Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931428F04Rik |
G |
A |
8: 105,282,123 (GRCm38) |
Q421* |
probably null |
Het |
Abca13 |
T |
C |
11: 9,277,974 (GRCm38) |
|
probably null |
Het |
Adamts20 |
A |
C |
15: 94,353,584 (GRCm38) |
S441A |
probably damaging |
Het |
Aen |
T |
A |
7: 78,907,301 (GRCm38) |
M299K |
probably damaging |
Het |
Akap3 |
T |
C |
6: 126,865,833 (GRCm38) |
S472P |
probably benign |
Het |
Ank3 |
T |
G |
10: 69,822,257 (GRCm38) |
V158G |
probably damaging |
Het |
Arfgap1 |
A |
G |
2: 180,981,162 (GRCm38) |
D324G |
probably benign |
Het |
Aste1 |
A |
T |
9: 105,403,415 (GRCm38) |
R448S |
probably benign |
Het |
Atp10a |
T |
A |
7: 58,658,618 (GRCm38) |
L55Q |
probably benign |
Het |
C1qtnf9 |
G |
A |
14: 60,779,450 (GRCm38) |
G143D |
probably damaging |
Het |
Camsap2 |
A |
G |
1: 136,280,388 (GRCm38) |
V1122A |
probably benign |
Het |
Cbl |
T |
C |
9: 44,233,779 (GRCm38) |
H37R |
probably damaging |
Het |
Cfap61 |
A |
C |
2: 146,129,149 (GRCm38) |
D893A |
probably benign |
Het |
Chd2 |
T |
A |
7: 73,478,715 (GRCm38) |
I841F |
probably damaging |
Het |
Chd9 |
A |
G |
8: 90,997,164 (GRCm38) |
T622A |
probably damaging |
Het |
Cntnap3 |
A |
G |
13: 64,748,577 (GRCm38) |
Y1028H |
probably benign |
Het |
Crybg2 |
A |
G |
4: 134,074,123 (GRCm38) |
T865A |
probably benign |
Het |
Cyp2c55 |
A |
G |
19: 39,042,067 (GRCm38) |
I448V |
probably benign |
Het |
Cyth1 |
T |
A |
11: 118,192,463 (GRCm38) |
|
probably null |
Het |
Dcaf13 |
C |
T |
15: 39,143,642 (GRCm38) |
R324* |
probably null |
Het |
Dhx37 |
C |
A |
5: 125,425,730 (GRCm38) |
R42L |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,763,933 (GRCm38) |
V450E |
probably damaging |
Het |
Ednrb |
A |
G |
14: 103,820,877 (GRCm38) |
L330P |
probably damaging |
Het |
Eml4 |
T |
A |
17: 83,477,741 (GRCm38) |
H778Q |
probably damaging |
Het |
Evx1 |
T |
A |
6: 52,315,990 (GRCm38) |
I227N |
probably damaging |
Het |
G3bp1 |
T |
A |
11: 55,497,940 (GRCm38) |
V326E |
probably benign |
Het |
Gata2 |
T |
C |
6: 88,200,747 (GRCm38) |
V253A |
probably benign |
Het |
Gbp2 |
A |
G |
3: 142,633,377 (GRCm38) |
N397D |
probably damaging |
Het |
Gm14401 |
C |
A |
2: 177,086,903 (GRCm38) |
H261N |
probably benign |
Het |
Hacd4 |
A |
T |
4: 88,398,152 (GRCm38) |
H243Q |
probably benign |
Het |
Hsd3b1 |
C |
A |
3: 98,852,939 (GRCm38) |
K245N |
possibly damaging |
Het |
Hyls1 |
G |
A |
9: 35,561,184 (GRCm38) |
S312F |
probably benign |
Het |
Ift27 |
A |
T |
15: 78,165,243 (GRCm38) |
C86S |
probably damaging |
Het |
Iqgap2 |
C |
T |
13: 95,675,372 (GRCm38) |
R707H |
probably damaging |
Het |
Irs3 |
T |
A |
5: 137,644,559 (GRCm38) |
S206C |
probably damaging |
Het |
Lefty2 |
C |
T |
1: 180,893,151 (GRCm38) |
|
probably benign |
Het |
Mark3 |
A |
G |
12: 111,624,487 (GRCm38) |
I162V |
probably damaging |
Het |
Mefv |
A |
C |
16: 3,716,046 (GRCm38) |
D120E |
probably damaging |
Het |
Mep1a |
G |
A |
17: 43,478,164 (GRCm38) |
H574Y |
probably benign |
Het |
Mre11a |
A |
G |
9: 14,799,657 (GRCm38) |
I45V |
probably benign |
Het |
Mtor |
A |
G |
4: 148,536,536 (GRCm38) |
N1797S |
possibly damaging |
Het |
Nav1 |
A |
C |
1: 135,532,406 (GRCm38) |
M393R |
probably benign |
Het |
Nod2 |
T |
C |
8: 88,664,639 (GRCm38) |
S510P |
possibly damaging |
Het |
Nos2 |
C |
T |
11: 78,928,579 (GRCm38) |
T39I |
probably benign |
Het |
Olfr474 |
T |
A |
7: 107,954,906 (GRCm38) |
H88Q |
probably benign |
Het |
Olfr93 |
A |
T |
17: 37,151,799 (GRCm38) |
Y58N |
probably damaging |
Het |
Pcdh7 |
A |
G |
5: 57,721,628 (GRCm38) |
S842G |
possibly damaging |
Het |
Pcdha11 |
T |
C |
18: 37,012,623 (GRCm38) |
V589A |
probably damaging |
Het |
Plaa |
A |
C |
4: 94,583,469 (GRCm38) |
V10G |
probably damaging |
Het |
Pprc1 |
T |
A |
19: 46,065,220 (GRCm38) |
|
probably benign |
Het |
Ptprt |
T |
C |
2: 161,560,269 (GRCm38) |
Y994C |
probably damaging |
Het |
Ripply2 |
T |
A |
9: 87,015,890 (GRCm38) |
W37R |
probably damaging |
Het |
Rpgrip1 |
A |
G |
14: 52,158,382 (GRCm38) |
D1227G |
probably damaging |
Het |
Scoc |
C |
T |
8: 83,437,631 (GRCm38) |
D10N |
possibly damaging |
Het |
Sdk2 |
A |
T |
11: 113,854,273 (GRCm38) |
I732N |
probably damaging |
Het |
Six2 |
T |
C |
17: 85,687,664 (GRCm38) |
K97E |
probably damaging |
Het |
Slit2 |
A |
C |
5: 48,259,647 (GRCm38) |
N1014H |
probably damaging |
Het |
Smc1b |
A |
C |
15: 85,089,665 (GRCm38) |
L930R |
probably damaging |
Het |
Spag16 |
T |
A |
1: 69,923,714 (GRCm38) |
M340K |
probably benign |
Het |
Spata31 |
C |
T |
13: 64,922,666 (GRCm38) |
S876L |
probably benign |
Het |
Spen |
A |
G |
4: 141,471,843 (GRCm38) |
Y3135H |
possibly damaging |
Het |
Spta1 |
A |
T |
1: 174,184,797 (GRCm38) |
|
probably null |
Het |
Stk3 |
G |
A |
15: 34,959,018 (GRCm38) |
T336I |
probably damaging |
Het |
Tas2r118 |
T |
A |
6: 23,969,877 (GRCm38) |
T62S |
probably benign |
Het |
Tmprss11d |
A |
G |
5: 86,306,310 (GRCm38) |
M212T |
probably damaging |
Het |
Trpc7 |
A |
G |
13: 56,776,158 (GRCm38) |
L738P |
probably damaging |
Het |
Ttll8 |
A |
G |
15: 88,917,246 (GRCm38) |
V413A |
possibly damaging |
Het |
Usb1 |
G |
A |
8: 95,333,533 (GRCm38) |
|
probably benign |
Het |
Vmn2r114 |
T |
C |
17: 23,310,625 (GRCm38) |
T168A |
possibly damaging |
Het |
Vmn2r60 |
C |
A |
7: 42,116,508 (GRCm38) |
P13H |
probably benign |
Het |
Wdr26 |
A |
G |
1: 181,203,147 (GRCm38) |
L194P |
probably damaging |
Het |
Zfhx2 |
G |
A |
14: 55,073,330 (GRCm38) |
Q636* |
probably null |
Het |
Zfyve26 |
A |
G |
12: 79,266,537 (GRCm38) |
Y25H |
probably benign |
Het |
|
Other mutations in Vmn1r238 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Vmn1r238
|
APN |
18 |
3,123,243 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01385:Vmn1r238
|
APN |
18 |
3,122,770 (GRCm38) |
missense |
possibly damaging |
0.83 |
IGL02716:Vmn1r238
|
APN |
18 |
3,123,124 (GRCm38) |
missense |
probably damaging |
1.00 |
R1219:Vmn1r238
|
UTSW |
18 |
3,123,135 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1568:Vmn1r238
|
UTSW |
18 |
3,123,358 (GRCm38) |
missense |
probably benign |
0.00 |
R1864:Vmn1r238
|
UTSW |
18 |
3,123,040 (GRCm38) |
nonsense |
probably null |
|
R3024:Vmn1r238
|
UTSW |
18 |
3,123,305 (GRCm38) |
missense |
probably benign |
0.13 |
R4291:Vmn1r238
|
UTSW |
18 |
3,123,214 (GRCm38) |
nonsense |
probably null |
|
R4304:Vmn1r238
|
UTSW |
18 |
3,123,040 (GRCm38) |
nonsense |
probably null |
|
R4586:Vmn1r238
|
UTSW |
18 |
3,123,294 (GRCm38) |
missense |
probably damaging |
1.00 |
R4664:Vmn1r238
|
UTSW |
18 |
3,123,300 (GRCm38) |
missense |
probably damaging |
0.99 |
R5123:Vmn1r238
|
UTSW |
18 |
3,123,243 (GRCm38) |
missense |
probably benign |
|
R5430:Vmn1r238
|
UTSW |
18 |
3,122,521 (GRCm38) |
missense |
possibly damaging |
0.63 |
R7186:Vmn1r238
|
UTSW |
18 |
3,122,661 (GRCm38) |
missense |
probably damaging |
0.99 |
R7206:Vmn1r238
|
UTSW |
18 |
3,122,623 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7308:Vmn1r238
|
UTSW |
18 |
3,122,875 (GRCm38) |
missense |
probably benign |
0.09 |
R7346:Vmn1r238
|
UTSW |
18 |
3,123,151 (GRCm38) |
missense |
probably damaging |
1.00 |
R7467:Vmn1r238
|
UTSW |
18 |
3,123,393 (GRCm38) |
missense |
probably benign |
0.10 |
R7571:Vmn1r238
|
UTSW |
18 |
3,122,721 (GRCm38) |
missense |
probably damaging |
1.00 |
R7808:Vmn1r238
|
UTSW |
18 |
3,123,033 (GRCm38) |
missense |
probably benign |
0.03 |
R8085:Vmn1r238
|
UTSW |
18 |
3,123,151 (GRCm38) |
missense |
probably damaging |
1.00 |
R8086:Vmn1r238
|
UTSW |
18 |
3,123,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R8325:Vmn1r238
|
UTSW |
18 |
3,122,529 (GRCm38) |
missense |
probably benign |
0.00 |
R8423:Vmn1r238
|
UTSW |
18 |
3,123,365 (GRCm38) |
nonsense |
probably null |
|
R8747:Vmn1r238
|
UTSW |
18 |
3,123,232 (GRCm38) |
missense |
possibly damaging |
0.87 |
R8930:Vmn1r238
|
UTSW |
18 |
3,123,127 (GRCm38) |
missense |
probably benign |
0.03 |
R8932:Vmn1r238
|
UTSW |
18 |
3,123,127 (GRCm38) |
missense |
probably benign |
0.03 |
R9279:Vmn1r238
|
UTSW |
18 |
3,122,994 (GRCm38) |
missense |
probably damaging |
0.99 |
R9382:Vmn1r238
|
UTSW |
18 |
3,122,676 (GRCm38) |
missense |
probably damaging |
0.99 |
R9644:Vmn1r238
|
UTSW |
18 |
3,122,635 (GRCm38) |
missense |
probably benign |
0.10 |
R9725:Vmn1r238
|
UTSW |
18 |
3,122,577 (GRCm38) |
missense |
probably benign |
0.00 |
Z1177:Vmn1r238
|
UTSW |
18 |
3,122,505 (GRCm38) |
missense |
probably benign |
0.00 |
|