Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr2 |
T |
G |
9: 121,738,333 (GRCm39) |
L236R |
probably damaging |
Het |
Agbl1 |
C |
T |
7: 76,069,793 (GRCm39) |
Q442* |
probably null |
Het |
Ahrr |
G |
A |
13: 74,405,614 (GRCm39) |
Q108* |
probably null |
Het |
Ankrd23 |
T |
C |
1: 36,570,726 (GRCm39) |
|
probably benign |
Het |
Art5 |
A |
G |
7: 101,747,104 (GRCm39) |
I225T |
probably damaging |
Het |
Asxl3 |
T |
C |
18: 22,656,031 (GRCm39) |
V1347A |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,905,994 (GRCm39) |
M1326V |
possibly damaging |
Het |
Bpifb6 |
A |
C |
2: 153,744,655 (GRCm39) |
N32T |
probably damaging |
Het |
Brip1 |
T |
A |
11: 85,952,653 (GRCm39) |
T1043S |
possibly damaging |
Het |
Cbx5 |
A |
T |
15: 103,121,532 (GRCm39) |
V35E |
probably damaging |
Het |
Ccdc175 |
T |
A |
12: 72,182,832 (GRCm39) |
M396L |
probably benign |
Het |
Ceacam3 |
G |
T |
7: 16,892,045 (GRCm39) |
E263* |
probably null |
Het |
Cyp4a12a |
A |
G |
4: 115,159,200 (GRCm39) |
T157A |
probably benign |
Het |
Dennd11 |
A |
T |
6: 40,399,828 (GRCm39) |
|
probably benign |
Het |
Derl3 |
T |
C |
10: 75,730,324 (GRCm39) |
V129A |
possibly damaging |
Het |
Dnajb1 |
T |
C |
8: 84,335,103 (GRCm39) |
I48T |
probably damaging |
Het |
Dop1b |
G |
A |
16: 93,556,543 (GRCm39) |
E349K |
probably benign |
Het |
Fkbp10 |
A |
T |
11: 100,313,580 (GRCm39) |
I285F |
probably benign |
Het |
Frrs1 |
A |
T |
3: 116,692,836 (GRCm39) |
T37S |
probably damaging |
Het |
Gata2 |
A |
G |
6: 88,181,677 (GRCm39) |
Y377C |
probably damaging |
Het |
Gm9789 |
T |
A |
16: 88,954,883 (GRCm39) |
|
probably benign |
Het |
Itpkb |
T |
A |
1: 180,160,933 (GRCm39) |
V353D |
probably benign |
Het |
Kcng4 |
T |
C |
8: 120,352,509 (GRCm39) |
E467G |
probably damaging |
Het |
Kdm3a |
A |
T |
6: 71,573,845 (GRCm39) |
I906N |
probably damaging |
Het |
Lama1 |
G |
A |
17: 68,111,531 (GRCm39) |
G2261R |
probably damaging |
Het |
Lef1 |
G |
T |
3: 130,993,965 (GRCm39) |
E314* |
probably null |
Het |
Lpin3 |
T |
C |
2: 160,745,518 (GRCm39) |
|
probably benign |
Het |
Mrtfb |
A |
G |
16: 13,218,676 (GRCm39) |
N452D |
possibly damaging |
Het |
Naaladl1 |
C |
T |
19: 6,164,896 (GRCm39) |
T628I |
possibly damaging |
Het |
Nell1 |
C |
T |
7: 49,929,281 (GRCm39) |
Q259* |
probably null |
Het |
Neu2 |
G |
T |
1: 87,524,698 (GRCm39) |
E228* |
probably null |
Het |
Or5b119 |
A |
T |
19: 13,456,835 (GRCm39) |
H242Q |
probably damaging |
Het |
Or5k15 |
A |
G |
16: 58,709,824 (GRCm39) |
F253S |
probably damaging |
Het |
Or8g21 |
T |
G |
9: 38,906,732 (GRCm39) |
|
probably benign |
Het |
Or8k20 |
T |
C |
2: 86,106,580 (GRCm39) |
N84D |
probably benign |
Het |
Osbpl6 |
T |
A |
2: 76,378,716 (GRCm39) |
D124E |
probably damaging |
Het |
Palm |
T |
C |
10: 79,652,617 (GRCm39) |
|
probably benign |
Het |
Parp8 |
C |
A |
13: 117,047,497 (GRCm39) |
|
probably benign |
Het |
Pax7 |
A |
G |
4: 139,556,798 (GRCm39) |
|
probably benign |
Het |
Pcnx3 |
G |
A |
19: 5,735,423 (GRCm39) |
R468W |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,702,722 (GRCm39) |
V818D |
probably damaging |
Het |
Piezo2 |
C |
T |
18: 63,241,147 (GRCm39) |
V694I |
probably damaging |
Het |
Plk1 |
A |
G |
7: 121,760,877 (GRCm39) |
|
probably benign |
Het |
Polb |
T |
C |
8: 23,130,367 (GRCm39) |
|
probably benign |
Het |
Rad54b |
A |
G |
4: 11,599,755 (GRCm39) |
T320A |
probably damaging |
Het |
Reg3b |
G |
A |
6: 78,349,183 (GRCm39) |
W103* |
probably null |
Het |
Slc17a3 |
T |
G |
13: 24,039,962 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
C |
T |
2: 127,071,962 (GRCm39) |
|
probably benign |
Het |
Stox2 |
T |
A |
8: 47,646,839 (GRCm39) |
H207L |
possibly damaging |
Het |
Tbx15 |
A |
C |
3: 99,259,514 (GRCm39) |
M462L |
possibly damaging |
Het |
Tcirg1 |
G |
A |
19: 3,948,811 (GRCm39) |
T458I |
probably damaging |
Het |
Tnfrsf25 |
A |
G |
4: 152,201,384 (GRCm39) |
|
probably benign |
Het |
Trank1 |
A |
G |
9: 111,195,155 (GRCm39) |
K1060E |
probably damaging |
Het |
Ttc16 |
T |
C |
2: 32,664,457 (GRCm39) |
D3G |
possibly damaging |
Het |
Vmn1r199 |
A |
C |
13: 22,567,299 (GRCm39) |
N155H |
probably damaging |
Het |
Vmn1r202 |
G |
A |
13: 22,685,640 (GRCm39) |
T259I |
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 |
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 |
153,110,358 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
R0792:Lamc1
|
UTSW |
1 |
153,110,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Lamc1
|
UTSW |
1 |
153,110,326 (GRCm39) |
missense |
possibly damaging |
0.94 |
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 |
153,097,392 (GRCm39) |
frame shift |
probably null |
|
R0961:Lamc1
|
UTSW |
1 |
153,097,446 (GRCm39) |
missense |
probably benign |
0.03 |
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 |
R2410:Lamc1
|
UTSW |
1 |
153,123,141 (GRCm39) |
missense |
possibly damaging |
0.61 |
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 |
|
|