Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
C |
A |
7: 41,274,996 (GRCm39) |
T233K |
possibly damaging |
Het |
Adamts9 |
A |
T |
6: 92,836,883 (GRCm39) |
M623K |
possibly damaging |
Het |
Arid1a |
T |
G |
4: 133,412,793 (GRCm39) |
D1467A |
unknown |
Het |
Cdhr2 |
A |
G |
13: 54,866,112 (GRCm39) |
D304G |
probably damaging |
Het |
Cenpj |
C |
T |
14: 56,790,487 (GRCm39) |
V521I |
probably benign |
Het |
Ciao2a |
A |
T |
9: 66,039,898 (GRCm39) |
I72L |
probably benign |
Het |
Csf2rb |
G |
T |
15: 78,232,714 (GRCm39) |
E674* |
probably null |
Het |
Dnai3 |
T |
C |
3: 145,750,674 (GRCm39) |
|
probably benign |
Het |
Edaradd |
C |
T |
13: 12,498,480 (GRCm39) |
|
probably null |
Het |
Emilin2 |
A |
G |
17: 71,559,854 (GRCm39) |
V1041A |
possibly damaging |
Het |
Fam135b |
A |
G |
15: 71,343,361 (GRCm39) |
V418A |
probably benign |
Het |
Gnas |
T |
A |
2: 174,183,504 (GRCm39) |
|
probably benign |
Het |
Grxcr1 |
A |
T |
5: 68,189,540 (GRCm39) |
N104Y |
possibly damaging |
Het |
Gtf2a1l |
T |
A |
17: 89,001,723 (GRCm39) |
L146Q |
probably damaging |
Het |
Hectd1 |
T |
A |
12: 51,837,181 (GRCm39) |
E791D |
probably damaging |
Het |
Ifi203 |
A |
G |
1: 173,765,306 (GRCm39) |
|
probably null |
Het |
Klk1b11 |
A |
G |
7: 43,649,243 (GRCm39) |
N260S |
probably damaging |
Het |
LTO1 |
G |
T |
7: 144,470,220 (GRCm39) |
V50F |
probably damaging |
Het |
Map4 |
A |
T |
9: 109,901,672 (GRCm39) |
|
probably benign |
Het |
Marveld2 |
C |
T |
13: 100,737,401 (GRCm39) |
V163M |
possibly damaging |
Het |
Med14 |
T |
C |
X: 12,613,003 (GRCm39) |
|
probably benign |
Het |
Mex3b |
A |
T |
7: 82,518,116 (GRCm39) |
I144F |
probably damaging |
Het |
Pde2a |
T |
A |
7: 101,133,796 (GRCm39) |
C92* |
probably null |
Het |
Phf6 |
T |
A |
X: 52,020,516 (GRCm39) |
Y103N |
probably damaging |
Het |
Rftn2 |
C |
A |
1: 55,243,444 (GRCm39) |
V275F |
probably damaging |
Het |
Skap1 |
C |
A |
11: 96,621,971 (GRCm39) |
Q296K |
probably damaging |
Het |
Skap1 |
T |
A |
11: 96,622,016 (GRCm39) |
F311I |
probably damaging |
Het |
Tas2r115 |
A |
G |
6: 132,714,741 (GRCm39) |
I70T |
probably benign |
Het |
Vav2 |
T |
C |
2: 27,167,250 (GRCm39) |
D613G |
probably benign |
Het |
Zranb3 |
T |
C |
1: 127,943,877 (GRCm39) |
E290G |
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 |
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 |
R3834:Ptprt
|
UTSW |
2 |
161,389,307 (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 |
|