Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 8,989,894 (GRCm39) |
T816S |
probably benign |
Het |
Aff4 |
G |
A |
11: 53,290,783 (GRCm39) |
S581N |
probably damaging |
Het |
Aimp2 |
G |
A |
5: 143,839,825 (GRCm39) |
A253V |
probably damaging |
Het |
Arl6ip4 |
T |
G |
5: 124,254,611 (GRCm39) |
S35A |
probably benign |
Het |
Atp1a4 |
A |
T |
1: 172,059,869 (GRCm39) |
Y787N |
probably damaging |
Het |
Btbd8 |
T |
G |
5: 107,658,293 (GRCm39) |
I1621R |
probably damaging |
Het |
Ccdc169 |
T |
C |
3: 55,058,334 (GRCm39) |
S13P |
probably damaging |
Het |
Ccdc186 |
G |
A |
19: 56,801,793 (GRCm39) |
S108F |
probably damaging |
Het |
Ccdc39 |
G |
A |
3: 33,893,282 (GRCm39) |
T101I |
probably benign |
Het |
Cdh13 |
G |
T |
8: 119,963,706 (GRCm39) |
|
probably null |
Het |
Clec1b |
A |
T |
6: 129,380,537 (GRCm39) |
E151V |
probably benign |
Het |
Cplx1 |
T |
A |
5: 108,673,435 (GRCm39) |
|
probably null |
Het |
Diablo |
T |
A |
5: 123,655,990 (GRCm39) |
I150F |
unknown |
Het |
Esp31 |
T |
C |
17: 38,955,582 (GRCm39) |
V75A |
probably benign |
Het |
Gm49336 |
G |
A |
14: 60,466,185 (GRCm39) |
L458F |
probably damaging |
Het |
Grin3b |
A |
T |
10: 79,808,972 (GRCm39) |
S241C |
possibly damaging |
Het |
Gxylt2 |
A |
G |
6: 100,727,432 (GRCm39) |
N182S |
probably damaging |
Het |
Hephl1 |
T |
G |
9: 14,972,090 (GRCm39) |
D950A |
probably benign |
Het |
Hkdc1 |
A |
G |
10: 62,234,612 (GRCm39) |
I556T |
possibly damaging |
Het |
Ints4 |
C |
A |
7: 97,134,227 (GRCm39) |
A53D |
probably damaging |
Het |
Kmt5c |
T |
C |
7: 4,745,712 (GRCm39) |
V124A |
possibly damaging |
Het |
Lrpprc |
T |
A |
17: 85,058,657 (GRCm39) |
Q734H |
probably benign |
Het |
Map1b |
T |
C |
13: 99,567,304 (GRCm39) |
T1806A |
unknown |
Het |
Mcmbp |
A |
T |
7: 128,308,855 (GRCm39) |
F389I |
probably damaging |
Het |
Mcrs1 |
C |
T |
15: 99,141,237 (GRCm39) |
G422S |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,632,185 (GRCm39) |
H173R |
probably damaging |
Het |
Mib1 |
G |
A |
18: 10,747,422 (GRCm39) |
G200S |
probably benign |
Het |
Myh13 |
A |
T |
11: 67,252,161 (GRCm39) |
Q1423L |
possibly damaging |
Het |
Myh2 |
A |
G |
11: 67,083,398 (GRCm39) |
R1454G |
possibly damaging |
Het |
Mylk4 |
C |
T |
13: 32,913,089 (GRCm39) |
V70I |
probably benign |
Het |
Myof |
A |
G |
19: 37,968,841 (GRCm39) |
V358A |
probably benign |
Het |
Ncor1 |
T |
A |
11: 62,324,494 (GRCm39) |
H47L |
probably damaging |
Het |
Ncor1 |
T |
A |
11: 62,324,492 (GRCm39) |
I48F |
probably benign |
Het |
Neurog2 |
G |
T |
3: 127,427,742 (GRCm39) |
R122L |
probably damaging |
Het |
Npdc1 |
T |
A |
2: 25,298,129 (GRCm39) |
L193Q |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,227,234 (GRCm39) |
N290D |
probably damaging |
Het |
Nynrin |
T |
C |
14: 56,109,120 (GRCm39) |
M1409T |
probably benign |
Het |
Oas1h |
T |
C |
5: 121,005,107 (GRCm39) |
L185P |
probably damaging |
Het |
Or10x4 |
A |
T |
1: 174,218,848 (GRCm39) |
Y71F |
probably damaging |
Het |
Or2z2 |
C |
T |
11: 58,346,757 (GRCm39) |
W6* |
probably null |
Het |
Or6c3 |
T |
A |
10: 129,309,374 (GRCm39) |
V271E |
possibly damaging |
Het |
Osbpl8 |
T |
A |
10: 111,128,974 (GRCm39) |
N853K |
probably benign |
Het |
Pcsk4 |
G |
T |
10: 80,159,557 (GRCm39) |
P405Q |
probably benign |
Het |
Piwil4 |
A |
C |
9: 14,650,685 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
T |
C |
15: 44,361,967 (GRCm39) |
Y547H |
probably damaging |
Het |
Prr36 |
TGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGC |
TGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGCTGGTCTGTGGAAGAGCGGCTTTGC |
8: 4,266,273 (GRCm39) |
|
probably benign |
Het |
Rft1 |
T |
C |
14: 30,382,156 (GRCm39) |
L51P |
probably damaging |
Het |
Rufy2 |
T |
G |
10: 62,833,660 (GRCm39) |
L241V |
possibly damaging |
Het |
Slc5a5 |
T |
C |
8: 71,343,934 (GRCm39) |
I155V |
possibly damaging |
Het |
Slc7a2 |
T |
G |
8: 41,351,991 (GRCm39) |
M18R |
probably damaging |
Het |
Snapc4 |
A |
G |
2: 26,259,375 (GRCm39) |
S592P |
probably benign |
Het |
Strn4 |
T |
C |
7: 16,550,533 (GRCm39) |
W86R |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,545,244 (GRCm39) |
N2457S |
probably damaging |
Het |
Tent4a |
T |
A |
13: 69,658,824 (GRCm39) |
D337V |
probably damaging |
Het |
Timd4 |
C |
A |
11: 46,706,309 (GRCm39) |
T37N |
possibly damaging |
Het |
Tmem268 |
T |
A |
4: 63,496,076 (GRCm39) |
N172K |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,773,949 (GRCm39) |
V2855D |
probably benign |
Het |
Tubb6 |
A |
T |
18: 67,534,598 (GRCm39) |
T166S |
probably damaging |
Het |
Tufm |
A |
G |
7: 126,088,034 (GRCm39) |
Y179C |
probably benign |
Het |
Tut7 |
T |
C |
13: 59,933,597 (GRCm39) |
N1302D |
probably benign |
Het |
Ube2r2 |
C |
T |
4: 41,190,715 (GRCm39) |
S203L |
possibly damaging |
Het |
Vldlr |
G |
T |
19: 27,217,946 (GRCm39) |
V465L |
probably benign |
Het |
Vmn2r16 |
C |
T |
5: 109,488,231 (GRCm39) |
T368M |
probably benign |
Het |
|
Other mutations in Vmn2r42 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02444:Vmn2r42
|
APN |
7 |
8,187,312 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02793:Vmn2r42
|
APN |
7 |
8,197,852 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02875:Vmn2r42
|
APN |
7 |
8,197,852 (GRCm39) |
missense |
probably benign |
0.00 |
R1743:Vmn2r42
|
UTSW |
7 |
8,187,264 (GRCm39) |
missense |
probably benign |
0.06 |
R3943:Vmn2r42
|
UTSW |
7 |
8,197,779 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4117:Vmn2r42
|
UTSW |
7 |
8,197,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Vmn2r42
|
UTSW |
7 |
8,187,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R5233:Vmn2r42
|
UTSW |
7 |
8,197,837 (GRCm39) |
nonsense |
probably null |
|
R6245:Vmn2r42
|
UTSW |
7 |
8,195,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6683:Vmn2r42
|
UTSW |
7 |
8,187,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R6709:Vmn2r42
|
UTSW |
7 |
8,195,618 (GRCm39) |
missense |
probably benign |
0.09 |
R7396:Vmn2r42
|
UTSW |
7 |
8,195,641 (GRCm39) |
missense |
probably benign |
0.00 |
R7450:Vmn2r42
|
UTSW |
7 |
8,187,220 (GRCm39) |
missense |
probably benign |
0.00 |
R7583:Vmn2r42
|
UTSW |
7 |
8,197,740 (GRCm39) |
nonsense |
probably null |
|
R7973:Vmn2r42
|
UTSW |
7 |
8,197,872 (GRCm39) |
missense |
probably benign |
0.03 |
R8777:Vmn2r42
|
UTSW |
7 |
8,195,692 (GRCm39) |
missense |
probably benign |
0.14 |
R8900:Vmn2r42
|
UTSW |
7 |
8,197,792 (GRCm39) |
missense |
probably benign |
0.15 |
R8972:Vmn2r42
|
UTSW |
7 |
8,187,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R9335:Vmn2r42
|
UTSW |
7 |
8,197,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R9453:Vmn2r42
|
UTSW |
7 |
8,187,295 (GRCm39) |
missense |
probably benign |
0.39 |
|