Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts8 |
G |
T |
9: 30,854,611 (GRCm39) |
R160L |
probably benign |
Het |
Atp11b |
T |
C |
3: 35,895,185 (GRCm39) |
S908P |
probably benign |
Het |
AW146154 |
C |
T |
7: 41,130,621 (GRCm39) |
G165D |
possibly damaging |
Het |
AW146154 |
C |
A |
7: 41,130,622 (GRCm39) |
G165C |
probably damaging |
Het |
Cachd1 |
G |
A |
4: 100,845,361 (GRCm39) |
G951D |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,435,683 (GRCm39) |
N250D |
probably benign |
Het |
Coch |
G |
C |
12: 51,650,031 (GRCm39) |
G340A |
possibly damaging |
Het |
Col18a1 |
A |
G |
10: 76,924,741 (GRCm39) |
V226A |
unknown |
Het |
Crocc2 |
G |
A |
1: 93,130,578 (GRCm39) |
R953Q |
possibly damaging |
Het |
Dgkh |
A |
T |
14: 78,824,558 (GRCm39) |
|
probably null |
Het |
Disp2 |
C |
T |
2: 118,617,452 (GRCm39) |
L149F |
possibly damaging |
Het |
Dpt |
T |
C |
1: 164,650,756 (GRCm39) |
F186S |
probably damaging |
Het |
Eif3l |
T |
G |
15: 78,961,066 (GRCm39) |
Y40D |
probably damaging |
Het |
Epha3 |
A |
C |
16: 63,403,873 (GRCm39) |
Y743D |
probably damaging |
Het |
Ercc6l2 |
A |
T |
13: 63,992,367 (GRCm39) |
Y272F |
probably benign |
Het |
Exoc2 |
G |
A |
13: 31,124,686 (GRCm39) |
L9F |
probably damaging |
Het |
Fkbp9 |
A |
G |
6: 56,833,289 (GRCm39) |
T259A |
probably benign |
Het |
Gm5622 |
A |
T |
14: 51,895,201 (GRCm39) |
K120M |
probably damaging |
Het |
Hectd1 |
A |
T |
12: 51,795,679 (GRCm39) |
F2250Y |
probably damaging |
Het |
Herc2 |
A |
G |
7: 55,879,427 (GRCm39) |
I4682V |
probably benign |
Het |
Kctd1 |
T |
A |
18: 15,140,901 (GRCm39) |
I610F |
possibly damaging |
Het |
Kif5a |
A |
T |
10: 127,075,178 (GRCm39) |
D478E |
probably benign |
Het |
Klf13 |
G |
T |
7: 63,541,497 (GRCm39) |
A210E |
probably damaging |
Het |
Klhl20 |
C |
A |
1: 160,921,354 (GRCm39) |
G543C |
probably damaging |
Het |
Krt78 |
T |
C |
15: 101,855,715 (GRCm39) |
T699A |
possibly damaging |
Het |
Lgr5 |
A |
T |
10: 115,311,102 (GRCm39) |
D231E |
probably benign |
Het |
Lonrf1 |
C |
A |
8: 36,715,769 (GRCm39) |
G289W |
probably damaging |
Het |
Lyst |
T |
C |
13: 13,808,894 (GRCm39) |
L188P |
probably damaging |
Het |
Mab21l2 |
T |
C |
3: 86,455,393 (GRCm39) |
|
probably benign |
Het |
Macf1 |
A |
G |
4: 123,303,875 (GRCm39) |
V209A |
possibly damaging |
Het |
Mctp1 |
A |
C |
13: 76,972,972 (GRCm39) |
R658S |
probably benign |
Het |
Mdfi |
T |
C |
17: 48,127,042 (GRCm39) |
T178A |
probably damaging |
Het |
Msln |
T |
A |
17: 25,971,942 (GRCm39) |
K92* |
probably null |
Het |
Msx3 |
T |
C |
7: 139,627,998 (GRCm39) |
H113R |
unknown |
Het |
Muc6 |
T |
A |
7: 141,226,729 (GRCm39) |
T1433S |
unknown |
Het |
Musk |
T |
A |
4: 58,373,110 (GRCm39) |
S693R |
probably benign |
Het |
Myh13 |
A |
G |
11: 67,225,613 (GRCm39) |
K296R |
probably benign |
Het |
Mylip |
A |
T |
13: 45,563,928 (GRCm39) |
H427L |
possibly damaging |
Het |
Nradd |
G |
T |
9: 110,451,179 (GRCm39) |
T63K |
possibly damaging |
Het |
Ntaq1 |
T |
G |
15: 58,015,983 (GRCm39) |
|
probably null |
Het |
Or5h17 |
A |
G |
16: 58,820,432 (GRCm39) |
N128S |
probably benign |
Het |
Or5p66 |
G |
T |
7: 107,885,620 (GRCm39) |
Q238K |
probably benign |
Het |
Osbp2 |
A |
G |
11: 3,662,521 (GRCm39) |
L187P |
probably damaging |
Het |
Oxct1 |
A |
G |
15: 4,158,350 (GRCm39) |
D428G |
probably damaging |
Het |
Oxsm |
G |
T |
14: 16,242,439 (GRCm38) |
S110* |
probably null |
Het |
Pard6a |
A |
G |
8: 106,429,642 (GRCm39) |
Q230R |
probably damaging |
Het |
Pkhd1 |
C |
A |
1: 20,683,639 (GRCm39) |
W38L |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,905,384 (GRCm39) |
N1093D |
probably damaging |
Het |
Rttn |
C |
T |
18: 89,071,672 (GRCm39) |
Q1240* |
probably null |
Het |
Serpina1d |
T |
C |
12: 103,730,087 (GRCm39) |
E365G |
probably damaging |
Het |
Sis |
A |
T |
3: 72,814,462 (GRCm39) |
H1589Q |
probably damaging |
Het |
Slc40a1 |
A |
T |
1: 45,957,528 (GRCm39) |
I152N |
probably damaging |
Het |
Slc44a5 |
C |
T |
3: 153,928,414 (GRCm39) |
P59S |
probably damaging |
Het |
Smarca4 |
T |
A |
9: 21,570,108 (GRCm39) |
|
probably null |
Het |
Smim33 |
A |
T |
18: 35,861,573 (GRCm39) |
D19V |
probably benign |
Het |
Spag9 |
A |
G |
11: 93,989,870 (GRCm39) |
Y930C |
probably benign |
Het |
Speg |
A |
G |
1: 75,391,997 (GRCm39) |
E1593G |
probably damaging |
Het |
St3gal5 |
G |
T |
6: 72,074,925 (GRCm39) |
A62S |
unknown |
Het |
Stx1a |
T |
C |
5: 135,066,431 (GRCm39) |
|
probably null |
Het |
Syne1 |
T |
A |
10: 5,178,021 (GRCm39) |
I4818F |
possibly damaging |
Het |
Tango6 |
A |
G |
8: 107,447,366 (GRCm39) |
H588R |
probably benign |
Het |
Tapt1 |
T |
C |
5: 44,336,307 (GRCm39) |
Y454C |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,066,753 (GRCm39) |
Y2282H |
probably benign |
Het |
Tle6 |
A |
T |
10: 81,431,792 (GRCm39) |
W151R |
probably damaging |
Het |
Tmem131l |
A |
T |
3: 83,834,438 (GRCm39) |
M715K |
possibly damaging |
Het |
Ubr1 |
T |
A |
2: 120,764,898 (GRCm39) |
R519* |
probably null |
Het |
Usp1 |
A |
T |
4: 98,816,578 (GRCm39) |
N93I |
probably damaging |
Het |
Vmn1r211 |
A |
T |
13: 23,035,953 (GRCm39) |
M238K |
probably damaging |
Het |
Vmn1r238 |
A |
G |
18: 3,123,151 (GRCm39) |
Y88H |
probably damaging |
Het |
Vmn2r62 |
A |
G |
7: 42,437,270 (GRCm39) |
Y405H |
probably damaging |
Het |
Vmn2r78 |
A |
G |
7: 86,603,998 (GRCm39) |
I725M |
probably benign |
Het |
Zfp12 |
C |
T |
5: 143,230,681 (GRCm39) |
T368M |
probably damaging |
Het |
|
Other mutations in Hnf1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01798:Hnf1a
|
APN |
5 |
115,091,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02192:Hnf1a
|
APN |
5 |
115,098,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03053:Hnf1a
|
APN |
5 |
115,108,792 (GRCm39) |
missense |
probably benign |
0.00 |
R0522:Hnf1a
|
UTSW |
5 |
115,088,747 (GRCm39) |
splice site |
probably benign |
|
R0543:Hnf1a
|
UTSW |
5 |
115,088,803 (GRCm39) |
missense |
probably benign |
|
R1498:Hnf1a
|
UTSW |
5 |
115,108,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R1827:Hnf1a
|
UTSW |
5 |
115,098,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Hnf1a
|
UTSW |
5 |
115,108,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R2408:Hnf1a
|
UTSW |
5 |
115,098,070 (GRCm39) |
splice site |
probably null |
|
R2898:Hnf1a
|
UTSW |
5 |
115,098,106 (GRCm39) |
nonsense |
probably null |
|
R4050:Hnf1a
|
UTSW |
5 |
115,108,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Hnf1a
|
UTSW |
5 |
115,093,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4859:Hnf1a
|
UTSW |
5 |
115,093,311 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4873:Hnf1a
|
UTSW |
5 |
115,108,732 (GRCm39) |
missense |
probably benign |
0.00 |
R4875:Hnf1a
|
UTSW |
5 |
115,108,732 (GRCm39) |
missense |
probably benign |
0.00 |
R6488:Hnf1a
|
UTSW |
5 |
115,094,020 (GRCm39) |
missense |
probably benign |
|
R7134:Hnf1a
|
UTSW |
5 |
115,091,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Hnf1a
|
UTSW |
5 |
115,098,233 (GRCm39) |
nonsense |
probably null |
|
R8093:Hnf1a
|
UTSW |
5 |
115,093,336 (GRCm39) |
missense |
probably benign |
|
R8360:Hnf1a
|
UTSW |
5 |
115,091,391 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8539:Hnf1a
|
UTSW |
5 |
115,108,576 (GRCm39) |
critical splice donor site |
probably null |
|
R9047:Hnf1a
|
UTSW |
5 |
115,088,882 (GRCm39) |
missense |
probably benign |
|
X0067:Hnf1a
|
UTSW |
5 |
115,093,539 (GRCm39) |
missense |
possibly damaging |
0.52 |
Z1176:Hnf1a
|
UTSW |
5 |
115,088,183 (GRCm39) |
frame shift |
probably null |
|
|