Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad8 |
A |
G |
9: 26,901,890 (GRCm39) |
L158P |
probably damaging |
Het |
Aco1 |
A |
G |
4: 40,197,576 (GRCm39) |
Q860R |
probably benign |
Het |
Actl11 |
A |
T |
9: 107,806,181 (GRCm39) |
Q168L |
possibly damaging |
Het |
Adam26b |
T |
C |
8: 43,972,975 (GRCm39) |
I676V |
probably benign |
Het |
Aldoart2 |
A |
C |
12: 55,612,920 (GRCm39) |
I282L |
probably benign |
Het |
Capns1 |
G |
T |
7: 29,889,565 (GRCm39) |
S211R |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,245,983 (GRCm39) |
V1158A |
probably damaging |
Het |
Cryl1 |
C |
T |
14: 57,523,821 (GRCm39) |
|
probably null |
Het |
Cxcr5 |
A |
G |
9: 44,425,607 (GRCm39) |
|
probably benign |
Het |
Dcaf13 |
A |
G |
15: 38,982,201 (GRCm39) |
K56E |
probably damaging |
Het |
Dlx6 |
T |
G |
6: 6,867,068 (GRCm39) |
S85A |
probably damaging |
Het |
Dsg2 |
C |
T |
18: 20,722,999 (GRCm39) |
|
probably benign |
Het |
Dync1li1 |
T |
A |
9: 114,549,665 (GRCm39) |
S412T |
possibly damaging |
Het |
Ebf3 |
C |
A |
7: 136,827,625 (GRCm39) |
|
probably benign |
Het |
Fads3 |
T |
C |
19: 10,030,366 (GRCm39) |
I168T |
probably benign |
Het |
Gm10295 |
G |
A |
7: 71,000,296 (GRCm39) |
P95S |
unknown |
Het |
Gm43638 |
T |
C |
5: 87,634,455 (GRCm39) |
T51A |
probably damaging |
Het |
Gm5114 |
G |
A |
7: 39,060,071 (GRCm39) |
|
probably benign |
Het |
Gucy2c |
G |
A |
6: 136,679,737 (GRCm39) |
T974M |
probably damaging |
Het |
Ighv1-19-1 |
T |
C |
12: 114,672,258 (GRCm39) |
|
probably benign |
Het |
Kri1 |
A |
T |
9: 21,191,723 (GRCm39) |
L173Q |
probably damaging |
Het |
Lztfl1 |
T |
C |
9: 123,531,338 (GRCm39) |
D210G |
probably benign |
Het |
Morc2a |
T |
A |
11: 3,638,149 (GRCm39) |
N958K |
probably damaging |
Het |
Msl3l2 |
G |
A |
10: 55,992,021 (GRCm39) |
A249T |
probably benign |
Het |
Nlrp4a |
A |
G |
7: 26,149,254 (GRCm39) |
E287G |
probably benign |
Het |
Nlrp9a |
A |
T |
7: 26,257,519 (GRCm39) |
N290I |
possibly damaging |
Het |
Or2b28 |
T |
G |
13: 21,531,185 (GRCm39) |
L29R |
probably damaging |
Het |
Or4e2 |
A |
G |
14: 52,688,484 (GRCm39) |
T205A |
probably benign |
Het |
Pcsk7 |
A |
G |
9: 45,840,005 (GRCm39) |
D731G |
probably benign |
Het |
Plppr5 |
T |
A |
3: 117,480,298 (GRCm39) |
|
probably benign |
Het |
Podxl |
T |
C |
6: 31,505,639 (GRCm39) |
T135A |
possibly damaging |
Het |
Pole |
T |
G |
5: 110,485,106 (GRCm39) |
C407G |
possibly damaging |
Het |
Prl |
C |
A |
13: 27,249,024 (GRCm39) |
N224K |
possibly damaging |
Het |
Prnp |
A |
T |
2: 131,778,340 (GRCm39) |
|
probably benign |
Het |
Proser2 |
A |
G |
2: 6,105,149 (GRCm39) |
*472R |
probably null |
Het |
Rhag |
T |
C |
17: 41,122,178 (GRCm39) |
S38P |
possibly damaging |
Het |
Rnf146 |
T |
C |
10: 29,223,856 (GRCm39) |
D10G |
probably damaging |
Het |
Rps3a1 |
T |
C |
3: 86,049,085 (GRCm39) |
D29G |
probably benign |
Het |
Sv2a |
A |
T |
3: 96,097,012 (GRCm39) |
I446F |
probably benign |
Het |
Tbc1d30 |
C |
A |
10: 121,103,319 (GRCm39) |
R571L |
probably damaging |
Het |
Tfrc |
T |
A |
16: 32,443,646 (GRCm39) |
|
probably null |
Het |
Tnfaip1 |
G |
A |
11: 78,419,129 (GRCm39) |
P156S |
probably damaging |
Het |
Vmn1r226 |
T |
C |
17: 20,908,166 (GRCm39) |
S133P |
probably damaging |
Het |
Wnt9b |
C |
T |
11: 103,622,836 (GRCm39) |
R189K |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,983,726 (GRCm39) |
H564R |
probably benign |
Het |
Zfp442 |
C |
A |
2: 150,251,267 (GRCm39) |
E211* |
probably null |
Het |
|
Other mutations in Or5al6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01106:Or5al6
|
APN |
2 |
85,976,560 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02193:Or5al6
|
APN |
2 |
85,977,059 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02730:Or5al6
|
APN |
2 |
85,976,443 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03032:Or5al6
|
APN |
2 |
85,977,043 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03165:Or5al6
|
APN |
2 |
85,976,412 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0388:Or5al6
|
UTSW |
2 |
85,976,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R2971:Or5al6
|
UTSW |
2 |
85,976,908 (GRCm39) |
missense |
probably damaging |
0.96 |
R4168:Or5al6
|
UTSW |
2 |
85,976,523 (GRCm39) |
missense |
probably benign |
0.03 |
R4532:Or5al6
|
UTSW |
2 |
85,976,274 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5024:Or5al6
|
UTSW |
2 |
85,976,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5175:Or5al6
|
UTSW |
2 |
85,976,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Or5al6
|
UTSW |
2 |
85,976,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Or5al6
|
UTSW |
2 |
85,976,613 (GRCm39) |
missense |
probably damaging |
0.97 |
R6033:Or5al6
|
UTSW |
2 |
85,976,613 (GRCm39) |
missense |
probably damaging |
0.97 |
R6137:Or5al6
|
UTSW |
2 |
85,976,313 (GRCm39) |
missense |
probably benign |
|
R6945:Or5al6
|
UTSW |
2 |
85,976,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Or5al6
|
UTSW |
2 |
85,976,681 (GRCm39) |
nonsense |
probably null |
|
R7065:Or5al6
|
UTSW |
2 |
85,976,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Or5al6
|
UTSW |
2 |
85,976,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R9039:Or5al6
|
UTSW |
2 |
85,976,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Or5al6
|
UTSW |
2 |
85,976,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R9745:Or5al6
|
UTSW |
2 |
85,976,251 (GRCm39) |
missense |
probably damaging |
0.99 |
|