Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak6 |
A |
T |
13: 100,790,722 (GRCm39) |
T18S |
probably damaging |
Het |
Aqp7 |
G |
A |
4: 41,035,510 (GRCm39) |
T115I |
probably benign |
Het |
Arhgap19 |
A |
G |
19: 41,773,227 (GRCm39) |
V275A |
possibly damaging |
Het |
Cebpz |
T |
A |
17: 79,242,040 (GRCm39) |
Q538L |
probably damaging |
Het |
Chgb |
A |
T |
2: 132,634,618 (GRCm39) |
I187F |
probably benign |
Het |
Cldn1 |
C |
A |
16: 26,190,167 (GRCm39) |
L70F |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,809,938 (GRCm39) |
D1230V |
probably damaging |
Het |
Csmd1 |
C |
T |
8: 16,003,703 (GRCm39) |
C2617Y |
probably damaging |
Het |
D7Ertd443e |
T |
A |
7: 133,951,110 (GRCm39) |
N188Y |
probably benign |
Het |
Ddx51 |
A |
G |
5: 110,802,790 (GRCm39) |
I214M |
probably benign |
Het |
Dlg5 |
A |
G |
14: 24,200,716 (GRCm39) |
V1328A |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,326,216 (GRCm39) |
C3639Y |
probably damaging |
Het |
Dync1i2 |
C |
T |
2: 71,081,326 (GRCm39) |
T511I |
probably benign |
Het |
Fam220a |
A |
T |
5: 143,549,212 (GRCm39) |
E208V |
probably damaging |
Het |
Gm4846 |
T |
C |
1: 166,311,594 (GRCm39) |
S422G |
probably benign |
Het |
Grin2c |
C |
T |
11: 115,141,115 (GRCm39) |
R1001Q |
probably benign |
Het |
H2-T3 |
T |
C |
17: 36,498,301 (GRCm39) |
E248G |
probably damaging |
Het |
Idi2 |
T |
C |
13: 9,008,518 (GRCm39) |
V92A |
probably benign |
Het |
Iqcd |
C |
T |
5: 120,740,571 (GRCm39) |
Q301* |
probably null |
Het |
Klhl26 |
T |
C |
8: 70,904,974 (GRCm39) |
D278G |
probably damaging |
Het |
Mok |
G |
T |
12: 110,774,503 (GRCm39) |
T228K |
probably damaging |
Het |
Or1e22 |
A |
G |
11: 73,377,008 (GRCm39) |
I214T |
probably damaging |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Pabpc1 |
T |
C |
15: 36,606,074 (GRCm39) |
I101V |
probably benign |
Het |
Ppargc1a |
G |
T |
5: 51,631,562 (GRCm39) |
Q356K |
probably damaging |
Het |
Rxfp1 |
C |
T |
3: 79,586,054 (GRCm39) |
C96Y |
probably damaging |
Het |
Scn11a |
A |
C |
9: 119,618,990 (GRCm39) |
V784G |
probably damaging |
Het |
Septin4 |
T |
C |
11: 87,458,723 (GRCm39) |
S366P |
probably benign |
Het |
Slc12a8 |
A |
G |
16: 33,410,679 (GRCm39) |
Y226C |
probably damaging |
Het |
Slc25a33 |
A |
G |
4: 149,846,914 (GRCm39) |
V49A |
possibly damaging |
Het |
Slc25a45 |
T |
C |
19: 5,934,451 (GRCm39) |
S140P |
probably benign |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Spty2d1 |
G |
T |
7: 46,647,845 (GRCm39) |
N361K |
possibly damaging |
Het |
Stk4 |
G |
A |
2: 163,941,674 (GRCm39) |
A297T |
probably benign |
Het |
Thsd7b |
T |
A |
1: 129,688,139 (GRCm39) |
N683K |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,299,829 (GRCm39) |
E141G |
probably benign |
Het |
Tmem125 |
A |
T |
4: 118,399,216 (GRCm39) |
C72S |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,572,437 (GRCm39) |
T26152K |
probably damaging |
Het |
Uhrf1 |
G |
A |
17: 56,627,259 (GRCm39) |
G643D |
possibly damaging |
Het |
Vmn2r50 |
C |
T |
7: 9,774,299 (GRCm39) |
M532I |
possibly damaging |
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 |
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 |
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 |
|