Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
Adgrf5 |
C |
A |
17: 43,766,157 (GRCm39) |
N1326K |
probably benign |
Het |
Ciita |
A |
G |
16: 10,328,568 (GRCm39) |
E284G |
probably damaging |
Het |
Ctbp2 |
T |
C |
7: 132,616,083 (GRCm39) |
Y284C |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,991,262 (GRCm39) |
D2368G |
probably damaging |
Het |
Enpp3 |
C |
T |
10: 24,650,716 (GRCm39) |
V807I |
probably benign |
Het |
Erich3 |
A |
G |
3: 154,439,240 (GRCm39) |
D491G |
probably damaging |
Het |
Ero1a |
C |
T |
14: 45,542,723 (GRCm39) |
V101I |
possibly damaging |
Het |
Fbxl7 |
A |
G |
15: 26,895,111 (GRCm39) |
Y9H |
possibly damaging |
Het |
Fzd2 |
A |
G |
11: 102,496,453 (GRCm39) |
Y299C |
possibly damaging |
Het |
Lrrc39 |
C |
T |
3: 116,374,899 (GRCm39) |
P327S |
probably benign |
Het |
Marf1 |
A |
T |
16: 13,933,691 (GRCm39) |
F1566I |
probably benign |
Het |
Me2 |
A |
T |
18: 73,924,183 (GRCm39) |
M343K |
probably damaging |
Het |
Mlxip |
T |
A |
5: 123,581,132 (GRCm39) |
W260R |
probably damaging |
Het |
Mrps17 |
T |
C |
5: 129,795,047 (GRCm39) |
V64A |
probably damaging |
Het |
Or4c118 |
A |
T |
2: 88,974,899 (GRCm39) |
I156N |
possibly damaging |
Het |
Phldb3 |
C |
T |
7: 24,323,719 (GRCm39) |
S450L |
probably benign |
Het |
Pi4k2a |
A |
G |
19: 42,093,316 (GRCm39) |
E219G |
possibly damaging |
Het |
Polr1a |
T |
C |
6: 71,951,866 (GRCm39) |
S1478P |
probably benign |
Het |
Rab14 |
T |
C |
2: 35,076,762 (GRCm39) |
|
probably null |
Het |
Rnf43 |
T |
C |
11: 87,623,085 (GRCm39) |
Y729H |
possibly damaging |
Het |
Sgms1 |
G |
A |
19: 32,137,072 (GRCm39) |
R165* |
probably null |
Het |
Sorbs1 |
T |
A |
19: 40,361,959 (GRCm39) |
I142F |
probably damaging |
Het |
Tmem255b |
A |
G |
8: 13,491,278 (GRCm39) |
I66V |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,996,123 (GRCm39) |
D175G |
probably damaging |
Het |
Zfp954 |
A |
T |
7: 7,120,808 (GRCm39) |
I74N |
probably benign |
Het |
|
Other mutations in Lamc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00950:Lamc1
|
APN |
1 |
153,116,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01397:Lamc1
|
APN |
1 |
153,126,880 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01661:Lamc1
|
APN |
1 |
153,097,319 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01894:Lamc1
|
APN |
1 |
153,122,828 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02000:Lamc1
|
APN |
1 |
153,116,179 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Lamc1
|
APN |
1 |
153,122,788 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02749:Lamc1
|
APN |
1 |
153,125,599 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02819:Lamc1
|
APN |
1 |
153,126,407 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02831:Lamc1
|
APN |
1 |
153,122,801 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03069:Lamc1
|
APN |
1 |
153,115,127 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03143:Lamc1
|
APN |
1 |
153,208,020 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03166:Lamc1
|
APN |
1 |
153,208,047 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03285:Lamc1
|
APN |
1 |
153,103,431 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03294:Lamc1
|
APN |
1 |
153,138,392 (GRCm39) |
missense |
probably damaging |
1.00 |
pride
|
UTSW |
1 |
153,123,030 (GRCm39) |
missense |
probably benign |
0.01 |
Stratum
|
UTSW |
1 |
153,126,870 (GRCm39) |
nonsense |
probably null |
|
tier
|
UTSW |
1 |
153,126,268 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Lamc1
|
UTSW |
1 |
153,119,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Lamc1
|
UTSW |
1 |
153,138,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0003:Lamc1
|
UTSW |
1 |
153,138,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Lamc1
|
UTSW |
1 |
153,138,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Lamc1
|
UTSW |
1 |
153,117,614 (GRCm39) |
unclassified |
probably benign |
|
R0078:Lamc1
|
UTSW |
1 |
153,104,936 (GRCm39) |
missense |
probably damaging |
0.96 |
R0157:Lamc1
|
UTSW |
1 |
153,138,353 (GRCm39) |
missense |
probably benign |
0.00 |
R0282:Lamc1
|
UTSW |
1 |
153,131,058 (GRCm39) |
missense |
probably benign |
|
R0374:Lamc1
|
UTSW |
1 |
153,126,811 (GRCm39) |
splice site |
probably benign |
|
R0494:Lamc1
|
UTSW |
1 |
153,122,682 (GRCm39) |
critical splice donor site |
probably null |
|
R0502:Lamc1
|
UTSW |
1 |
153,122,678 (GRCm39) |
splice site |
probably benign |
|
R0755:Lamc1
|
UTSW |
1 |
153,123,196 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0791:Lamc1
|
UTSW |
1 |
153,110,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0791:Lamc1
|
UTSW |
1 |
153,110,326 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0791:Lamc1
|
UTSW |
1 |
153,110,358 (GRCm39) |
missense |
probably benign |
0.01 |
R0792:Lamc1
|
UTSW |
1 |
153,110,326 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0792:Lamc1
|
UTSW |
1 |
153,110,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Lamc1
|
UTSW |
1 |
153,110,358 (GRCm39) |
missense |
probably benign |
0.01 |
R0892:Lamc1
|
UTSW |
1 |
153,208,000 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0941:Lamc1
|
UTSW |
1 |
153,208,020 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0961:Lamc1
|
UTSW |
1 |
153,097,446 (GRCm39) |
missense |
probably benign |
0.03 |
R0961:Lamc1
|
UTSW |
1 |
153,097,392 (GRCm39) |
frame shift |
probably null |
|
R0963:Lamc1
|
UTSW |
1 |
153,119,132 (GRCm39) |
missense |
probably benign |
|
R1127:Lamc1
|
UTSW |
1 |
153,126,205 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1173:Lamc1
|
UTSW |
1 |
153,122,977 (GRCm39) |
splice site |
probably benign |
|
R1175:Lamc1
|
UTSW |
1 |
153,122,977 (GRCm39) |
splice site |
probably benign |
|
R1449:Lamc1
|
UTSW |
1 |
153,126,241 (GRCm39) |
missense |
probably benign |
|
R1481:Lamc1
|
UTSW |
1 |
153,097,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Lamc1
|
UTSW |
1 |
153,118,489 (GRCm39) |
missense |
probably benign |
0.34 |
R1583:Lamc1
|
UTSW |
1 |
153,119,224 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1643:Lamc1
|
UTSW |
1 |
153,133,818 (GRCm39) |
splice site |
probably benign |
|
R1652:Lamc1
|
UTSW |
1 |
153,125,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Lamc1
|
UTSW |
1 |
153,122,995 (GRCm39) |
missense |
probably benign |
0.04 |
R1854:Lamc1
|
UTSW |
1 |
153,125,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R2018:Lamc1
|
UTSW |
1 |
153,118,378 (GRCm39) |
missense |
probably benign |
0.07 |
R2170:Lamc1
|
UTSW |
1 |
153,124,888 (GRCm39) |
missense |
probably benign |
0.07 |
R3438:Lamc1
|
UTSW |
1 |
153,102,161 (GRCm39) |
missense |
probably benign |
0.04 |
R3615:Lamc1
|
UTSW |
1 |
153,126,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R3616:Lamc1
|
UTSW |
1 |
153,126,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R3699:Lamc1
|
UTSW |
1 |
153,130,951 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3811:Lamc1
|
UTSW |
1 |
153,138,454 (GRCm39) |
splice site |
probably null |
|
R4285:Lamc1
|
UTSW |
1 |
153,110,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R4431:Lamc1
|
UTSW |
1 |
153,097,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Lamc1
|
UTSW |
1 |
153,123,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R4625:Lamc1
|
UTSW |
1 |
153,118,442 (GRCm39) |
missense |
probably benign |
0.04 |
R4649:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4650:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4651:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4652:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4653:Lamc1
|
UTSW |
1 |
153,104,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R4784:Lamc1
|
UTSW |
1 |
153,107,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Lamc1
|
UTSW |
1 |
153,107,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4853:Lamc1
|
UTSW |
1 |
153,104,846 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5216:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5218:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Lamc1
|
UTSW |
1 |
153,103,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5468:Lamc1
|
UTSW |
1 |
153,109,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R5597:Lamc1
|
UTSW |
1 |
153,127,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Lamc1
|
UTSW |
1 |
153,123,030 (GRCm39) |
missense |
probably benign |
0.01 |
R6233:Lamc1
|
UTSW |
1 |
153,099,412 (GRCm39) |
missense |
probably benign |
|
R6431:Lamc1
|
UTSW |
1 |
153,097,417 (GRCm39) |
missense |
probably benign |
0.21 |
R6636:Lamc1
|
UTSW |
1 |
153,117,721 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6888:Lamc1
|
UTSW |
1 |
153,138,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Lamc1
|
UTSW |
1 |
153,102,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7240:Lamc1
|
UTSW |
1 |
153,110,396 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7388:Lamc1
|
UTSW |
1 |
153,124,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Lamc1
|
UTSW |
1 |
153,208,011 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7570:Lamc1
|
UTSW |
1 |
153,119,021 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7583:Lamc1
|
UTSW |
1 |
153,118,978 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7597:Lamc1
|
UTSW |
1 |
153,116,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7635:Lamc1
|
UTSW |
1 |
153,124,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R7976:Lamc1
|
UTSW |
1 |
153,123,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Lamc1
|
UTSW |
1 |
153,097,358 (GRCm39) |
missense |
probably benign |
0.04 |
R8207:Lamc1
|
UTSW |
1 |
153,126,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R8219:Lamc1
|
UTSW |
1 |
153,123,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Lamc1
|
UTSW |
1 |
153,099,500 (GRCm39) |
missense |
probably benign |
0.04 |
R8315:Lamc1
|
UTSW |
1 |
153,119,167 (GRCm39) |
missense |
probably benign |
0.00 |
R8417:Lamc1
|
UTSW |
1 |
153,106,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R8685:Lamc1
|
UTSW |
1 |
153,109,288 (GRCm39) |
missense |
probably benign |
0.31 |
R8827:Lamc1
|
UTSW |
1 |
153,097,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Lamc1
|
UTSW |
1 |
153,207,993 (GRCm39) |
missense |
probably benign |
0.00 |
R9061:Lamc1
|
UTSW |
1 |
153,126,870 (GRCm39) |
nonsense |
probably null |
|
R9141:Lamc1
|
UTSW |
1 |
153,123,196 (GRCm39) |
missense |
probably benign |
0.01 |
R9187:Lamc1
|
UTSW |
1 |
153,097,434 (GRCm39) |
nonsense |
probably null |
|
R9206:Lamc1
|
UTSW |
1 |
153,126,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R9222:Lamc1
|
UTSW |
1 |
153,119,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R9297:Lamc1
|
UTSW |
1 |
153,127,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Lamc1
|
UTSW |
1 |
153,127,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Lamc1
|
UTSW |
1 |
153,115,009 (GRCm39) |
missense |
probably benign |
|
|