Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930022D16Rik |
A |
G |
11: 109,308,786 (GRCm39) |
T51A |
unknown |
Het |
Acaa1a |
A |
G |
9: 119,178,604 (GRCm39) |
|
probably null |
Het |
Clasp2 |
T |
C |
9: 113,642,332 (GRCm39) |
S280P |
probably damaging |
Het |
Cnga3 |
T |
C |
1: 37,300,359 (GRCm39) |
S398P |
probably damaging |
Het |
Cngb3 |
T |
G |
4: 19,280,946 (GRCm39) |
L5R |
probably damaging |
Het |
Cyp2c65 |
T |
C |
19: 39,070,662 (GRCm39) |
F282L |
possibly damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Dnm2 |
T |
C |
9: 21,416,942 (GRCm39) |
F825S |
probably benign |
Het |
Egfem1 |
T |
A |
3: 29,716,560 (GRCm39) |
C343* |
probably null |
Het |
Fah |
T |
A |
7: 84,242,468 (GRCm39) |
D280V |
probably benign |
Het |
Fiz1 |
C |
T |
7: 5,011,400 (GRCm39) |
A373T |
possibly damaging |
Het |
Flg |
A |
T |
3: 93,200,290 (GRCm39) |
|
probably benign |
Het |
Flnb |
A |
G |
14: 7,929,138 (GRCm38) |
R1956G |
possibly damaging |
Het |
Mterf2 |
A |
G |
10: 84,955,970 (GRCm39) |
F218S |
probably damaging |
Het |
Nlrp1a |
A |
G |
11: 70,996,899 (GRCm39) |
V868A |
probably benign |
Het |
Nrip2 |
T |
A |
6: 128,381,911 (GRCm39) |
C85* |
probably null |
Het |
Ogfrl1 |
T |
G |
1: 23,408,944 (GRCm39) |
K427N |
probably benign |
Het |
Or1o1 |
G |
A |
17: 37,716,796 (GRCm39) |
R119H |
probably benign |
Het |
Or51v14 |
T |
A |
7: 103,261,183 (GRCm39) |
I126F |
possibly damaging |
Het |
Palm |
A |
C |
10: 79,645,365 (GRCm39) |
N111H |
probably benign |
Het |
Pipox |
T |
C |
11: 77,772,005 (GRCm39) |
D373G |
possibly damaging |
Het |
Plec |
C |
T |
15: 76,059,287 (GRCm39) |
G3540D |
probably damaging |
Het |
Psd3 |
T |
C |
8: 68,416,197 (GRCm39) |
T567A |
probably damaging |
Het |
Psg28 |
T |
C |
7: 18,164,469 (GRCm39) |
Y81C |
probably damaging |
Het |
Rarres1 |
A |
T |
3: 67,398,366 (GRCm39) |
N131K |
probably damaging |
Het |
Rbbp8nl |
G |
A |
2: 179,922,752 (GRCm39) |
H214Y |
probably damaging |
Het |
Styxl2 |
T |
C |
1: 165,928,454 (GRCm39) |
E386G |
possibly damaging |
Het |
Tas2r135 |
A |
G |
6: 42,382,952 (GRCm39) |
T164A |
probably benign |
Het |
Tmco3 |
G |
T |
8: 13,370,894 (GRCm39) |
|
probably benign |
Het |
Tnpo2 |
T |
A |
8: 85,771,831 (GRCm39) |
M259K |
possibly damaging |
Het |
Tns4 |
T |
C |
11: 98,971,093 (GRCm39) |
R206G |
probably benign |
Het |
Trim60 |
G |
T |
8: 65,453,248 (GRCm39) |
L334I |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,560,754 (GRCm39) |
T29216A |
probably damaging |
Het |
Urb2 |
G |
T |
8: 124,757,864 (GRCm39) |
E1190D |
probably damaging |
Het |
Vmn1r60 |
T |
A |
7: 5,547,446 (GRCm39) |
N218I |
probably benign |
Het |
Vps25 |
T |
G |
11: 101,149,835 (GRCm39) |
V125G |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,978,855 (GRCm39) |
D455G |
probably benign |
Het |
Ythdf2 |
A |
T |
4: 131,932,911 (GRCm39) |
M83K |
probably benign |
Het |
|
Other mutations in 1700013G24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01547:1700013G24Rik
|
APN |
4 |
137,182,573 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02646:1700013G24Rik
|
APN |
4 |
137,182,101 (GRCm39) |
nonsense |
probably null |
|
R0526:1700013G24Rik
|
UTSW |
4 |
137,182,535 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1449:1700013G24Rik
|
UTSW |
4 |
137,182,666 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3743:1700013G24Rik
|
UTSW |
4 |
137,182,348 (GRCm39) |
missense |
probably damaging |
0.96 |
R5357:1700013G24Rik
|
UTSW |
4 |
137,182,463 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6265:1700013G24Rik
|
UTSW |
4 |
137,181,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R6720:1700013G24Rik
|
UTSW |
4 |
137,181,997 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6988:1700013G24Rik
|
UTSW |
4 |
137,181,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:1700013G24Rik
|
UTSW |
4 |
137,181,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R7825:1700013G24Rik
|
UTSW |
4 |
137,182,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:1700013G24Rik
|
UTSW |
4 |
137,182,553 (GRCm39) |
missense |
probably benign |
|
R9536:1700013G24Rik
|
UTSW |
4 |
137,182,623 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:1700013G24Rik
|
UTSW |
4 |
137,182,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|