Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A430033K04Rik |
A |
G |
5: 138,645,366 (GRCm39) |
Y417C |
probably damaging |
Het |
Adam28 |
T |
A |
14: 68,859,569 (GRCm39) |
H548L |
possibly damaging |
Het |
Agbl3 |
A |
T |
6: 34,823,771 (GRCm39) |
D812V |
probably damaging |
Het |
Aopep |
A |
T |
13: 63,163,237 (GRCm39) |
D86V |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,098,203 (GRCm39) |
L305Q |
probably damaging |
Het |
Arhgef38 |
A |
G |
3: 132,837,812 (GRCm39) |
V706A |
probably benign |
Het |
Arl15 |
A |
G |
13: 114,291,288 (GRCm39) |
I171V |
probably benign |
Het |
Cacna1s |
C |
A |
1: 136,012,011 (GRCm39) |
Y237* |
probably null |
Het |
Ccnt1 |
T |
C |
15: 98,462,990 (GRCm39) |
T61A |
possibly damaging |
Het |
Col25a1 |
T |
A |
3: 129,975,433 (GRCm39) |
|
probably benign |
Het |
Col4a1 |
T |
A |
8: 11,290,077 (GRCm39) |
|
probably benign |
Het |
Dcun1d1 |
T |
C |
3: 35,970,455 (GRCm39) |
E130G |
possibly damaging |
Het |
Dnah7b |
G |
A |
1: 46,181,309 (GRCm39) |
M1065I |
probably benign |
Het |
Ephb2 |
T |
G |
4: 136,384,795 (GRCm39) |
K872T |
probably damaging |
Het |
Fga |
G |
A |
3: 82,938,981 (GRCm39) |
G452D |
probably damaging |
Het |
Flrt1 |
T |
A |
19: 7,074,277 (GRCm39) |
N90I |
probably damaging |
Het |
Fut10 |
T |
A |
8: 31,685,319 (GRCm39) |
|
probably null |
Het |
Gm4553 |
T |
C |
7: 141,718,964 (GRCm39) |
S155G |
unknown |
Het |
Gpr137b |
T |
C |
13: 13,549,000 (GRCm39) |
|
probably benign |
Het |
Gprc5d |
G |
A |
6: 135,093,488 (GRCm39) |
Q140* |
probably null |
Het |
Ifi27l2b |
T |
C |
12: 103,417,476 (GRCm39) |
K237R |
unknown |
Het |
Ipo8 |
A |
T |
6: 148,684,284 (GRCm39) |
M836K |
possibly damaging |
Het |
Kcnq4 |
G |
A |
4: 120,555,213 (GRCm39) |
Q657* |
probably null |
Het |
Lama1 |
A |
T |
17: 68,120,943 (GRCm39) |
H2693L |
probably benign |
Het |
Lrrc23 |
A |
G |
6: 124,755,889 (GRCm39) |
W40R |
probably damaging |
Het |
Minar1 |
T |
C |
9: 89,485,196 (GRCm39) |
D67G |
probably damaging |
Het |
Morn2 |
C |
A |
17: 80,602,933 (GRCm39) |
|
probably benign |
Het |
Ms4a6b |
T |
A |
19: 11,506,854 (GRCm39) |
N214K |
possibly damaging |
Het |
Nags |
A |
T |
11: 102,039,892 (GRCm39) |
S527C |
probably damaging |
Het |
Ndst1 |
C |
T |
18: 60,841,028 (GRCm39) |
G218D |
probably damaging |
Het |
Or10j5 |
G |
A |
1: 172,785,045 (GRCm39) |
V228M |
probably benign |
Het |
Or5b94 |
T |
A |
19: 12,651,924 (GRCm39) |
Y118* |
probably null |
Het |
Oxa1l |
G |
T |
14: 54,600,802 (GRCm39) |
G92* |
probably null |
Het |
Parp16 |
A |
T |
9: 65,137,245 (GRCm39) |
E157V |
probably damaging |
Het |
Pcdh17 |
A |
T |
14: 84,684,984 (GRCm39) |
I484F |
probably damaging |
Het |
Pex16 |
A |
G |
2: 92,209,580 (GRCm39) |
R263G |
probably benign |
Het |
Pkd1l3 |
G |
A |
8: 110,356,869 (GRCm39) |
E765K |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,640,350 (GRCm39) |
V532A |
probably damaging |
Het |
Polq |
A |
G |
16: 36,885,609 (GRCm39) |
|
probably benign |
Het |
Pramel5 |
T |
C |
4: 143,998,191 (GRCm39) |
T351A |
probably damaging |
Het |
Prokr1 |
A |
T |
6: 87,565,593 (GRCm39) |
I84N |
probably damaging |
Het |
Prss30 |
A |
T |
17: 24,192,695 (GRCm39) |
S162T |
probably benign |
Het |
Ranbp2 |
A |
G |
10: 58,287,806 (GRCm39) |
K25E |
probably damaging |
Het |
Rapsn |
A |
G |
2: 90,866,205 (GRCm39) |
T22A |
probably damaging |
Het |
Rhoj |
G |
T |
12: 75,355,680 (GRCm39) |
G9V |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,340,169 (GRCm39) |
R3467G |
probably benign |
Het |
Rreb1 |
C |
A |
13: 38,113,622 (GRCm39) |
S327* |
probably null |
Het |
Scn5a |
G |
A |
9: 119,315,290 (GRCm39) |
P1806L |
probably damaging |
Het |
Sema6a |
C |
A |
18: 47,423,042 (GRCm39) |
|
probably null |
Het |
Stag3 |
G |
A |
5: 138,295,921 (GRCm39) |
E416K |
probably benign |
Het |
Stpg1 |
T |
A |
4: 135,256,856 (GRCm39) |
S216T |
possibly damaging |
Het |
Tfeb |
C |
A |
17: 48,102,589 (GRCm39) |
N426K |
probably benign |
Het |
Trp53bp1 |
G |
T |
2: 121,087,060 (GRCm39) |
Q199K |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,155,877 (GRCm39) |
D2234G |
probably damaging |
Het |
Ush1c |
T |
G |
7: 45,846,194 (GRCm39) |
Q866P |
probably benign |
Het |
Vdr |
T |
A |
15: 97,782,735 (GRCm39) |
D29V |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,853,224 (GRCm39) |
V2439A |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,342,942 (GRCm39) |
S1728P |
possibly damaging |
Het |
Zfp9 |
A |
G |
6: 118,441,436 (GRCm39) |
S409P |
probably damaging |
Het |
|
Other mutations in Or8h7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01674:Or8h7
|
APN |
2 |
86,721,093 (GRCm39) |
missense |
probably benign |
|
IGL02089:Or8h7
|
APN |
2 |
86,721,460 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02201:Or8h7
|
APN |
2 |
86,721,420 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02426:Or8h7
|
APN |
2 |
86,720,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02469:Or8h7
|
APN |
2 |
86,721,499 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02489:Or8h7
|
APN |
2 |
86,721,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02817:Or8h7
|
APN |
2 |
86,720,937 (GRCm39) |
missense |
probably benign |
|
R0042:Or8h7
|
UTSW |
2 |
86,720,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:Or8h7
|
UTSW |
2 |
86,720,763 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1867:Or8h7
|
UTSW |
2 |
86,720,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R2412:Or8h7
|
UTSW |
2 |
86,721,178 (GRCm39) |
missense |
probably benign |
0.01 |
R4465:Or8h7
|
UTSW |
2 |
86,721,494 (GRCm39) |
missense |
probably benign |
|
R4520:Or8h7
|
UTSW |
2 |
86,721,363 (GRCm39) |
missense |
probably benign |
0.20 |
R5185:Or8h7
|
UTSW |
2 |
86,720,946 (GRCm39) |
missense |
probably benign |
0.42 |
R5329:Or8h7
|
UTSW |
2 |
86,720,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Or8h7
|
UTSW |
2 |
86,720,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Or8h7
|
UTSW |
2 |
86,720,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Or8h7
|
UTSW |
2 |
86,720,676 (GRCm39) |
missense |
probably damaging |
0.99 |
R6288:Or8h7
|
UTSW |
2 |
86,721,226 (GRCm39) |
missense |
probably benign |
0.01 |
R6906:Or8h7
|
UTSW |
2 |
86,721,091 (GRCm39) |
missense |
probably benign |
|
R7161:Or8h7
|
UTSW |
2 |
86,720,993 (GRCm39) |
missense |
probably benign |
0.01 |
R7256:Or8h7
|
UTSW |
2 |
86,720,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R7404:Or8h7
|
UTSW |
2 |
86,721,217 (GRCm39) |
missense |
probably benign |
0.05 |
R9236:Or8h7
|
UTSW |
2 |
86,720,622 (GRCm39) |
missense |
probably benign |
|
R9356:Or8h7
|
UTSW |
2 |
86,720,605 (GRCm39) |
missense |
probably benign |
|
R9542:Or8h7
|
UTSW |
2 |
86,720,813 (GRCm39) |
missense |
probably benign |
0.00 |
R9630:Or8h7
|
UTSW |
2 |
86,720,956 (GRCm39) |
missense |
probably damaging |
0.97 |
|