Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
C |
A |
10: 76,290,536 (GRCm39) |
|
probably benign |
Het |
Acot10 |
G |
A |
15: 20,665,868 (GRCm39) |
T291I |
probably benign |
Het |
Adam34l |
T |
G |
8: 44,080,125 (GRCm39) |
H33P |
possibly damaging |
Het |
Atp13a3 |
A |
G |
16: 30,157,439 (GRCm39) |
|
probably null |
Het |
Atp2a1 |
C |
T |
7: 126,049,399 (GRCm39) |
V548M |
possibly damaging |
Het |
Bsn |
G |
A |
9: 107,992,812 (GRCm39) |
S980L |
probably damaging |
Het |
Ccdc158 |
A |
G |
5: 92,797,865 (GRCm39) |
M425T |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,147,143 (GRCm39) |
L2733S |
probably damaging |
Het |
Chd3 |
C |
T |
11: 69,251,874 (GRCm39) |
|
probably null |
Het |
Cimap1d |
T |
C |
10: 79,475,811 (GRCm39) |
N251S |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,260,448 (GRCm39) |
|
probably benign |
Het |
Elfn2 |
T |
C |
15: 78,556,082 (GRCm39) |
K822E |
probably damaging |
Het |
Eps15l1 |
G |
A |
8: 73,112,240 (GRCm39) |
S764L |
probably benign |
Het |
Etl4 |
C |
A |
2: 20,806,348 (GRCm39) |
|
probably benign |
Het |
Faap24 |
C |
A |
7: 35,092,376 (GRCm39) |
K180N |
probably damaging |
Het |
Fhod1 |
G |
A |
8: 106,057,862 (GRCm39) |
R888W |
probably damaging |
Het |
Fus |
T |
C |
7: 127,581,009 (GRCm39) |
|
probably benign |
Het |
Gm3453 |
T |
C |
14: 5,976,168 (GRCm38) |
E201G |
possibly damaging |
Het |
Gnpat |
G |
T |
8: 125,597,644 (GRCm39) |
D69Y |
probably benign |
Het |
Gpaa1 |
T |
A |
15: 76,217,019 (GRCm39) |
|
probably benign |
Het |
Gsta1 |
A |
T |
9: 78,149,819 (GRCm39) |
K211* |
probably null |
Het |
Lct |
G |
T |
1: 128,227,948 (GRCm39) |
Q1182K |
probably damaging |
Het |
Mroh1 |
T |
C |
15: 76,311,836 (GRCm39) |
L523P |
probably damaging |
Het |
Mrpl46 |
A |
G |
7: 78,425,200 (GRCm39) |
|
probably benign |
Het |
Mst1r |
G |
T |
9: 107,785,403 (GRCm39) |
V354F |
possibly damaging |
Het |
Myo15b |
A |
G |
11: 115,772,127 (GRCm39) |
D299G |
probably damaging |
Het |
Myo6 |
G |
A |
9: 80,171,516 (GRCm39) |
V506I |
possibly damaging |
Het |
Nadk |
A |
C |
4: 155,671,933 (GRCm39) |
K271Q |
probably benign |
Het |
Nbas |
A |
G |
12: 13,412,542 (GRCm39) |
R954G |
probably benign |
Het |
Nbr1 |
T |
A |
11: 101,462,805 (GRCm39) |
|
probably null |
Het |
Nup88 |
T |
C |
11: 70,835,698 (GRCm39) |
D587G |
possibly damaging |
Het |
Oas1a |
A |
T |
5: 121,043,727 (GRCm39) |
F135Y |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,885,339 (GRCm39) |
|
probably benign |
Het |
Or4k42 |
T |
G |
2: 111,320,465 (GRCm39) |
I13L |
probably benign |
Het |
Parp14 |
G |
A |
16: 35,678,903 (GRCm39) |
T355I |
probably benign |
Het |
Pou5f2 |
T |
C |
13: 78,173,237 (GRCm39) |
S60P |
probably benign |
Het |
Prp2 |
A |
G |
6: 132,576,788 (GRCm39) |
N25S |
unknown |
Het |
Ptprq |
A |
T |
10: 107,503,321 (GRCm39) |
F779Y |
probably benign |
Het |
Rims2 |
C |
T |
15: 39,398,334 (GRCm39) |
R1078C |
probably damaging |
Het |
Rnf38 |
G |
T |
4: 44,129,619 (GRCm39) |
S425* |
probably null |
Het |
Rps21 |
T |
A |
2: 179,899,840 (GRCm39) |
I59N |
probably damaging |
Het |
Scn5a |
A |
T |
9: 119,324,751 (GRCm39) |
F1359Y |
probably damaging |
Het |
Slc35b2 |
A |
G |
17: 45,875,694 (GRCm39) |
E67G |
probably damaging |
Het |
Slc37a2 |
A |
G |
9: 37,166,611 (GRCm39) |
F15L |
probably benign |
Het |
Snapc4 |
A |
C |
2: 26,260,847 (GRCm39) |
N465K |
probably benign |
Het |
Spata31f1a |
C |
T |
4: 42,850,696 (GRCm39) |
E487K |
probably benign |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Taco1 |
A |
G |
11: 105,960,353 (GRCm39) |
N98S |
probably benign |
Het |
Tcea3 |
T |
C |
4: 135,985,299 (GRCm39) |
|
probably null |
Het |
Thada |
T |
C |
17: 84,751,456 (GRCm39) |
S507G |
probably benign |
Het |
Tmem132b |
T |
A |
5: 125,864,611 (GRCm39) |
C906S |
probably damaging |
Het |
Trpm2 |
A |
T |
10: 77,765,112 (GRCm39) |
I963N |
possibly damaging |
Het |
Usp10 |
A |
G |
8: 120,673,825 (GRCm39) |
T397A |
probably benign |
Het |
Usp3 |
G |
A |
9: 66,449,832 (GRCm39) |
R160* |
probably null |
Het |
Utp15 |
T |
C |
13: 98,394,460 (GRCm39) |
Y144C |
probably damaging |
Het |
Xpc |
G |
A |
6: 91,483,831 (GRCm39) |
R172W |
probably damaging |
Het |
|
Other mutations in Pdgfd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00545:Pdgfd
|
APN |
9 |
6,288,621 (GRCm39) |
nonsense |
probably null |
|
IGL00806:Pdgfd
|
APN |
9 |
6,288,667 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01481:Pdgfd
|
APN |
9 |
6,337,271 (GRCm39) |
missense |
probably null |
0.62 |
IGL01704:Pdgfd
|
APN |
9 |
6,337,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03022:Pdgfd
|
APN |
9 |
6,288,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R0122:Pdgfd
|
UTSW |
9 |
6,293,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R0408:Pdgfd
|
UTSW |
9 |
6,293,928 (GRCm39) |
nonsense |
probably null |
|
R0542:Pdgfd
|
UTSW |
9 |
6,359,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Pdgfd
|
UTSW |
9 |
6,359,706 (GRCm39) |
missense |
probably damaging |
0.98 |
R1376:Pdgfd
|
UTSW |
9 |
6,376,994 (GRCm39) |
missense |
probably benign |
0.00 |
R1376:Pdgfd
|
UTSW |
9 |
6,376,994 (GRCm39) |
missense |
probably benign |
0.00 |
R1563:Pdgfd
|
UTSW |
9 |
6,293,939 (GRCm39) |
critical splice donor site |
probably null |
|
R2513:Pdgfd
|
UTSW |
9 |
6,359,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R3751:Pdgfd
|
UTSW |
9 |
6,337,447 (GRCm39) |
splice site |
probably benign |
|
R3831:Pdgfd
|
UTSW |
9 |
6,359,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R3832:Pdgfd
|
UTSW |
9 |
6,359,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R3833:Pdgfd
|
UTSW |
9 |
6,359,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4691:Pdgfd
|
UTSW |
9 |
6,288,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6280:Pdgfd
|
UTSW |
9 |
6,288,627 (GRCm39) |
missense |
probably benign |
0.00 |
R6622:Pdgfd
|
UTSW |
9 |
6,293,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7488:Pdgfd
|
UTSW |
9 |
6,359,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7581:Pdgfd
|
UTSW |
9 |
6,293,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7873:Pdgfd
|
UTSW |
9 |
6,337,271 (GRCm39) |
missense |
probably benign |
0.06 |
R7883:Pdgfd
|
UTSW |
9 |
6,293,939 (GRCm39) |
critical splice donor site |
probably null |
|
R8498:Pdgfd
|
UTSW |
9 |
6,288,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R8788:Pdgfd
|
UTSW |
9 |
6,377,000 (GRCm39) |
missense |
probably benign |
0.00 |
R9147:Pdgfd
|
UTSW |
9 |
6,333,328 (GRCm39) |
missense |
probably benign |
0.09 |
R9148:Pdgfd
|
UTSW |
9 |
6,333,328 (GRCm39) |
missense |
probably benign |
0.09 |
R9386:Pdgfd
|
UTSW |
9 |
6,293,903 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9747:Pdgfd
|
UTSW |
9 |
6,337,310 (GRCm39) |
missense |
probably benign |
0.09 |
RF009:Pdgfd
|
UTSW |
9 |
6,288,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|