Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
A |
G |
9: 103,972,824 (GRCm39) |
T506A |
probably damaging |
Het |
Ankib1 |
A |
C |
5: 3,743,479 (GRCm39) |
D845E |
probably benign |
Het |
Atxn2 |
T |
C |
5: 121,919,399 (GRCm39) |
V369A |
possibly damaging |
Het |
Ccdc50 |
T |
A |
16: 27,225,534 (GRCm39) |
|
probably benign |
Het |
Clec2g |
A |
G |
6: 128,957,224 (GRCm39) |
I61V |
possibly damaging |
Het |
Col16a1 |
G |
A |
4: 129,955,172 (GRCm39) |
|
probably benign |
Het |
Dapk2 |
A |
G |
9: 66,139,096 (GRCm39) |
Y139C |
probably damaging |
Het |
Ecpas |
A |
G |
4: 58,840,757 (GRCm39) |
V667A |
probably damaging |
Het |
Fnip1 |
T |
C |
11: 54,384,177 (GRCm39) |
L334P |
probably damaging |
Het |
Igf1r |
A |
G |
7: 67,839,739 (GRCm39) |
E682G |
possibly damaging |
Het |
Ints8 |
T |
C |
4: 11,241,627 (GRCm39) |
E272G |
possibly damaging |
Het |
Jph2 |
G |
A |
2: 163,217,699 (GRCm39) |
P326S |
probably damaging |
Het |
Krtap1-4 |
T |
C |
11: 99,473,940 (GRCm39) |
|
probably benign |
Het |
Lrrk1 |
A |
G |
7: 65,958,439 (GRCm39) |
V320A |
probably benign |
Het |
Myh6 |
A |
C |
14: 55,191,381 (GRCm39) |
I820S |
possibly damaging |
Het |
Napg |
A |
T |
18: 63,119,319 (GRCm39) |
T110S |
probably damaging |
Het |
Nova1 |
G |
A |
12: 46,767,475 (GRCm39) |
Q56* |
probably null |
Het |
Phyhip |
A |
G |
14: 70,699,367 (GRCm39) |
|
probably null |
Het |
Pkd2l2 |
C |
A |
18: 34,549,970 (GRCm39) |
S205* |
probably null |
Het |
Ppp2r1a |
G |
T |
17: 21,179,265 (GRCm39) |
C101F |
probably benign |
Het |
Serpinb3c |
G |
A |
1: 107,200,872 (GRCm39) |
R182* |
probably null |
Het |
St18 |
A |
C |
1: 6,872,540 (GRCm39) |
|
probably benign |
Het |
St6galnac4 |
C |
T |
2: 32,487,096 (GRCm39) |
R264C |
possibly damaging |
Het |
Tmem168 |
T |
C |
6: 13,603,261 (GRCm39) |
Y35C |
probably benign |
Het |
Tmem219 |
A |
G |
7: 126,496,220 (GRCm39) |
L74P |
probably damaging |
Het |
Trpc4 |
T |
A |
3: 54,206,667 (GRCm39) |
N622K |
probably damaging |
Het |
Trpm6 |
A |
C |
19: 18,807,376 (GRCm39) |
|
probably benign |
Het |
Ttl |
C |
A |
2: 128,908,213 (GRCm39) |
F49L |
possibly damaging |
Het |
Tut7 |
C |
T |
13: 59,964,156 (GRCm39) |
D250N |
probably damaging |
Het |
Vmn1r123 |
A |
T |
7: 20,896,968 (GRCm39) |
I287F |
possibly damaging |
Het |
Vmn2r97 |
T |
G |
17: 19,149,432 (GRCm39) |
I273M |
probably damaging |
Het |
Wdr5 |
C |
A |
2: 27,410,437 (GRCm39) |
|
probably benign |
Het |
Zfp37 |
C |
A |
4: 62,110,548 (GRCm39) |
C172F |
possibly 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 |
IGL02471:Lrp5
|
APN |
19 |
3,652,408 (GRCm39) |
missense |
probably benign |
0.31 |
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 |
|
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 |
|
|