
probably benign |
|
IGL02980:Adam28
|
UTSW |
14 |
68,857,255 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4453001:Adam28
|
UTSW |
14 |
68,872,325 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:Adam28
|
UTSW |
14 |
68,874,822 (GRCm39) |
missense |
probably benign |
0.33 |
R0321:Adam28
|
UTSW |
14 |
68,855,200 (GRCm39) |
missense |
probably damaging |
0.97 |
R0329:Adam28
|
UTSW |
14 |
68,855,188 (GRCm39) |
missense |
probably damaging |
0.96 |
R0494:Adam28
|
UTSW |
14 |
68,868,241 (GRCm39) |
splice site |
probably benign |
|
R0605:Adam28
|
UTSW |
14 |
68,844,049 (GRCm39) |
unclassified |
probably benign |
|
R0732:Adam28
|
UTSW |
14 |
68,874,796 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Adam28
|
UTSW |
14 |
68,845,387 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1319:Adam28
|
UTSW |
14 |
68,846,578 (GRCm39) |
missense |
probably benign |
0.28 |
R1745:Adam28
|
UTSW |
14 |
68,870,620 (GRCm39) |
missense |
probably benign |
0.04 |
R1836:Adam28
|
UTSW |
14 |
68,886,870 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1838:Adam28
|
UTSW |
14 |
68,876,659 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1839:Adam28
|
UTSW |
14 |
68,876,659 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1850:Adam28
|
UTSW |
14 |
68,876,644 (GRCm39) |
missense |
probably benign |
0.01 |
R1912:Adam28
|
UTSW |
14 |
68,881,780 (GRCm39) |
missense |
probably benign |
0.24 |
R2830:Adam28
|
UTSW |
14 |
68,864,363 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2889:Adam28
|
UTSW |
14 |
68,872,294 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3977:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R3978:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R3979:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R4282:Adam28
|
UTSW |
14 |
68,885,155 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4416:Adam28
|
UTSW |
14 |
68,859,531 (GRCm39) |
critical splice donor site |
probably null |
|
R4690:Adam28
|
UTSW |
14 |
68,879,497 (GRCm39) |
missense |
probably benign |
0.01 |
R4768:Adam28
|
UTSW |
14 |
68,872,264 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4883:Adam28
|
UTSW |
14 |
68,875,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R5054:Adam28
|
UTSW |
14 |
68,855,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R5710:Adam28
|
UTSW |
14 |
68,847,357 (GRCm39) |
missense |
probably damaging |
0.96 |
R5835:Adam28
|
UTSW |
14 |
68,893,130 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6002:Adam28
|
UTSW |
14 |
68,879,511 (GRCm39) |
missense |
probably benign |
|
R6054:Adam28
|
UTSW |
14 |
68,879,601 (GRCm39) |
missense |
probably benign |
0.01 |
R6349:Adam28
|
UTSW |
14 |
68,870,621 (GRCm39) |
missense |
probably benign |
0.29 |
R6449:Adam28
|
UTSW |
14 |
68,868,116 (GRCm39) |
missense |
probably benign |
0.31 |
R6455:Adam28
|
UTSW |
14 |
68,870,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Adam28
|
UTSW |
14 |
68,855,576 (GRCm39) |
missense |
probably benign |
0.04 |
R6833:Adam28
|
UTSW |
14 |
68,855,576 (GRCm39) |
missense |
probably benign |
0.04 |
R7212:Adam28
|
UTSW |
14 |
68,874,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R7411:Adam28
|
UTSW |
14 |
68,864,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Adam28
|
UTSW |
14 |
68,864,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Adam28
|
UTSW |
14 |
68,868,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R7649:Adam28
|
UTSW |
14 |
68,872,282 (GRCm39) |
missense |
probably benign |
0.12 |
R7765:Adam28
|
UTSW |
14 |
68,846,555 (GRCm39) |
critical splice donor site |
probably null |
|
R8469:Adam28
|
UTSW |
14 |
68,844,029 (GRCm39) |
missense |
probably benign |
0.16 |
R8520:Adam28
|
UTSW |
14 |
68,879,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R9026:Adam28
|
UTSW |
14 |
68,846,593 (GRCm39) |
missense |
probably benign |
0.16 |
R9163:Adam28
|
UTSW |
14 |
68,866,531 (GRCm39) |
missense |
probably damaging |
0.98 |
R9264:Adam28
|
UTSW |
14 |
68,844,914 (GRCm39) |
missense |
probably benign |
|
R9304:Adam28
|
UTSW |
14 |
68,874,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Adam28
|
UTSW |
14 |
68,879,479 (GRCm39) |
missense |
probably benign |
0.36 |
R9441:Adam28
|
UTSW |
14 |
68,874,943 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Adam28
|
UTSW |
14 |
68,864,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|