Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,207,220 (GRCm39) |
T324A |
probably benign |
Het |
Aadat |
G |
A |
8: 60,979,635 (GRCm39) |
V166I |
probably benign |
Het |
Abca17 |
C |
T |
17: 24,565,207 (GRCm39) |
S75N |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,411,624 (GRCm39) |
T376A |
probably damaging |
Het |
Atp5po |
CTTTGACG |
C |
16: 91,723,804 (GRCm39) |
|
probably null |
Het |
Atp5po |
TTTGACGGT |
TT |
16: 91,723,805 (GRCm39) |
|
probably null |
Het |
Car9 |
A |
G |
4: 43,507,180 (GRCm39) |
E42G |
probably benign |
Het |
Ccdc168 |
A |
G |
1: 44,096,520 (GRCm39) |
V1526A |
probably benign |
Het |
Cep41 |
T |
C |
6: 30,680,345 (GRCm39) |
K9R |
probably null |
Het |
Cfap20dc |
T |
A |
14: 8,518,635 (GRCm38) |
T274S |
probably benign |
Het |
Ckm |
A |
G |
7: 19,149,398 (GRCm39) |
T141A |
probably benign |
Het |
Clcc1 |
G |
T |
3: 108,581,976 (GRCm39) |
R360S |
probably benign |
Het |
Clcn3 |
A |
C |
8: 61,390,503 (GRCm39) |
I146R |
probably damaging |
Het |
Crlf1 |
A |
G |
8: 70,951,466 (GRCm39) |
D115G |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 30,987,970 (GRCm39) |
I3483F |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,406,641 (GRCm39) |
*386Q |
probably null |
Het |
Eftud2 |
A |
G |
11: 102,730,262 (GRCm39) |
V899A |
probably benign |
Het |
Ephx3 |
C |
G |
17: 32,408,290 (GRCm39) |
D45H |
probably benign |
Het |
Faap100 |
A |
G |
11: 120,267,688 (GRCm39) |
S362P |
probably damaging |
Het |
Fdps |
A |
T |
3: 89,006,655 (GRCm39) |
D78E |
probably benign |
Het |
Fsd1l |
T |
G |
4: 53,694,760 (GRCm39) |
W405G |
probably damaging |
Het |
Fsd1l |
T |
C |
4: 53,701,093 (GRCm39) |
V485A |
possibly damaging |
Het |
Gm12887 |
C |
T |
4: 121,473,701 (GRCm39) |
V50M |
probably benign |
Het |
Gm45785 |
T |
C |
7: 140,398,616 (GRCm39) |
I94V |
unknown |
Het |
Hcls1 |
C |
T |
16: 36,777,000 (GRCm39) |
A230V |
probably benign |
Het |
Hmcn1 |
A |
C |
1: 150,522,343 (GRCm39) |
V3519G |
probably benign |
Het |
Hmgcs1 |
A |
G |
13: 120,165,963 (GRCm39) |
Y360C |
probably benign |
Het |
Hsd17b13 |
A |
G |
5: 104,113,639 (GRCm39) |
|
probably null |
Het |
Ift57 |
T |
A |
16: 49,557,085 (GRCm39) |
D235E |
possibly damaging |
Het |
Il22b |
A |
G |
10: 118,130,138 (GRCm39) |
C89R |
probably damaging |
Het |
Iqcn |
G |
A |
8: 71,161,353 (GRCm39) |
G182D |
probably damaging |
Het |
Krt9 |
T |
A |
11: 100,079,547 (GRCm39) |
Y615F |
unknown |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Marco |
T |
C |
1: 120,421,814 (GRCm39) |
E130G |
probably damaging |
Het |
Ms4a18 |
A |
T |
19: 10,988,804 (GRCm39) |
L184Q |
probably damaging |
Het |
Mtus1 |
A |
T |
8: 41,535,923 (GRCm39) |
S598T |
probably damaging |
Het |
Nbeal2 |
C |
A |
9: 110,463,436 (GRCm39) |
R1265L |
probably damaging |
Het |
Odf2 |
G |
T |
2: 29,816,815 (GRCm39) |
G754C |
probably benign |
Het |
Or2m12 |
T |
G |
16: 19,105,100 (GRCm39) |
Y131S |
probably benign |
Het |
Or4x13 |
C |
A |
2: 90,231,917 (GRCm39) |
T304K |
probably benign |
Het |
Or5w11 |
T |
C |
2: 87,459,076 (GRCm39) |
S90P |
probably benign |
Het |
Or6c69b |
A |
T |
10: 129,626,789 (GRCm39) |
I223N |
probably damaging |
Het |
Paqr8 |
G |
A |
1: 21,005,128 (GRCm39) |
W94* |
probably null |
Het |
Pkd1 |
G |
A |
17: 24,813,932 (GRCm39) |
G4132D |
probably damaging |
Het |
Pom121l2 |
A |
G |
13: 22,168,506 (GRCm39) |
M926V |
probably benign |
Het |
Postn |
A |
T |
3: 54,273,336 (GRCm39) |
Y79F |
probably damaging |
Het |
Prl7d1 |
T |
C |
13: 27,893,182 (GRCm39) |
E242G |
probably benign |
Het |
Rcor3 |
G |
T |
1: 191,810,181 (GRCm39) |
H165Q |
possibly damaging |
Het |
Rnf157 |
A |
G |
11: 116,250,718 (GRCm39) |
V161A |
probably damaging |
Het |
Rnf38 |
G |
A |
4: 44,143,584 (GRCm39) |
T150M |
probably damaging |
Het |
Scn4b |
T |
A |
9: 45,058,013 (GRCm39) |
V35E |
probably damaging |
Het |
Serpina3i |
T |
C |
12: 104,231,672 (GRCm39) |
I103T |
probably damaging |
Het |
Shcbp1 |
T |
A |
8: 4,794,518 (GRCm39) |
D425V |
probably damaging |
Het |
Sidt2 |
T |
C |
9: 45,852,658 (GRCm39) |
T776A |
possibly damaging |
Het |
Siglecg |
A |
G |
7: 43,061,856 (GRCm39) |
D534G |
probably benign |
Het |
Sipa1l3 |
T |
A |
7: 29,077,439 (GRCm39) |
T778S |
probably benign |
Het |
Slc13a1 |
A |
G |
6: 24,108,203 (GRCm39) |
V291A |
probably benign |
Het |
Stra6l |
A |
G |
4: 45,881,454 (GRCm39) |
I439V |
probably benign |
Het |
Tdrd7 |
G |
A |
4: 46,005,319 (GRCm39) |
S375N |
probably benign |
Het |
Tut7 |
A |
T |
13: 59,947,798 (GRCm39) |
M841K |
probably benign |
Het |
Vmn1r192 |
T |
A |
13: 22,372,191 (GRCm39) |
I10L |
probably benign |
Het |
Xirp2 |
G |
T |
2: 67,347,322 (GRCm39) |
A3188S |
probably damaging |
Het |
Zfp219 |
A |
G |
14: 52,246,200 (GRCm39) |
V309A |
probably damaging |
Het |
Zfp341 |
C |
A |
2: 154,469,907 (GRCm39) |
P197T |
probably damaging |
Het |
Zfp628 |
G |
A |
7: 4,922,549 (GRCm39) |
R257H |
probably benign |
Het |
Zfp644 |
T |
G |
5: 106,784,324 (GRCm39) |
Y741S |
probably benign |
Het |
|