Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c20 |
A |
G |
13: 4,562,664 (GRCm39) |
|
probably null |
Het |
Alg5 |
T |
C |
3: 54,652,140 (GRCm39) |
|
probably benign |
Het |
App |
A |
T |
16: 84,762,599 (GRCm39) |
F675I |
probably damaging |
Het |
Atad1 |
C |
A |
19: 32,675,968 (GRCm39) |
C152F |
probably benign |
Het |
Atp2a3 |
A |
C |
11: 72,873,613 (GRCm39) |
I829L |
probably damaging |
Het |
B3galt1 |
C |
T |
2: 67,949,050 (GRCm39) |
S255L |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,964,754 (GRCm39) |
V1417A |
possibly damaging |
Het |
Cast |
T |
A |
13: 74,885,093 (GRCm39) |
T219S |
probably damaging |
Het |
Cep95 |
A |
T |
11: 106,709,043 (GRCm39) |
I705F |
probably damaging |
Het |
Cnot3 |
C |
T |
7: 3,653,854 (GRCm39) |
A2V |
probably damaging |
Het |
Col1a1 |
A |
G |
11: 94,840,204 (GRCm39) |
D1084G |
unknown |
Het |
Col5a3 |
G |
A |
9: 20,697,685 (GRCm39) |
Q873* |
probably null |
Het |
Cubn |
C |
T |
2: 13,386,738 (GRCm39) |
G1509D |
probably damaging |
Het |
Defb10 |
T |
A |
8: 22,351,952 (GRCm39) |
C66S |
possibly damaging |
Het |
Dennd4b |
T |
C |
3: 90,186,993 (GRCm39) |
|
probably null |
Het |
Dido1 |
G |
A |
2: 180,331,319 (GRCm39) |
T43M |
possibly damaging |
Het |
Hmcn1 |
C |
T |
1: 150,506,091 (GRCm39) |
V3812I |
probably benign |
Het |
Islr2 |
T |
C |
9: 58,107,069 (GRCm39) |
T64A |
probably benign |
Het |
Kif2b |
A |
T |
11: 91,467,206 (GRCm39) |
I359N |
probably damaging |
Het |
Kit |
A |
C |
5: 75,806,619 (GRCm39) |
N704T |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 78,918,343 (GRCm39) |
F604L |
probably damaging |
Het |
Lrrn1 |
A |
G |
6: 107,545,269 (GRCm39) |
T356A |
probably benign |
Het |
Mrps17 |
G |
A |
5: 129,793,829 (GRCm39) |
V8I |
probably benign |
Het |
Nop56 |
T |
A |
2: 130,117,915 (GRCm39) |
H130Q |
possibly damaging |
Het |
Plg |
T |
A |
17: 12,630,380 (GRCm39) |
L639Q |
probably damaging |
Het |
Ppcdc |
A |
G |
9: 57,322,423 (GRCm39) |
F159L |
probably benign |
Het |
Ppp1ca |
A |
G |
19: 4,244,519 (GRCm39) |
T193A |
probably benign |
Het |
Prpf39 |
A |
G |
12: 65,090,037 (GRCm39) |
D117G |
probably damaging |
Het |
Ranbp2 |
C |
A |
10: 58,289,145 (GRCm39) |
T51K |
possibly damaging |
Het |
Sytl2 |
A |
G |
7: 90,031,844 (GRCm39) |
|
probably benign |
Het |
Tenm2 |
T |
A |
11: 35,915,085 (GRCm39) |
I2150F |
probably damaging |
Het |
Wdr11 |
T |
G |
7: 129,194,817 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Lrp5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
|
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 |
|
|