Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067P10Rik |
A |
G |
17: 48,400,991 (GRCm39) |
E92G |
probably benign |
Het |
Abca13 |
C |
T |
11: 9,416,429 (GRCm39) |
Q4064* |
probably null |
Het |
Abca14 |
G |
A |
7: 119,815,524 (GRCm39) |
M257I |
probably benign |
Het |
Acsm2 |
T |
A |
7: 119,174,855 (GRCm39) |
C207S |
probably damaging |
Het |
Actr3 |
A |
G |
1: 125,344,018 (GRCm39) |
I67T |
probably benign |
Het |
Adcy7 |
T |
C |
8: 89,046,835 (GRCm39) |
V606A |
probably benign |
Het |
Ahnak2 |
G |
A |
12: 112,751,570 (GRCm39) |
S54F |
probably damaging |
Het |
Ano6 |
T |
C |
15: 95,870,388 (GRCm39) |
S848P |
probably damaging |
Het |
Atg3 |
C |
T |
16: 44,992,123 (GRCm39) |
|
probably benign |
Het |
Atp8b1 |
T |
A |
18: 64,697,597 (GRCm39) |
S416C |
probably damaging |
Het |
C2cd5 |
A |
G |
6: 142,987,072 (GRCm39) |
|
probably benign |
Het |
Capn11 |
A |
T |
17: 45,954,735 (GRCm39) |
V134E |
probably damaging |
Het |
Ccnd3 |
A |
G |
17: 47,909,033 (GRCm39) |
|
probably null |
Het |
Chaf1b |
T |
A |
16: 93,684,998 (GRCm39) |
V149E |
probably damaging |
Het |
Col5a2 |
T |
A |
1: 45,542,074 (GRCm39) |
M1L |
unknown |
Het |
Copa |
T |
C |
1: 171,931,694 (GRCm39) |
I315T |
probably benign |
Het |
Cyp3a57 |
A |
G |
5: 145,318,077 (GRCm39) |
M353V |
probably damaging |
Het |
Dcaf6 |
T |
C |
1: 165,160,942 (GRCm39) |
M828V |
probably damaging |
Het |
Dock2 |
T |
A |
11: 34,232,761 (GRCm39) |
K1080* |
probably null |
Het |
Dock6 |
A |
G |
9: 21,726,038 (GRCm39) |
V1424A |
probably benign |
Het |
Foxp4 |
G |
C |
17: 48,191,278 (GRCm39) |
|
probably benign |
Het |
Galnt9 |
T |
A |
5: 110,736,196 (GRCm39) |
S171T |
probably damaging |
Het |
Glt6d1 |
A |
G |
2: 25,684,260 (GRCm39) |
Y249H |
probably damaging |
Het |
Gm37240 |
A |
T |
3: 84,434,998 (GRCm39) |
Y104N |
probably damaging |
Het |
Gpx8 |
C |
T |
13: 113,182,149 (GRCm39) |
E95K |
possibly damaging |
Het |
Grm1 |
T |
C |
10: 10,565,450 (GRCm39) |
T953A |
probably benign |
Het |
Helz |
T |
C |
11: 107,494,889 (GRCm39) |
|
probably benign |
Het |
Hif3a |
T |
C |
7: 16,788,647 (GRCm39) |
Y108C |
probably damaging |
Het |
Kcnj13 |
A |
T |
1: 87,316,939 (GRCm39) |
L58Q |
probably damaging |
Het |
Mfsd14b |
A |
T |
13: 65,243,485 (GRCm39) |
V53D |
probably damaging |
Het |
Mrps7 |
G |
C |
11: 115,494,952 (GRCm39) |
|
probably benign |
Het |
Mug1 |
G |
A |
6: 121,856,259 (GRCm39) |
G1013D |
probably damaging |
Het |
Or52h7 |
T |
A |
7: 104,214,038 (GRCm39) |
Y203* |
probably null |
Het |
Or6c8 |
A |
T |
10: 128,915,484 (GRCm39) |
M116K |
probably damaging |
Het |
Pax6 |
T |
C |
2: 105,521,955 (GRCm39) |
I19T |
probably benign |
Het |
Pde8b |
G |
A |
13: 95,184,304 (GRCm39) |
R416C |
probably damaging |
Het |
Prl2c2 |
G |
C |
13: 13,176,786 (GRCm39) |
T47R |
probably damaging |
Het |
Pygl |
G |
A |
12: 70,246,504 (GRCm39) |
R348W |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,731,309 (GRCm39) |
D1874V |
probably damaging |
Het |
Shf |
G |
A |
2: 122,199,163 (GRCm39) |
P51S |
probably damaging |
Het |
Sncaip |
T |
C |
18: 53,001,958 (GRCm39) |
S160P |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,133,719 (GRCm39) |
V79A |
probably damaging |
Het |
Sptlc3 |
A |
T |
2: 139,431,480 (GRCm39) |
Y334F |
possibly damaging |
Het |
Supt16 |
A |
G |
14: 52,409,916 (GRCm39) |
Y764H |
probably benign |
Het |
Syne3 |
A |
T |
12: 104,921,841 (GRCm39) |
V438E |
possibly damaging |
Het |
Tagap1 |
T |
C |
17: 7,224,210 (GRCm39) |
D162G |
probably damaging |
Het |
Terb1 |
T |
C |
8: 105,225,122 (GRCm39) |
|
probably benign |
Het |
Themis3 |
C |
A |
17: 66,866,949 (GRCm39) |
R97L |
probably benign |
Het |
Tnk1 |
T |
A |
11: 69,747,372 (GRCm39) |
E86D |
possibly damaging |
Het |
Tnpo3 |
A |
G |
6: 29,557,043 (GRCm39) |
L53P |
probably damaging |
Het |
Trpc6 |
G |
A |
9: 8,658,305 (GRCm39) |
R725K |
probably benign |
Het |
Ttll11 |
T |
G |
2: 35,685,391 (GRCm39) |
T566P |
probably damaging |
Het |
Unc5c |
A |
T |
3: 141,533,310 (GRCm39) |
T779S |
possibly damaging |
Het |
Zfp42 |
A |
G |
8: 43,748,638 (GRCm39) |
C288R |
possibly damaging |
Het |
Zfp763 |
G |
A |
17: 33,240,477 (GRCm39) |
T52I |
probably damaging |
Het |
|
Other mutations in Foxa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00696:Foxa1
|
APN |
12 |
57,589,443 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02371:Foxa1
|
APN |
12 |
57,589,486 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03150:Foxa1
|
APN |
12 |
57,589,082 (GRCm39) |
missense |
probably benign |
0.41 |
PIT4377001:Foxa1
|
UTSW |
12 |
57,589,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1347:Foxa1
|
UTSW |
12 |
57,589,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R1347:Foxa1
|
UTSW |
12 |
57,589,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R1598:Foxa1
|
UTSW |
12 |
57,589,473 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1809:Foxa1
|
UTSW |
12 |
57,589,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Foxa1
|
UTSW |
12 |
57,589,077 (GRCm39) |
missense |
probably benign |
0.00 |
R5667:Foxa1
|
UTSW |
12 |
57,589,081 (GRCm39) |
missense |
probably benign |
0.01 |
R5782:Foxa1
|
UTSW |
12 |
57,589,302 (GRCm39) |
missense |
probably benign |
0.00 |
R6174:Foxa1
|
UTSW |
12 |
57,589,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Foxa1
|
UTSW |
12 |
57,589,396 (GRCm39) |
missense |
probably benign |
0.32 |
R6781:Foxa1
|
UTSW |
12 |
57,590,043 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6995:Foxa1
|
UTSW |
12 |
57,589,264 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Foxa1
|
UTSW |
12 |
57,590,077 (GRCm39) |
missense |
probably benign |
0.03 |
R7864:Foxa1
|
UTSW |
12 |
57,589,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R8257:Foxa1
|
UTSW |
12 |
57,589,932 (GRCm39) |
missense |
probably benign |
0.22 |
R8464:Foxa1
|
UTSW |
12 |
57,589,246 (GRCm39) |
missense |
probably benign |
0.00 |
X0020:Foxa1
|
UTSW |
12 |
57,590,098 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Foxa1
|
UTSW |
12 |
57,589,203 (GRCm39) |
missense |
probably benign |
0.09 |
|