Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
C |
1: 71,298,945 (GRCm39) |
|
probably null |
Het |
Adgra3 |
T |
C |
5: 50,183,128 (GRCm39) |
|
probably benign |
Het |
Anxa7 |
A |
T |
14: 20,510,227 (GRCm39) |
L386M |
probably damaging |
Het |
Ap2b1 |
A |
G |
11: 83,212,793 (GRCm39) |
M58V |
possibly damaging |
Het |
Arfip2 |
A |
G |
7: 105,285,578 (GRCm39) |
L224P |
probably damaging |
Het |
Arhgap20 |
A |
G |
9: 51,750,251 (GRCm39) |
N373S |
possibly damaging |
Het |
Asph |
T |
C |
4: 9,635,918 (GRCm39) |
D73G |
probably damaging |
Het |
Atp1a2 |
T |
A |
1: 172,116,909 (GRCm39) |
E236V |
probably damaging |
Het |
Atp2a1 |
A |
G |
7: 126,057,116 (GRCm39) |
S170P |
probably damaging |
Het |
Atp4a |
C |
G |
7: 30,419,526 (GRCm39) |
R659G |
probably benign |
Het |
B4galnt3 |
C |
T |
6: 120,191,999 (GRCm39) |
R578H |
probably benign |
Het |
Ccdc178 |
C |
A |
18: 21,978,081 (GRCm39) |
|
probably null |
Het |
Ccnh |
T |
A |
13: 85,354,312 (GRCm39) |
M252K |
probably damaging |
Het |
Clec4b2 |
A |
G |
6: 123,181,131 (GRCm39) |
D172G |
probably benign |
Het |
Col1a1 |
A |
G |
11: 94,828,895 (GRCm39) |
E79G |
unknown |
Het |
Csf3r |
A |
G |
4: 125,923,642 (GRCm39) |
N51D |
probably benign |
Het |
Cul7 |
C |
T |
17: 46,974,299 (GRCm39) |
L1489F |
probably damaging |
Het |
Cyp2b13 |
G |
A |
7: 25,786,010 (GRCm39) |
C309Y |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,001,327 (GRCm39) |
|
probably benign |
Het |
Edn1 |
A |
G |
13: 42,458,741 (GRCm39) |
T135A |
probably benign |
Het |
Ephb2 |
A |
G |
4: 136,498,368 (GRCm39) |
I237T |
probably damaging |
Het |
Fam111a |
T |
A |
19: 12,561,444 (GRCm39) |
F12L |
probably benign |
Het |
Gabra6 |
A |
G |
11: 42,205,798 (GRCm39) |
S353P |
probably benign |
Het |
Gm4847 |
T |
C |
1: 166,469,857 (GRCm39) |
D72G |
probably damaging |
Het |
Grhl3 |
A |
G |
4: 135,279,860 (GRCm39) |
I398T |
probably damaging |
Het |
Gtdc1 |
T |
C |
2: 44,455,550 (GRCm39) |
|
probably benign |
Het |
Kel |
A |
C |
6: 41,678,998 (GRCm39) |
|
probably benign |
Het |
L3mbtl3 |
C |
T |
10: 26,189,768 (GRCm39) |
D499N |
unknown |
Het |
Lama1 |
T |
A |
17: 68,105,508 (GRCm39) |
|
probably benign |
Het |
Mamdc2 |
T |
A |
19: 23,288,223 (GRCm39) |
E605V |
probably benign |
Het |
Nolc1 |
G |
A |
19: 46,069,817 (GRCm39) |
|
probably benign |
Het |
Nudt12 |
A |
T |
17: 59,314,634 (GRCm39) |
S317T |
possibly damaging |
Het |
Optn |
C |
T |
2: 5,028,926 (GRCm39) |
G526R |
probably damaging |
Het |
Or4k35 |
A |
T |
2: 111,100,659 (GRCm39) |
C18S |
probably benign |
Het |
Or5w20 |
A |
G |
2: 87,727,434 (GRCm39) |
K297R |
possibly damaging |
Het |
Or8g23 |
T |
A |
9: 38,971,056 (GRCm39) |
K302M |
probably damaging |
Het |
Or8k38 |
A |
G |
2: 86,488,163 (GRCm39) |
V213A |
probably benign |
Het |
Pbld1 |
C |
T |
10: 62,907,282 (GRCm39) |
|
probably benign |
Het |
Prl8a9 |
T |
G |
13: 27,744,589 (GRCm39) |
N84T |
probably benign |
Het |
Psph |
T |
A |
5: 129,868,633 (GRCm39) |
|
probably benign |
Het |
Sbf2 |
A |
G |
7: 110,088,426 (GRCm39) |
|
probably null |
Het |
Senp6 |
A |
G |
9: 80,023,952 (GRCm39) |
D405G |
probably benign |
Het |
Serpinb1a |
T |
A |
13: 33,032,754 (GRCm39) |
|
probably benign |
Het |
Slc2a9 |
T |
C |
5: 38,556,086 (GRCm39) |
I287V |
probably benign |
Het |
Sptbn2 |
T |
C |
19: 4,795,321 (GRCm39) |
F1593S |
probably damaging |
Het |
Tcf21 |
T |
C |
10: 22,695,706 (GRCm39) |
T33A |
probably benign |
Het |
Tdrd3 |
A |
T |
14: 87,776,915 (GRCm39) |
Q727L |
probably damaging |
Het |
Tecpr1 |
C |
T |
5: 144,147,017 (GRCm39) |
E450K |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,795,694 (GRCm39) |
T532I |
probably damaging |
Het |
Tg |
A |
T |
15: 66,612,630 (GRCm39) |
Q396L |
probably benign |
Het |
Tmtc3 |
A |
G |
10: 100,294,770 (GRCm39) |
|
probably benign |
Het |
Twnk |
T |
C |
19: 44,997,704 (GRCm39) |
|
probably benign |
Het |
Ubac1 |
A |
G |
2: 25,898,871 (GRCm39) |
|
probably null |
Het |
Ubn2 |
T |
C |
6: 38,429,793 (GRCm39) |
|
probably benign |
Het |
Zfp944 |
T |
A |
17: 22,558,249 (GRCm39) |
T333S |
possibly damaging |
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 |
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 |
R5258: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 |
|