Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,197,179 (GRCm39) |
F251I |
possibly damaging |
Het |
Abcb11 |
C |
T |
2: 69,108,146 (GRCm39) |
G717D |
probably benign |
Het |
Abcc1 |
G |
A |
16: 14,207,763 (GRCm39) |
W47* |
probably null |
Het |
Ahnak2 |
A |
G |
12: 112,748,641 (GRCm39) |
I402T |
|
Het |
Ankfy1 |
G |
A |
11: 72,650,769 (GRCm39) |
R984Q |
probably benign |
Het |
Apaf1 |
A |
G |
10: 90,890,242 (GRCm39) |
I598T |
probably benign |
Het |
Apobec1 |
G |
T |
6: 122,558,521 (GRCm39) |
P78Q |
possibly damaging |
Het |
Asap1 |
A |
T |
15: 63,991,974 (GRCm39) |
I737N |
probably benign |
Het |
Aste1 |
T |
A |
9: 105,279,904 (GRCm39) |
|
probably null |
Het |
Bcr |
A |
C |
10: 74,996,162 (GRCm39) |
D902A |
possibly damaging |
Het |
Bicra |
T |
C |
7: 15,723,367 (GRCm39) |
|
probably null |
Het |
Ccdc27 |
T |
C |
4: 154,117,424 (GRCm39) |
T508A |
probably benign |
Het |
Ccz1 |
T |
A |
5: 143,928,401 (GRCm39) |
N383I |
probably damaging |
Het |
Cdh24 |
T |
C |
14: 54,869,637 (GRCm39) |
D760G |
possibly damaging |
Het |
Cdhr2 |
T |
C |
13: 54,865,728 (GRCm39) |
I242T |
probably benign |
Het |
Cdk4 |
T |
A |
10: 126,900,106 (GRCm39) |
M1K |
probably null |
Het |
Cfap96 |
A |
G |
8: 46,415,331 (GRCm39) |
V225A |
probably benign |
Het |
Cntn5 |
A |
T |
9: 9,970,570 (GRCm39) |
S302T |
probably damaging |
Het |
Col25a1 |
G |
T |
3: 130,378,350 (GRCm39) |
G601V |
probably damaging |
Het |
Cpb1 |
A |
G |
3: 20,324,488 (GRCm39) |
L62P |
possibly damaging |
Het |
Cpne1 |
T |
C |
2: 155,919,857 (GRCm39) |
T264A |
probably benign |
Het |
Cpvl |
T |
A |
6: 53,924,727 (GRCm39) |
N198Y |
probably damaging |
Het |
Cyp2u1 |
A |
C |
3: 131,091,596 (GRCm39) |
L308R |
probably damaging |
Het |
Ddx54 |
G |
T |
5: 120,762,789 (GRCm39) |
V637L |
probably benign |
Het |
Dglucy |
C |
A |
12: 100,823,310 (GRCm39) |
P472T |
possibly damaging |
Het |
Dync2h1 |
A |
G |
9: 7,124,855 (GRCm39) |
Y2006H |
probably benign |
Het |
Eif5b |
T |
C |
1: 38,089,387 (GRCm39) |
M1121T |
possibly damaging |
Het |
Emsy |
A |
G |
7: 98,264,762 (GRCm39) |
V545A |
possibly damaging |
Het |
Ezh1 |
G |
A |
11: 101,091,726 (GRCm39) |
L480F |
possibly damaging |
Het |
Fbln2 |
T |
A |
6: 91,242,845 (GRCm39) |
|
probably null |
Het |
Gja10 |
T |
A |
4: 32,602,058 (GRCm39) |
K109* |
probably null |
Het |
Gm28042 |
A |
G |
2: 119,870,438 (GRCm39) |
N762S |
probably benign |
Het |
Gnb1l |
C |
A |
16: 18,359,220 (GRCm39) |
P7Q |
possibly damaging |
Het |
Grem2 |
A |
T |
1: 174,664,685 (GRCm39) |
S55T |
probably damaging |
Het |
Gsn |
A |
T |
2: 35,186,433 (GRCm39) |
N393I |
possibly damaging |
Het |
H6pd |
T |
A |
4: 150,067,093 (GRCm39) |
Q439L |
probably benign |
Het |
Hmcn2 |
G |
A |
2: 31,310,842 (GRCm39) |
G3362E |
probably damaging |
Het |
Ighv11-2 |
T |
C |
12: 114,011,978 (GRCm39) |
Y79C |
probably damaging |
Het |
Ikzf2 |
T |
A |
1: 69,578,544 (GRCm39) |
N322Y |
probably benign |
Het |
Il25 |
A |
G |
14: 55,170,459 (GRCm39) |
I11V |
probably benign |
Het |
Jak2 |
C |
T |
19: 29,275,783 (GRCm39) |
T741I |
probably damaging |
Het |
Kdm3b |
T |
C |
18: 34,957,934 (GRCm39) |
S1300P |
probably damaging |
Het |
Ldb3 |
T |
A |
14: 34,289,402 (GRCm39) |
Q268L |
probably damaging |
Het |
Lrrc23 |
T |
A |
6: 124,756,075 (GRCm39) |
D6V |
unknown |
Het |
Megf10 |
A |
G |
18: 57,324,187 (GRCm39) |
Y76C |
probably damaging |
Het |
Neb |
A |
T |
2: 52,110,233 (GRCm39) |
M205K |
probably benign |
Het |
Or12e8 |
T |
C |
2: 87,188,597 (GRCm39) |
S270P |
probably damaging |
Het |
Or6c2b |
G |
T |
10: 128,947,605 (GRCm39) |
Q230K |
probably benign |
Het |
Or8a1 |
A |
G |
9: 37,641,983 (GRCm39) |
S99P |
probably damaging |
Het |
Pcnx3 |
G |
A |
19: 5,717,487 (GRCm39) |
R1541W |
possibly damaging |
Het |
Pdgfd |
A |
G |
9: 6,359,739 (GRCm39) |
Y270C |
probably damaging |
Het |
Pds5b |
A |
T |
5: 150,646,802 (GRCm39) |
D197V |
probably damaging |
Het |
Pknox2 |
A |
G |
9: 36,866,127 (GRCm39) |
M30T |
probably benign |
Het |
Plekhg1 |
A |
T |
10: 3,907,491 (GRCm39) |
S858C |
|
Het |
Por |
A |
T |
5: 135,762,498 (GRCm39) |
E400D |
probably benign |
Het |
Pou2af2 |
C |
A |
9: 51,201,360 (GRCm39) |
R232L |
probably damaging |
Het |
Psip1 |
A |
G |
4: 83,391,275 (GRCm39) |
|
probably null |
Het |
Retreg1 |
G |
T |
15: 25,889,628 (GRCm39) |
V111F |
|
Het |
Rock1 |
G |
A |
18: 10,122,762 (GRCm39) |
A353V |
probably damaging |
Het |
Rpl6 |
C |
G |
5: 121,346,591 (GRCm39) |
R231G |
probably benign |
Het |
Scn7a |
C |
T |
2: 66,587,574 (GRCm39) |
R43H |
probably benign |
Het |
Scnn1g |
T |
A |
7: 121,362,657 (GRCm39) |
N488K |
probably benign |
Het |
Slc24a1 |
A |
G |
9: 64,831,764 (GRCm39) |
V1111A |
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,029,285 (GRCm39) |
S356L |
probably benign |
Het |
Spata31e2 |
T |
C |
1: 26,723,039 (GRCm39) |
T714A |
possibly damaging |
Het |
Ssbp2 |
T |
A |
13: 91,823,209 (GRCm39) |
N201K |
probably damaging |
Het |
Tfdp2 |
A |
G |
9: 96,179,695 (GRCm39) |
N43D |
probably damaging |
Het |
Tmprss11d |
A |
G |
5: 86,474,309 (GRCm39) |
I216T |
probably damaging |
Het |
Tmprss4 |
A |
G |
9: 45,086,853 (GRCm39) |
S303P |
probably benign |
Het |
Tnpo2 |
A |
G |
8: 85,781,663 (GRCm39) |
E815G |
probably benign |
Het |
Trav6-1 |
A |
C |
14: 52,875,972 (GRCm39) |
M1L |
possibly damaging |
Het |
Trpm3 |
T |
C |
19: 22,955,937 (GRCm39) |
V1133A |
probably damaging |
Het |
Trpv1 |
C |
T |
11: 73,129,355 (GRCm39) |
P91S |
probably benign |
Het |
Trpv2 |
T |
C |
11: 62,480,576 (GRCm39) |
Y338H |
probably damaging |
Het |
Txnip |
T |
C |
3: 96,467,539 (GRCm39) |
M336T |
probably benign |
Het |
Vmn1r61 |
A |
T |
7: 5,613,767 (GRCm39) |
H182Q |
possibly damaging |
Het |
Wwp1 |
G |
T |
4: 19,627,660 (GRCm39) |
T745K |
probably damaging |
Het |
Xkr5 |
C |
A |
8: 18,983,608 (GRCm39) |
E645* |
probably null |
Het |
Zfp451 |
C |
T |
1: 33,818,221 (GRCm39) |
R303H |
probably benign |
Het |
Zyg11b |
T |
C |
4: 108,123,655 (GRCm39) |
H104R |
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 |
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 |
R8880:Vmn2r105
|
UTSW |
17 |
20,429,229 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|