Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
T |
G |
8: 25,137,799 (GRCm39) |
|
probably null |
Het |
Adgb |
A |
T |
10: 10,318,409 (GRCm39) |
Y138* |
probably null |
Het |
Adra1d |
T |
C |
2: 131,388,092 (GRCm39) |
R488G |
possibly damaging |
Het |
Ahnak |
G |
A |
19: 8,979,739 (GRCm39) |
G341E |
probably damaging |
Het |
Ankmy1 |
T |
C |
1: 92,808,838 (GRCm39) |
D690G |
probably damaging |
Het |
Arhgef38 |
C |
T |
3: 132,838,225 (GRCm39) |
E21K |
probably damaging |
Het |
Atp8b2 |
T |
C |
3: 89,857,155 (GRCm39) |
M402V |
probably damaging |
Het |
Atp8b4 |
G |
T |
2: 126,167,314 (GRCm39) |
H1062N |
probably benign |
Het |
Bdnf |
A |
G |
2: 109,554,139 (GRCm39) |
H131R |
probably damaging |
Het |
Cblb |
C |
T |
16: 51,956,192 (GRCm39) |
T265M |
probably damaging |
Het |
Cenpe |
T |
A |
3: 134,945,519 (GRCm39) |
M1011K |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,781,410 (GRCm39) |
Y711* |
probably null |
Het |
Clca4a |
A |
G |
3: 144,658,690 (GRCm39) |
Y842H |
probably benign |
Het |
Clspn |
T |
A |
4: 126,475,310 (GRCm39) |
M1021K |
probably benign |
Het |
Cpne8 |
G |
T |
15: 90,503,845 (GRCm39) |
R107S |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Dna2 |
C |
T |
10: 62,784,966 (GRCm39) |
R28W |
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,409,323 (GRCm39) |
N3580K |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,359,123 (GRCm39) |
I298T |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,157,553 (GRCm39) |
K858R |
probably null |
Het |
Fasn |
A |
T |
11: 120,704,075 (GRCm39) |
V1448E |
possibly damaging |
Het |
Gins2 |
T |
C |
8: 121,308,939 (GRCm39) |
D105G |
probably damaging |
Het |
Insr |
A |
T |
8: 3,215,576 (GRCm39) |
D975E |
probably benign |
Het |
Klrc3 |
T |
C |
6: 129,616,510 (GRCm39) |
D169G |
probably benign |
Het |
Krt76 |
T |
A |
15: 101,793,443 (GRCm39) |
S532C |
unknown |
Het |
Lamp3 |
A |
T |
16: 19,492,275 (GRCm39) |
M323K |
probably damaging |
Het |
Lgmn |
T |
C |
12: 102,360,868 (GRCm39) |
I423M |
possibly damaging |
Het |
Lpgat1 |
A |
T |
1: 191,508,538 (GRCm39) |
T359S |
possibly damaging |
Het |
Lrguk |
T |
A |
6: 34,063,373 (GRCm39) |
I466N |
probably damaging |
Het |
Magi3 |
A |
C |
3: 103,996,843 (GRCm39) |
M234R |
probably benign |
Het |
Myh14 |
G |
A |
7: 44,261,122 (GRCm39) |
R1042* |
probably null |
Het |
Nfia |
T |
G |
4: 97,999,461 (GRCm39) |
Y378D |
possibly damaging |
Het |
Npffr1 |
T |
A |
10: 61,462,012 (GRCm39) |
S383T |
possibly damaging |
Het |
Or4f57 |
C |
A |
2: 111,790,585 (GRCm39) |
V278F |
probably benign |
Het |
Or52n4 |
T |
A |
7: 104,293,977 (GRCm39) |
I199F |
probably benign |
Het |
Or5b112 |
C |
A |
19: 13,319,539 (GRCm39) |
P139Q |
probably benign |
Het |
Or9s14 |
T |
C |
1: 92,535,676 (GRCm39) |
L39P |
probably damaging |
Het |
Osr1 |
G |
A |
12: 9,629,798 (GRCm39) |
|
probably null |
Het |
Pde4b |
A |
C |
4: 102,454,896 (GRCm39) |
R375S |
probably damaging |
Het |
Pde8a |
A |
G |
7: 80,942,011 (GRCm39) |
E150G |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,408,897 (GRCm39) |
|
probably null |
Het |
Ppp3ca |
A |
G |
3: 136,634,305 (GRCm39) |
T422A |
probably benign |
Het |
Proser1 |
T |
C |
3: 53,385,180 (GRCm39) |
V354A |
possibly damaging |
Het |
Rgs20 |
G |
T |
1: 5,091,050 (GRCm39) |
R127S |
probably benign |
Het |
Sanbr |
T |
C |
11: 23,539,971 (GRCm39) |
K48E |
probably damaging |
Het |
Sec22a |
T |
C |
16: 35,167,998 (GRCm39) |
D171G |
probably benign |
Het |
Secisbp2 |
A |
G |
13: 51,827,143 (GRCm39) |
E417G |
possibly damaging |
Het |
Serpinb6b |
T |
C |
13: 33,158,895 (GRCm39) |
L32S |
probably damaging |
Het |
Sf3b1 |
C |
G |
1: 55,058,554 (GRCm39) |
E12Q |
possibly damaging |
Het |
Slc39a10 |
A |
T |
1: 46,865,375 (GRCm39) |
S487T |
probably benign |
Het |
Slc6a1 |
G |
T |
6: 114,284,731 (GRCm39) |
G263V |
probably damaging |
Het |
Spag6 |
A |
G |
2: 18,737,925 (GRCm39) |
D265G |
probably benign |
Het |
Spata31e2 |
T |
C |
1: 26,724,950 (GRCm39) |
T77A |
probably benign |
Het |
Sybu |
G |
T |
15: 44,582,228 (GRCm39) |
S132* |
probably null |
Het |
Virma |
T |
C |
4: 11,528,776 (GRCm39) |
S1288P |
probably damaging |
Het |
Vmn1r229 |
T |
A |
17: 21,035,067 (GRCm39) |
V104D |
probably damaging |
Het |
Vmn1r238 |
T |
C |
18: 3,123,358 (GRCm39) |
T19A |
probably benign |
Het |
Vmn2r86 |
C |
T |
10: 130,289,010 (GRCm39) |
V164I |
probably benign |
Het |
Wfdc13 |
G |
T |
2: 164,528,854 (GRCm39) |
A64S |
probably damaging |
Het |
Zfp873 |
C |
A |
10: 81,896,113 (GRCm39) |
H318Q |
probably damaging |
Het |
Zyg11a |
A |
G |
4: 108,040,843 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ghdc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1489:Ghdc
|
UTSW |
11 |
100,659,083 (GRCm39) |
missense |
probably benign |
0.39 |
R1945:Ghdc
|
UTSW |
11 |
100,660,031 (GRCm39) |
missense |
probably benign |
0.10 |
R1999:Ghdc
|
UTSW |
11 |
100,660,018 (GRCm39) |
missense |
probably benign |
0.04 |
R2150:Ghdc
|
UTSW |
11 |
100,660,018 (GRCm39) |
missense |
probably benign |
0.04 |
R4779:Ghdc
|
UTSW |
11 |
100,660,929 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4807:Ghdc
|
UTSW |
11 |
100,661,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Ghdc
|
UTSW |
11 |
100,657,814 (GRCm39) |
missense |
probably benign |
0.26 |
R4952:Ghdc
|
UTSW |
11 |
100,659,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Ghdc
|
UTSW |
11 |
100,657,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5220:Ghdc
|
UTSW |
11 |
100,660,543 (GRCm39) |
missense |
probably damaging |
0.98 |
R5422:Ghdc
|
UTSW |
11 |
100,660,020 (GRCm39) |
missense |
probably benign |
0.03 |
R5926:Ghdc
|
UTSW |
11 |
100,659,063 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6165:Ghdc
|
UTSW |
11 |
100,659,928 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7076:Ghdc
|
UTSW |
11 |
100,660,540 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7299:Ghdc
|
UTSW |
11 |
100,658,942 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7314:Ghdc
|
UTSW |
11 |
100,659,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R7655:Ghdc
|
UTSW |
11 |
100,660,493 (GRCm39) |
missense |
probably benign |
0.04 |
R7656:Ghdc
|
UTSW |
11 |
100,660,493 (GRCm39) |
missense |
probably benign |
0.04 |
R9419:Ghdc
|
UTSW |
11 |
100,661,081 (GRCm39) |
missense |
probably damaging |
0.96 |
R9556:Ghdc
|
UTSW |
11 |
100,658,861 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9684:Ghdc
|
UTSW |
11 |
100,661,091 (GRCm39) |
missense |
probably benign |
0.02 |
R9710:Ghdc
|
UTSW |
11 |
100,658,863 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Ghdc
|
UTSW |
11 |
100,660,243 (GRCm39) |
missense |
probably benign |
0.00 |
|