Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
T |
G |
1: 58,373,928 (GRCm39) |
|
probably null |
Het |
Col18a1 |
G |
A |
10: 76,949,146 (GRCm39) |
A122V |
possibly damaging |
Het |
Dnai3 |
A |
T |
3: 145,753,903 (GRCm39) |
I719N |
possibly damaging |
Het |
Dtnb |
T |
A |
12: 3,698,380 (GRCm39) |
H289Q |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 38,944,744 (GRCm39) |
K1212N |
probably damaging |
Het |
Gm10392 |
T |
C |
11: 77,409,294 (GRCm39) |
H44R |
possibly damaging |
Het |
Herc2 |
G |
A |
7: 55,787,562 (GRCm39) |
A1740T |
possibly damaging |
Het |
Knl1 |
A |
C |
2: 118,901,411 (GRCm39) |
E1037D |
probably damaging |
Het |
Lsg1 |
A |
T |
16: 30,390,292 (GRCm39) |
D274E |
probably benign |
Het |
Msantd3 |
A |
G |
4: 48,552,686 (GRCm39) |
K92E |
probably damaging |
Het |
Nap1l4 |
G |
A |
7: 143,077,998 (GRCm39) |
T312I |
probably benign |
Het |
Nlrp3 |
A |
G |
11: 59,456,802 (GRCm39) |
E988G |
probably damaging |
Het |
Or11g2 |
C |
T |
14: 50,856,255 (GRCm39) |
T192I |
probably benign |
Het |
Palm3 |
C |
T |
8: 84,754,941 (GRCm39) |
T151I |
possibly damaging |
Het |
Pde1b |
T |
C |
15: 103,430,484 (GRCm39) |
W144R |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,207,730 (GRCm39) |
L1427P |
probably damaging |
Het |
Rasal1 |
A |
T |
5: 120,804,496 (GRCm39) |
H456L |
possibly damaging |
Het |
Sec16a |
C |
T |
2: 26,320,142 (GRCm39) |
G1432D |
possibly damaging |
Het |
Shc1 |
A |
G |
3: 89,331,917 (GRCm39) |
|
probably null |
Het |
Skint5 |
T |
A |
4: 113,335,156 (GRCm39) |
I1452F |
unknown |
Het |
Slc35b4 |
C |
A |
6: 34,135,476 (GRCm39) |
V279L |
probably benign |
Het |
Snx9 |
T |
C |
17: 5,958,873 (GRCm39) |
V283A |
probably damaging |
Het |
Stra6l |
T |
C |
4: 45,882,728 (GRCm39) |
F480L |
possibly damaging |
Het |
Stt3a |
A |
G |
9: 36,670,041 (GRCm39) |
Y132H |
probably damaging |
Het |
Sv2c |
T |
A |
13: 96,125,649 (GRCm39) |
I363F |
probably damaging |
Het |
Tnfrsf21 |
C |
T |
17: 43,398,820 (GRCm39) |
T642I |
probably damaging |
Het |
Tubgcp2 |
G |
A |
7: 139,584,897 (GRCm39) |
|
probably benign |
Het |
Usp47 |
A |
G |
7: 111,692,132 (GRCm39) |
N845D |
probably benign |
Het |
Wdr20 |
A |
T |
12: 110,759,544 (GRCm39) |
|
probably benign |
Het |
Zfp518b |
A |
G |
5: 38,830,061 (GRCm39) |
V648A |
probably damaging |
Het |
Zfp687 |
A |
T |
3: 94,916,084 (GRCm39) |
S927T |
probably benign |
Het |
|
Other mutations in Ifna1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02630:Ifna1
|
APN |
4 |
88,768,496 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02675:Ifna1
|
APN |
4 |
88,768,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02680:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02681:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02709:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02712:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02721:Ifna1
|
APN |
4 |
88,768,523 (GRCm39) |
missense |
probably benign |
0.01 |
R1630:Ifna1
|
UTSW |
4 |
88,768,566 (GRCm39) |
missense |
probably benign |
0.00 |
R2897:Ifna1
|
UTSW |
4 |
88,768,450 (GRCm39) |
missense |
probably benign |
|
R6150:Ifna1
|
UTSW |
4 |
88,768,349 (GRCm39) |
missense |
probably null |
0.34 |
R8233:Ifna1
|
UTSW |
4 |
88,768,628 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9181:Ifna1
|
UTSW |
4 |
88,768,453 (GRCm39) |
missense |
probably benign |
0.13 |
|