Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,433,890 (GRCm39) |
R4148S |
probably benign |
Het |
Acoxl |
T |
A |
2: 127,886,311 (GRCm39) |
L182Q |
possibly damaging |
Het |
Aldh7a1 |
T |
C |
18: 56,665,088 (GRCm39) |
T364A |
possibly damaging |
Het |
App |
T |
C |
16: 84,853,322 (GRCm39) |
D252G |
unknown |
Het |
Arid1a |
A |
G |
4: 133,408,672 (GRCm39) |
I1945T |
unknown |
Het |
Arsk |
C |
T |
13: 76,213,398 (GRCm39) |
|
probably null |
Het |
Atad2b |
G |
A |
12: 4,993,251 (GRCm39) |
G257S |
probably benign |
Het |
Best1 |
C |
A |
19: 9,969,062 (GRCm39) |
R218L |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,312,300 (GRCm39) |
|
probably null |
Het |
Cdh13 |
C |
T |
8: 119,484,129 (GRCm39) |
T130I |
possibly damaging |
Het |
Cela2a |
T |
C |
4: 141,552,902 (GRCm39) |
E25G |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,632,314 (GRCm39) |
I346F |
probably damaging |
Het |
Chil6 |
C |
T |
3: 106,297,244 (GRCm39) |
G299D |
possibly damaging |
Het |
Cic |
G |
A |
7: 24,972,327 (GRCm39) |
R686H |
probably damaging |
Het |
Cnpy1 |
T |
C |
5: 28,450,738 (GRCm39) |
I23V |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,707,011 (GRCm39) |
Y2034F |
unknown |
Het |
Coq10b |
T |
C |
1: 55,110,903 (GRCm39) |
Y224H |
probably benign |
Het |
Cryge |
G |
T |
1: 65,090,211 (GRCm39) |
|
probably benign |
Het |
Cyb5rl |
T |
G |
4: 106,941,510 (GRCm39) |
S252A |
probably benign |
Het |
Cyp2ab1 |
T |
A |
16: 20,133,814 (GRCm39) |
R125S |
probably damaging |
Het |
Dclk1 |
G |
A |
3: 55,387,811 (GRCm39) |
G86R |
probably damaging |
Het |
Dmtn |
A |
G |
14: 70,842,254 (GRCm39) |
M382T |
probably damaging |
Het |
Dnaaf8 |
A |
G |
16: 4,794,138 (GRCm39) |
|
noncoding transcript |
Het |
Dnah12 |
T |
A |
14: 26,437,784 (GRCm39) |
L471* |
probably null |
Het |
Dock10 |
A |
T |
1: 80,526,874 (GRCm39) |
S782T |
probably benign |
Het |
Egfem1 |
C |
A |
3: 29,206,032 (GRCm39) |
H90N |
possibly damaging |
Het |
Ephb6 |
T |
A |
6: 41,595,079 (GRCm39) |
W698R |
probably benign |
Het |
Exoc4 |
T |
A |
6: 33,895,343 (GRCm39) |
C787S |
probably damaging |
Het |
Exosc8 |
A |
T |
3: 54,639,523 (GRCm39) |
|
probably benign |
Het |
Galc |
T |
A |
12: 98,193,533 (GRCm39) |
Q352L |
probably benign |
Het |
Galns |
A |
G |
8: 123,327,272 (GRCm39) |
Y167H |
probably damaging |
Het |
Glb1l |
T |
C |
1: 75,185,528 (GRCm39) |
|
probably benign |
Het |
Gm6185 |
A |
T |
1: 161,033,750 (GRCm39) |
|
noncoding transcript |
Het |
Gm7694 |
T |
C |
1: 170,128,794 (GRCm39) |
N245S |
probably benign |
Het |
Gmcl1 |
T |
G |
6: 86,681,538 (GRCm39) |
K385N |
possibly damaging |
Het |
Gramd1c |
A |
T |
16: 43,810,200 (GRCm39) |
W463R |
probably damaging |
Het |
Gtpbp8 |
C |
G |
16: 44,566,433 (GRCm39) |
A90P |
probably benign |
Het |
H2bc11 |
G |
T |
13: 22,227,421 (GRCm39) |
|
probably benign |
Het |
Hcar1 |
T |
C |
5: 124,016,731 (GRCm39) |
E320G |
probably benign |
Het |
Hhatl |
T |
C |
9: 121,618,077 (GRCm39) |
D226G |
probably damaging |
Het |
Hoxc5 |
T |
A |
15: 102,923,801 (GRCm39) |
I199N |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,059,845 (GRCm39) |
D121G |
probably damaging |
Het |
Il5ra |
T |
A |
6: 106,715,432 (GRCm39) |
H134L |
probably benign |
Het |
Isl2 |
T |
A |
9: 55,452,271 (GRCm39) |
I281N |
possibly damaging |
Het |
Kcnk13 |
T |
C |
12: 99,932,383 (GRCm39) |
F60L |
probably damaging |
Het |
Kdelr3 |
C |
T |
15: 79,409,066 (GRCm39) |
T85M |
possibly damaging |
Het |
Kdf1 |
A |
T |
4: 133,255,676 (GRCm39) |
H131L |
probably damaging |
Het |
Mipol1 |
T |
A |
12: 57,379,087 (GRCm39) |
L182I |
probably damaging |
Het |
Morc1 |
T |
G |
16: 48,381,980 (GRCm39) |
S513R |
probably benign |
Het |
Moxd2 |
A |
T |
6: 40,855,756 (GRCm39) |
L611H |
probably damaging |
Het |
Mpped2 |
T |
C |
2: 106,529,724 (GRCm39) |
|
probably benign |
Het |
Mrpl51 |
T |
C |
6: 125,170,270 (GRCm39) |
V92A |
probably benign |
Het |
Mrps26 |
G |
A |
2: 130,405,681 (GRCm39) |
|
probably benign |
Het |
Mrps5 |
A |
G |
2: 127,432,665 (GRCm39) |
T29A |
probably benign |
Het |
Mustn1 |
A |
G |
14: 30,601,517 (GRCm39) |
|
probably benign |
Het |
Ncor2 |
G |
A |
5: 125,110,431 (GRCm39) |
P858S |
possibly damaging |
Het |
Nfasc |
A |
G |
1: 132,529,759 (GRCm39) |
F807S |
probably damaging |
Het |
Nup50 |
G |
A |
15: 84,823,912 (GRCm39) |
V422I |
probably benign |
Het |
Or10x1 |
T |
A |
1: 174,196,562 (GRCm39) |
F26L |
probably benign |
Het |
Or13a25 |
A |
T |
7: 140,247,226 (GRCm39) |
M2L |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,493,883 (GRCm39) |
H159L |
probably damaging |
Het |
Or2ag13 |
A |
T |
7: 106,473,221 (GRCm39) |
V77D |
probably damaging |
Het |
Or3a1d |
C |
A |
11: 74,237,769 (GRCm39) |
V214L |
probably benign |
Het |
Or4c107 |
A |
G |
2: 88,788,930 (GRCm39) |
N40S |
probably damaging |
Het |
Or8b44 |
T |
A |
9: 38,410,319 (GRCm39) |
M118K |
probably damaging |
Het |
Or8u9 |
T |
A |
2: 86,002,015 (GRCm39) |
I49F |
probably damaging |
Het |
Osbpl8 |
T |
A |
10: 111,040,661 (GRCm39) |
M1K |
probably null |
Het |
Pcdhb22 |
A |
C |
18: 37,652,087 (GRCm39) |
D185A |
possibly damaging |
Het |
Pcdhga8 |
G |
T |
18: 37,949,457 (GRCm39) |
R291L |
probably damaging |
Het |
Saysd1 |
A |
T |
14: 20,127,672 (GRCm39) |
L84Q |
possibly damaging |
Het |
Slc41a1 |
T |
C |
1: 131,758,508 (GRCm39) |
I50T |
probably benign |
Het |
Smg7 |
G |
A |
1: 152,720,020 (GRCm39) |
P834S |
probably benign |
Het |
Speer4a1 |
C |
T |
5: 26,243,210 (GRCm39) |
V92M |
probably damaging |
Het |
Srf |
T |
C |
17: 46,860,400 (GRCm39) |
T461A |
probably benign |
Het |
Ssu72 |
A |
G |
4: 155,800,053 (GRCm39) |
D72G |
possibly damaging |
Het |
Suco |
T |
C |
1: 161,661,761 (GRCm39) |
E890G |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,763,656 (GRCm39) |
|
probably null |
Het |
Tm6sf1 |
A |
G |
7: 81,515,091 (GRCm39) |
E7G |
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,378,616 (GRCm39) |
K240R |
probably benign |
Het |
Tmem52 |
T |
A |
4: 155,554,825 (GRCm39) |
Y149* |
probably null |
Het |
Tpgs2 |
A |
T |
18: 25,284,305 (GRCm39) |
Y68N |
possibly damaging |
Het |
Vmn1r205 |
T |
A |
13: 22,777,074 (GRCm39) |
E9D |
probably benign |
Het |
Vmn2r32 |
A |
G |
7: 7,482,953 (GRCm39) |
V7A |
possibly damaging |
Het |
Vps39 |
G |
A |
2: 120,152,312 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
T |
6: 13,196,047 (GRCm39) |
V326D |
possibly damaging |
Het |
Zfp641 |
T |
A |
15: 98,186,598 (GRCm39) |
S342C |
probably damaging |
Het |
Zfp961 |
T |
C |
8: 72,722,847 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn2r80 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01084:Vmn2r80
|
APN |
10 |
79,030,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01325:Vmn2r80
|
APN |
10 |
79,030,081 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01611:Vmn2r80
|
APN |
10 |
79,007,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01799:Vmn2r80
|
APN |
10 |
79,007,385 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01877:Vmn2r80
|
APN |
10 |
79,007,334 (GRCm39) |
splice site |
probably null |
|
IGL02673:Vmn2r80
|
APN |
10 |
79,005,318 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02756:Vmn2r80
|
APN |
10 |
79,030,145 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Vmn2r80
|
APN |
10 |
79,007,439 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03382:Vmn2r80
|
APN |
10 |
79,005,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R0071:Vmn2r80
|
UTSW |
10 |
79,007,566 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0071:Vmn2r80
|
UTSW |
10 |
79,007,566 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0129:Vmn2r80
|
UTSW |
10 |
79,005,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Vmn2r80
|
UTSW |
10 |
78,984,773 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0567:Vmn2r80
|
UTSW |
10 |
79,030,665 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1510:Vmn2r80
|
UTSW |
10 |
79,005,553 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1519:Vmn2r80
|
UTSW |
10 |
79,030,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R1520:Vmn2r80
|
UTSW |
10 |
79,030,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1627:Vmn2r80
|
UTSW |
10 |
79,030,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Vmn2r80
|
UTSW |
10 |
79,030,223 (GRCm39) |
missense |
probably benign |
0.04 |
R2116:Vmn2r80
|
UTSW |
10 |
79,030,558 (GRCm39) |
missense |
probably benign |
0.09 |
R2237:Vmn2r80
|
UTSW |
10 |
79,004,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R2308:Vmn2r80
|
UTSW |
10 |
79,007,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R2893:Vmn2r80
|
UTSW |
10 |
78,984,699 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3408:Vmn2r80
|
UTSW |
10 |
79,004,227 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4502:Vmn2r80
|
UTSW |
10 |
78,984,764 (GRCm39) |
missense |
probably benign |
0.00 |
R4685:Vmn2r80
|
UTSW |
10 |
79,030,162 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4947:Vmn2r80
|
UTSW |
10 |
79,030,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Vmn2r80
|
UTSW |
10 |
79,030,292 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5217:Vmn2r80
|
UTSW |
10 |
79,004,980 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5226:Vmn2r80
|
UTSW |
10 |
79,029,874 (GRCm39) |
missense |
probably benign |
0.36 |
R5512:Vmn2r80
|
UTSW |
10 |
79,004,066 (GRCm39) |
missense |
probably benign |
0.00 |
R5618:Vmn2r80
|
UTSW |
10 |
78,984,755 (GRCm39) |
missense |
probably benign |
|
R5959:Vmn2r80
|
UTSW |
10 |
79,005,313 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Vmn2r80
|
UTSW |
10 |
78,984,854 (GRCm39) |
missense |
probably benign |
0.00 |
R6110:Vmn2r80
|
UTSW |
10 |
79,017,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R6270:Vmn2r80
|
UTSW |
10 |
79,030,159 (GRCm39) |
missense |
probably benign |
0.00 |
R6508:Vmn2r80
|
UTSW |
10 |
79,030,290 (GRCm39) |
missense |
probably benign |
0.03 |
R6843:Vmn2r80
|
UTSW |
10 |
79,005,502 (GRCm39) |
missense |
probably benign |
0.08 |
R6894:Vmn2r80
|
UTSW |
10 |
79,005,438 (GRCm39) |
missense |
probably benign |
0.06 |
R7048:Vmn2r80
|
UTSW |
10 |
79,030,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Vmn2r80
|
UTSW |
10 |
79,030,654 (GRCm39) |
missense |
probably benign |
0.00 |
R7262:Vmn2r80
|
UTSW |
10 |
79,005,579 (GRCm39) |
missense |
probably damaging |
0.98 |
R7559:Vmn2r80
|
UTSW |
10 |
79,030,459 (GRCm39) |
missense |
probably benign |
0.00 |
R7622:Vmn2r80
|
UTSW |
10 |
79,030,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8003:Vmn2r80
|
UTSW |
10 |
78,984,711 (GRCm39) |
missense |
probably benign |
0.16 |
R8207:Vmn2r80
|
UTSW |
10 |
79,030,150 (GRCm39) |
nonsense |
probably null |
|
R8330:Vmn2r80
|
UTSW |
10 |
79,007,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8337:Vmn2r80
|
UTSW |
10 |
78,984,707 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Vmn2r80
|
UTSW |
10 |
78,984,710 (GRCm39) |
missense |
probably benign |
|
R8688:Vmn2r80
|
UTSW |
10 |
79,004,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Vmn2r80
|
UTSW |
10 |
79,017,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Vmn2r80
|
UTSW |
10 |
79,005,378 (GRCm39) |
missense |
probably benign |
0.05 |
R9125:Vmn2r80
|
UTSW |
10 |
78,984,760 (GRCm39) |
missense |
probably benign |
0.12 |
R9147:Vmn2r80
|
UTSW |
10 |
79,030,687 (GRCm39) |
missense |
probably damaging |
0.98 |
R9148:Vmn2r80
|
UTSW |
10 |
79,030,687 (GRCm39) |
missense |
probably damaging |
0.98 |
R9187:Vmn2r80
|
UTSW |
10 |
79,030,438 (GRCm39) |
missense |
probably benign |
0.20 |
R9218:Vmn2r80
|
UTSW |
10 |
79,030,270 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9553:Vmn2r80
|
UTSW |
10 |
78,984,743 (GRCm39) |
missense |
probably benign |
|
R9612:Vmn2r80
|
UTSW |
10 |
79,030,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R9677:Vmn2r80
|
UTSW |
10 |
78,984,672 (GRCm39) |
missense |
probably benign |
0.15 |
R9769:Vmn2r80
|
UTSW |
10 |
79,005,443 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r80
|
UTSW |
10 |
79,030,441 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r80
|
UTSW |
10 |
79,030,232 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1176:Vmn2r80
|
UTSW |
10 |
79,005,311 (GRCm39) |
missense |
not run |
|
Z1176:Vmn2r80
|
UTSW |
10 |
79,030,605 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn2r80
|
UTSW |
10 |
79,005,311 (GRCm39) |
missense |
not run |
|
|