Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,668,711 (GRCm39) |
S701P |
probably damaging |
Het |
Acsl1 |
A |
G |
8: 46,961,397 (GRCm39) |
K114R |
probably benign |
Het |
Adam11 |
A |
G |
11: 102,663,495 (GRCm39) |
N275D |
probably damaging |
Het |
Adamts20 |
C |
T |
15: 94,180,943 (GRCm39) |
C1666Y |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,987,541 (GRCm39) |
I2942L |
possibly damaging |
Het |
Ank1 |
A |
G |
8: 23,576,993 (GRCm39) |
H195R |
probably damaging |
Het |
Ank2 |
T |
C |
3: 126,752,667 (GRCm39) |
T350A |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,008,946 (GRCm39) |
N243K |
possibly damaging |
Het |
Atp10b |
C |
T |
11: 43,088,339 (GRCm39) |
T315I |
probably benign |
Het |
Avl9 |
C |
T |
6: 56,730,825 (GRCm39) |
S583F |
probably damaging |
Het |
Bclaf1 |
A |
G |
10: 20,207,892 (GRCm39) |
K700E |
possibly damaging |
Het |
Brd10 |
C |
A |
19: 29,731,911 (GRCm39) |
C367F |
possibly damaging |
Het |
Cacna1i |
G |
A |
15: 80,246,318 (GRCm39) |
E571K |
probably benign |
Het |
Casp1 |
T |
A |
9: 5,299,322 (GRCm39) |
V17E |
probably damaging |
Het |
Ccdc115 |
A |
T |
1: 34,478,001 (GRCm39) |
D76E |
probably benign |
Het |
Ccdc150 |
A |
T |
1: 54,299,107 (GRCm39) |
R28* |
probably null |
Het |
Cd36 |
T |
G |
5: 18,019,732 (GRCm39) |
E123A |
probably benign |
Het |
Cd5l |
A |
C |
3: 87,275,104 (GRCm39) |
Q214H |
probably benign |
Het |
Cfap46 |
T |
A |
7: 139,191,907 (GRCm39) |
H2370L |
unknown |
Het |
Cftr |
C |
A |
6: 18,285,636 (GRCm39) |
T1148K |
possibly damaging |
Het |
Col15a1 |
T |
A |
4: 47,312,208 (GRCm39) |
L1341Q |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,661,239 (GRCm39) |
E290G |
probably benign |
Het |
D6Wsu163e |
A |
G |
6: 126,938,977 (GRCm39) |
E404G |
probably benign |
Het |
Dchs1 |
A |
T |
7: 105,412,682 (GRCm39) |
D1239E |
probably damaging |
Het |
Dennd4b |
C |
T |
3: 90,177,828 (GRCm39) |
T430I |
possibly damaging |
Het |
Dmgdh |
C |
T |
13: 93,825,154 (GRCm39) |
P159L |
probably damaging |
Het |
Dmrt3 |
G |
A |
19: 25,600,003 (GRCm39) |
D283N |
probably damaging |
Het |
Dnttip1 |
A |
G |
2: 164,607,100 (GRCm39) |
D247G |
probably damaging |
Het |
Efhc1 |
A |
T |
1: 21,048,928 (GRCm39) |
D447V |
probably damaging |
Het |
Ehhadh |
T |
C |
16: 21,585,138 (GRCm39) |
K248E |
probably benign |
Het |
Eif4enif1 |
T |
C |
11: 3,163,267 (GRCm39) |
L34P |
probably damaging |
Het |
Fer |
T |
C |
17: 64,214,376 (GRCm39) |
M103T |
probably benign |
Het |
Gabrg1 |
T |
C |
5: 70,938,029 (GRCm39) |
M197V |
probably damaging |
Het |
Galnt5 |
C |
A |
2: 57,889,477 (GRCm39) |
T359K |
probably benign |
Het |
Gm8108 |
G |
T |
14: 4,110,527 (GRCm38) |
|
probably benign |
Het |
Gna12 |
T |
C |
5: 140,746,602 (GRCm39) |
N281S |
probably damaging |
Het |
Golgb1 |
C |
T |
16: 36,713,769 (GRCm39) |
T250I |
probably damaging |
Het |
Gpd1 |
A |
G |
15: 99,618,004 (GRCm39) |
K130E |
probably benign |
Het |
Gys2 |
A |
T |
6: 142,395,181 (GRCm39) |
M428K |
possibly damaging |
Het |
Hey2 |
A |
C |
10: 30,709,824 (GRCm39) |
S310A |
probably benign |
Het |
Ifi47 |
T |
C |
11: 48,987,367 (GRCm39) |
V378A |
possibly damaging |
Het |
Ighv8-12 |
A |
G |
12: 115,611,640 (GRCm39) |
S95P |
probably damaging |
Het |
Igkv1-131 |
G |
T |
6: 67,743,215 (GRCm39) |
T56K |
probably damaging |
Het |
Igsf23 |
T |
C |
7: 19,675,839 (GRCm39) |
N127S |
probably benign |
Het |
Iqgap2 |
T |
A |
13: 95,821,505 (GRCm39) |
N546I |
probably damaging |
Het |
Irf9 |
A |
G |
14: 55,844,045 (GRCm39) |
H270R |
probably benign |
Het |
Itga6 |
C |
T |
2: 71,656,871 (GRCm39) |
S375L |
probably damaging |
Het |
Jak1 |
T |
C |
4: 101,016,087 (GRCm39) |
E857G |
probably benign |
Het |
Kbtbd8 |
A |
G |
6: 95,098,838 (GRCm39) |
T116A |
possibly damaging |
Het |
Kif5a |
T |
C |
10: 127,074,622 (GRCm39) |
I570V |
probably benign |
Het |
Klhdc10 |
T |
C |
6: 30,439,859 (GRCm39) |
M154T |
possibly damaging |
Het |
Krtap6-2 |
A |
G |
16: 89,216,776 (GRCm39) |
Y64H |
unknown |
Het |
Lce1l |
C |
T |
3: 92,757,828 (GRCm39) |
C10Y |
unknown |
Het |
Lrrc72 |
A |
G |
12: 36,264,371 (GRCm39) |
Y29H |
probably damaging |
Het |
Ltbp2 |
A |
T |
12: 84,915,515 (GRCm39) |
N181K |
probably damaging |
Het |
Ly75 |
A |
G |
2: 60,136,672 (GRCm39) |
|
probably null |
Het |
Mpped1 |
A |
G |
15: 83,684,305 (GRCm39) |
Y109C |
probably damaging |
Het |
Mrgpra2a |
C |
T |
7: 47,076,458 (GRCm39) |
V267I |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,698 (GRCm38) |
V1524E |
probably benign |
Het |
Nabp2 |
T |
A |
10: 128,237,610 (GRCm39) |
R208* |
probably null |
Het |
Ndst3 |
A |
G |
3: 123,340,461 (GRCm39) |
F786L |
possibly damaging |
Het |
Nos2 |
C |
T |
11: 78,822,472 (GRCm39) |
P123S |
probably damaging |
Het |
Nrcam |
T |
A |
12: 44,645,192 (GRCm39) |
V1198E |
probably damaging |
Het |
Oacyl |
A |
G |
18: 65,880,962 (GRCm39) |
Q592R |
possibly damaging |
Het |
Or10ak9 |
C |
T |
4: 118,726,217 (GRCm39) |
P80S |
probably damaging |
Het |
Or5as1 |
T |
A |
2: 86,980,898 (GRCm39) |
T36S |
probably benign |
Het |
Pcdhgc4 |
A |
G |
18: 37,951,026 (GRCm39) |
Y814C |
probably benign |
Het |
Pcm1 |
A |
C |
8: 41,757,135 (GRCm39) |
H1349P |
probably benign |
Het |
Pcsk6 |
T |
A |
7: 65,633,470 (GRCm39) |
D567E |
probably damaging |
Het |
Pdgfd |
T |
C |
9: 6,337,310 (GRCm39) |
V214A |
probably benign |
Het |
Plekhg3 |
A |
T |
12: 76,611,367 (GRCm39) |
N270I |
probably damaging |
Het |
Rasgrf1 |
T |
A |
9: 89,877,047 (GRCm39) |
V804E |
probably benign |
Het |
Rbl1 |
G |
T |
2: 157,033,966 (GRCm39) |
L371I |
probably damaging |
Het |
Rcl1 |
T |
A |
19: 29,105,482 (GRCm39) |
I223N |
probably damaging |
Het |
Saa4 |
C |
T |
7: 46,381,077 (GRCm39) |
G15E |
probably damaging |
Het |
Selenbp1 |
T |
C |
3: 94,844,648 (GRCm39) |
S102P |
probably damaging |
Het |
Setx |
G |
T |
2: 29,064,377 (GRCm39) |
E232* |
probably null |
Het |
Sik2 |
A |
G |
9: 50,810,058 (GRCm39) |
F502L |
possibly damaging |
Het |
Slamf9 |
A |
T |
1: 172,305,782 (GRCm39) |
I272F |
unknown |
Het |
Slc33a1 |
A |
T |
3: 63,861,424 (GRCm39) |
D259E |
probably benign |
Het |
Slc41a3 |
A |
G |
6: 90,621,138 (GRCm39) |
I393V |
probably benign |
Het |
Slk |
A |
G |
19: 47,608,346 (GRCm39) |
D433G |
possibly damaging |
Het |
Spata13 |
C |
T |
14: 60,929,240 (GRCm39) |
P266L |
probably benign |
Het |
Speer4c1 |
T |
A |
5: 15,916,652 (GRCm39) |
Q105L |
probably benign |
Het |
Srgap1 |
T |
A |
10: 121,761,771 (GRCm39) |
I126F |
probably damaging |
Het |
Srgap1 |
A |
G |
10: 121,628,579 (GRCm39) |
S818P |
probably benign |
Het |
Tbpl2 |
A |
T |
2: 23,981,104 (GRCm39) |
C232* |
probably null |
Het |
Tctn3 |
T |
G |
19: 40,599,743 (GRCm39) |
N153T |
possibly damaging |
Het |
Tdrd1 |
T |
A |
19: 56,847,101 (GRCm39) |
V914E |
probably benign |
Het |
Tmem200b |
A |
G |
4: 131,649,359 (GRCm39) |
H93R |
possibly damaging |
Het |
Tmem33 |
T |
G |
5: 67,425,922 (GRCm39) |
N155K |
possibly damaging |
Het |
Tmprss15 |
T |
C |
16: 78,884,400 (GRCm39) |
D94G |
probably benign |
Het |
Tnpo2 |
A |
G |
8: 85,781,988 (GRCm39) |
D869G |
probably benign |
Het |
Traf6 |
C |
T |
2: 101,527,029 (GRCm39) |
R260* |
probably null |
Het |
Ttn |
C |
T |
2: 76,594,293 (GRCm39) |
V20552I |
possibly damaging |
Het |
Vmn2r102 |
T |
A |
17: 19,898,129 (GRCm39) |
D381E |
probably benign |
Het |
Vmn2r92 |
T |
C |
17: 18,405,201 (GRCm39) |
F782L |
possibly damaging |
Het |
Zfc3h1 |
G |
A |
10: 115,244,821 (GRCm39) |
D765N |
possibly damaging |
Het |
Zfp472 |
T |
A |
17: 33,196,271 (GRCm39) |
H115Q |
possibly damaging |
Het |
Zmynd11 |
T |
A |
13: 9,739,244 (GRCm39) |
N514I |
probably benign |
Het |
|
Other mutations in Adamts19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00156:Adamts19
|
APN |
18 |
59,157,537 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00331:Adamts19
|
APN |
18 |
59,140,397 (GRCm39) |
splice site |
probably benign |
|
IGL00970:Adamts19
|
APN |
18 |
59,144,149 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01328:Adamts19
|
APN |
18 |
59,181,954 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01385:Adamts19
|
APN |
18 |
59,105,851 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01529:Adamts19
|
APN |
18 |
59,096,535 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01535:Adamts19
|
APN |
18 |
59,101,891 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01557:Adamts19
|
APN |
18 |
59,101,792 (GRCm39) |
splice site |
probably null |
|
IGL01705:Adamts19
|
APN |
18 |
59,166,038 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01803:Adamts19
|
APN |
18 |
59,085,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02116:Adamts19
|
APN |
18 |
58,970,571 (GRCm39) |
missense |
probably benign |
|
IGL02131:Adamts19
|
APN |
18 |
59,185,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02312:Adamts19
|
APN |
18 |
59,060,369 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Adamts19
|
APN |
18 |
59,103,005 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02866:Adamts19
|
APN |
18 |
59,181,914 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02964:Adamts19
|
APN |
18 |
59,122,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Adamts19
|
APN |
18 |
59,157,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Adamts19
|
APN |
18 |
59,036,080 (GRCm39) |
missense |
probably benign |
0.05 |
R0081:Adamts19
|
UTSW |
18 |
59,036,137 (GRCm39) |
critical splice donor site |
probably null |
|
R0194:Adamts19
|
UTSW |
18 |
59,144,220 (GRCm39) |
missense |
probably null |
1.00 |
R0195:Adamts19
|
UTSW |
18 |
59,102,942 (GRCm39) |
splice site |
probably benign |
|
R0541:Adamts19
|
UTSW |
18 |
59,060,372 (GRCm39) |
critical splice donor site |
probably null |
|
R0659:Adamts19
|
UTSW |
18 |
59,140,565 (GRCm39) |
splice site |
probably benign |
|
R0967:Adamts19
|
UTSW |
18 |
59,105,812 (GRCm39) |
nonsense |
probably null |
|
R1512:Adamts19
|
UTSW |
18 |
59,181,917 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1536:Adamts19
|
UTSW |
18 |
59,185,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1582:Adamts19
|
UTSW |
18 |
59,103,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R1629:Adamts19
|
UTSW |
18 |
59,087,691 (GRCm39) |
missense |
probably damaging |
0.97 |
R1653:Adamts19
|
UTSW |
18 |
59,023,365 (GRCm39) |
missense |
probably benign |
0.00 |
R1718:Adamts19
|
UTSW |
18 |
59,105,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R1733:Adamts19
|
UTSW |
18 |
59,165,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Adamts19
|
UTSW |
18 |
59,140,444 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1776:Adamts19
|
UTSW |
18 |
59,087,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Adamts19
|
UTSW |
18 |
59,166,017 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1958:Adamts19
|
UTSW |
18 |
59,103,078 (GRCm39) |
missense |
probably benign |
0.09 |
R1994:Adamts19
|
UTSW |
18 |
59,105,903 (GRCm39) |
critical splice donor site |
probably null |
|
R2177:Adamts19
|
UTSW |
18 |
59,087,626 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3730:Adamts19
|
UTSW |
18 |
59,033,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Adamts19
|
UTSW |
18 |
59,075,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4772:Adamts19
|
UTSW |
18 |
58,970,848 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4822:Adamts19
|
UTSW |
18 |
59,023,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R4891:Adamts19
|
UTSW |
18 |
59,166,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Adamts19
|
UTSW |
18 |
59,164,876 (GRCm39) |
nonsense |
probably null |
|
R5116:Adamts19
|
UTSW |
18 |
59,036,066 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5205:Adamts19
|
UTSW |
18 |
59,101,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Adamts19
|
UTSW |
18 |
59,185,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5781:Adamts19
|
UTSW |
18 |
58,971,040 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5792:Adamts19
|
UTSW |
18 |
58,970,584 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6082:Adamts19
|
UTSW |
18 |
59,101,846 (GRCm39) |
missense |
probably benign |
0.18 |
R6088:Adamts19
|
UTSW |
18 |
59,035,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7060:Adamts19
|
UTSW |
18 |
58,970,712 (GRCm39) |
nonsense |
probably null |
|
R7251:Adamts19
|
UTSW |
18 |
58,970,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Adamts19
|
UTSW |
18 |
58,970,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Adamts19
|
UTSW |
18 |
59,144,094 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7991:Adamts19
|
UTSW |
18 |
59,185,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Adamts19
|
UTSW |
18 |
59,140,559 (GRCm39) |
critical splice donor site |
probably null |
|
R8297:Adamts19
|
UTSW |
18 |
58,970,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R8336:Adamts19
|
UTSW |
18 |
59,140,444 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8358:Adamts19
|
UTSW |
18 |
59,181,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Adamts19
|
UTSW |
18 |
59,023,497 (GRCm39) |
nonsense |
probably null |
|
R9051:Adamts19
|
UTSW |
18 |
59,034,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Adamts19
|
UTSW |
18 |
59,103,013 (GRCm39) |
missense |
probably damaging |
0.98 |
R9423:Adamts19
|
UTSW |
18 |
59,023,427 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9610:Adamts19
|
UTSW |
18 |
59,023,399 (GRCm39) |
missense |
probably benign |
0.26 |
R9611:Adamts19
|
UTSW |
18 |
59,023,399 (GRCm39) |
missense |
probably benign |
0.26 |
R9686:Adamts19
|
UTSW |
18 |
58,971,093 (GRCm39) |
missense |
probably benign |
0.00 |
R9697:Adamts19
|
UTSW |
18 |
59,101,834 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Adamts19
|
UTSW |
18 |
59,023,446 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Adamts19
|
UTSW |
18 |
58,971,147 (GRCm39) |
missense |
probably damaging |
1.00 |
|