Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
G |
T |
1: 71,297,357 (GRCm39) |
H2378N |
probably benign |
Het |
Btaf1 |
C |
A |
19: 36,977,592 (GRCm39) |
A1470E |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,394,793 (GRCm39) |
D228G |
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cldn18 |
T |
C |
9: 99,578,128 (GRCm39) |
D205G |
probably benign |
Het |
Clip2 |
T |
C |
5: 134,546,876 (GRCm39) |
T231A |
probably benign |
Het |
Cltc |
A |
G |
11: 86,608,860 (GRCm39) |
V723A |
probably damaging |
Het |
Cpa3 |
C |
T |
3: 20,282,971 (GRCm39) |
|
probably null |
Het |
Cyfip2 |
T |
G |
11: 46,091,630 (GRCm39) |
T1097P |
possibly damaging |
Het |
Dnah9 |
T |
A |
11: 65,838,444 (GRCm39) |
R667* |
probably null |
Het |
Dock10 |
T |
C |
1: 80,493,339 (GRCm39) |
E1878G |
probably damaging |
Het |
Ermap |
G |
A |
4: 119,037,160 (GRCm39) |
H353Y |
probably damaging |
Het |
Etfa |
A |
T |
9: 55,393,984 (GRCm39) |
|
probably null |
Het |
F5 |
C |
T |
1: 164,001,860 (GRCm39) |
P188S |
probably damaging |
Het |
Foxq1 |
G |
A |
13: 31,743,326 (GRCm39) |
E143K |
possibly damaging |
Het |
Gsr |
C |
T |
8: 34,172,612 (GRCm39) |
|
probably benign |
Het |
Hebp1 |
T |
A |
6: 135,132,274 (GRCm39) |
Y31F |
probably benign |
Het |
Ighv1-14 |
T |
C |
12: 114,610,457 (GRCm39) |
|
noncoding transcript |
Het |
Lamb1 |
T |
A |
12: 31,370,907 (GRCm39) |
D1319E |
probably damaging |
Het |
Manba |
G |
A |
3: 135,212,769 (GRCm39) |
|
probably benign |
Het |
Mknk2 |
A |
T |
10: 80,503,955 (GRCm39) |
F319I |
probably damaging |
Het |
Mup6 |
A |
T |
4: 60,003,971 (GRCm39) |
|
probably benign |
Het |
Nalcn |
T |
C |
14: 123,560,726 (GRCm39) |
T784A |
probably benign |
Het |
Nt5dc1 |
T |
C |
10: 34,279,721 (GRCm39) |
E107G |
probably benign |
Het |
Or11h6 |
A |
T |
14: 50,880,214 (GRCm39) |
I159F |
probably benign |
Het |
Or56b34 |
T |
A |
7: 104,938,252 (GRCm39) |
F317L |
probably benign |
Het |
Or9q2 |
G |
A |
19: 13,772,589 (GRCm39) |
P129S |
probably damaging |
Het |
Phldb1 |
T |
C |
9: 44,622,530 (GRCm39) |
E41G |
probably damaging |
Het |
Ptk2 |
T |
C |
15: 73,170,036 (GRCm39) |
D309G |
probably benign |
Het |
Rab11fip5 |
A |
G |
6: 85,325,207 (GRCm39) |
S367P |
probably damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,310,275 (GRCm39) |
N224K |
probably benign |
Het |
Rchy1 |
A |
T |
5: 92,105,405 (GRCm39) |
C65* |
probably null |
Het |
Rgs18 |
T |
C |
1: 144,650,359 (GRCm39) |
D56G |
probably benign |
Het |
Rtraf |
A |
C |
14: 19,862,296 (GRCm39) |
L197R |
probably damaging |
Het |
Slc44a5 |
G |
T |
3: 153,962,213 (GRCm39) |
W382L |
probably damaging |
Het |
Snx24 |
C |
T |
18: 53,518,241 (GRCm39) |
|
probably benign |
Het |
Sphkap |
T |
C |
1: 83,253,897 (GRCm39) |
D1284G |
probably damaging |
Het |
Tmem54 |
A |
G |
4: 129,002,111 (GRCm39) |
M53V |
probably benign |
Het |
Trip6 |
G |
A |
5: 137,308,618 (GRCm39) |
P414S |
probably benign |
Het |
Vmn1r38 |
A |
G |
6: 66,753,751 (GRCm39) |
Y122H |
probably benign |
Het |
Wapl |
T |
A |
14: 34,413,877 (GRCm39) |
N246K |
possibly damaging |
Het |
Zfp12 |
G |
A |
5: 143,230,551 (GRCm39) |
G293R |
probably damaging |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
probably benign |
Het |
Zfp446 |
T |
G |
7: 12,716,181 (GRCm39) |
V209G |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
|
Other mutations in Lrp5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00834:Lrp5
|
APN |
19 |
3,699,404 (GRCm39) |
missense |
probably benign |
|
IGL00902:Lrp5
|
APN |
19 |
3,650,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02032:Lrp5
|
APN |
19 |
3,665,886 (GRCm39) |
splice site |
probably benign |
|
IGL02331:Lrp5
|
APN |
19 |
3,641,816 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02401:Lrp5
|
APN |
19 |
3,643,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02572:Lrp5
|
APN |
19 |
3,664,283 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02637:Lrp5
|
APN |
19 |
3,680,269 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02696:Lrp5
|
APN |
19 |
3,652,253 (GRCm39) |
missense |
probably benign |
|
IGL02742:Lrp5
|
APN |
19 |
3,654,022 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02804:Lrp5
|
APN |
19 |
3,650,777 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03089:Lrp5
|
APN |
19 |
3,670,314 (GRCm39) |
splice site |
probably null |
|
IGL03243:Lrp5
|
APN |
19 |
3,680,159 (GRCm39) |
missense |
probably benign |
0.12 |
Contrarian
|
UTSW |
19 |
3,709,355 (GRCm39) |
missense |
probably damaging |
1.00 |
Contrarian2
|
UTSW |
19 |
3,702,296 (GRCm39) |
missense |
probably damaging |
1.00 |
lucent
|
UTSW |
19 |
3,736,353 (GRCm39) |
critical splice donor site |
probably null |
|
Microtome
|
UTSW |
19 |
3,672,638 (GRCm39) |
missense |
probably damaging |
1.00 |
r18
|
UTSW |
19 |
0 () |
small insertion |
|
|
Spicule
|
UTSW |
19 |
3,662,197 (GRCm39) |
critical splice donor site |
probably null |
|
Stirrup
|
UTSW |
19 |
3,650,753 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4494001:Lrp5
|
UTSW |
19 |
3,660,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Lrp5
|
UTSW |
19 |
3,647,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Lrp5
|
UTSW |
19 |
3,678,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Lrp5
|
UTSW |
19 |
3,650,777 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0883:Lrp5
|
UTSW |
19 |
3,655,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1086:Lrp5
|
UTSW |
19 |
3,699,476 (GRCm39) |
missense |
probably benign |
0.28 |
R1417:Lrp5
|
UTSW |
19 |
3,636,425 (GRCm39) |
missense |
probably benign |
0.04 |
R1468:Lrp5
|
UTSW |
19 |
3,670,191 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1468:Lrp5
|
UTSW |
19 |
3,670,191 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1533:Lrp5
|
UTSW |
19 |
3,664,234 (GRCm39) |
missense |
probably benign |
0.17 |
R1538:Lrp5
|
UTSW |
19 |
3,697,585 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1856:Lrp5
|
UTSW |
19 |
3,647,346 (GRCm39) |
missense |
probably benign |
0.18 |
R1930:Lrp5
|
UTSW |
19 |
3,660,131 (GRCm39) |
missense |
probably benign |
0.02 |
R1931:Lrp5
|
UTSW |
19 |
3,660,131 (GRCm39) |
missense |
probably benign |
0.02 |
R1932:Lrp5
|
UTSW |
19 |
3,660,131 (GRCm39) |
missense |
probably benign |
0.02 |
R1951:Lrp5
|
UTSW |
19 |
3,670,298 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2016:Lrp5
|
UTSW |
19 |
3,660,056 (GRCm39) |
missense |
probably benign |
0.04 |
R2131:Lrp5
|
UTSW |
19 |
3,672,708 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2153:Lrp5
|
UTSW |
19 |
3,664,339 (GRCm39) |
missense |
probably benign |
0.22 |
R2403:Lrp5
|
UTSW |
19 |
3,647,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R3158:Lrp5
|
UTSW |
19 |
3,665,849 (GRCm39) |
missense |
probably damaging |
0.97 |
R3771:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R3772:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R3825:Lrp5
|
UTSW |
19 |
3,655,290 (GRCm39) |
nonsense |
probably null |
|
R3887:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R3893:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R3917:Lrp5
|
UTSW |
19 |
3,662,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R4279:Lrp5
|
UTSW |
19 |
3,641,778 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4714:Lrp5
|
UTSW |
19 |
3,709,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Lrp5
|
UTSW |
19 |
3,664,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5102:Lrp5
|
UTSW |
19 |
3,709,304 (GRCm39) |
missense |
probably damaging |
0.96 |
R5138:Lrp5
|
UTSW |
19 |
3,678,319 (GRCm39) |
missense |
probably benign |
0.03 |
R5497:Lrp5
|
UTSW |
19 |
3,652,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5632:Lrp5
|
UTSW |
19 |
3,672,512 (GRCm39) |
missense |
probably benign |
|
R5887:Lrp5
|
UTSW |
19 |
3,654,094 (GRCm39) |
missense |
probably benign |
0.01 |
R5950:Lrp5
|
UTSW |
19 |
3,652,333 (GRCm39) |
missense |
probably benign |
0.17 |
R5987:Lrp5
|
UTSW |
19 |
3,678,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R6080:Lrp5
|
UTSW |
19 |
3,678,316 (GRCm39) |
missense |
probably benign |
0.32 |
R6181:Lrp5
|
UTSW |
19 |
3,678,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6236:Lrp5
|
UTSW |
19 |
3,680,483 (GRCm39) |
splice site |
probably null |
|
R6332:Lrp5
|
UTSW |
19 |
3,709,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R6511:Lrp5
|
UTSW |
19 |
3,702,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R6641:Lrp5
|
UTSW |
19 |
3,702,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R6791:Lrp5
|
UTSW |
19 |
3,650,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R6865:Lrp5
|
UTSW |
19 |
3,670,013 (GRCm39) |
critical splice donor site |
probably null |
|
R6906:Lrp5
|
UTSW |
19 |
3,672,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R6922:Lrp5
|
UTSW |
19 |
3,655,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7091:Lrp5
|
UTSW |
19 |
3,680,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Lrp5
|
UTSW |
19 |
3,641,774 (GRCm39) |
missense |
probably damaging |
0.99 |
R7368:Lrp5
|
UTSW |
19 |
3,670,085 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7381:Lrp5
|
UTSW |
19 |
3,643,588 (GRCm39) |
missense |
probably benign |
0.20 |
R7385:Lrp5
|
UTSW |
19 |
3,662,197 (GRCm39) |
critical splice donor site |
probably null |
|
R7392:Lrp5
|
UTSW |
19 |
3,660,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Lrp5
|
UTSW |
19 |
3,699,439 (GRCm39) |
missense |
probably benign |
0.01 |
R7585:Lrp5
|
UTSW |
19 |
3,654,094 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7662:Lrp5
|
UTSW |
19 |
3,736,353 (GRCm39) |
critical splice donor site |
probably null |
|
R7984:Lrp5
|
UTSW |
19 |
3,662,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Lrp5
|
UTSW |
19 |
3,647,337 (GRCm39) |
missense |
probably damaging |
0.98 |
R8391:Lrp5
|
UTSW |
19 |
3,654,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Lrp5
|
UTSW |
19 |
3,641,015 (GRCm39) |
missense |
probably damaging |
0.98 |
R8885:Lrp5
|
UTSW |
19 |
3,702,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Lrp5
|
UTSW |
19 |
3,680,156 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9263:Lrp5
|
UTSW |
19 |
3,654,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9376:Lrp5
|
UTSW |
19 |
3,670,286 (GRCm39) |
missense |
probably benign |
0.00 |
R9400:Lrp5
|
UTSW |
19 |
3,635,272 (GRCm39) |
missense |
probably benign |
0.00 |
R9536:Lrp5
|
UTSW |
19 |
3,672,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Lrp5
|
UTSW |
19 |
3,641,712 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Lrp5
|
UTSW |
19 |
3,678,345 (GRCm39) |
nonsense |
probably null |
|
|