Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl1 |
T |
A |
7: 76,239,252 (GRCm39) |
F584Y |
probably damaging |
Het |
Amer2 |
C |
A |
14: 60,616,001 (GRCm39) |
D65E |
probably damaging |
Het |
Arhgap28 |
A |
T |
17: 68,159,930 (GRCm39) |
L623Q |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,447,328 (GRCm39) |
T407A |
possibly damaging |
Het |
Cmpk2 |
A |
G |
12: 26,521,442 (GRCm39) |
D238G |
possibly damaging |
Het |
Fam169a |
C |
A |
13: 97,243,497 (GRCm39) |
Q176K |
possibly damaging |
Het |
Fbxo17 |
T |
A |
7: 28,434,782 (GRCm39) |
I189N |
probably damaging |
Het |
Gm5581 |
T |
A |
6: 131,145,044 (GRCm39) |
|
noncoding transcript |
Het |
Gpcpd1 |
C |
T |
2: 132,375,993 (GRCm39) |
|
probably null |
Het |
Lhx2 |
A |
G |
2: 38,244,628 (GRCm39) |
Y123C |
probably damaging |
Het |
Llgl1 |
C |
A |
11: 60,602,180 (GRCm39) |
T741N |
possibly damaging |
Het |
Macc1 |
A |
G |
12: 119,410,603 (GRCm39) |
Q457R |
probably benign |
Het |
Mthfd2l |
A |
G |
5: 91,168,067 (GRCm39) |
T321A |
probably damaging |
Het |
Myo6 |
T |
C |
9: 80,153,837 (GRCm39) |
F271S |
probably damaging |
Het |
Ncoa6 |
A |
G |
2: 155,247,427 (GRCm39) |
V1959A |
probably benign |
Het |
Npsr1 |
A |
G |
9: 24,224,535 (GRCm39) |
D304G |
probably benign |
Het |
Nup205 |
T |
C |
6: 35,185,104 (GRCm39) |
V841A |
probably damaging |
Het |
Or10c1 |
A |
G |
17: 37,522,568 (GRCm39) |
Y59H |
probably damaging |
Het |
Or1j20 |
A |
T |
2: 36,760,537 (GRCm39) |
|
probably benign |
Het |
Osbpl9 |
A |
G |
4: 109,029,529 (GRCm39) |
|
probably benign |
Het |
Ptgs1 |
A |
T |
2: 36,127,717 (GRCm39) |
H92L |
probably damaging |
Het |
Rasd1 |
T |
A |
11: 59,855,181 (GRCm39) |
I100F |
possibly damaging |
Het |
Rbm26 |
T |
C |
14: 105,388,758 (GRCm39) |
T378A |
probably damaging |
Het |
Slc12a3 |
T |
C |
8: 95,078,386 (GRCm39) |
S805P |
possibly damaging |
Het |
Smarcal1 |
G |
A |
1: 72,665,625 (GRCm39) |
V708I |
probably benign |
Het |
Strn |
A |
G |
17: 78,974,652 (GRCm39) |
S408P |
probably damaging |
Het |
Suclg1 |
A |
G |
6: 73,247,975 (GRCm39) |
N232S |
probably benign |
Het |
Tmbim1 |
A |
G |
1: 74,332,225 (GRCm39) |
Y101H |
probably damaging |
Het |
Ube3a |
T |
A |
7: 58,935,895 (GRCm39) |
L614Q |
probably damaging |
Het |
Wrn |
A |
G |
8: 33,826,149 (GRCm39) |
L171P |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,737,904 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Pdgfra |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Pdgfra
|
APN |
5 |
75,324,340 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00574:Pdgfra
|
APN |
5 |
75,341,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00906:Pdgfra
|
APN |
5 |
75,340,834 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00964:Pdgfra
|
APN |
5 |
75,335,726 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01467:Pdgfra
|
APN |
5 |
75,346,292 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01485:Pdgfra
|
APN |
5 |
75,324,313 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01556:Pdgfra
|
APN |
5 |
75,338,352 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01949:Pdgfra
|
APN |
5 |
75,331,326 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02066:Pdgfra
|
APN |
5 |
75,331,241 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02271:Pdgfra
|
APN |
5 |
75,348,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Pdgfra
|
APN |
5 |
75,355,618 (GRCm39) |
nonsense |
probably null |
|
IGL02858:Pdgfra
|
APN |
5 |
75,355,635 (GRCm39) |
missense |
probably damaging |
1.00 |
Pony_express
|
UTSW |
5 |
75,349,895 (GRCm39) |
nonsense |
probably null |
|
P0033:Pdgfra
|
UTSW |
5 |
75,353,222 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Pdgfra
|
UTSW |
5 |
75,340,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R0134:Pdgfra
|
UTSW |
5 |
75,327,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Pdgfra
|
UTSW |
5 |
75,324,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Pdgfra
|
UTSW |
5 |
75,328,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0331:Pdgfra
|
UTSW |
5 |
75,355,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R0467:Pdgfra
|
UTSW |
5 |
75,355,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Pdgfra
|
UTSW |
5 |
75,331,434 (GRCm39) |
missense |
probably benign |
0.00 |
R0608:Pdgfra
|
UTSW |
5 |
75,324,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R0765:Pdgfra
|
UTSW |
5 |
75,348,648 (GRCm39) |
unclassified |
probably benign |
|
R1171:Pdgfra
|
UTSW |
5 |
75,334,108 (GRCm39) |
missense |
probably damaging |
0.98 |
R1372:Pdgfra
|
UTSW |
5 |
75,349,924 (GRCm39) |
missense |
probably damaging |
0.96 |
R1530:Pdgfra
|
UTSW |
5 |
75,349,671 (GRCm39) |
splice site |
probably null |
|
R1585:Pdgfra
|
UTSW |
5 |
75,353,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Pdgfra
|
UTSW |
5 |
75,349,681 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1836:Pdgfra
|
UTSW |
5 |
75,343,675 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1868:Pdgfra
|
UTSW |
5 |
75,331,534 (GRCm39) |
missense |
probably benign |
0.43 |
R1923:Pdgfra
|
UTSW |
5 |
75,324,394 (GRCm39) |
missense |
probably benign |
0.03 |
R2075:Pdgfra
|
UTSW |
5 |
75,348,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Pdgfra
|
UTSW |
5 |
75,346,184 (GRCm39) |
missense |
probably benign |
0.03 |
R2262:Pdgfra
|
UTSW |
5 |
75,346,184 (GRCm39) |
missense |
probably benign |
0.03 |
R3028:Pdgfra
|
UTSW |
5 |
75,335,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Pdgfra
|
UTSW |
5 |
75,328,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R3692:Pdgfra
|
UTSW |
5 |
75,349,948 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3701:Pdgfra
|
UTSW |
5 |
75,340,881 (GRCm39) |
nonsense |
probably null |
|
R3890:Pdgfra
|
UTSW |
5 |
75,328,588 (GRCm39) |
missense |
probably null |
0.57 |
R3901:Pdgfra
|
UTSW |
5 |
75,353,169 (GRCm39) |
missense |
probably benign |
0.10 |
R3902:Pdgfra
|
UTSW |
5 |
75,353,169 (GRCm39) |
missense |
probably benign |
0.10 |
R4272:Pdgfra
|
UTSW |
5 |
75,343,731 (GRCm39) |
missense |
probably benign |
0.05 |
R4532:Pdgfra
|
UTSW |
5 |
75,341,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Pdgfra
|
UTSW |
5 |
75,322,932 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4753:Pdgfra
|
UTSW |
5 |
75,342,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Pdgfra
|
UTSW |
5 |
75,349,972 (GRCm39) |
missense |
probably benign |
|
R4796:Pdgfra
|
UTSW |
5 |
75,349,972 (GRCm39) |
missense |
probably benign |
|
R4884:Pdgfra
|
UTSW |
5 |
75,349,973 (GRCm39) |
missense |
probably benign |
0.07 |
R4936:Pdgfra
|
UTSW |
5 |
75,355,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R5625:Pdgfra
|
UTSW |
5 |
75,349,998 (GRCm39) |
critical splice donor site |
probably null |
|
R5666:Pdgfra
|
UTSW |
5 |
75,334,156 (GRCm39) |
missense |
probably benign |
0.00 |
R5670:Pdgfra
|
UTSW |
5 |
75,334,156 (GRCm39) |
missense |
probably benign |
0.00 |
R5714:Pdgfra
|
UTSW |
5 |
75,346,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5836:Pdgfra
|
UTSW |
5 |
75,324,435 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6126:Pdgfra
|
UTSW |
5 |
75,331,190 (GRCm39) |
missense |
probably benign |
0.09 |
R6141:Pdgfra
|
UTSW |
5 |
75,334,057 (GRCm39) |
missense |
probably damaging |
0.98 |
R6297:Pdgfra
|
UTSW |
5 |
75,334,135 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6363:Pdgfra
|
UTSW |
5 |
75,331,497 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6376:Pdgfra
|
UTSW |
5 |
75,327,180 (GRCm39) |
missense |
probably benign |
0.02 |
R6485:Pdgfra
|
UTSW |
5 |
75,335,735 (GRCm39) |
splice site |
probably null |
|
R6612:Pdgfra
|
UTSW |
5 |
75,328,503 (GRCm39) |
missense |
probably benign |
0.01 |
R6641:Pdgfra
|
UTSW |
5 |
75,322,762 (GRCm39) |
intron |
probably benign |
|
R6954:Pdgfra
|
UTSW |
5 |
75,334,055 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7110:Pdgfra
|
UTSW |
5 |
75,349,895 (GRCm39) |
nonsense |
probably null |
|
R7192:Pdgfra
|
UTSW |
5 |
75,343,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Pdgfra
|
UTSW |
5 |
75,342,312 (GRCm39) |
missense |
probably benign |
0.05 |
R7347:Pdgfra
|
UTSW |
5 |
75,343,759 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7476:Pdgfra
|
UTSW |
5 |
75,331,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Pdgfra
|
UTSW |
5 |
75,355,675 (GRCm39) |
nonsense |
probably null |
|
R7609:Pdgfra
|
UTSW |
5 |
75,327,382 (GRCm39) |
missense |
probably benign |
0.10 |
R7925:Pdgfra
|
UTSW |
5 |
75,353,079 (GRCm39) |
splice site |
probably benign |
|
R8141:Pdgfra
|
UTSW |
5 |
75,338,387 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8490:Pdgfra
|
UTSW |
5 |
75,331,329 (GRCm39) |
critical splice donor site |
probably null |
|
R8886:Pdgfra
|
UTSW |
5 |
75,343,734 (GRCm39) |
missense |
probably benign |
0.03 |
R9234:Pdgfra
|
UTSW |
5 |
75,324,262 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9339:Pdgfra
|
UTSW |
5 |
75,355,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9459:Pdgfra
|
UTSW |
5 |
75,353,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Pdgfra
|
UTSW |
5 |
75,328,588 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9519:Pdgfra
|
UTSW |
5 |
75,337,350 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Pdgfra
|
UTSW |
5 |
75,327,238 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Pdgfra
|
UTSW |
5 |
75,342,335 (GRCm39) |
missense |
probably null |
1.00 |
|