Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700088E04Rik |
T |
C |
15: 79,135,203 (GRCm38) |
D179G |
probably benign |
Het |
Adh7 |
C |
T |
3: 138,221,729 (GRCm38) |
A12V |
probably benign |
Het |
Ankhd1 |
T |
A |
18: 36,634,346 (GRCm38) |
N1179K |
probably damaging |
Het |
Ankrd50 |
T |
C |
3: 38,457,187 (GRCm38) |
T344A |
probably benign |
Het |
Aplf |
T |
C |
6: 87,646,291 (GRCm38) |
T269A |
probably benign |
Het |
C87977 |
G |
A |
4: 144,207,124 (GRCm38) |
T471I |
probably damaging |
Het |
Cavin4 |
T |
C |
4: 48,663,637 (GRCm38) |
S6P |
probably damaging |
Het |
Ces2g |
T |
C |
8: 104,967,462 (GRCm38) |
|
probably null |
Het |
Cyp2c66 |
A |
T |
19: 39,163,368 (GRCm38) |
N176Y |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,923,030 (GRCm38) |
D3980V |
probably damaging |
Het |
Drc7 |
G |
T |
8: 95,072,788 (GRCm38) |
E530D |
probably damaging |
Het |
Dst |
A |
G |
1: 34,275,277 (GRCm38) |
T6434A |
probably damaging |
Het |
Dtx3l |
A |
G |
16: 35,938,757 (GRCm38) |
S41P |
possibly damaging |
Het |
Eef1b2 |
G |
A |
1: 63,179,457 (GRCm38) |
|
probably null |
Het |
Eml3 |
C |
T |
19: 8,936,308 (GRCm38) |
T43I |
probably damaging |
Het |
Fam110b |
T |
A |
4: 5,799,434 (GRCm38) |
L284Q |
probably damaging |
Het |
Gm5538 |
G |
A |
3: 59,751,893 (GRCm38) |
E256K |
probably benign |
Het |
Gpr33 |
A |
C |
12: 52,023,469 (GRCm38) |
H262Q |
probably damaging |
Het |
Igfals |
T |
G |
17: 24,880,481 (GRCm38) |
L182R |
probably damaging |
Het |
Mgea5 |
G |
A |
19: 45,752,155 (GRCm38) |
R914* |
probably null |
Het |
Muc4 |
T |
A |
16: 32,750,525 (GRCm38) |
H134Q |
possibly damaging |
Het |
Nckap1 |
C |
T |
2: 80,517,942 (GRCm38) |
S889N |
probably benign |
Het |
Nxn |
A |
T |
11: 76,274,069 (GRCm38) |
C205* |
probably null |
Het |
Olfr323 |
T |
C |
11: 58,625,458 (GRCm38) |
E196G |
probably damaging |
Het |
Olfr651 |
C |
A |
7: 104,553,086 (GRCm38) |
H56N |
possibly damaging |
Het |
Pamr1 |
A |
T |
2: 102,639,353 (GRCm38) |
I415F |
possibly damaging |
Het |
Ppp4r4 |
G |
A |
12: 103,579,068 (GRCm38) |
G200E |
probably damaging |
Het |
Prdm16 |
C |
A |
4: 154,528,799 (GRCm38) |
S57I |
probably damaging |
Het |
Psmd11 |
A |
G |
11: 80,471,584 (GRCm38) |
K157R |
possibly damaging |
Het |
Ptprn2 |
G |
A |
12: 117,212,008 (GRCm38) |
|
probably null |
Het |
Pus7 |
G |
A |
5: 23,768,795 (GRCm38) |
H234Y |
probably benign |
Het |
Rd3l |
A |
G |
12: 111,980,283 (GRCm38) |
Y20H |
probably benign |
Het |
Stk31 |
A |
G |
6: 49,409,207 (GRCm38) |
D160G |
probably damaging |
Het |
Sycp2 |
C |
T |
2: 178,374,366 (GRCm38) |
E768K |
possibly damaging |
Het |
Tango6 |
T |
C |
8: 106,688,895 (GRCm38) |
V116A |
probably benign |
Het |
Ttn |
C |
T |
2: 76,867,230 (GRCm38) |
|
probably benign |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,290,932 (GRCm38) |
|
probably null |
Het |
Xylb |
T |
C |
9: 119,383,377 (GRCm38) |
I427T |
probably damaging |
Het |
Zc3h7a |
T |
G |
16: 11,139,075 (GRCm38) |
D890A |
probably damaging |
Het |
|
Other mutations in Lamc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00950:Lamc1
|
APN |
1 |
153,240,495 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01397:Lamc1
|
APN |
1 |
153,251,134 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01661:Lamc1
|
APN |
1 |
153,221,573 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01894:Lamc1
|
APN |
1 |
153,247,082 (GRCm38) |
missense |
possibly damaging |
0.51 |
IGL02000:Lamc1
|
APN |
1 |
153,240,433 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02649:Lamc1
|
APN |
1 |
153,247,042 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL02749:Lamc1
|
APN |
1 |
153,249,853 (GRCm38) |
missense |
possibly damaging |
0.51 |
IGL02819:Lamc1
|
APN |
1 |
153,250,661 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02831:Lamc1
|
APN |
1 |
153,247,055 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03069:Lamc1
|
APN |
1 |
153,239,381 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03143:Lamc1
|
APN |
1 |
153,332,274 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03166:Lamc1
|
APN |
1 |
153,332,301 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03285:Lamc1
|
APN |
1 |
153,227,685 (GRCm38) |
missense |
possibly damaging |
0.96 |
IGL03294:Lamc1
|
APN |
1 |
153,262,646 (GRCm38) |
missense |
probably damaging |
1.00 |
pride
|
UTSW |
1 |
153,247,284 (GRCm38) |
missense |
probably benign |
0.01 |
Stratum
|
UTSW |
1 |
153,251,124 (GRCm38) |
nonsense |
probably null |
|
tier
|
UTSW |
1 |
153,250,522 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4280001:Lamc1
|
UTSW |
1 |
153,243,471 (GRCm38) |
missense |
probably damaging |
1.00 |
R0003:Lamc1
|
UTSW |
1 |
153,262,439 (GRCm38) |
missense |
probably damaging |
0.99 |
R0003:Lamc1
|
UTSW |
1 |
153,262,439 (GRCm38) |
missense |
probably damaging |
0.99 |
R0027:Lamc1
|
UTSW |
1 |
153,262,583 (GRCm38) |
missense |
probably damaging |
1.00 |
R0060:Lamc1
|
UTSW |
1 |
153,241,868 (GRCm38) |
unclassified |
probably benign |
|
R0078:Lamc1
|
UTSW |
1 |
153,229,190 (GRCm38) |
missense |
probably damaging |
0.96 |
R0157:Lamc1
|
UTSW |
1 |
153,262,607 (GRCm38) |
missense |
probably benign |
0.00 |
R0282:Lamc1
|
UTSW |
1 |
153,255,312 (GRCm38) |
missense |
probably benign |
|
R0374:Lamc1
|
UTSW |
1 |
153,251,065 (GRCm38) |
splice site |
probably benign |
|
R0494:Lamc1
|
UTSW |
1 |
153,246,936 (GRCm38) |
critical splice donor site |
probably null |
|
R0502:Lamc1
|
UTSW |
1 |
153,246,932 (GRCm38) |
splice site |
probably benign |
|
R0755:Lamc1
|
UTSW |
1 |
153,247,450 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0791:Lamc1
|
UTSW |
1 |
153,234,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R0791:Lamc1
|
UTSW |
1 |
153,234,580 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0791:Lamc1
|
UTSW |
1 |
153,234,612 (GRCm38) |
missense |
probably benign |
0.01 |
R0792:Lamc1
|
UTSW |
1 |
153,234,580 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0792:Lamc1
|
UTSW |
1 |
153,234,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R0792:Lamc1
|
UTSW |
1 |
153,234,612 (GRCm38) |
missense |
probably benign |
0.01 |
R0892:Lamc1
|
UTSW |
1 |
153,332,254 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0941:Lamc1
|
UTSW |
1 |
153,332,274 (GRCm38) |
missense |
possibly damaging |
0.72 |
R0961:Lamc1
|
UTSW |
1 |
153,221,700 (GRCm38) |
missense |
probably benign |
0.03 |
R0961:Lamc1
|
UTSW |
1 |
153,221,646 (GRCm38) |
frame shift |
probably null |
|
R0963:Lamc1
|
UTSW |
1 |
153,243,386 (GRCm38) |
missense |
probably benign |
|
R1173:Lamc1
|
UTSW |
1 |
153,247,231 (GRCm38) |
splice site |
probably benign |
|
R1175:Lamc1
|
UTSW |
1 |
153,247,231 (GRCm38) |
splice site |
probably benign |
|
R1449:Lamc1
|
UTSW |
1 |
153,250,495 (GRCm38) |
missense |
probably benign |
|
R1481:Lamc1
|
UTSW |
1 |
153,221,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R1565:Lamc1
|
UTSW |
1 |
153,242,743 (GRCm38) |
missense |
probably benign |
0.34 |
R1583:Lamc1
|
UTSW |
1 |
153,243,478 (GRCm38) |
critical splice acceptor site |
probably null |
|
R1643:Lamc1
|
UTSW |
1 |
153,258,072 (GRCm38) |
splice site |
probably benign |
|
R1652:Lamc1
|
UTSW |
1 |
153,249,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R1691:Lamc1
|
UTSW |
1 |
153,247,249 (GRCm38) |
missense |
probably benign |
0.04 |
R1854:Lamc1
|
UTSW |
1 |
153,249,872 (GRCm38) |
missense |
probably damaging |
0.99 |
R2018:Lamc1
|
UTSW |
1 |
153,242,632 (GRCm38) |
missense |
probably benign |
0.07 |
R2170:Lamc1
|
UTSW |
1 |
153,249,142 (GRCm38) |
missense |
probably benign |
0.07 |
R2410:Lamc1
|
UTSW |
1 |
153,247,395 (GRCm38) |
missense |
possibly damaging |
0.61 |
R3438:Lamc1
|
UTSW |
1 |
153,226,415 (GRCm38) |
missense |
probably benign |
0.04 |
R3615:Lamc1
|
UTSW |
1 |
153,251,150 (GRCm38) |
missense |
probably damaging |
1.00 |
R3616:Lamc1
|
UTSW |
1 |
153,251,150 (GRCm38) |
missense |
probably damaging |
1.00 |
R3699:Lamc1
|
UTSW |
1 |
153,255,205 (GRCm38) |
missense |
possibly damaging |
0.79 |
R3811:Lamc1
|
UTSW |
1 |
153,262,708 (GRCm38) |
splice site |
probably null |
|
R4285:Lamc1
|
UTSW |
1 |
153,234,552 (GRCm38) |
missense |
probably damaging |
0.99 |
R4431:Lamc1
|
UTSW |
1 |
153,221,528 (GRCm38) |
missense |
probably damaging |
1.00 |
R4579:Lamc1
|
UTSW |
1 |
153,247,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R4625:Lamc1
|
UTSW |
1 |
153,242,696 (GRCm38) |
missense |
probably benign |
0.04 |
R4649:Lamc1
|
UTSW |
1 |
153,228,777 (GRCm38) |
missense |
probably damaging |
0.99 |
R4650:Lamc1
|
UTSW |
1 |
153,228,777 (GRCm38) |
missense |
probably damaging |
0.99 |
R4651:Lamc1
|
UTSW |
1 |
153,228,777 (GRCm38) |
missense |
probably damaging |
0.99 |
R4652:Lamc1
|
UTSW |
1 |
153,228,777 (GRCm38) |
missense |
probably damaging |
0.99 |
R4653:Lamc1
|
UTSW |
1 |
153,228,777 (GRCm38) |
missense |
probably damaging |
0.99 |
R4784:Lamc1
|
UTSW |
1 |
153,231,740 (GRCm38) |
missense |
probably damaging |
1.00 |
R4785:Lamc1
|
UTSW |
1 |
153,231,740 (GRCm38) |
missense |
probably damaging |
1.00 |
R4853:Lamc1
|
UTSW |
1 |
153,229,100 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5216:Lamc1
|
UTSW |
1 |
153,227,696 (GRCm38) |
missense |
probably damaging |
1.00 |
R5217:Lamc1
|
UTSW |
1 |
153,227,696 (GRCm38) |
missense |
probably damaging |
1.00 |
R5218:Lamc1
|
UTSW |
1 |
153,227,696 (GRCm38) |
missense |
probably damaging |
1.00 |
R5219:Lamc1
|
UTSW |
1 |
153,227,696 (GRCm38) |
missense |
probably damaging |
1.00 |
R5468:Lamc1
|
UTSW |
1 |
153,233,564 (GRCm38) |
missense |
probably damaging |
0.99 |
R5597:Lamc1
|
UTSW |
1 |
153,251,970 (GRCm38) |
missense |
probably damaging |
1.00 |
R5754:Lamc1
|
UTSW |
1 |
153,247,284 (GRCm38) |
missense |
probably benign |
0.01 |
R6233:Lamc1
|
UTSW |
1 |
153,223,666 (GRCm38) |
missense |
probably benign |
|
R6431:Lamc1
|
UTSW |
1 |
153,221,671 (GRCm38) |
missense |
probably benign |
0.21 |
R6636:Lamc1
|
UTSW |
1 |
153,241,975 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6888:Lamc1
|
UTSW |
1 |
153,262,492 (GRCm38) |
missense |
probably damaging |
1.00 |
R7161:Lamc1
|
UTSW |
1 |
153,226,454 (GRCm38) |
missense |
probably damaging |
1.00 |
R7240:Lamc1
|
UTSW |
1 |
153,234,650 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7388:Lamc1
|
UTSW |
1 |
153,249,076 (GRCm38) |
missense |
probably damaging |
1.00 |
R7474:Lamc1
|
UTSW |
1 |
153,332,265 (GRCm38) |
missense |
possibly damaging |
0.81 |
R7570:Lamc1
|
UTSW |
1 |
153,243,275 (GRCm38) |
missense |
possibly damaging |
0.64 |
R7583:Lamc1
|
UTSW |
1 |
153,243,232 (GRCm38) |
missense |
possibly damaging |
0.71 |
R7597:Lamc1
|
UTSW |
1 |
153,240,454 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7635:Lamc1
|
UTSW |
1 |
153,249,060 (GRCm38) |
missense |
probably damaging |
1.00 |
R7976:Lamc1
|
UTSW |
1 |
153,247,268 (GRCm38) |
missense |
probably damaging |
1.00 |
R8012:Lamc1
|
UTSW |
1 |
153,221,612 (GRCm38) |
missense |
probably benign |
0.04 |
R8207:Lamc1
|
UTSW |
1 |
153,250,522 (GRCm38) |
missense |
probably damaging |
1.00 |
R8219:Lamc1
|
UTSW |
1 |
153,247,327 (GRCm38) |
missense |
probably damaging |
1.00 |
R8227:Lamc1
|
UTSW |
1 |
153,223,754 (GRCm38) |
missense |
probably benign |
0.04 |
R8315:Lamc1
|
UTSW |
1 |
153,243,421 (GRCm38) |
missense |
probably benign |
0.00 |
R8417:Lamc1
|
UTSW |
1 |
153,230,769 (GRCm38) |
missense |
probably damaging |
1.00 |
R8685:Lamc1
|
UTSW |
1 |
153,233,542 (GRCm38) |
missense |
probably benign |
0.31 |
R8827:Lamc1
|
UTSW |
1 |
153,221,678 (GRCm38) |
missense |
probably damaging |
1.00 |
R8995:Lamc1
|
UTSW |
1 |
153,332,247 (GRCm38) |
missense |
probably benign |
0.00 |
R9061:Lamc1
|
UTSW |
1 |
153,251,124 (GRCm38) |
nonsense |
probably null |
|
R9141:Lamc1
|
UTSW |
1 |
153,247,450 (GRCm38) |
missense |
probably benign |
0.01 |
R9187:Lamc1
|
UTSW |
1 |
153,221,688 (GRCm38) |
nonsense |
probably null |
|
R9206:Lamc1
|
UTSW |
1 |
153,250,451 (GRCm38) |
missense |
probably damaging |
1.00 |
R9222:Lamc1
|
UTSW |
1 |
153,243,341 (GRCm38) |
missense |
probably damaging |
0.96 |
R9297:Lamc1
|
UTSW |
1 |
153,252,000 (GRCm38) |
missense |
probably damaging |
1.00 |
R9318:Lamc1
|
UTSW |
1 |
153,252,000 (GRCm38) |
missense |
probably damaging |
1.00 |
R9377:Lamc1
|
UTSW |
1 |
153,239,263 (GRCm38) |
missense |
probably benign |
|
|