Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,984,787 (GRCm39) |
M2024V |
probably benign |
Het |
Ahnak2 |
T |
A |
12: 112,745,831 (GRCm39) |
Q1673L |
|
Het |
Atic |
G |
T |
1: 71,602,946 (GRCm39) |
V107L |
probably benign |
Het |
B2m |
A |
G |
2: 121,981,416 (GRCm39) |
N44D |
probably damaging |
Het |
Bud13 |
A |
G |
9: 46,209,799 (GRCm39) |
D636G |
probably damaging |
Het |
Cenpk |
T |
C |
13: 104,386,025 (GRCm39) |
*307Q |
probably null |
Het |
Cep68 |
A |
G |
11: 20,189,438 (GRCm39) |
S525P |
probably benign |
Het |
Clca3a1 |
A |
G |
3: 144,733,193 (GRCm39) |
L105P |
probably damaging |
Het |
Cntnap5a |
A |
T |
1: 116,220,079 (GRCm39) |
M630L |
probably benign |
Het |
Cpb2 |
A |
G |
14: 75,520,782 (GRCm39) |
Y399C |
probably damaging |
Het |
Dars2 |
G |
T |
1: 160,874,454 (GRCm39) |
P412T |
possibly damaging |
Het |
E2f8 |
A |
T |
7: 48,517,927 (GRCm39) |
I665N |
probably damaging |
Het |
Epha4 |
A |
T |
1: 77,364,553 (GRCm39) |
I652N |
probably damaging |
Het |
Ermn |
ACTTCTTCTTCTTCTTCTTCTTC |
ACTTCTTCTTCTTCTTCTTC |
2: 57,938,079 (GRCm39) |
|
probably benign |
Het |
Flrt3 |
T |
C |
2: 140,502,387 (GRCm39) |
T414A |
probably benign |
Het |
Fmn1 |
A |
T |
2: 113,271,956 (GRCm39) |
Q108L |
unknown |
Het |
Fosb |
T |
C |
7: 19,041,199 (GRCm39) |
D98G |
possibly damaging |
Het |
Gm5773 |
T |
C |
3: 93,680,850 (GRCm39) |
L174S |
probably damaging |
Het |
Hectd3 |
T |
A |
4: 116,854,124 (GRCm39) |
V258E |
possibly damaging |
Het |
Inf2 |
T |
A |
12: 112,571,821 (GRCm39) |
W617R |
unknown |
Het |
Irf7 |
T |
A |
7: 140,843,599 (GRCm39) |
I358F |
probably damaging |
Het |
Lipo3 |
A |
G |
19: 33,535,663 (GRCm39) |
|
probably null |
Het |
Lrig2 |
A |
T |
3: 104,404,829 (GRCm39) |
L93* |
probably null |
Het |
Lzts1 |
C |
T |
8: 69,588,331 (GRCm39) |
V542M |
probably damaging |
Het |
Mefv |
T |
A |
16: 3,533,386 (GRCm39) |
H295L |
probably benign |
Het |
Naf1 |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
8: 67,313,200 (GRCm39) |
|
probably benign |
Het |
Nat8f6 |
G |
C |
6: 85,786,112 (GRCm39) |
S12R |
probably benign |
Het |
Nipal4 |
G |
T |
11: 46,057,062 (GRCm39) |
N14K |
probably benign |
Het |
Nlrp4c |
T |
A |
7: 6,095,595 (GRCm39) |
C824* |
probably null |
Het |
Npat |
T |
C |
9: 53,460,210 (GRCm39) |
S53P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,477,464 (GRCm39) |
E549G |
probably damaging |
Het |
Or10a5 |
T |
C |
7: 106,635,554 (GRCm39) |
L64P |
probably damaging |
Het |
Or1r1 |
T |
C |
11: 73,874,576 (GRCm39) |
N286S |
probably damaging |
Het |
Or4a80 |
T |
C |
2: 89,583,103 (GRCm39) |
K23R |
probably benign |
Het |
Or4f62 |
A |
T |
2: 111,987,060 (GRCm39) |
I255F |
probably damaging |
Het |
Or5p55 |
T |
A |
7: 107,566,811 (GRCm39) |
V69E |
probably damaging |
Het |
Or6c6b |
T |
C |
10: 129,147,559 (GRCm39) |
M61T |
probably benign |
Het |
Or6z6 |
C |
A |
7: 6,490,919 (GRCm39) |
W311L |
probably benign |
Het |
Pcdhb11 |
T |
A |
18: 37,555,672 (GRCm39) |
I334K |
probably damaging |
Het |
Pcdhb4 |
T |
C |
18: 37,442,505 (GRCm39) |
L605P |
probably damaging |
Het |
Pced1a |
G |
T |
2: 130,263,979 (GRCm39) |
H224Q |
probably damaging |
Het |
Pde6b |
C |
A |
5: 108,575,008 (GRCm39) |
S623* |
probably null |
Het |
Pgr |
T |
C |
9: 8,946,883 (GRCm39) |
L708P |
probably damaging |
Het |
Pnpla1 |
T |
C |
17: 29,097,455 (GRCm39) |
I207T |
possibly damaging |
Het |
Prkag3 |
A |
T |
1: 74,786,425 (GRCm39) |
D173E |
probably benign |
Het |
Prrt4 |
A |
G |
6: 29,176,516 (GRCm39) |
F270L |
probably benign |
Het |
Ptdss2 |
C |
A |
7: 140,732,997 (GRCm39) |
P260Q |
possibly damaging |
Het |
Rftn1 |
T |
A |
17: 50,354,435 (GRCm39) |
N309I |
probably damaging |
Het |
Rgs12 |
T |
C |
5: 35,183,287 (GRCm39) |
V978A |
possibly damaging |
Het |
Rnf111 |
T |
C |
9: 70,348,125 (GRCm39) |
Y816C |
probably damaging |
Het |
Rnf208 |
C |
T |
2: 25,133,326 (GRCm39) |
P7S |
probably damaging |
Het |
Rnf24 |
T |
C |
2: 131,155,215 (GRCm39) |
D4G |
probably damaging |
Het |
Ryr2 |
T |
A |
13: 11,570,349 (GRCm39) |
I4925L |
probably benign |
Het |
S1pr5 |
A |
T |
9: 21,156,378 (GRCm39) |
V16D |
possibly damaging |
Het |
Scgb1b24 |
A |
G |
7: 33,443,566 (GRCm39) |
D75G |
possibly damaging |
Het |
Setdb2 |
A |
T |
14: 59,660,794 (GRCm39) |
C116* |
probably null |
Het |
Sh3rf2 |
G |
A |
18: 42,234,604 (GRCm39) |
R129Q |
probably damaging |
Het |
Spata31d1d |
C |
T |
13: 59,875,007 (GRCm39) |
V843I |
probably benign |
Het |
Steap3 |
A |
C |
1: 120,169,248 (GRCm39) |
F350V |
probably benign |
Het |
Tecrl |
T |
A |
5: 83,502,915 (GRCm39) |
|
probably benign |
Het |
Tex15 |
T |
A |
8: 34,066,590 (GRCm39) |
S2007T |
possibly damaging |
Het |
Tomm7 |
C |
A |
5: 24,049,155 (GRCm39) |
|
probably benign |
Het |
Trpv1 |
A |
C |
11: 73,135,030 (GRCm39) |
N409T |
possibly damaging |
Het |
Try5 |
T |
A |
6: 41,288,299 (GRCm39) |
Y218F |
probably benign |
Het |
Tspan5 |
A |
T |
3: 138,603,883 (GRCm39) |
I196F |
possibly damaging |
Het |
Wdhd1 |
A |
T |
14: 47,489,405 (GRCm39) |
C709* |
probably null |
Het |
|
Other mutations in Or12e8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01142:Or12e8
|
APN |
2 |
87,187,889 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01680:Or12e8
|
APN |
2 |
87,188,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02210:Or12e8
|
APN |
2 |
87,188,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Or12e8
|
UTSW |
2 |
87,188,026 (GRCm39) |
nonsense |
probably null |
|
R0849:Or12e8
|
UTSW |
2 |
87,188,609 (GRCm39) |
missense |
probably benign |
0.00 |
R1298:Or12e8
|
UTSW |
2 |
87,188,414 (GRCm39) |
missense |
probably benign |
0.20 |
R2309:Or12e8
|
UTSW |
2 |
87,188,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4237:Or12e8
|
UTSW |
2 |
87,188,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Or12e8
|
UTSW |
2 |
87,188,419 (GRCm39) |
missense |
probably benign |
0.00 |
R5679:Or12e8
|
UTSW |
2 |
87,187,889 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5939:Or12e8
|
UTSW |
2 |
87,188,048 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6269:Or12e8
|
UTSW |
2 |
87,677,218 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6551:Or12e8
|
UTSW |
2 |
87,677,005 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7024:Or12e8
|
UTSW |
2 |
87,188,066 (GRCm39) |
missense |
probably benign |
0.06 |
R7242:Or12e8
|
UTSW |
2 |
87,188,426 (GRCm39) |
missense |
probably benign |
0.13 |
R7359:Or12e8
|
UTSW |
2 |
87,188,555 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7488:Or12e8
|
UTSW |
2 |
87,188,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7646:Or12e8
|
UTSW |
2 |
87,188,102 (GRCm39) |
missense |
probably benign |
0.00 |
R7711:Or12e8
|
UTSW |
2 |
87,187,871 (GRCm39) |
missense |
probably benign |
0.02 |
R8963:Or12e8
|
UTSW |
2 |
87,187,950 (GRCm39) |
missense |
possibly damaging |
0.94 |
|