Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9830107B12Rik |
A |
T |
17: 48,439,167 (GRCm39) |
L130I |
probably benign |
Het |
Abca9 |
A |
G |
11: 110,035,610 (GRCm39) |
V670A |
probably benign |
Het |
Adad1 |
A |
G |
3: 37,146,182 (GRCm39) |
N517D |
probably damaging |
Het |
Ankle2 |
T |
C |
5: 110,379,245 (GRCm39) |
L48P |
probably benign |
Het |
Aoc3 |
A |
T |
11: 101,228,485 (GRCm39) |
|
probably benign |
Het |
Areg |
A |
G |
5: 91,291,363 (GRCm39) |
K102R |
probably benign |
Het |
Bmp1 |
T |
C |
14: 70,745,963 (GRCm39) |
T167A |
probably damaging |
Het |
C4b |
C |
T |
17: 34,953,525 (GRCm39) |
G986D |
probably benign |
Het |
Caml |
G |
T |
13: 55,772,955 (GRCm39) |
G200C |
probably damaging |
Het |
Ccdc40 |
A |
C |
11: 119,122,358 (GRCm39) |
R53S |
probably benign |
Het |
Cdh22 |
T |
A |
2: 164,985,576 (GRCm39) |
I337L |
probably benign |
Het |
Col12a1 |
A |
T |
9: 79,554,883 (GRCm39) |
V2065D |
probably benign |
Het |
Copg2 |
A |
G |
6: 30,788,531 (GRCm39) |
S591P |
probably benign |
Het |
Cyp2d34 |
G |
A |
15: 82,500,526 (GRCm39) |
P438S |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,421,931 (GRCm39) |
D163G |
probably damaging |
Het |
Depdc1b |
T |
C |
13: 108,500,177 (GRCm39) |
V230A |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,132,790 (GRCm39) |
L1300H |
probably damaging |
Het |
Dnah10 |
G |
T |
5: 124,839,933 (GRCm39) |
|
probably null |
Het |
Dsc2 |
A |
T |
18: 20,174,876 (GRCm39) |
D466E |
probably damaging |
Het |
Dthd1 |
A |
G |
5: 62,984,411 (GRCm39) |
D372G |
probably damaging |
Het |
Eeig2 |
A |
T |
3: 108,934,571 (GRCm39) |
F23I |
probably benign |
Het |
Eogt |
G |
T |
6: 97,111,265 (GRCm39) |
Q199K |
probably benign |
Het |
Epha6 |
C |
A |
16: 59,486,960 (GRCm39) |
R1029L |
possibly damaging |
Het |
Eppin |
C |
A |
2: 164,431,243 (GRCm39) |
E128* |
probably null |
Het |
Fgf20 |
T |
C |
8: 40,739,652 (GRCm39) |
R33G |
probably benign |
Het |
Fgg |
A |
G |
3: 82,917,397 (GRCm39) |
N142S |
probably damaging |
Het |
Fhip2a |
C |
A |
19: 57,359,619 (GRCm39) |
P53Q |
probably damaging |
Het |
Gba1 |
C |
T |
3: 89,115,951 (GRCm39) |
|
probably null |
Het |
Gli2 |
A |
G |
1: 118,765,241 (GRCm39) |
V970A |
probably damaging |
Het |
Gramd1b |
A |
T |
9: 40,219,289 (GRCm39) |
V508D |
probably damaging |
Het |
Gucy2c |
T |
A |
6: 136,685,319 (GRCm39) |
D898V |
probably damaging |
Het |
Kcnj15 |
T |
C |
16: 95,096,653 (GRCm39) |
Y92H |
probably damaging |
Het |
L3mbtl3 |
A |
T |
10: 26,158,693 (GRCm39) |
S652T |
unknown |
Het |
Ldb2 |
G |
T |
5: 44,633,893 (GRCm39) |
Q326K |
probably benign |
Het |
Lipi |
C |
A |
16: 75,357,689 (GRCm39) |
R292L |
probably benign |
Het |
Lrrc36 |
G |
A |
8: 106,176,246 (GRCm39) |
V207I |
possibly damaging |
Het |
Lyplal1 |
C |
T |
1: 185,820,949 (GRCm39) |
G166D |
probably benign |
Het |
Map1b |
A |
T |
13: 99,566,810 (GRCm39) |
Y1970* |
probably null |
Het |
Map2 |
A |
G |
1: 66,464,628 (GRCm39) |
N287D |
probably damaging |
Het |
Map3k11 |
G |
T |
19: 5,747,499 (GRCm39) |
Q578H |
probably damaging |
Het |
Map3k11 |
A |
T |
19: 5,747,498 (GRCm39) |
Q578L |
probably benign |
Het |
Map4k4 |
G |
A |
1: 40,056,351 (GRCm39) |
S1012N |
probably benign |
Het |
Mapk13 |
A |
T |
17: 28,988,426 (GRCm39) |
N15Y |
probably damaging |
Het |
Mapk15 |
G |
A |
15: 75,867,759 (GRCm39) |
A125T |
probably damaging |
Het |
Mrgprb1 |
C |
A |
7: 48,097,456 (GRCm39) |
R152L |
possibly damaging |
Het |
Mtrex |
C |
A |
13: 113,058,273 (GRCm39) |
E53* |
probably null |
Het |
Muc5ac |
T |
G |
7: 141,344,840 (GRCm39) |
Y104D |
possibly damaging |
Het |
Myo1h |
A |
G |
5: 114,486,440 (GRCm39) |
N566S |
possibly damaging |
Het |
Myo1h |
C |
A |
5: 114,489,737 (GRCm39) |
H647Q |
probably benign |
Het |
Neo1 |
A |
G |
9: 58,796,324 (GRCm39) |
I1201T |
possibly damaging |
Het |
Nlgn1 |
T |
C |
3: 25,490,186 (GRCm39) |
T514A |
probably benign |
Het |
Or10al4 |
A |
G |
17: 38,037,587 (GRCm39) |
Y224C |
probably damaging |
Het |
Or12j4 |
A |
T |
7: 140,046,981 (GRCm39) |
Y289F |
probably damaging |
Het |
Or8d4 |
T |
A |
9: 40,039,018 (GRCm39) |
K80* |
probably null |
Het |
Orc2 |
A |
T |
1: 58,539,468 (GRCm39) |
L57* |
probably null |
Het |
Otoa |
G |
A |
7: 120,744,791 (GRCm39) |
V850M |
probably damaging |
Het |
Pcnx3 |
T |
C |
19: 5,717,247 (GRCm39) |
T1579A |
possibly damaging |
Het |
Pde5a |
A |
T |
3: 122,616,742 (GRCm39) |
Y564F |
probably damaging |
Het |
Pdxk |
A |
C |
10: 78,283,753 (GRCm39) |
I147S |
probably damaging |
Het |
Pfdn5 |
A |
G |
15: 102,237,187 (GRCm39) |
D108G |
probably benign |
Het |
Pink1 |
T |
C |
4: 138,044,621 (GRCm39) |
D342G |
probably damaging |
Het |
Prkacb |
A |
T |
3: 146,443,753 (GRCm39) |
V336E |
probably damaging |
Het |
Ptpro |
C |
A |
6: 137,393,834 (GRCm39) |
S13* |
probably null |
Het |
Rfng |
A |
G |
11: 120,673,476 (GRCm39) |
L215P |
probably damaging |
Het |
Rpn2 |
T |
C |
2: 157,144,345 (GRCm39) |
F336L |
possibly damaging |
Het |
Sacs |
A |
G |
14: 61,449,246 (GRCm39) |
|
probably null |
Het |
Sirpb1a |
T |
A |
3: 15,482,097 (GRCm39) |
Y77F |
probably benign |
Het |
Slc30a8 |
A |
G |
15: 52,196,971 (GRCm39) |
D294G |
probably benign |
Het |
Sox13 |
T |
C |
1: 133,316,672 (GRCm39) |
I212V |
probably benign |
Het |
Srebf2 |
T |
A |
15: 82,069,549 (GRCm39) |
I657N |
possibly damaging |
Het |
Srsf6 |
C |
A |
2: 162,775,629 (GRCm39) |
T146K |
probably benign |
Het |
Strn4 |
T |
C |
7: 16,558,088 (GRCm39) |
V162A |
possibly damaging |
Het |
Sulf2 |
T |
C |
2: 165,974,525 (GRCm39) |
D53G |
probably damaging |
Het |
Tbc1d8 |
T |
A |
1: 39,411,789 (GRCm39) |
I1016F |
probably damaging |
Het |
Tfrc |
G |
T |
16: 32,437,475 (GRCm39) |
A278S |
probably damaging |
Het |
Tnrc6a |
T |
G |
7: 122,783,512 (GRCm39) |
|
probably null |
Het |
Vmn1r83 |
T |
C |
7: 12,055,695 (GRCm39) |
I121V |
probably benign |
Het |
Vps13d |
T |
C |
4: 144,858,225 (GRCm39) |
S2200G |
possibly damaging |
Het |
Washc2 |
T |
A |
6: 116,206,230 (GRCm39) |
D397E |
probably damaging |
Het |
Wipf3 |
T |
C |
6: 54,462,540 (GRCm39) |
L250P |
probably damaging |
Het |
Xirp1 |
A |
G |
9: 119,848,748 (GRCm39) |
F45S |
probably damaging |
Het |
Xpo5 |
A |
G |
17: 46,547,889 (GRCm39) |
T910A |
probably benign |
Het |
Zfp235 |
T |
C |
7: 23,841,101 (GRCm39) |
Y507H |
probably damaging |
Het |
|
Other mutations in Or7a42 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01022:Or7a42
|
APN |
10 |
78,791,188 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01480:Or7a42
|
APN |
10 |
78,791,978 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02505:Or7a42
|
APN |
10 |
78,791,767 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02543:Or7a42
|
APN |
10 |
78,791,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03323:Or7a42
|
APN |
10 |
78,791,434 (GRCm39) |
missense |
probably benign |
|
PIT4466001:Or7a42
|
UTSW |
10 |
78,791,676 (GRCm39) |
missense |
probably benign |
0.00 |
R1496:Or7a42
|
UTSW |
10 |
78,791,682 (GRCm39) |
missense |
probably benign |
0.41 |
R1754:Or7a42
|
UTSW |
10 |
78,791,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R1878:Or7a42
|
UTSW |
10 |
78,791,639 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2760:Or7a42
|
UTSW |
10 |
78,791,876 (GRCm39) |
missense |
probably damaging |
0.99 |
R4202:Or7a42
|
UTSW |
10 |
78,791,129 (GRCm39) |
missense |
probably benign |
|
R4206:Or7a42
|
UTSW |
10 |
78,791,117 (GRCm39) |
missense |
probably benign |
0.00 |
R4517:Or7a42
|
UTSW |
10 |
78,791,877 (GRCm39) |
nonsense |
probably null |
|
R4799:Or7a42
|
UTSW |
10 |
78,791,931 (GRCm39) |
missense |
probably null |
0.92 |
R4979:Or7a42
|
UTSW |
10 |
78,791,766 (GRCm39) |
nonsense |
probably null |
|
R5008:Or7a42
|
UTSW |
10 |
78,791,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R5700:Or7a42
|
UTSW |
10 |
78,791,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R5876:Or7a42
|
UTSW |
10 |
78,791,191 (GRCm39) |
missense |
probably benign |
0.15 |
R6439:Or7a42
|
UTSW |
10 |
78,791,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R6930:Or7a42
|
UTSW |
10 |
78,791,615 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7110:Or7a42
|
UTSW |
10 |
78,791,284 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7405:Or7a42
|
UTSW |
10 |
78,791,531 (GRCm39) |
missense |
probably benign |
0.14 |
R7524:Or7a42
|
UTSW |
10 |
78,791,325 (GRCm39) |
nonsense |
probably null |
|
R8198:Or7a42
|
UTSW |
10 |
78,791,558 (GRCm39) |
missense |
probably damaging |
0.97 |
R9227:Or7a42
|
UTSW |
10 |
78,791,929 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9230:Or7a42
|
UTSW |
10 |
78,791,929 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1176:Or7a42
|
UTSW |
10 |
78,791,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|