Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atg2a |
T |
C |
19: 6,299,959 (GRCm39) |
|
probably null |
Het |
Bfsp1 |
T |
C |
2: 143,704,566 (GRCm39) |
T96A |
probably benign |
Het |
Btnl1 |
A |
G |
17: 34,601,239 (GRCm39) |
E322G |
possibly damaging |
Het |
Cand2 |
T |
C |
6: 115,766,568 (GRCm39) |
V391A |
probably damaging |
Het |
Ccdc169 |
A |
G |
3: 55,078,702 (GRCm39) |
M188V |
probably benign |
Het |
Cngb1 |
T |
C |
8: 95,968,987 (GRCm39) |
I1174V |
probably benign |
Het |
Cpeb4 |
T |
C |
11: 31,822,316 (GRCm39) |
V10A |
possibly damaging |
Het |
Cpt1b |
T |
C |
15: 89,307,942 (GRCm39) |
T206A |
probably benign |
Het |
Dapk3 |
T |
C |
10: 81,025,999 (GRCm39) |
S97P |
probably benign |
Het |
Drc3 |
T |
C |
11: 60,261,404 (GRCm39) |
L185P |
probably damaging |
Het |
Efr3b |
T |
C |
12: 4,042,923 (GRCm39) |
|
probably null |
Het |
Erbb3 |
T |
A |
10: 128,409,088 (GRCm39) |
I742F |
probably damaging |
Het |
Fktn |
A |
G |
4: 53,720,181 (GRCm39) |
Y65C |
probably benign |
Het |
Fstl5 |
G |
A |
3: 76,496,302 (GRCm39) |
G355D |
probably damaging |
Het |
Grm8 |
A |
T |
6: 27,363,115 (GRCm39) |
I800N |
probably damaging |
Het |
Gss |
C |
T |
2: 155,409,773 (GRCm39) |
R221H |
probably benign |
Het |
H2-M10.4 |
A |
T |
17: 36,771,359 (GRCm39) |
V273D |
probably damaging |
Het |
Large1 |
C |
A |
8: 73,774,945 (GRCm39) |
W255L |
possibly damaging |
Het |
Meig1 |
T |
C |
2: 3,410,288 (GRCm39) |
K71E |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,619,396 (GRCm39) |
N1760D |
probably benign |
Het |
Ncapd2 |
A |
T |
6: 125,166,781 (GRCm39) |
N24K |
probably damaging |
Het |
Nphp3 |
A |
C |
9: 103,903,167 (GRCm39) |
S715R |
probably benign |
Het |
Papolg |
T |
G |
11: 23,841,869 (GRCm39) |
H18P |
probably damaging |
Het |
Psd |
T |
C |
19: 46,308,098 (GRCm39) |
H667R |
possibly damaging |
Het |
Rita1 |
C |
T |
5: 120,747,858 (GRCm39) |
A147T |
probably damaging |
Het |
Rtp1 |
T |
C |
16: 23,249,943 (GRCm39) |
S103P |
probably damaging |
Het |
Snx21 |
T |
C |
2: 164,634,310 (GRCm39) |
|
probably benign |
Het |
Tiam1 |
G |
T |
16: 89,596,924 (GRCm39) |
H301N |
probably benign |
Het |
Trcg1 |
A |
T |
9: 57,147,676 (GRCm39) |
I11F |
possibly damaging |
Het |
Trpm6 |
A |
G |
19: 18,831,581 (GRCm39) |
K1482R |
probably benign |
Het |
Tyw1 |
G |
T |
5: 130,295,921 (GRCm39) |
G116V |
probably benign |
Het |
Zfp341 |
T |
C |
2: 154,474,224 (GRCm39) |
C343R |
possibly damaging |
Het |
|
Other mutations in Spmip3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01385:Spmip3
|
APN |
1 |
177,568,640 (GRCm39) |
missense |
probably benign |
|
IGL01542:Spmip3
|
APN |
1 |
177,570,950 (GRCm39) |
missense |
possibly damaging |
0.94 |
N/A:Spmip3
|
UTSW |
1 |
177,561,100 (GRCm39) |
missense |
probably damaging |
0.99 |
R0850:Spmip3
|
UTSW |
1 |
177,568,571 (GRCm39) |
missense |
probably benign |
|
R7739:Spmip3
|
UTSW |
1 |
177,570,828 (GRCm39) |
missense |
probably damaging |
0.97 |
R9426:Spmip3
|
UTSW |
1 |
177,570,834 (GRCm39) |
nonsense |
probably null |
|
R9485:Spmip3
|
UTSW |
1 |
177,580,545 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Spmip3
|
UTSW |
1 |
177,568,583 (GRCm39) |
missense |
possibly damaging |
0.95 |
|