Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,385,266 (GRCm39) |
D233V |
probably damaging |
Het |
Abca13 |
A |
T |
11: 9,199,684 (GRCm39) |
T128S |
possibly damaging |
Het |
Abca16 |
T |
G |
7: 120,035,992 (GRCm39) |
|
probably null |
Het |
Abcc8 |
T |
C |
7: 45,757,811 (GRCm39) |
I1313V |
probably benign |
Het |
Abcc8 |
C |
T |
7: 45,806,572 (GRCm39) |
V379I |
probably benign |
Het |
Acp3 |
T |
C |
9: 104,186,674 (GRCm39) |
I266V |
probably benign |
Het |
Asf1b |
C |
T |
8: 84,695,896 (GRCm39) |
T179I |
probably benign |
Het |
B3gnt7 |
A |
G |
1: 86,233,287 (GRCm39) |
K61E |
possibly damaging |
Het |
Card11 |
G |
A |
5: 140,862,180 (GRCm39) |
P1039L |
possibly damaging |
Het |
Cd1d2 |
C |
G |
3: 86,894,954 (GRCm39) |
R147G |
possibly damaging |
Het |
Cfap68 |
T |
C |
9: 50,675,633 (GRCm39) |
|
probably benign |
Het |
Cfap69 |
T |
C |
5: 5,654,271 (GRCm39) |
|
probably null |
Het |
Ddx46 |
T |
C |
13: 55,800,837 (GRCm39) |
F331L |
possibly damaging |
Het |
Dkk4 |
C |
A |
8: 23,117,031 (GRCm39) |
L215I |
probably damaging |
Het |
Dnhd1 |
C |
T |
7: 105,323,244 (GRCm39) |
T584I |
probably benign |
Het |
Dock3 |
T |
C |
9: 106,874,124 (GRCm39) |
Y449C |
probably damaging |
Het |
Gm12887 |
T |
C |
4: 121,472,897 (GRCm39) |
K82E |
probably benign |
Het |
Gm4787 |
G |
C |
12: 81,424,604 (GRCm39) |
T518S |
probably benign |
Het |
Igkv4-80 |
T |
A |
6: 68,993,811 (GRCm39) |
T27S |
probably benign |
Het |
Invs |
A |
G |
4: 48,396,374 (GRCm39) |
D349G |
possibly damaging |
Het |
Lbhd1 |
A |
G |
19: 8,861,453 (GRCm39) |
|
probably benign |
Het |
Lipo3 |
T |
A |
19: 33,591,243 (GRCm39) |
|
probably benign |
Het |
Llgl1 |
G |
C |
11: 60,602,389 (GRCm39) |
|
probably null |
Het |
Lyzl6 |
T |
A |
11: 103,525,899 (GRCm39) |
I74F |
probably damaging |
Het |
Map3k6 |
T |
C |
4: 132,974,953 (GRCm39) |
V662A |
possibly damaging |
Het |
Megf8 |
T |
A |
7: 25,047,751 (GRCm39) |
F1645I |
possibly damaging |
Het |
Mfsd4b2 |
T |
A |
10: 39,798,017 (GRCm39) |
M113L |
probably benign |
Het |
Mib1 |
G |
A |
18: 10,795,856 (GRCm39) |
|
probably null |
Het |
Mrps6 |
T |
A |
16: 91,896,543 (GRCm39) |
V36E |
probably damaging |
Het |
Nhsl1 |
C |
A |
10: 18,400,070 (GRCm39) |
S432* |
probably null |
Het |
Nle1 |
T |
C |
11: 82,795,772 (GRCm39) |
D225G |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,069,622 (GRCm39) |
S508T |
probably benign |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or5d37 |
A |
T |
2: 87,923,762 (GRCm39) |
Y173N |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,819,066 (GRCm39) |
E496G |
probably damaging |
Het |
Prdm16 |
A |
T |
4: 154,451,671 (GRCm39) |
D179E |
possibly damaging |
Het |
Psca |
A |
T |
15: 74,588,240 (GRCm39) |
I56F |
probably damaging |
Het |
Ptprg |
A |
G |
14: 12,142,431 (GRCm38) |
T361A |
probably benign |
Het |
Ptrhd1 |
A |
G |
12: 4,286,481 (GRCm39) |
Y124C |
probably damaging |
Het |
Sesn1 |
C |
T |
10: 41,770,984 (GRCm39) |
P172S |
probably benign |
Het |
Sspo |
T |
C |
6: 48,453,428 (GRCm39) |
V2872A |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,529,824 (GRCm39) |
L2027H |
probably damaging |
Het |
Tas2r114 |
T |
A |
6: 131,666,504 (GRCm39) |
I175F |
probably benign |
Het |
Tex2 |
T |
A |
11: 106,458,585 (GRCm39) |
|
probably benign |
Het |
Tfdp1 |
C |
T |
8: 13,419,529 (GRCm39) |
T86M |
possibly damaging |
Het |
Trav14-1 |
C |
T |
14: 53,791,730 (GRCm39) |
H27Y |
probably benign |
Het |
Trim24 |
A |
T |
6: 37,896,335 (GRCm39) |
Q264L |
probably benign |
Het |
Vmn2r90 |
A |
G |
17: 17,933,114 (GRCm39) |
I225V |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,794,567 (GRCm39) |
T2326A |
possibly damaging |
Het |
Zfp354b |
A |
C |
11: 50,813,917 (GRCm39) |
I336S |
probably benign |
Het |
Zfp407 |
C |
T |
18: 84,334,051 (GRCm39) |
V1761I |
probably damaging |
Het |
Zfp958 |
A |
T |
8: 4,678,456 (GRCm39) |
E160D |
probably benign |
Het |
|
Other mutations in Foxi2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01101:Foxi2
|
APN |
7 |
135,013,736 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02984:Foxi2
|
UTSW |
7 |
135,012,127 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0030:Foxi2
|
UTSW |
7 |
135,013,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R0030:Foxi2
|
UTSW |
7 |
135,013,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R0121:Foxi2
|
UTSW |
7 |
135,013,640 (GRCm39) |
missense |
probably benign |
|
R0830:Foxi2
|
UTSW |
7 |
135,013,459 (GRCm39) |
missense |
probably benign |
|
R2059:Foxi2
|
UTSW |
7 |
135,012,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R3615:Foxi2
|
UTSW |
7 |
135,012,180 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3616:Foxi2
|
UTSW |
7 |
135,012,180 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4021:Foxi2
|
UTSW |
7 |
135,012,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Foxi2
|
UTSW |
7 |
135,012,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Foxi2
|
UTSW |
7 |
135,013,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R5257:Foxi2
|
UTSW |
7 |
135,012,256 (GRCm39) |
missense |
probably benign |
0.19 |
R5561:Foxi2
|
UTSW |
7 |
135,013,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R5611:Foxi2
|
UTSW |
7 |
135,013,433 (GRCm39) |
missense |
probably benign |
0.00 |
R5667:Foxi2
|
UTSW |
7 |
135,012,668 (GRCm39) |
splice site |
probably null |
|
R7492:Foxi2
|
UTSW |
7 |
135,012,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R8726:Foxi2
|
UTSW |
7 |
135,012,133 (GRCm39) |
missense |
probably damaging |
0.98 |
R9205:Foxi2
|
UTSW |
7 |
135,013,525 (GRCm39) |
missense |
probably benign |
|
R9644:Foxi2
|
UTSW |
7 |
135,013,727 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Foxi2
|
UTSW |
7 |
135,013,687 (GRCm39) |
missense |
probably benign |
0.32 |
Z1177:Foxi2
|
UTSW |
7 |
135,012,144 (GRCm39) |
missense |
probably benign |
0.40 |
|