Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
C |
T |
11: 9,238,529 (GRCm39) |
T709I |
possibly damaging |
Het |
Acte1 |
T |
A |
7: 143,447,910 (GRCm39) |
M251K |
possibly damaging |
Het |
Arhgef1 |
T |
A |
7: 24,612,854 (GRCm39) |
Y185* |
probably null |
Het |
Atxn7l1 |
T |
C |
12: 33,392,077 (GRCm39) |
S218P |
probably benign |
Het |
Cd200r2 |
T |
A |
16: 44,729,723 (GRCm39) |
L126Q |
probably damaging |
Het |
Cdc6 |
T |
A |
11: 98,811,641 (GRCm39) |
|
probably null |
Het |
Cenph |
T |
C |
13: 100,898,381 (GRCm39) |
N174S |
probably benign |
Het |
Cep192 |
A |
G |
18: 67,936,207 (GRCm39) |
R49G |
possibly damaging |
Het |
Edrf1 |
A |
G |
7: 133,258,699 (GRCm39) |
T692A |
probably benign |
Het |
Frem2 |
A |
T |
3: 53,562,220 (GRCm39) |
H762Q |
probably benign |
Het |
Gli2 |
T |
C |
1: 118,764,596 (GRCm39) |
D1185G |
probably damaging |
Het |
Hsd3b2 |
T |
A |
3: 98,619,183 (GRCm39) |
Y254F |
possibly damaging |
Het |
Itgal |
C |
A |
7: 126,929,351 (GRCm39) |
Y1089* |
probably null |
Het |
Klf11 |
T |
G |
12: 24,703,631 (GRCm39) |
V22G |
probably benign |
Het |
Morc3 |
T |
C |
16: 93,667,749 (GRCm39) |
V636A |
probably benign |
Het |
Nin |
T |
A |
12: 70,102,210 (GRCm39) |
D330V |
probably damaging |
Het |
Nlrp4a |
G |
T |
7: 26,148,703 (GRCm39) |
K103N |
possibly damaging |
Het |
Ntsr2 |
T |
A |
12: 16,703,661 (GRCm39) |
V54E |
probably damaging |
Het |
Or7g27 |
C |
A |
9: 19,250,545 (GRCm39) |
A263E |
probably benign |
Het |
Prr19 |
T |
C |
7: 25,003,462 (GRCm39) |
S359P |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,745,274 (GRCm39) |
K2040E |
probably damaging |
Het |
Ryr2 |
C |
A |
13: 11,762,544 (GRCm39) |
|
probably benign |
Het |
Sema4a |
G |
T |
3: 88,357,050 (GRCm39) |
A307E |
probably damaging |
Het |
Setd5 |
T |
A |
6: 113,127,976 (GRCm39) |
S1310T |
probably benign |
Het |
Tph1 |
A |
T |
7: 46,303,185 (GRCm39) |
D264E |
probably benign |
Het |
Zc3h6 |
T |
C |
2: 128,858,501 (GRCm39) |
L844P |
probably damaging |
Het |
|
Other mutations in Pdha2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01064:Pdha2
|
APN |
3 |
140,916,776 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02037:Pdha2
|
APN |
3 |
140,916,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0352:Pdha2
|
UTSW |
3 |
140,917,457 (GRCm39) |
missense |
probably benign |
|
R1164:Pdha2
|
UTSW |
3 |
140,917,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Pdha2
|
UTSW |
3 |
140,916,960 (GRCm39) |
nonsense |
probably null |
|
R3826:Pdha2
|
UTSW |
3 |
140,916,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6002:Pdha2
|
UTSW |
3 |
140,917,457 (GRCm39) |
missense |
probably benign |
|
R8169:Pdha2
|
UTSW |
3 |
140,917,155 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8672:Pdha2
|
UTSW |
3 |
140,917,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Pdha2
|
UTSW |
3 |
140,917,649 (GRCm39) |
start gained |
probably benign |
|
R9141:Pdha2
|
UTSW |
3 |
140,917,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R9322:Pdha2
|
UTSW |
3 |
140,916,550 (GRCm39) |
missense |
probably benign |
0.00 |
|