Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
G |
A |
16: 16,936,196 (GRCm39) |
P176L |
probably damaging |
Het |
4932414N04Rik |
A |
G |
2: 68,561,467 (GRCm39) |
M265V |
probably benign |
Het |
A2ml1 |
T |
C |
6: 128,524,173 (GRCm39) |
E1153G |
possibly damaging |
Het |
Adam22 |
T |
C |
5: 8,184,845 (GRCm39) |
T452A |
probably benign |
Het |
Ambra1 |
A |
G |
2: 91,597,432 (GRCm39) |
T56A |
possibly damaging |
Het |
Atp1a4 |
A |
G |
1: 172,062,103 (GRCm39) |
V674A |
possibly damaging |
Het |
Ccnb1 |
A |
T |
13: 100,919,994 (GRCm39) |
Y172* |
probably null |
Het |
Chrdl2 |
A |
T |
7: 99,683,821 (GRCm39) |
T416S |
possibly damaging |
Het |
Col6a5 |
A |
G |
9: 105,805,621 (GRCm39) |
L1095P |
unknown |
Het |
Dhx16 |
T |
C |
17: 36,200,361 (GRCm39) |
C901R |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,656,371 (GRCm39) |
T732A |
probably benign |
Het |
Dnah12 |
A |
C |
14: 26,495,069 (GRCm39) |
I1376L |
probably damaging |
Het |
Dock2 |
A |
T |
11: 34,217,949 (GRCm39) |
L1207Q |
probably damaging |
Het |
Eif2ak1 |
A |
T |
5: 143,816,278 (GRCm39) |
H192L |
probably benign |
Het |
Evi5 |
T |
A |
5: 107,969,750 (GRCm39) |
T54S |
probably benign |
Het |
Fam151a |
T |
C |
4: 106,592,795 (GRCm39) |
|
probably null |
Het |
Fam98a |
C |
T |
17: 75,847,187 (GRCm39) |
|
probably null |
Het |
Frmd4a |
G |
A |
2: 4,570,988 (GRCm39) |
R306K |
probably damaging |
Het |
Fxyd7 |
C |
A |
7: 30,744,432 (GRCm39) |
V28L |
possibly damaging |
Het |
Gabrb1 |
T |
A |
5: 72,294,073 (GRCm39) |
I449K |
probably damaging |
Het |
Gkn3 |
G |
T |
6: 87,360,493 (GRCm39) |
D167E |
possibly damaging |
Het |
Gm14496 |
A |
T |
2: 181,638,144 (GRCm39) |
Y406F |
probably damaging |
Het |
Gm8603 |
T |
A |
17: 13,737,073 (GRCm39) |
|
noncoding transcript |
Het |
Hecw1 |
T |
C |
13: 14,438,743 (GRCm39) |
N880S |
possibly damaging |
Het |
Hivep2 |
C |
A |
10: 14,003,548 (GRCm39) |
Q49K |
possibly damaging |
Het |
Hscb |
T |
A |
5: 110,987,492 (GRCm39) |
S35C |
probably damaging |
Het |
Hspa12a |
T |
G |
19: 58,793,113 (GRCm39) |
K357N |
probably benign |
Het |
Kcnu1 |
A |
T |
8: 26,427,588 (GRCm39) |
I302F |
probably damaging |
Het |
Krtap5-3 |
T |
A |
7: 141,756,215 (GRCm39) |
C351S |
unknown |
Het |
Mvd |
A |
G |
8: 123,164,747 (GRCm39) |
V142A |
probably benign |
Het |
Myo1f |
A |
T |
17: 33,797,246 (GRCm39) |
I143L |
probably benign |
Het |
Ncoa7 |
T |
A |
10: 30,565,849 (GRCm39) |
E599D |
possibly damaging |
Het |
Nfasc |
A |
T |
1: 132,538,104 (GRCm39) |
C495* |
probably null |
Het |
Nfx1 |
G |
A |
4: 41,018,019 (GRCm39) |
G920E |
probably damaging |
Het |
Nlrp4g |
T |
G |
9: 124,348,980 (GRCm38) |
|
noncoding transcript |
Het |
Nup85 |
T |
A |
11: 115,468,757 (GRCm39) |
V200E |
probably damaging |
Het |
Or2z2 |
T |
A |
11: 58,345,906 (GRCm39) |
I290F |
probably damaging |
Het |
Or5an1c |
T |
C |
19: 12,218,120 (GRCm39) |
M302V |
probably benign |
Het |
Pask |
T |
C |
1: 93,238,606 (GRCm39) |
Q1293R |
possibly damaging |
Het |
Ppfia2 |
T |
A |
10: 106,636,646 (GRCm39) |
S232T |
probably benign |
Het |
Prr12 |
G |
A |
7: 44,695,612 (GRCm39) |
R1285W |
unknown |
Het |
Rimoc1 |
C |
T |
15: 4,015,848 (GRCm39) |
V239I |
probably benign |
Het |
Rxylt1 |
A |
T |
10: 121,930,548 (GRCm39) |
D126E |
probably damaging |
Het |
Slc1a1 |
T |
A |
19: 28,880,153 (GRCm39) |
F278I |
possibly damaging |
Het |
Sos1 |
G |
T |
17: 80,705,719 (GRCm39) |
T1284N |
probably damaging |
Het |
Sp2 |
T |
A |
11: 96,847,036 (GRCm39) |
Q475L |
probably damaging |
Het |
Sspo |
A |
T |
6: 48,444,917 (GRCm39) |
T2134S |
possibly damaging |
Het |
Tbx1 |
C |
A |
16: 18,401,552 (GRCm39) |
A300S |
probably benign |
Het |
Uap1 |
A |
C |
1: 169,994,281 (GRCm39) |
V65G |
probably benign |
Het |
Ubr2 |
G |
A |
17: 47,278,123 (GRCm39) |
T738I |
probably benign |
Het |
Uvrag |
A |
T |
7: 98,758,297 (GRCm39) |
Y81* |
probably null |
Het |
Vmn2r116 |
T |
G |
17: 23,603,907 (GRCm39) |
I44S |
probably benign |
Het |
Xkr8 |
A |
T |
4: 132,455,688 (GRCm39) |
Y228* |
probably null |
Het |
Zbtb20 |
A |
G |
16: 43,430,025 (GRCm39) |
I106V |
possibly damaging |
Het |
Zc3h7a |
C |
T |
16: 10,964,259 (GRCm39) |
S683N |
probably benign |
Het |
Zfp146 |
A |
T |
7: 29,861,905 (GRCm39) |
C46S |
possibly damaging |
Het |
Zfp871 |
T |
C |
17: 32,994,662 (GRCm39) |
E152G |
possibly damaging |
Het |
Zfp90 |
T |
C |
8: 107,146,156 (GRCm39) |
V57A |
probably damaging |
Het |
Zhx3 |
A |
T |
2: 160,621,718 (GRCm39) |
N816K |
probably damaging |
Het |
|
Other mutations in Spmip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01590:Spmip2
|
APN |
3 |
79,356,647 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02152:Spmip2
|
APN |
3 |
79,252,839 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02170:Spmip2
|
APN |
3 |
79,356,741 (GRCm39) |
splice site |
probably benign |
|
IGL02253:Spmip2
|
APN |
3 |
79,356,742 (GRCm39) |
splice site |
probably benign |
|
IGL02253:Spmip2
|
APN |
3 |
79,356,741 (GRCm39) |
splice site |
probably benign |
|
R0139:Spmip2
|
UTSW |
3 |
79,313,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Spmip2
|
UTSW |
3 |
79,313,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Spmip2
|
UTSW |
3 |
79,313,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R6408:Spmip2
|
UTSW |
3 |
79,356,706 (GRCm39) |
missense |
probably benign |
0.34 |
R6767:Spmip2
|
UTSW |
3 |
79,337,330 (GRCm39) |
missense |
probably benign |
0.00 |
R7711:Spmip2
|
UTSW |
3 |
79,313,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8945:Spmip2
|
UTSW |
3 |
79,252,812 (GRCm39) |
missense |
probably benign |
|
R9088:Spmip2
|
UTSW |
3 |
79,337,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Spmip2
|
UTSW |
3 |
79,356,616 (GRCm39) |
missense |
probably benign |
0.00 |
R9656:Spmip2
|
UTSW |
3 |
79,313,183 (GRCm39) |
missense |
probably benign |
0.04 |
R9687:Spmip2
|
UTSW |
3 |
79,337,299 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9707:Spmip2
|
UTSW |
3 |
79,313,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|