Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
C |
T |
14: 32,382,837 (GRCm39) |
V1043I |
probably benign |
Het |
5031439G07Rik |
T |
A |
15: 84,839,867 (GRCm39) |
I176F |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,454,764 (GRCm39) |
M527K |
probably benign |
Het |
Atp10b |
C |
T |
11: 43,106,811 (GRCm39) |
T615I |
probably benign |
Het |
Atxn2 |
A |
G |
5: 121,948,973 (GRCm39) |
T1117A |
probably benign |
Het |
AU021092 |
A |
T |
16: 5,032,585 (GRCm39) |
|
probably benign |
Het |
Bcam |
C |
T |
7: 19,492,671 (GRCm39) |
V505M |
probably damaging |
Het |
Bco2 |
A |
T |
9: 50,461,962 (GRCm39) |
L14Q |
probably damaging |
Het |
Caps2 |
T |
G |
10: 112,030,824 (GRCm39) |
|
probably benign |
Het |
Cblb |
T |
C |
16: 51,986,368 (GRCm39) |
V537A |
probably benign |
Het |
Ccdc141 |
A |
T |
2: 76,845,556 (GRCm39) |
N1170K |
probably benign |
Het |
Ccdc154 |
T |
G |
17: 25,389,129 (GRCm39) |
D442E |
probably benign |
Het |
Col24a1 |
A |
G |
3: 145,019,798 (GRCm39) |
I60V |
probably null |
Het |
Crb1 |
A |
T |
1: 139,164,886 (GRCm39) |
N1140K |
probably benign |
Het |
Ddhd1 |
G |
A |
14: 45,846,430 (GRCm39) |
P621S |
probably benign |
Het |
Ddx46 |
A |
T |
13: 55,814,033 (GRCm39) |
N663I |
probably benign |
Het |
Dgki |
C |
T |
6: 37,011,652 (GRCm39) |
|
probably benign |
Het |
Disp2 |
T |
C |
2: 118,621,239 (GRCm39) |
F657S |
probably damaging |
Het |
Dnajc2 |
T |
C |
5: 21,973,670 (GRCm39) |
E262G |
probably damaging |
Het |
Dvl2 |
T |
A |
11: 69,898,761 (GRCm39) |
L408Q |
possibly damaging |
Het |
Egflam |
T |
C |
15: 7,267,249 (GRCm39) |
D712G |
probably damaging |
Het |
Entpd7 |
A |
G |
19: 43,692,846 (GRCm39) |
|
probably benign |
Het |
Epb41 |
A |
T |
4: 131,695,104 (GRCm39) |
W28R |
|
Het |
Fabp9 |
C |
T |
3: 10,262,231 (GRCm39) |
|
probably benign |
Het |
Fkbp15 |
T |
A |
4: 62,232,602 (GRCm39) |
M657L |
probably benign |
Het |
Gfy |
A |
C |
7: 44,827,784 (GRCm39) |
L104R |
possibly damaging |
Het |
Gm4884 |
A |
T |
7: 40,693,911 (GRCm39) |
I627F |
probably damaging |
Het |
Gm9195 |
A |
T |
14: 72,691,320 (GRCm39) |
S1643T |
unknown |
Het |
Gpsm2 |
C |
T |
3: 108,610,335 (GRCm39) |
A42T |
possibly damaging |
Het |
Gvin2 |
T |
C |
7: 105,551,120 (GRCm39) |
K644R |
probably benign |
Het |
Gys2 |
T |
C |
6: 142,402,113 (GRCm39) |
Y242C |
probably damaging |
Het |
Hbs1l |
A |
G |
10: 21,185,868 (GRCm39) |
N430S |
probably damaging |
Het |
Idh3b |
A |
T |
2: 130,126,004 (GRCm39) |
|
probably benign |
Het |
Igdcc3 |
C |
T |
9: 65,088,550 (GRCm39) |
A384V |
probably benign |
Het |
Ighv3-4 |
C |
T |
12: 114,217,535 (GRCm39) |
D19N |
possibly damaging |
Het |
Igkv19-93 |
G |
T |
6: 68,713,494 (GRCm39) |
A45E |
probably damaging |
Het |
Il10ra |
G |
A |
9: 45,175,631 (GRCm39) |
T230M |
probably damaging |
Het |
Kalrn |
A |
G |
16: 34,038,305 (GRCm39) |
V1009A |
probably damaging |
Het |
Kcnma1 |
G |
T |
14: 23,417,718 (GRCm39) |
A837D |
probably damaging |
Het |
Kif7 |
T |
A |
7: 79,348,650 (GRCm39) |
R1231S |
probably benign |
Het |
Klhdc1 |
A |
G |
12: 69,298,817 (GRCm39) |
D134G |
possibly damaging |
Het |
Klk14 |
T |
C |
7: 43,343,459 (GRCm39) |
V97A |
probably damaging |
Het |
Lamb3 |
G |
A |
1: 193,003,363 (GRCm39) |
V101M |
possibly damaging |
Het |
Lrrc7 |
C |
T |
3: 157,867,381 (GRCm39) |
E787K |
probably damaging |
Het |
Mep1a |
A |
G |
17: 43,808,808 (GRCm39) |
I94T |
possibly damaging |
Het |
Mtrex |
T |
A |
13: 113,051,034 (GRCm39) |
K180N |
probably benign |
Het |
Ncr1 |
C |
T |
7: 4,341,336 (GRCm39) |
S109L |
probably benign |
Het |
Nell2 |
A |
T |
15: 95,129,329 (GRCm39) |
M678K |
probably damaging |
Het |
Or12j5 |
C |
A |
7: 140,084,172 (GRCm39) |
A67S |
probably benign |
Het |
Or14c42-ps1 |
G |
A |
7: 86,211,549 (GRCm39) |
C203Y |
unknown |
Het |
Or2m13 |
A |
T |
16: 19,226,396 (GRCm39) |
Y123* |
probably null |
Het |
Or8g19 |
T |
A |
9: 39,055,899 (GRCm39) |
F168I |
probably damaging |
Het |
Pnpla1 |
A |
C |
17: 29,098,438 (GRCm39) |
Y248S |
probably damaging |
Het |
Pramel27 |
T |
C |
4: 143,573,140 (GRCm39) |
|
probably null |
Het |
Prdm10 |
T |
C |
9: 31,264,742 (GRCm39) |
F726L |
probably damaging |
Het |
Prdm16 |
T |
C |
4: 154,613,370 (GRCm39) |
N19S |
probably damaging |
Het |
Prss44 |
A |
G |
9: 110,643,263 (GRCm39) |
R53G |
probably benign |
Het |
Rasgrp1 |
C |
T |
2: 117,115,425 (GRCm39) |
R721Q |
probably benign |
Het |
Rassf1 |
A |
T |
9: 107,434,740 (GRCm39) |
N149I |
probably damaging |
Het |
Rbp3 |
A |
C |
14: 33,678,796 (GRCm39) |
T915P |
probably benign |
Het |
Reg3g |
A |
T |
6: 78,444,788 (GRCm39) |
D63E |
probably benign |
Het |
Relch |
T |
C |
1: 105,592,220 (GRCm39) |
Y130H |
probably damaging |
Het |
Rgs3 |
C |
A |
4: 62,543,373 (GRCm39) |
T236K |
probably damaging |
Het |
Rin2 |
T |
C |
2: 145,690,772 (GRCm39) |
F147L |
probably damaging |
Het |
Slc17a1 |
T |
C |
13: 24,062,732 (GRCm39) |
I266T |
probably benign |
Het |
Slc34a3 |
A |
T |
2: 25,119,267 (GRCm39) |
N534K |
probably benign |
Het |
Smc2 |
A |
T |
4: 52,462,856 (GRCm39) |
E615D |
probably benign |
Het |
Snx16 |
A |
C |
3: 10,484,193 (GRCm39) |
D343E |
probably benign |
Het |
St18 |
T |
A |
1: 6,865,619 (GRCm39) |
Y32* |
probably null |
Het |
Svep1 |
C |
T |
4: 58,064,204 (GRCm39) |
V3260I |
possibly damaging |
Het |
Synm |
C |
T |
7: 67,386,456 (GRCm39) |
R402H |
possibly damaging |
Het |
Tacc2 |
A |
T |
7: 130,318,564 (GRCm39) |
E67V |
possibly damaging |
Het |
Tarbp1 |
G |
T |
8: 127,198,044 (GRCm39) |
N302K |
probably damaging |
Het |
Tenm2 |
A |
G |
11: 35,942,788 (GRCm39) |
S1294P |
probably damaging |
Het |
Ttk |
T |
C |
9: 83,751,304 (GRCm39) |
S794P |
probably damaging |
Het |
Ulk1 |
G |
A |
5: 110,934,288 (GRCm39) |
A999V |
probably damaging |
Het |
Upf2 |
A |
G |
2: 6,030,983 (GRCm39) |
I808V |
unknown |
Het |
Ush2a |
A |
G |
1: 188,460,733 (GRCm39) |
T2665A |
probably benign |
Het |
Usp8 |
A |
G |
2: 126,590,229 (GRCm39) |
K672E |
probably damaging |
Het |
Vps33a |
T |
C |
5: 123,707,506 (GRCm39) |
M154V |
probably damaging |
Het |
Wdfy4 |
A |
C |
14: 32,795,492 (GRCm39) |
Y2083* |
probably null |
Het |
Zc3hav1 |
A |
G |
6: 38,288,212 (GRCm39) |
F875L |
probably benign |
Het |
Zfp979 |
T |
C |
4: 147,697,836 (GRCm39) |
N291S |
probably benign |
Het |
Zp2 |
T |
A |
7: 119,742,835 (GRCm39) |
Y99F |
possibly damaging |
Het |
|
Other mutations in Vmn2r105 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01433:Vmn2r105
|
APN |
17 |
20,448,817 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01909:Vmn2r105
|
APN |
17 |
20,444,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01925:Vmn2r105
|
APN |
17 |
20,428,973 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02021:Vmn2r105
|
APN |
17 |
20,448,157 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02828:Vmn2r105
|
APN |
17 |
20,429,345 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02838:Vmn2r105
|
APN |
17 |
20,447,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03343:Vmn2r105
|
APN |
17 |
20,446,631 (GRCm39) |
nonsense |
probably null |
|
R0096:Vmn2r105
|
UTSW |
17 |
20,447,741 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0096:Vmn2r105
|
UTSW |
17 |
20,447,741 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0212:Vmn2r105
|
UTSW |
17 |
20,428,827 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0268:Vmn2r105
|
UTSW |
17 |
20,428,938 (GRCm39) |
missense |
probably benign |
0.18 |
R0271:Vmn2r105
|
UTSW |
17 |
20,454,965 (GRCm39) |
missense |
probably damaging |
0.96 |
R0613:Vmn2r105
|
UTSW |
17 |
20,428,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0765:Vmn2r105
|
UTSW |
17 |
20,448,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R0765:Vmn2r105
|
UTSW |
17 |
20,447,973 (GRCm39) |
missense |
probably benign |
0.20 |
R1162:Vmn2r105
|
UTSW |
17 |
20,447,973 (GRCm39) |
missense |
probably benign |
0.20 |
R1263:Vmn2r105
|
UTSW |
17 |
20,428,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R1363:Vmn2r105
|
UTSW |
17 |
20,428,932 (GRCm39) |
missense |
probably benign |
0.00 |
R1464:Vmn2r105
|
UTSW |
17 |
20,449,004 (GRCm39) |
splice site |
probably benign |
|
R2029:Vmn2r105
|
UTSW |
17 |
20,444,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R2420:Vmn2r105
|
UTSW |
17 |
20,448,097 (GRCm39) |
missense |
probably benign |
0.15 |
R2421:Vmn2r105
|
UTSW |
17 |
20,448,097 (GRCm39) |
missense |
probably benign |
0.15 |
R2422:Vmn2r105
|
UTSW |
17 |
20,448,097 (GRCm39) |
missense |
probably benign |
0.15 |
R2570:Vmn2r105
|
UTSW |
17 |
20,447,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Vmn2r105
|
UTSW |
17 |
20,428,952 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3848:Vmn2r105
|
UTSW |
17 |
20,428,952 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4030:Vmn2r105
|
UTSW |
17 |
20,429,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R4275:Vmn2r105
|
UTSW |
17 |
20,448,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R4551:Vmn2r105
|
UTSW |
17 |
20,446,613 (GRCm39) |
missense |
probably benign |
|
R4801:Vmn2r105
|
UTSW |
17 |
20,447,556 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Vmn2r105
|
UTSW |
17 |
20,447,556 (GRCm39) |
missense |
probably benign |
0.00 |
R4816:Vmn2r105
|
UTSW |
17 |
20,428,953 (GRCm39) |
missense |
probably benign |
0.27 |
R4929:Vmn2r105
|
UTSW |
17 |
20,448,280 (GRCm39) |
missense |
probably benign |
0.44 |
R5022:Vmn2r105
|
UTSW |
17 |
20,428,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R5475:Vmn2r105
|
UTSW |
17 |
20,455,044 (GRCm39) |
missense |
probably benign |
|
R5576:Vmn2r105
|
UTSW |
17 |
20,444,836 (GRCm39) |
critical splice donor site |
probably null |
|
R5795:Vmn2r105
|
UTSW |
17 |
20,448,998 (GRCm39) |
missense |
probably benign |
0.00 |
R5895:Vmn2r105
|
UTSW |
17 |
20,448,929 (GRCm39) |
missense |
probably benign |
0.10 |
R6017:Vmn2r105
|
UTSW |
17 |
20,428,889 (GRCm39) |
missense |
probably damaging |
0.97 |
R6210:Vmn2r105
|
UTSW |
17 |
20,448,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R6491:Vmn2r105
|
UTSW |
17 |
20,447,992 (GRCm39) |
nonsense |
probably null |
|
R6542:Vmn2r105
|
UTSW |
17 |
20,448,803 (GRCm39) |
missense |
probably benign |
0.03 |
R6729:Vmn2r105
|
UTSW |
17 |
20,428,605 (GRCm39) |
missense |
probably damaging |
0.99 |
R7020:Vmn2r105
|
UTSW |
17 |
20,429,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Vmn2r105
|
UTSW |
17 |
20,428,874 (GRCm39) |
missense |
probably damaging |
0.97 |
R7488:Vmn2r105
|
UTSW |
17 |
20,429,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Vmn2r105
|
UTSW |
17 |
20,448,827 (GRCm39) |
missense |
probably benign |
0.02 |
R7555:Vmn2r105
|
UTSW |
17 |
20,447,937 (GRCm39) |
missense |
probably damaging |
0.98 |
R7863:Vmn2r105
|
UTSW |
17 |
20,428,937 (GRCm39) |
missense |
probably benign |
0.18 |
R8137:Vmn2r105
|
UTSW |
17 |
20,454,966 (GRCm39) |
missense |
probably benign |
0.02 |
R8166:Vmn2r105
|
UTSW |
17 |
20,428,904 (GRCm39) |
missense |
probably benign |
0.07 |
R8186:Vmn2r105
|
UTSW |
17 |
20,444,880 (GRCm39) |
nonsense |
probably null |
|
R8214:Vmn2r105
|
UTSW |
17 |
20,448,775 (GRCm39) |
missense |
probably benign |
0.02 |
R8497:Vmn2r105
|
UTSW |
17 |
20,455,134 (GRCm39) |
start codon destroyed |
probably null |
0.75 |
R8850:Vmn2r105
|
UTSW |
17 |
20,428,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R9272:Vmn2r105
|
UTSW |
17 |
20,447,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R9506:Vmn2r105
|
UTSW |
17 |
20,429,404 (GRCm39) |
missense |
probably benign |
0.00 |
R9549:Vmn2r105
|
UTSW |
17 |
20,448,023 (GRCm39) |
missense |
probably benign |
0.12 |
|