Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
A |
G |
2: 35,245,002 (GRCm39) |
Y117H |
probably benign |
Het |
a |
A |
G |
2: 154,892,612 (GRCm39) |
D97G |
probably damaging |
Het |
Cdca7l |
T |
C |
12: 117,836,098 (GRCm39) |
S190P |
probably damaging |
Het |
Chst9 |
T |
A |
18: 15,586,086 (GRCm39) |
Y159F |
possibly damaging |
Het |
Col26a1 |
G |
A |
5: 136,911,708 (GRCm39) |
R52C |
probably damaging |
Het |
Dchs2 |
A |
T |
3: 83,263,701 (GRCm39) |
D3323V |
possibly damaging |
Het |
Dennd11 |
T |
C |
6: 40,395,775 (GRCm39) |
|
probably benign |
Het |
Dqx1 |
T |
A |
6: 83,035,619 (GRCm39) |
I44N |
probably damaging |
Het |
Edc4 |
A |
G |
8: 106,613,992 (GRCm39) |
D415G |
probably damaging |
Het |
Enpp3 |
T |
A |
10: 24,650,733 (GRCm39) |
D801V |
probably damaging |
Het |
Fam13b |
G |
A |
18: 34,584,446 (GRCm39) |
R573C |
probably damaging |
Het |
Fgfr2 |
A |
T |
7: 129,798,002 (GRCm39) |
I415N |
possibly damaging |
Het |
Gm32742 |
T |
A |
9: 51,067,230 (GRCm39) |
M366L |
probably benign |
Het |
Gm49336 |
A |
T |
14: 60,457,515 (GRCm39) |
S563T |
possibly damaging |
Het |
Gm5475 |
T |
C |
15: 100,324,892 (GRCm39) |
F107L |
unknown |
Het |
Lamp3 |
T |
C |
16: 19,474,252 (GRCm39) |
D374G |
probably damaging |
Het |
Lin9 |
T |
C |
1: 180,496,450 (GRCm39) |
|
probably null |
Het |
Mef2d |
T |
C |
3: 88,074,956 (GRCm39) |
S381P |
probably benign |
Het |
Mpo |
A |
G |
11: 87,693,538 (GRCm39) |
I639V |
possibly damaging |
Het |
Mrgprh |
T |
C |
17: 13,096,375 (GRCm39) |
I205T |
probably benign |
Het |
Ncapd2 |
T |
C |
6: 125,154,476 (GRCm39) |
D580G |
probably benign |
Het |
Nkain4 |
T |
A |
2: 180,585,920 (GRCm39) |
I48F |
probably damaging |
Het |
Notch4 |
C |
A |
17: 34,806,579 (GRCm39) |
R1839S |
probably damaging |
Het |
Nr6a1 |
A |
G |
2: 38,650,244 (GRCm39) |
Y129H |
probably damaging |
Het |
Nras |
T |
C |
3: 102,966,176 (GRCm39) |
|
probably benign |
Het |
Or7g19 |
T |
A |
9: 18,856,286 (GRCm39) |
I114N |
possibly damaging |
Het |
Robo1 |
G |
T |
16: 72,821,141 (GRCm39) |
E1294* |
probably null |
Het |
Septin8 |
A |
G |
11: 53,428,343 (GRCm39) |
K331R |
probably benign |
Het |
Shmt2 |
A |
G |
10: 127,356,785 (GRCm39) |
|
probably null |
Het |
Skint6 |
A |
C |
4: 112,661,885 (GRCm39) |
L1233R |
possibly damaging |
Het |
Slc41a3 |
A |
T |
6: 90,621,165 (GRCm39) |
T402S |
probably benign |
Het |
Slc9a2 |
A |
G |
1: 40,781,889 (GRCm39) |
T373A |
probably damaging |
Het |
Spata31d1b |
T |
C |
13: 59,863,283 (GRCm39) |
C144R |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,181,783 (GRCm39) |
V4184A |
possibly damaging |
Het |
Tenm4 |
G |
A |
7: 96,544,239 (GRCm39) |
R2122H |
probably damaging |
Het |
Tlnrd1 |
A |
T |
7: 83,532,316 (GRCm39) |
D38E |
probably benign |
Het |
Tnnc2 |
C |
T |
2: 164,620,135 (GRCm39) |
A6T |
probably benign |
Het |
Usp9y |
A |
G |
Y: 1,356,320 (GRCm39) |
V1127A |
probably benign |
Het |
Ylpm1 |
T |
C |
12: 85,077,195 (GRCm39) |
Y1307H |
probably damaging |
Het |
Zfp266 |
T |
C |
9: 20,411,509 (GRCm39) |
S223G |
probably benign |
Het |
|
Other mutations in Mfsd9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00946:Mfsd9
|
APN |
1 |
40,812,940 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01453:Mfsd9
|
APN |
1 |
40,829,638 (GRCm39) |
splice site |
probably benign |
|
R0631:Mfsd9
|
UTSW |
1 |
40,829,634 (GRCm39) |
splice site |
probably benign |
|
R1644:Mfsd9
|
UTSW |
1 |
40,812,958 (GRCm39) |
missense |
probably benign |
0.39 |
R4204:Mfsd9
|
UTSW |
1 |
40,820,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R4761:Mfsd9
|
UTSW |
1 |
40,813,635 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4777:Mfsd9
|
UTSW |
1 |
40,820,700 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5109:Mfsd9
|
UTSW |
1 |
40,813,365 (GRCm39) |
missense |
probably damaging |
0.98 |
R6712:Mfsd9
|
UTSW |
1 |
40,825,601 (GRCm39) |
splice site |
probably null |
|
R8776-TAIL:Mfsd9
|
UTSW |
1 |
40,812,915 (GRCm39) |
makesense |
probably null |
|
R8839:Mfsd9
|
UTSW |
1 |
40,813,554 (GRCm39) |
missense |
probably benign |
|
R9411:Mfsd9
|
UTSW |
1 |
40,829,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R9478:Mfsd9
|
UTSW |
1 |
40,812,941 (GRCm39) |
missense |
probably benign |
0.00 |
R9499:Mfsd9
|
UTSW |
1 |
40,813,152 (GRCm39) |
missense |
probably damaging |
0.96 |
R9551:Mfsd9
|
UTSW |
1 |
40,813,152 (GRCm39) |
missense |
probably damaging |
0.96 |
|