Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adh6a |
G |
A |
3: 138,033,275 (GRCm39) |
|
probably null |
Het |
Bptf |
T |
C |
11: 106,964,683 (GRCm39) |
T1389A |
probably benign |
Het |
Cfap54 |
A |
G |
10: 92,636,985 (GRCm39) |
|
probably benign |
Het |
Cimip3 |
AC |
A |
17: 47,744,348 (GRCm39) |
|
probably benign |
Het |
Coq5 |
G |
T |
5: 115,422,635 (GRCm39) |
G180W |
probably damaging |
Het |
Cyp2d34 |
A |
G |
15: 82,500,947 (GRCm39) |
|
probably null |
Het |
Cyp2j13 |
C |
T |
4: 95,944,794 (GRCm39) |
|
probably null |
Het |
Fam114a1 |
C |
T |
5: 65,163,416 (GRCm39) |
T197I |
possibly damaging |
Het |
Fbxo44 |
A |
G |
4: 148,240,707 (GRCm39) |
Y227H |
probably damaging |
Het |
Gm5114 |
T |
A |
7: 39,058,161 (GRCm39) |
H486L |
possibly damaging |
Het |
Grik4 |
T |
C |
9: 42,540,419 (GRCm39) |
R254G |
probably benign |
Het |
Iqcm |
T |
C |
8: 76,304,380 (GRCm39) |
I47T |
possibly damaging |
Het |
Kif20b |
A |
G |
19: 34,912,428 (GRCm39) |
Y278C |
probably damaging |
Het |
Lbhd1 |
G |
A |
19: 8,861,421 (GRCm39) |
C43Y |
probably benign |
Het |
Lrfn5 |
T |
A |
12: 61,886,816 (GRCm39) |
D201E |
probably damaging |
Het |
Map1a |
G |
A |
2: 121,137,803 (GRCm39) |
G2635D |
probably damaging |
Het |
Ms4a4a |
A |
T |
19: 11,356,219 (GRCm39) |
M35L |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,412,918 (GRCm39) |
I1955F |
unknown |
Het |
Mug2 |
T |
C |
6: 122,026,746 (GRCm39) |
|
probably null |
Het |
Nav2 |
T |
A |
7: 49,195,606 (GRCm39) |
I994N |
possibly damaging |
Het |
Ngly1 |
T |
C |
14: 16,290,766 (GRCm38) |
|
probably benign |
Het |
Nr1i2 |
T |
C |
16: 38,074,291 (GRCm39) |
|
probably null |
Het |
Or51f5 |
A |
G |
7: 102,424,493 (GRCm39) |
Y254C |
probably damaging |
Het |
Or52h9 |
T |
A |
7: 104,202,552 (GRCm39) |
V142D |
probably benign |
Het |
Or5p69 |
A |
T |
7: 107,967,279 (GRCm39) |
D194V |
probably damaging |
Het |
Oxct2a |
C |
T |
4: 123,216,266 (GRCm39) |
V372I |
probably benign |
Het |
Pax6 |
G |
A |
2: 105,526,795 (GRCm39) |
E234K |
probably benign |
Het |
Pramel14 |
T |
A |
4: 143,720,796 (GRCm39) |
K48N |
probably benign |
Het |
Prkdc |
A |
G |
16: 15,609,810 (GRCm39) |
E3138G |
probably damaging |
Het |
Ptprc |
T |
A |
1: 138,011,305 (GRCm39) |
N584I |
probably damaging |
Het |
Rps20 |
A |
T |
4: 3,834,610 (GRCm39) |
I84N |
probably damaging |
Het |
Scd3 |
A |
G |
19: 44,230,156 (GRCm39) |
Y313C |
probably damaging |
Het |
Sertad2 |
T |
C |
11: 20,598,482 (GRCm39) |
I226T |
probably benign |
Het |
Slc15a2 |
A |
T |
16: 36,592,490 (GRCm39) |
C191* |
probably null |
Het |
Slco1a1 |
G |
T |
6: 141,889,163 (GRCm39) |
Q50K |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,785,776 (GRCm39) |
I622N |
possibly damaging |
Het |
Tmc4 |
C |
T |
7: 3,675,006 (GRCm39) |
V222M |
probably benign |
Het |
Tmem145 |
T |
C |
7: 25,010,786 (GRCm39) |
F359L |
probably damaging |
Het |
Tmem238 |
C |
A |
7: 4,792,078 (GRCm39) |
R155L |
possibly damaging |
Het |
Vmn1r32 |
C |
A |
6: 66,530,647 (GRCm39) |
C43F |
probably benign |
Het |
Vmn2r104 |
C |
T |
17: 20,250,183 (GRCm39) |
R696K |
probably benign |
Het |
|
Other mutations in Ptprt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ptprt
|
APN |
2 |
161,652,544 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00565:Ptprt
|
APN |
2 |
161,402,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00925:Ptprt
|
APN |
2 |
161,498,083 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01344:Ptprt
|
APN |
2 |
161,393,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01432:Ptprt
|
APN |
2 |
162,109,999 (GRCm39) |
splice site |
probably benign |
|
IGL02008:Ptprt
|
APN |
2 |
161,769,593 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02040:Ptprt
|
APN |
2 |
162,079,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Ptprt
|
APN |
2 |
161,397,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02231:Ptprt
|
APN |
2 |
162,119,966 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02231:Ptprt
|
APN |
2 |
162,079,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Ptprt
|
APN |
2 |
161,372,437 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02277:Ptprt
|
APN |
2 |
161,389,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02447:Ptprt
|
APN |
2 |
162,120,027 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02601:Ptprt
|
APN |
2 |
161,608,227 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02623:Ptprt
|
APN |
2 |
161,449,372 (GRCm39) |
splice site |
probably benign |
|
IGL03379:Ptprt
|
APN |
2 |
161,397,379 (GRCm39) |
nonsense |
probably null |
|
Poverina
|
UTSW |
2 |
161,743,417 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03055:Ptprt
|
UTSW |
2 |
161,375,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R0064:Ptprt
|
UTSW |
2 |
161,769,711 (GRCm39) |
splice site |
probably benign |
|
R0129:Ptprt
|
UTSW |
2 |
162,119,990 (GRCm39) |
missense |
probably benign |
0.35 |
R0131:Ptprt
|
UTSW |
2 |
162,120,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0131:Ptprt
|
UTSW |
2 |
162,120,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0132:Ptprt
|
UTSW |
2 |
162,120,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0316:Ptprt
|
UTSW |
2 |
161,449,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Ptprt
|
UTSW |
2 |
161,395,742 (GRCm39) |
missense |
probably damaging |
0.96 |
R0488:Ptprt
|
UTSW |
2 |
161,395,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R0573:Ptprt
|
UTSW |
2 |
161,393,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Ptprt
|
UTSW |
2 |
161,654,040 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0834:Ptprt
|
UTSW |
2 |
161,654,059 (GRCm39) |
splice site |
probably null |
|
R1023:Ptprt
|
UTSW |
2 |
161,400,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Ptprt
|
UTSW |
2 |
161,769,692 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1253:Ptprt
|
UTSW |
2 |
162,120,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Ptprt
|
UTSW |
2 |
161,769,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1515:Ptprt
|
UTSW |
2 |
162,079,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Ptprt
|
UTSW |
2 |
161,652,469 (GRCm39) |
critical splice donor site |
probably null |
|
R1939:Ptprt
|
UTSW |
2 |
161,769,560 (GRCm39) |
missense |
probably benign |
0.45 |
R1987:Ptprt
|
UTSW |
2 |
161,608,241 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1987:Ptprt
|
UTSW |
2 |
161,400,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Ptprt
|
UTSW |
2 |
161,376,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Ptprt
|
UTSW |
2 |
161,653,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2421:Ptprt
|
UTSW |
2 |
162,119,960 (GRCm39) |
splice site |
probably benign |
|
R3432:Ptprt
|
UTSW |
2 |
161,769,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R3619:Ptprt
|
UTSW |
2 |
161,408,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R3757:Ptprt
|
UTSW |
2 |
161,653,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3758:Ptprt
|
UTSW |
2 |
161,653,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Ptprt
|
UTSW |
2 |
161,389,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R3915:Ptprt
|
UTSW |
2 |
161,397,475 (GRCm39) |
splice site |
probably benign |
|
R4003:Ptprt
|
UTSW |
2 |
161,408,037 (GRCm39) |
splice site |
probably benign |
|
R4387:Ptprt
|
UTSW |
2 |
161,769,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R4519:Ptprt
|
UTSW |
2 |
161,406,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Ptprt
|
UTSW |
2 |
161,395,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Ptprt
|
UTSW |
2 |
161,743,366 (GRCm39) |
critical splice donor site |
probably null |
|
R4866:Ptprt
|
UTSW |
2 |
161,402,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Ptprt
|
UTSW |
2 |
162,080,095 (GRCm39) |
missense |
probably benign |
0.01 |
R5173:Ptprt
|
UTSW |
2 |
161,769,676 (GRCm39) |
missense |
probably benign |
0.01 |
R5215:Ptprt
|
UTSW |
2 |
162,120,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R5383:Ptprt
|
UTSW |
2 |
161,539,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Ptprt
|
UTSW |
2 |
161,769,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Ptprt
|
UTSW |
2 |
162,120,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5711:Ptprt
|
UTSW |
2 |
161,652,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R5735:Ptprt
|
UTSW |
2 |
161,376,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R5834:Ptprt
|
UTSW |
2 |
161,402,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Ptprt
|
UTSW |
2 |
161,977,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R5926:Ptprt
|
UTSW |
2 |
161,406,606 (GRCm39) |
missense |
probably benign |
0.00 |
R6210:Ptprt
|
UTSW |
2 |
162,109,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Ptprt
|
UTSW |
2 |
161,743,417 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6298:Ptprt
|
UTSW |
2 |
161,395,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Ptprt
|
UTSW |
2 |
161,395,703 (GRCm39) |
missense |
probably damaging |
0.98 |
R6499:Ptprt
|
UTSW |
2 |
161,376,507 (GRCm39) |
missense |
probably benign |
0.32 |
R6613:Ptprt
|
UTSW |
2 |
161,372,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Ptprt
|
UTSW |
2 |
161,395,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R7218:Ptprt
|
UTSW |
2 |
161,389,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Ptprt
|
UTSW |
2 |
161,375,443 (GRCm39) |
missense |
probably benign |
0.15 |
R7576:Ptprt
|
UTSW |
2 |
161,449,225 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7733:Ptprt
|
UTSW |
2 |
161,417,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R7735:Ptprt
|
UTSW |
2 |
161,417,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R7813:Ptprt
|
UTSW |
2 |
161,372,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R8031:Ptprt
|
UTSW |
2 |
161,977,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R8074:Ptprt
|
UTSW |
2 |
161,769,581 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8151:Ptprt
|
UTSW |
2 |
162,120,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8236:Ptprt
|
UTSW |
2 |
161,528,988 (GRCm39) |
critical splice donor site |
probably null |
|
R8308:Ptprt
|
UTSW |
2 |
161,769,566 (GRCm39) |
missense |
probably benign |
0.00 |
R8348:Ptprt
|
UTSW |
2 |
161,400,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Ptprt
|
UTSW |
2 |
161,393,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Ptprt
|
UTSW |
2 |
161,743,451 (GRCm39) |
missense |
probably benign |
0.05 |
R8448:Ptprt
|
UTSW |
2 |
161,400,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8512:Ptprt
|
UTSW |
2 |
161,400,783 (GRCm39) |
missense |
probably benign |
0.00 |
R8715:Ptprt
|
UTSW |
2 |
161,372,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Ptprt
|
UTSW |
2 |
161,608,314 (GRCm39) |
missense |
probably benign |
0.04 |
R9046:Ptprt
|
UTSW |
2 |
161,372,361 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9222:Ptprt
|
UTSW |
2 |
161,402,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R9297:Ptprt
|
UTSW |
2 |
161,417,698 (GRCm39) |
missense |
probably benign |
|
R9318:Ptprt
|
UTSW |
2 |
161,417,698 (GRCm39) |
missense |
probably benign |
|
R9476:Ptprt
|
UTSW |
2 |
161,397,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Ptprt
|
UTSW |
2 |
161,397,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Ptprt
|
UTSW |
2 |
161,395,732 (GRCm39) |
missense |
probably benign |
0.10 |
X0064:Ptprt
|
UTSW |
2 |
161,769,403 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ptprt
|
UTSW |
2 |
162,080,041 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1177:Ptprt
|
UTSW |
2 |
162,204,868 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Ptprt
|
UTSW |
2 |
161,574,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|