Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
T |
C |
3: 36,139,564 (GRCm39) |
V388A |
probably damaging |
Het |
Acp3 |
T |
C |
9: 104,197,201 (GRCm39) |
E146G |
probably damaging |
Het |
Adap2 |
A |
T |
11: 80,066,905 (GRCm39) |
R276S |
probably damaging |
Het |
Agbl3 |
A |
T |
6: 34,816,270 (GRCm39) |
M727L |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,977,628 (GRCm39) |
|
probably benign |
Het |
Ankmy1 |
G |
T |
1: 92,813,948 (GRCm39) |
D410E |
probably damaging |
Het |
Ankra2 |
T |
C |
13: 98,402,962 (GRCm39) |
S70P |
probably damaging |
Het |
Aox4 |
T |
C |
1: 58,302,556 (GRCm39) |
|
probably null |
Het |
Arl13b |
G |
A |
16: 62,622,096 (GRCm39) |
T399I |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,966,636 (GRCm39) |
D652E |
possibly damaging |
Het |
Atad2 |
T |
G |
15: 57,984,345 (GRCm39) |
M328L |
probably benign |
Het |
Ccnb1 |
T |
C |
13: 100,916,642 (GRCm39) |
|
probably null |
Het |
Ccr2 |
G |
C |
9: 123,905,976 (GRCm39) |
K85N |
possibly damaging |
Het |
Ccr2 |
A |
T |
9: 123,906,163 (GRCm39) |
T148S |
possibly damaging |
Het |
Cdc20b |
T |
C |
13: 113,192,484 (GRCm39) |
V59A |
probably benign |
Het |
Cdin1 |
C |
T |
2: 115,473,172 (GRCm39) |
R101W |
probably damaging |
Het |
Cdkl3 |
T |
C |
11: 51,923,243 (GRCm39) |
S507P |
possibly damaging |
Het |
Celf6 |
C |
A |
9: 59,510,161 (GRCm39) |
T86K |
probably benign |
Het |
Ces1g |
A |
G |
8: 94,060,317 (GRCm39) |
F101L |
probably benign |
Het |
Cimap1d |
T |
C |
10: 79,476,099 (GRCm39) |
D155G |
probably damaging |
Het |
Cntnap3 |
C |
T |
13: 65,006,492 (GRCm39) |
D107N |
probably benign |
Het |
Col15a1 |
A |
T |
4: 47,262,950 (GRCm39) |
D534V |
probably damaging |
Het |
Col27a1 |
A |
G |
4: 63,218,978 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,710,527 (GRCm39) |
T1687A |
probably benign |
Het |
Cstf3 |
A |
G |
2: 104,479,950 (GRCm39) |
I272M |
possibly damaging |
Het |
Cyp2d40 |
T |
C |
15: 82,645,418 (GRCm39) |
T150A |
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,934,483 (GRCm39) |
F1489L |
possibly damaging |
Het |
Dop1b |
A |
T |
16: 93,567,325 (GRCm39) |
T1251S |
probably benign |
Het |
Dtx2 |
G |
A |
5: 136,057,957 (GRCm39) |
G421R |
probably damaging |
Het |
Epb41l3 |
T |
A |
17: 69,554,654 (GRCm39) |
D251E |
probably benign |
Het |
Erg |
A |
C |
16: 95,161,842 (GRCm39) |
Y305* |
probably null |
Het |
Exosc4 |
G |
A |
15: 76,213,766 (GRCm39) |
A197T |
probably benign |
Het |
Fam227b |
T |
A |
2: 125,942,829 (GRCm39) |
I323L |
probably benign |
Het |
Far1 |
G |
T |
7: 113,153,503 (GRCm39) |
|
probably benign |
Het |
Fmod |
A |
G |
1: 133,968,934 (GRCm39) |
I325V |
possibly damaging |
Het |
Fshr |
C |
G |
17: 89,316,713 (GRCm39) |
S169T |
probably benign |
Het |
Gm4076 |
G |
T |
13: 85,275,345 (GRCm39) |
|
noncoding transcript |
Het |
Gm5134 |
A |
T |
10: 75,828,359 (GRCm39) |
Y313F |
probably benign |
Het |
H2-Q6 |
T |
A |
17: 35,644,179 (GRCm39) |
F54I |
probably damaging |
Het |
Hcrtr2 |
C |
A |
9: 76,161,954 (GRCm39) |
L145F |
probably damaging |
Het |
Hepacam2 |
A |
G |
6: 3,476,121 (GRCm39) |
L268P |
probably damaging |
Het |
Herc2 |
C |
A |
7: 55,834,117 (GRCm39) |
C3107* |
probably null |
Het |
Herc4 |
T |
C |
10: 63,099,811 (GRCm39) |
V78A |
probably damaging |
Het |
Hyal5 |
T |
C |
6: 24,877,920 (GRCm39) |
W339R |
probably damaging |
Het |
Igfbp6 |
T |
A |
15: 102,056,419 (GRCm39) |
|
probably null |
Het |
Il18rap |
A |
T |
1: 40,564,218 (GRCm39) |
H112L |
probably benign |
Het |
Il1r2 |
T |
A |
1: 40,162,309 (GRCm39) |
Y317* |
probably null |
Het |
Ints8 |
C |
A |
4: 11,246,097 (GRCm39) |
V190L |
probably benign |
Het |
Ipo11 |
T |
C |
13: 107,061,595 (GRCm39) |
T22A |
probably benign |
Het |
Itgb4 |
C |
A |
11: 115,870,521 (GRCm39) |
R117S |
probably benign |
Het |
Lcorl |
C |
G |
5: 45,891,711 (GRCm39) |
G214A |
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,289,019 (GRCm39) |
|
probably null |
Het |
Lyst |
T |
A |
13: 13,791,298 (GRCm39) |
L54I |
probably damaging |
Het |
Mcm9 |
T |
C |
10: 53,414,250 (GRCm39) |
T1015A |
probably benign |
Het |
Mef2d |
T |
A |
3: 88,063,825 (GRCm39) |
I84N |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,119,913 (GRCm39) |
N261S |
probably damaging |
Het |
Mpdz |
T |
C |
4: 81,210,768 (GRCm39) |
T1693A |
probably benign |
Het |
Mss51 |
T |
A |
14: 20,534,756 (GRCm39) |
Q338L |
possibly damaging |
Het |
Mstn |
T |
A |
1: 53,103,143 (GRCm39) |
Y160N |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,226,735 (GRCm39) |
T1431A |
probably benign |
Het |
Nek9 |
A |
T |
12: 85,348,657 (GRCm39) |
M959K |
probably benign |
Het |
Or2ak6 |
G |
A |
11: 58,593,069 (GRCm39) |
V181I |
probably benign |
Het |
Or4f58 |
A |
T |
2: 111,851,777 (GRCm39) |
C141S |
probably damaging |
Het |
Or8b47 |
A |
T |
9: 38,435,801 (GRCm39) |
M258L |
probably benign |
Het |
Otog |
G |
T |
7: 45,923,256 (GRCm39) |
G1044W |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,123,671 (GRCm39) |
T833M |
probably damaging |
Het |
Pdcd10 |
T |
C |
3: 75,434,958 (GRCm39) |
K111R |
probably damaging |
Het |
Pde5a |
A |
G |
3: 122,542,107 (GRCm39) |
N199S |
probably damaging |
Het |
Plekhg1 |
T |
C |
10: 3,887,971 (GRCm39) |
V355A |
probably damaging |
Het |
Podn |
G |
T |
4: 107,878,791 (GRCm39) |
L359I |
probably damaging |
Het |
Psd |
T |
C |
19: 46,310,600 (GRCm39) |
E483G |
probably damaging |
Het |
Ptch2 |
T |
A |
4: 116,968,340 (GRCm39) |
L905* |
probably null |
Het |
Rxfp2 |
T |
A |
5: 149,989,880 (GRCm39) |
N420K |
probably damaging |
Het |
Scpppq1 |
C |
A |
5: 104,222,747 (GRCm39) |
G24* |
probably null |
Het |
Sde2 |
T |
A |
1: 180,689,992 (GRCm39) |
D237E |
probably benign |
Het |
Serpina1d |
A |
T |
12: 103,732,016 (GRCm39) |
L281Q |
probably damaging |
Het |
Serpina9 |
T |
C |
12: 103,967,729 (GRCm39) |
N222S |
probably benign |
Het |
Sh3bgrl2 |
A |
G |
9: 83,459,612 (GRCm39) |
K57E |
probably damaging |
Het |
Shc3 |
C |
T |
13: 51,634,264 (GRCm39) |
|
probably benign |
Het |
Sik3 |
T |
C |
9: 46,120,038 (GRCm39) |
M659T |
possibly damaging |
Het |
Slc23a2 |
A |
G |
2: 131,913,937 (GRCm39) |
L280P |
probably damaging |
Het |
Smchd1 |
G |
T |
17: 71,694,083 (GRCm39) |
Q1221K |
probably benign |
Het |
Spmip2 |
T |
A |
3: 79,313,093 (GRCm39) |
W56R |
probably damaging |
Het |
Spocd1 |
A |
G |
4: 129,849,263 (GRCm39) |
N694S |
possibly damaging |
Het |
Styxl2 |
C |
A |
1: 165,926,670 (GRCm39) |
V981L |
probably benign |
Het |
Tecta |
T |
C |
9: 42,263,359 (GRCm39) |
D1409G |
probably damaging |
Het |
Tmem131 |
A |
T |
1: 36,880,754 (GRCm39) |
V172D |
probably damaging |
Het |
Trpm3 |
T |
C |
19: 22,964,237 (GRCm39) |
M1244T |
possibly damaging |
Het |
Ugcg |
G |
C |
4: 59,217,036 (GRCm39) |
V187L |
possibly damaging |
Het |
Usp17le |
T |
C |
7: 104,417,708 (GRCm39) |
N478S |
probably benign |
Het |
Usp36 |
A |
G |
11: 118,164,397 (GRCm39) |
V205A |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,615,077 (GRCm39) |
H1176L |
probably benign |
Het |
Zfyve28 |
C |
T |
5: 34,389,550 (GRCm39) |
D217N |
possibly damaging |
Het |
Zranb3 |
A |
C |
1: 127,882,817 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn1r25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01867:Vmn1r25
|
APN |
6 |
57,956,196 (GRCm39) |
missense |
probably damaging |
0.99 |
R0299:Vmn1r25
|
UTSW |
6 |
57,955,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Vmn1r25
|
UTSW |
6 |
57,955,696 (GRCm39) |
missense |
probably benign |
0.01 |
R1294:Vmn1r25
|
UTSW |
6 |
57,955,464 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1562:Vmn1r25
|
UTSW |
6 |
57,955,786 (GRCm39) |
missense |
probably benign |
0.03 |
R1661:Vmn1r25
|
UTSW |
6 |
57,955,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1665:Vmn1r25
|
UTSW |
6 |
57,955,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Vmn1r25
|
UTSW |
6 |
57,955,912 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2221:Vmn1r25
|
UTSW |
6 |
57,956,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Vmn1r25
|
UTSW |
6 |
57,956,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2374:Vmn1r25
|
UTSW |
6 |
57,955,543 (GRCm39) |
missense |
probably benign |
0.10 |
R4073:Vmn1r25
|
UTSW |
6 |
57,955,572 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4398:Vmn1r25
|
UTSW |
6 |
57,955,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Vmn1r25
|
UTSW |
6 |
57,955,480 (GRCm39) |
missense |
probably benign |
0.02 |
R4779:Vmn1r25
|
UTSW |
6 |
57,956,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R5397:Vmn1r25
|
UTSW |
6 |
57,956,060 (GRCm39) |
nonsense |
probably null |
|
R6113:Vmn1r25
|
UTSW |
6 |
57,955,557 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Vmn1r25
|
UTSW |
6 |
57,955,996 (GRCm39) |
missense |
probably benign |
0.22 |
R7407:Vmn1r25
|
UTSW |
6 |
57,956,044 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7748:Vmn1r25
|
UTSW |
6 |
57,955,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8001:Vmn1r25
|
UTSW |
6 |
57,956,065 (GRCm39) |
nonsense |
probably null |
|
R8472:Vmn1r25
|
UTSW |
6 |
57,955,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9235:Vmn1r25
|
UTSW |
6 |
57,955,488 (GRCm39) |
missense |
probably damaging |
0.96 |
R9651:Vmn1r25
|
UTSW |
6 |
57,956,306 (GRCm39) |
unclassified |
probably benign |
|
|