Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam9 |
A |
T |
8: 25,486,774 (GRCm39) |
I168N |
probably benign |
Het |
Adamts20 |
G |
A |
15: 94,245,571 (GRCm39) |
A577V |
probably benign |
Het |
Agtr1a |
A |
T |
13: 30,565,279 (GRCm39) |
S115C |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,618,692 (GRCm39) |
Y1720C |
probably damaging |
Het |
Ano6 |
A |
T |
15: 95,818,252 (GRCm39) |
T353S |
probably damaging |
Het |
App |
A |
G |
16: 84,876,840 (GRCm39) |
F184L |
probably damaging |
Het |
Arhgef38 |
T |
A |
3: 132,843,232 (GRCm39) |
Y446F |
probably benign |
Het |
Aspg |
T |
A |
12: 112,078,693 (GRCm39) |
Y57* |
probably null |
Het |
Atp1a4 |
G |
A |
1: 172,067,774 (GRCm39) |
|
probably benign |
Het |
Bdp1 |
G |
A |
13: 100,195,459 (GRCm39) |
|
probably benign |
Het |
Bicd2 |
T |
A |
13: 49,531,717 (GRCm39) |
S246T |
possibly damaging |
Het |
Brd10 |
T |
A |
19: 29,695,381 (GRCm39) |
I1438F |
probably benign |
Het |
Bsn |
T |
A |
9: 107,984,011 (GRCm39) |
M3348L |
unknown |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,704,322 (GRCm39) |
I820V |
probably benign |
Het |
Cdc40 |
A |
G |
10: 40,720,952 (GRCm39) |
|
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,159,493 (GRCm39) |
E2094G |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,305,922 (GRCm39) |
N2061Y |
probably damaging |
Het |
Cfap206 |
G |
A |
4: 34,711,391 (GRCm39) |
A502V |
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,870,599 (GRCm39) |
T29A |
probably benign |
Het |
Cfap57 |
T |
C |
4: 118,470,117 (GRCm39) |
|
probably null |
Het |
Chd5 |
A |
G |
4: 152,432,441 (GRCm39) |
E43G |
possibly damaging |
Het |
Clk1 |
G |
A |
1: 58,453,558 (GRCm39) |
H343Y |
probably benign |
Het |
Cntn4 |
A |
C |
6: 106,527,447 (GRCm39) |
K443T |
probably damaging |
Het |
Csn2 |
G |
A |
5: 87,842,811 (GRCm39) |
A72V |
possibly damaging |
Het |
Ctdp1 |
T |
A |
18: 80,493,457 (GRCm39) |
H346L |
probably benign |
Het |
Ctif |
A |
T |
18: 75,698,083 (GRCm39) |
N192K |
probably damaging |
Het |
Ddr2 |
G |
A |
1: 169,823,135 (GRCm39) |
A383V |
probably benign |
Het |
Derl3 |
C |
T |
10: 75,731,076 (GRCm39) |
|
probably benign |
Het |
Dgkh |
T |
C |
14: 78,821,919 (GRCm39) |
I865V |
probably damaging |
Het |
Dip2b |
C |
T |
15: 100,069,532 (GRCm39) |
A619V |
probably damaging |
Het |
Elapor1 |
T |
A |
3: 108,376,851 (GRCm39) |
H509L |
probably benign |
Het |
Eml1 |
A |
G |
12: 108,496,585 (GRCm39) |
T614A |
possibly damaging |
Het |
Eogt |
G |
C |
6: 97,092,970 (GRCm39) |
Y402* |
probably null |
Het |
Erbb4 |
A |
G |
1: 68,298,449 (GRCm39) |
V647A |
probably damaging |
Het |
Esm1 |
G |
T |
13: 113,350,036 (GRCm39) |
|
probably null |
Het |
Fbxo31 |
A |
G |
8: 122,282,103 (GRCm39) |
|
probably benign |
Het |
Fbxw5 |
T |
A |
2: 25,394,630 (GRCm39) |
D201E |
possibly damaging |
Het |
Fgfr1 |
G |
A |
8: 26,045,760 (GRCm39) |
D123N |
probably benign |
Het |
G530012D18Rik |
A |
C |
1: 85,504,757 (GRCm39) |
|
probably benign |
Het |
Gnat1 |
G |
A |
9: 107,556,662 (GRCm39) |
T29I |
probably damaging |
Het |
Gtf2ird2 |
A |
T |
5: 134,221,597 (GRCm39) |
R67* |
probably null |
Het |
Il22b |
A |
T |
10: 118,130,142 (GRCm39) |
D87E |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,867,457 (GRCm39) |
T729A |
probably benign |
Het |
Klrc2 |
A |
T |
6: 129,635,659 (GRCm39) |
S156R |
probably damaging |
Het |
Krt76 |
A |
T |
15: 101,795,784 (GRCm39) |
L462Q |
probably damaging |
Het |
Lama3 |
C |
A |
18: 12,589,907 (GRCm39) |
|
probably benign |
Het |
Lin28a |
A |
T |
4: 133,735,319 (GRCm39) |
S56T |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,276,323 (GRCm39) |
|
probably benign |
Het |
Macrod2 |
C |
T |
2: 142,059,594 (GRCm39) |
|
probably benign |
Het |
Mansc1 |
C |
T |
6: 134,594,424 (GRCm39) |
|
probably benign |
Het |
Map1b |
G |
T |
13: 99,566,274 (GRCm39) |
S2149* |
probably null |
Het |
Mgst1 |
A |
T |
6: 138,124,667 (GRCm39) |
T34S |
probably benign |
Het |
Mlf2 |
C |
T |
6: 124,911,354 (GRCm39) |
T123M |
probably damaging |
Het |
Mospd2 |
C |
T |
X: 163,731,253 (GRCm39) |
|
probably benign |
Het |
Mrpl15 |
A |
T |
1: 4,847,834 (GRCm39) |
V155E |
probably damaging |
Het |
Mstn |
A |
T |
1: 53,100,953 (GRCm39) |
Y10F |
possibly damaging |
Het |
Myo1g |
C |
T |
11: 6,470,794 (GRCm39) |
V21M |
probably damaging |
Het |
Myom2 |
T |
C |
8: 15,149,326 (GRCm39) |
I599T |
probably benign |
Het |
Ndc80 |
A |
T |
17: 71,803,241 (GRCm39) |
N633K |
probably benign |
Het |
Nhs |
C |
A |
X: 160,620,296 (GRCm39) |
V1487L |
possibly damaging |
Het |
Npc1 |
T |
C |
18: 12,352,382 (GRCm39) |
T106A |
probably benign |
Het |
Nup133 |
C |
T |
8: 124,675,747 (GRCm39) |
V57M |
probably benign |
Het |
Nup98 |
T |
A |
7: 101,809,923 (GRCm39) |
T536S |
probably damaging |
Het |
Oprm1 |
T |
C |
10: 6,782,652 (GRCm39) |
|
probably benign |
Het |
Or5j1 |
T |
C |
2: 86,879,492 (GRCm39) |
I29M |
probably benign |
Het |
Or6c219 |
T |
A |
10: 129,780,980 (GRCm39) |
H317L |
probably benign |
Het |
Or8j3 |
A |
G |
2: 86,029,069 (GRCm39) |
V9A |
probably benign |
Het |
Ostf1 |
C |
T |
19: 18,581,571 (GRCm39) |
V14I |
unknown |
Het |
Pcdhb14 |
C |
A |
18: 37,581,921 (GRCm39) |
D342E |
probably damaging |
Het |
Pdia3 |
G |
A |
2: 121,262,858 (GRCm39) |
G275S |
probably damaging |
Het |
Plce1 |
G |
A |
19: 38,705,135 (GRCm39) |
V847M |
probably damaging |
Het |
Pon3 |
A |
G |
6: 5,230,444 (GRCm39) |
M288T |
probably benign |
Het |
Psd2 |
A |
T |
18: 36,111,627 (GRCm39) |
D84V |
possibly damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,712,448 (GRCm39) |
K1808E |
probably damaging |
Het |
Ramp3 |
T |
C |
11: 6,626,476 (GRCm39) |
|
probably benign |
Het |
Rasgrf1 |
T |
A |
9: 89,833,062 (GRCm39) |
|
probably benign |
Het |
Rictor |
A |
G |
15: 6,803,467 (GRCm39) |
|
probably benign |
Het |
Rptor |
A |
T |
11: 119,775,780 (GRCm39) |
I984F |
probably benign |
Het |
Slc1a6 |
C |
T |
10: 78,631,842 (GRCm39) |
P223S |
probably benign |
Het |
Taar8b |
A |
C |
10: 23,967,924 (GRCm39) |
V90G |
probably damaging |
Het |
Tbc1d21 |
A |
G |
9: 58,267,160 (GRCm39) |
V327A |
probably benign |
Het |
Tex21 |
T |
C |
12: 76,250,940 (GRCm39) |
T499A |
probably benign |
Het |
Tg |
A |
T |
15: 66,550,638 (GRCm39) |
D256V |
probably damaging |
Het |
Tmf1 |
A |
G |
6: 97,153,453 (GRCm39) |
S207P |
probably benign |
Het |
Tpr |
A |
G |
1: 150,269,158 (GRCm39) |
|
probably benign |
Het |
Ufd1 |
A |
G |
16: 18,633,637 (GRCm39) |
T21A |
probably damaging |
Het |
Unc13a |
T |
C |
8: 72,108,929 (GRCm39) |
D115G |
possibly damaging |
Het |
Usb1 |
T |
A |
8: 96,070,669 (GRCm39) |
F198L |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,573,902 (GRCm39) |
|
probably benign |
Het |
Vars1 |
A |
G |
17: 35,233,276 (GRCm39) |
N954S |
probably damaging |
Het |
Wdr17 |
C |
T |
8: 55,146,131 (GRCm39) |
A90T |
possibly damaging |
Het |
Wdr33 |
C |
T |
18: 31,968,429 (GRCm39) |
|
probably benign |
Het |
Zfp236 |
A |
G |
18: 82,658,369 (GRCm39) |
|
probably benign |
Het |
Zfp445 |
A |
T |
9: 122,690,823 (GRCm39) |
V124E |
probably damaging |
Het |
Zfp616 |
A |
T |
11: 73,975,648 (GRCm39) |
H639L |
probably damaging |
Het |
Zfyve16 |
C |
A |
13: 92,657,985 (GRCm39) |
S642I |
probably damaging |
Het |
Zswim5 |
C |
T |
4: 116,842,943 (GRCm39) |
T896I |
possibly damaging |
Het |
|
Other mutations in Pdpr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Pdpr
|
APN |
8 |
111,828,704 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01116:Pdpr
|
APN |
8 |
111,839,342 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01353:Pdpr
|
APN |
8 |
111,847,910 (GRCm39) |
splice site |
probably null |
|
IGL01681:Pdpr
|
APN |
8 |
111,859,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01785:Pdpr
|
APN |
8 |
111,856,288 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02115:Pdpr
|
APN |
8 |
111,830,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02292:Pdpr
|
APN |
8 |
111,852,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02749:Pdpr
|
APN |
8 |
111,844,722 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03296:Pdpr
|
APN |
8 |
111,841,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1510:Pdpr
|
UTSW |
8 |
111,851,107 (GRCm39) |
splice site |
probably benign |
|
R1837:Pdpr
|
UTSW |
8 |
111,861,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Pdpr
|
UTSW |
8 |
111,861,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Pdpr
|
UTSW |
8 |
111,844,668 (GRCm39) |
missense |
probably damaging |
0.97 |
R4214:Pdpr
|
UTSW |
8 |
111,856,212 (GRCm39) |
intron |
probably benign |
|
R4812:Pdpr
|
UTSW |
8 |
111,843,349 (GRCm39) |
missense |
probably benign |
0.00 |
R4863:Pdpr
|
UTSW |
8 |
111,828,583 (GRCm39) |
missense |
probably benign |
0.01 |
R4998:Pdpr
|
UTSW |
8 |
111,841,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Pdpr
|
UTSW |
8 |
111,850,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R5665:Pdpr
|
UTSW |
8 |
111,841,443 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5739:Pdpr
|
UTSW |
8 |
111,861,252 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6675:Pdpr
|
UTSW |
8 |
111,828,532 (GRCm39) |
nonsense |
probably null |
|
R6785:Pdpr
|
UTSW |
8 |
111,851,243 (GRCm39) |
missense |
probably benign |
0.00 |
R6889:Pdpr
|
UTSW |
8 |
111,851,245 (GRCm39) |
critical splice donor site |
probably null |
|
R7397:Pdpr
|
UTSW |
8 |
111,839,385 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7543:Pdpr
|
UTSW |
8 |
111,859,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R7634:Pdpr
|
UTSW |
8 |
111,852,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Pdpr
|
UTSW |
8 |
111,850,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Pdpr
|
UTSW |
8 |
111,852,240 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8833:Pdpr
|
UTSW |
8 |
111,852,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9283:Pdpr
|
UTSW |
8 |
111,856,268 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9487:Pdpr
|
UTSW |
8 |
111,852,925 (GRCm39) |
missense |
probably benign |
0.00 |
|