Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931422A03Rik |
A |
G |
2: 103,823,101 (GRCm39) |
C61R |
probably benign |
Het |
4933427D14Rik |
A |
G |
11: 72,080,422 (GRCm39) |
F415L |
probably benign |
Het |
Abcc2 |
G |
A |
19: 43,825,052 (GRCm39) |
G1446D |
possibly damaging |
Het |
Acaca |
A |
T |
11: 84,229,283 (GRCm39) |
E1703D |
possibly damaging |
Het |
Acap3 |
T |
C |
4: 155,990,415 (GRCm39) |
*834Q |
probably null |
Het |
Adam22 |
A |
G |
5: 8,166,554 (GRCm39) |
S726P |
probably benign |
Het |
Adamtsl3 |
T |
C |
7: 82,244,745 (GRCm39) |
|
probably null |
Het |
Adgrg6 |
T |
A |
10: 14,296,188 (GRCm39) |
I1071F |
probably benign |
Het |
Agxt2 |
A |
T |
15: 10,373,825 (GRCm39) |
D77V |
probably benign |
Het |
Ahnak |
C |
A |
19: 8,990,710 (GRCm39) |
S3998* |
probably null |
Het |
Asns |
T |
A |
6: 7,676,085 (GRCm39) |
I462F |
probably damaging |
Het |
Barx2 |
G |
C |
9: 31,824,280 (GRCm39) |
C36W |
probably damaging |
Het |
Bnc2 |
A |
G |
4: 84,211,883 (GRCm39) |
V162A |
possibly damaging |
Het |
Bptf |
A |
G |
11: 107,022,295 (GRCm39) |
S152P |
unknown |
Het |
Brpf3 |
T |
C |
17: 29,029,510 (GRCm39) |
L490P |
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,220,568 (GRCm39) |
D1052G |
probably benign |
Het |
Ccn1 |
T |
A |
3: 145,354,584 (GRCm39) |
N109I |
probably damaging |
Het |
Cdk17 |
A |
G |
10: 93,064,565 (GRCm39) |
H311R |
probably damaging |
Het |
Cenpj |
G |
A |
14: 56,772,975 (GRCm39) |
R1022C |
probably damaging |
Het |
Cog5 |
A |
G |
12: 31,969,703 (GRCm39) |
D741G |
possibly damaging |
Het |
Csmd2 |
T |
A |
4: 128,445,743 (GRCm39) |
|
probably benign |
Het |
Dnah17 |
G |
A |
11: 117,961,283 (GRCm39) |
Q2568* |
probably null |
Het |
Dspp |
A |
G |
5: 104,326,433 (GRCm39) |
D932G |
unknown |
Het |
Dtwd2 |
T |
C |
18: 49,833,385 (GRCm39) |
T223A |
probably damaging |
Het |
Fzd8 |
A |
G |
18: 9,213,686 (GRCm39) |
N256S |
possibly damaging |
Het |
Gm10800 |
AAGAAAACTGAAAATCAT |
A |
2: 98,497,379 (GRCm39) |
|
probably benign |
Het |
Gm9936 |
T |
C |
5: 114,995,515 (GRCm39) |
Y34C |
unknown |
Het |
Gstcd |
T |
A |
3: 132,777,822 (GRCm39) |
K330* |
probably null |
Het |
Igf2bp1 |
A |
G |
11: 95,861,606 (GRCm39) |
V277A |
possibly damaging |
Het |
Kidins220 |
G |
A |
12: 25,051,593 (GRCm39) |
V332I |
probably benign |
Het |
Kif24 |
T |
C |
4: 41,394,233 (GRCm39) |
H1014R |
probably benign |
Het |
Lrrc43 |
T |
C |
5: 123,646,142 (GRCm39) |
Y639H |
possibly damaging |
Het |
Med22 |
T |
C |
2: 26,800,313 (GRCm39) |
T39A |
probably benign |
Het |
Morn3 |
T |
C |
5: 123,179,177 (GRCm39) |
Y91C |
probably damaging |
Het |
Myo1a |
T |
C |
10: 127,542,707 (GRCm39) |
M115T |
probably damaging |
Het |
Or1e32 |
T |
A |
11: 73,705,882 (GRCm39) |
I9F |
probably benign |
Het |
Or52n2b |
C |
T |
7: 104,565,708 (GRCm39) |
R265H |
probably benign |
Het |
Pdcl |
T |
C |
2: 37,247,317 (GRCm39) |
D24G |
probably benign |
Het |
Pde10a |
G |
A |
17: 9,163,772 (GRCm39) |
C250Y |
probably benign |
Het |
Pla2g10 |
A |
T |
16: 13,548,254 (GRCm39) |
L8M |
unknown |
Het |
Plch2 |
A |
T |
4: 155,069,860 (GRCm39) |
|
probably benign |
Het |
Ppp1r42 |
T |
C |
1: 10,055,894 (GRCm39) |
K198R |
probably benign |
Het |
Prlh |
G |
T |
1: 90,880,897 (GRCm39) |
R23L |
possibly damaging |
Het |
Ranbp2 |
C |
A |
10: 58,312,049 (GRCm39) |
T923K |
probably damaging |
Het |
Rps11 |
T |
C |
7: 44,772,616 (GRCm39) |
N65S |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,603,116 (GRCm39) |
T2463A |
probably benign |
Het |
Shank2 |
C |
T |
7: 143,729,485 (GRCm39) |
|
probably benign |
Het |
Slc12a1 |
T |
A |
2: 125,002,518 (GRCm39) |
V166E |
probably damaging |
Het |
Slc6a9 |
C |
T |
4: 117,714,452 (GRCm39) |
R97C |
unknown |
Het |
Slpi |
A |
C |
2: 164,197,975 (GRCm39) |
M1R |
probably null |
Het |
Syne2 |
T |
A |
12: 75,972,095 (GRCm39) |
V994D |
probably benign |
Het |
Tacc3 |
T |
C |
5: 33,825,553 (GRCm39) |
Y435H |
probably damaging |
Het |
Tpgs2 |
T |
A |
18: 25,274,679 (GRCm39) |
Q132L |
probably benign |
Het |
Usp13 |
T |
A |
3: 32,956,114 (GRCm39) |
I462N |
probably benign |
Het |
Zfp281 |
C |
T |
1: 136,553,334 (GRCm39) |
A104V |
probably benign |
Het |
Zfp40 |
A |
G |
17: 23,395,157 (GRCm39) |
C477R |
probably damaging |
Het |
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