Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl1 |
T |
C |
8: 84,649,704 (GRCm39) |
Y121H |
possibly damaging |
Het |
Agbl5 |
G |
A |
5: 31,051,247 (GRCm39) |
|
probably null |
Het |
Atp13a2 |
T |
A |
4: 140,731,671 (GRCm39) |
|
probably null |
Het |
Cd69 |
A |
T |
6: 129,248,379 (GRCm39) |
S36T |
probably damaging |
Het |
Ceacam5 |
A |
T |
7: 17,449,005 (GRCm39) |
I124L |
probably benign |
Het |
Cerkl |
T |
C |
2: 79,223,328 (GRCm39) |
H131R |
probably benign |
Het |
Cfap57 |
A |
T |
4: 118,453,085 (GRCm39) |
N539K |
probably benign |
Het |
Cyp4x1 |
C |
A |
4: 114,979,174 (GRCm39) |
W141L |
probably damaging |
Het |
Dlgap1 |
T |
C |
17: 70,823,993 (GRCm39) |
|
probably null |
Het |
Dnaaf9 |
G |
A |
2: 130,656,222 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
C |
1: 34,296,954 (GRCm39) |
I5781T |
possibly damaging |
Het |
Epha2 |
T |
A |
4: 141,035,867 (GRCm39) |
V101E |
probably damaging |
Het |
Exph5 |
T |
C |
9: 53,285,613 (GRCm39) |
F898S |
possibly damaging |
Het |
Fyco1 |
G |
A |
9: 123,623,836 (GRCm39) |
R1398* |
probably null |
Het |
Gemin6 |
T |
G |
17: 80,535,178 (GRCm39) |
V46G |
probably damaging |
Het |
Grb10 |
T |
C |
11: 11,886,746 (GRCm39) |
I508V |
probably benign |
Het |
Igf1r |
C |
A |
7: 67,833,258 (GRCm39) |
Q473K |
probably damaging |
Het |
Ighv1-66 |
T |
A |
12: 115,556,755 (GRCm39) |
D109V |
probably damaging |
Het |
Ipmk |
C |
A |
10: 71,199,304 (GRCm39) |
T55K |
probably benign |
Het |
Kdm2b |
A |
G |
5: 123,087,225 (GRCm39) |
Y192H |
probably damaging |
Het |
Krt32 |
A |
T |
11: 99,977,497 (GRCm39) |
|
probably null |
Het |
Kti12 |
T |
A |
4: 108,705,620 (GRCm39) |
L178Q |
possibly damaging |
Het |
Mchr1 |
A |
T |
15: 81,122,211 (GRCm39) |
K320N |
possibly damaging |
Het |
Mdn1 |
T |
C |
4: 32,685,783 (GRCm39) |
L858S |
probably damaging |
Het |
Myo3a |
T |
A |
2: 22,464,353 (GRCm39) |
F198Y |
probably damaging |
Het |
Ncam2 |
C |
T |
16: 81,231,766 (GRCm39) |
R77* |
probably null |
Het |
Nfatc1 |
T |
C |
18: 80,696,744 (GRCm39) |
T647A |
probably benign |
Het |
Nuf2 |
A |
G |
1: 169,326,453 (GRCm39) |
Y433H |
probably damaging |
Het |
Nup210l |
T |
C |
3: 90,061,972 (GRCm39) |
V717A |
probably benign |
Het |
Or3a1b |
A |
G |
11: 74,012,484 (GRCm39) |
Y123C |
probably damaging |
Het |
Or5h17 |
A |
T |
16: 58,820,268 (GRCm39) |
L73F |
probably benign |
Het |
Pbrm1 |
A |
G |
14: 30,811,520 (GRCm39) |
Y1210C |
probably damaging |
Het |
Pcdhb6 |
A |
G |
18: 37,467,402 (GRCm39) |
I108V |
probably benign |
Het |
Plac8 |
T |
A |
5: 100,710,584 (GRCm39) |
T6S |
probably benign |
Het |
Plbd1 |
A |
T |
6: 136,594,298 (GRCm39) |
V317E |
probably benign |
Het |
Rars1 |
A |
T |
11: 35,708,195 (GRCm39) |
Y406* |
probably null |
Het |
Scamp3 |
T |
C |
3: 89,084,929 (GRCm39) |
F11L |
possibly damaging |
Het |
Sctr |
A |
G |
1: 119,964,146 (GRCm39) |
N142S |
probably benign |
Het |
Sh2d4a |
T |
C |
8: 68,749,349 (GRCm39) |
S128P |
probably benign |
Het |
Snrnp70 |
C |
T |
7: 45,026,601 (GRCm39) |
|
probably benign |
Het |
Taf3 |
T |
C |
2: 9,945,816 (GRCm39) |
K596R |
probably damaging |
Het |
Tango6 |
T |
C |
8: 107,422,230 (GRCm39) |
|
probably null |
Het |
Taok3 |
A |
G |
5: 117,411,822 (GRCm39) |
T414A |
probably benign |
Het |
Tmem104 |
G |
A |
11: 115,079,149 (GRCm39) |
|
probably null |
Het |
Tmem231 |
T |
A |
8: 112,645,042 (GRCm39) |
S155C |
possibly damaging |
Het |
Tssk3 |
G |
A |
4: 129,383,343 (GRCm39) |
R110W |
possibly damaging |
Het |
Ugt2b37 |
T |
C |
5: 87,388,759 (GRCm39) |
T485A |
probably benign |
Het |
Unc5b |
T |
C |
10: 60,613,974 (GRCm39) |
K292E |
possibly damaging |
Het |
Upf3a |
T |
A |
8: 13,845,497 (GRCm39) |
|
probably null |
Het |
Usp24 |
T |
A |
4: 106,229,918 (GRCm39) |
V797E |
probably damaging |
Het |
Vcan |
T |
C |
13: 89,839,929 (GRCm39) |
T1872A |
possibly damaging |
Het |
Vmn1r195 |
A |
G |
13: 22,463,120 (GRCm39) |
M197V |
probably damaging |
Het |
Vmn2r40 |
T |
A |
7: 8,911,203 (GRCm39) |
T697S |
probably benign |
Het |
Xab2 |
A |
T |
8: 3,661,718 (GRCm39) |
D578E |
probably benign |
Het |
Xpo7 |
A |
T |
14: 70,909,090 (GRCm39) |
Y810* |
probably null |
Het |
Zcchc2 |
A |
G |
1: 105,951,426 (GRCm39) |
N587S |
probably benign |
Het |
Zfp189 |
C |
T |
4: 49,529,739 (GRCm39) |
R281* |
probably null |
Het |
Zranb1 |
T |
C |
7: 132,585,678 (GRCm39) |
*735R |
probably null |
Het |
|
Other mutations in Or6c35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01121:Or6c35
|
APN |
10 |
129,168,804 (GRCm39) |
missense |
probably benign |
|
IGL01636:Or6c35
|
APN |
10 |
129,168,752 (GRCm39) |
start codon destroyed |
probably damaging |
0.96 |
IGL01744:Or6c35
|
APN |
10 |
129,169,326 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01867:Or6c35
|
APN |
10 |
129,169,232 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02002:Or6c35
|
APN |
10 |
129,168,996 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02423:Or6c35
|
APN |
10 |
129,169,397 (GRCm39) |
missense |
probably benign |
0.00 |
R2036:Or6c35
|
UTSW |
10 |
129,169,541 (GRCm39) |
missense |
probably benign |
0.43 |
R2099:Or6c35
|
UTSW |
10 |
129,169,152 (GRCm39) |
missense |
probably damaging |
0.96 |
R2273:Or6c35
|
UTSW |
10 |
129,169,326 (GRCm39) |
missense |
probably benign |
0.05 |
R2274:Or6c35
|
UTSW |
10 |
129,169,326 (GRCm39) |
missense |
probably benign |
0.05 |
R3841:Or6c35
|
UTSW |
10 |
129,169,202 (GRCm39) |
missense |
probably benign |
0.00 |
R4585:Or6c35
|
UTSW |
10 |
129,169,142 (GRCm39) |
missense |
probably benign |
0.08 |
R4586:Or6c35
|
UTSW |
10 |
129,169,142 (GRCm39) |
missense |
probably benign |
0.08 |
R6052:Or6c35
|
UTSW |
10 |
129,169,071 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6414:Or6c35
|
UTSW |
10 |
129,169,578 (GRCm39) |
missense |
probably benign |
0.23 |
R6468:Or6c35
|
UTSW |
10 |
129,169,580 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6647:Or6c35
|
UTSW |
10 |
129,169,033 (GRCm39) |
nonsense |
probably null |
|
R8099:Or6c35
|
UTSW |
10 |
129,168,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R9151:Or6c35
|
UTSW |
10 |
129,169,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R9617:Or6c35
|
UTSW |
10 |
129,168,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R9649:Or6c35
|
UTSW |
10 |
129,169,368 (GRCm39) |
missense |
possibly damaging |
0.68 |
T0975:Or6c35
|
UTSW |
10 |
129,169,314 (GRCm39) |
missense |
probably benign |
0.31 |
|