Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
G |
A |
4: 53,059,253 (GRCm39) |
|
probably benign |
Het |
Actl6a |
T |
C |
3: 32,776,759 (GRCm39) |
|
probably benign |
Het |
Aoc1l1 |
A |
T |
6: 48,952,767 (GRCm39) |
T231S |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,385,371 (GRCm39) |
|
probably benign |
Het |
Arrdc3 |
A |
G |
13: 81,031,973 (GRCm39) |
T69A |
probably damaging |
Het |
Bbs2 |
T |
C |
8: 94,808,627 (GRCm39) |
K360R |
probably null |
Het |
Cdh8 |
A |
T |
8: 100,006,250 (GRCm39) |
N112K |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,228,809 (GRCm39) |
F474I |
probably damaging |
Het |
Dync1i1 |
G |
A |
6: 5,915,876 (GRCm39) |
D253N |
probably damaging |
Het |
Fam151b |
T |
C |
13: 92,610,480 (GRCm39) |
D103G |
probably damaging |
Het |
Fam227b |
A |
G |
2: 125,845,759 (GRCm39) |
L410P |
probably damaging |
Het |
Ihh |
A |
T |
1: 74,990,372 (GRCm39) |
M1K |
probably null |
Het |
Itga6 |
A |
G |
2: 71,669,060 (GRCm39) |
T617A |
probably benign |
Het |
Itpr1 |
T |
A |
6: 108,363,609 (GRCm39) |
C744S |
probably benign |
Het |
Kif5a |
T |
C |
10: 127,081,311 (GRCm39) |
I208V |
probably benign |
Het |
Lpin3 |
T |
A |
2: 160,734,310 (GRCm39) |
|
probably null |
Het |
Macf1 |
T |
A |
4: 123,270,309 (GRCm39) |
E6612V |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Ncdn |
T |
C |
4: 126,643,833 (GRCm39) |
K330E |
probably benign |
Het |
Neb |
C |
T |
2: 52,073,287 (GRCm39) |
D1975N |
possibly damaging |
Het |
Nell1 |
T |
A |
7: 50,503,621 (GRCm39) |
N675K |
possibly damaging |
Het |
Nlrp6 |
GAGAAGAAGAAGAAGAAGAAGA |
GAGAAGAAGAAGAAGAAGA |
7: 140,504,026 (GRCm39) |
|
probably benign |
Het |
Or4f47 |
G |
A |
2: 111,972,968 (GRCm39) |
R226H |
probably benign |
Het |
Rnf43 |
A |
G |
11: 87,625,003 (GRCm39) |
E737G |
possibly damaging |
Het |
Sardh |
C |
A |
2: 27,129,473 (GRCm39) |
W275L |
probably damaging |
Het |
Sel1l2 |
C |
T |
2: 140,071,979 (GRCm39) |
|
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,176,712 (GRCm39) |
H1185Y |
probably damaging |
Het |
Skp2 |
G |
A |
15: 9,117,012 (GRCm39) |
Q298* |
probably null |
Het |
Spag16 |
G |
A |
1: 69,934,439 (GRCm39) |
|
probably benign |
Het |
Spink14 |
A |
G |
18: 44,161,896 (GRCm39) |
|
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Stx12 |
T |
A |
4: 132,598,960 (GRCm39) |
I43L |
probably benign |
Het |
Tmc1 |
T |
A |
19: 20,793,548 (GRCm39) |
I538F |
possibly damaging |
Het |
Tollip |
T |
C |
7: 141,438,292 (GRCm39) |
M209V |
probably benign |
Het |
Ttn |
A |
T |
2: 76,643,312 (GRCm39) |
S13202R |
probably damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,786,211 (GRCm39) |
V338D |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,263,471 (GRCm39) |
L767P |
probably damaging |
Het |
Zfp202 |
C |
T |
9: 40,122,792 (GRCm39) |
T518I |
probably damaging |
Het |
|
Other mutations in Lama4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Lama4
|
APN |
10 |
38,941,591 (GRCm39) |
splice site |
probably benign |
|
IGL00091:Lama4
|
APN |
10 |
38,948,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00429:Lama4
|
APN |
10 |
38,887,022 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL00430:Lama4
|
APN |
10 |
38,921,700 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01074:Lama4
|
APN |
10 |
38,974,484 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01386:Lama4
|
APN |
10 |
38,887,060 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01603:Lama4
|
APN |
10 |
38,941,642 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01643:Lama4
|
APN |
10 |
38,932,846 (GRCm39) |
missense |
probably benign |
|
IGL01655:Lama4
|
APN |
10 |
38,936,209 (GRCm39) |
missense |
probably benign |
|
IGL01954:Lama4
|
APN |
10 |
38,963,295 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01984:Lama4
|
APN |
10 |
38,951,525 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02193:Lama4
|
APN |
10 |
38,918,670 (GRCm39) |
missense |
probably benign |
|
IGL02290:Lama4
|
APN |
10 |
38,893,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02441:Lama4
|
APN |
10 |
38,937,441 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02549:Lama4
|
APN |
10 |
38,936,200 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02797:Lama4
|
APN |
10 |
38,932,920 (GRCm39) |
missense |
probably null |
0.00 |
IGL02819:Lama4
|
APN |
10 |
38,902,565 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03122:Lama4
|
APN |
10 |
38,943,959 (GRCm39) |
missense |
probably benign |
|
IGL03184:Lama4
|
APN |
10 |
38,954,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03307:Lama4
|
APN |
10 |
38,893,379 (GRCm39) |
missense |
probably benign |
|
BB006:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4585001:Lama4
|
UTSW |
10 |
38,950,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Lama4
|
UTSW |
10 |
38,936,218 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0015:Lama4
|
UTSW |
10 |
38,951,432 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0015:Lama4
|
UTSW |
10 |
38,951,432 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0035:Lama4
|
UTSW |
10 |
38,948,734 (GRCm39) |
missense |
probably benign |
0.01 |
R0141:Lama4
|
UTSW |
10 |
38,968,274 (GRCm39) |
missense |
probably benign |
0.05 |
R0257:Lama4
|
UTSW |
10 |
38,970,880 (GRCm39) |
splice site |
probably benign |
|
R0267:Lama4
|
UTSW |
10 |
38,904,635 (GRCm39) |
missense |
probably damaging |
0.96 |
R0557:Lama4
|
UTSW |
10 |
38,964,393 (GRCm39) |
missense |
probably benign |
0.38 |
R1052:Lama4
|
UTSW |
10 |
38,968,241 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1248:Lama4
|
UTSW |
10 |
38,932,843 (GRCm39) |
missense |
probably damaging |
0.99 |
R1249:Lama4
|
UTSW |
10 |
38,951,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R1291:Lama4
|
UTSW |
10 |
38,924,065 (GRCm39) |
missense |
probably benign |
0.00 |
R1307:Lama4
|
UTSW |
10 |
38,946,028 (GRCm39) |
missense |
probably benign |
0.06 |
R1404:Lama4
|
UTSW |
10 |
38,937,387 (GRCm39) |
missense |
probably benign |
0.09 |
R1443:Lama4
|
UTSW |
10 |
38,949,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Lama4
|
UTSW |
10 |
38,964,876 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1616:Lama4
|
UTSW |
10 |
38,951,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Lama4
|
UTSW |
10 |
38,956,559 (GRCm39) |
missense |
probably benign |
0.09 |
R1748:Lama4
|
UTSW |
10 |
38,941,615 (GRCm39) |
missense |
probably benign |
0.01 |
R1768:Lama4
|
UTSW |
10 |
38,979,497 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1772:Lama4
|
UTSW |
10 |
38,936,220 (GRCm39) |
missense |
probably benign |
0.00 |
R1813:Lama4
|
UTSW |
10 |
38,936,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Lama4
|
UTSW |
10 |
38,909,121 (GRCm39) |
splice site |
probably benign |
|
R1897:Lama4
|
UTSW |
10 |
38,936,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1907:Lama4
|
UTSW |
10 |
38,948,754 (GRCm39) |
missense |
probably benign |
0.13 |
R1943:Lama4
|
UTSW |
10 |
38,973,134 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2041:Lama4
|
UTSW |
10 |
38,945,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R2242:Lama4
|
UTSW |
10 |
38,902,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R2300:Lama4
|
UTSW |
10 |
38,963,316 (GRCm39) |
missense |
probably benign |
|
R2326:Lama4
|
UTSW |
10 |
38,918,563 (GRCm39) |
splice site |
probably null |
|
R2570:Lama4
|
UTSW |
10 |
38,982,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2570:Lama4
|
UTSW |
10 |
38,951,354 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2571:Lama4
|
UTSW |
10 |
38,918,671 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2887:Lama4
|
UTSW |
10 |
38,968,250 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2926:Lama4
|
UTSW |
10 |
38,954,828 (GRCm39) |
missense |
probably benign |
0.16 |
R3237:Lama4
|
UTSW |
10 |
38,973,175 (GRCm39) |
missense |
probably damaging |
0.97 |
R4095:Lama4
|
UTSW |
10 |
38,973,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4151:Lama4
|
UTSW |
10 |
38,881,424 (GRCm39) |
missense |
probably benign |
0.00 |
R4470:Lama4
|
UTSW |
10 |
38,956,492 (GRCm39) |
nonsense |
probably null |
|
R4812:Lama4
|
UTSW |
10 |
38,948,765 (GRCm39) |
missense |
probably benign |
|
R4822:Lama4
|
UTSW |
10 |
38,909,049 (GRCm39) |
missense |
probably benign |
0.01 |
R4997:Lama4
|
UTSW |
10 |
38,968,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R5119:Lama4
|
UTSW |
10 |
38,924,050 (GRCm39) |
missense |
probably benign |
0.00 |
R5468:Lama4
|
UTSW |
10 |
38,948,678 (GRCm39) |
splice site |
probably null |
|
R5909:Lama4
|
UTSW |
10 |
38,948,855 (GRCm39) |
missense |
probably benign |
0.00 |
R5917:Lama4
|
UTSW |
10 |
38,924,028 (GRCm39) |
missense |
probably benign |
0.10 |
R5927:Lama4
|
UTSW |
10 |
38,948,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Lama4
|
UTSW |
10 |
38,906,444 (GRCm39) |
missense |
probably benign |
0.03 |
R6051:Lama4
|
UTSW |
10 |
38,943,898 (GRCm39) |
missense |
probably benign |
0.01 |
R6277:Lama4
|
UTSW |
10 |
38,982,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6294:Lama4
|
UTSW |
10 |
38,951,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6372:Lama4
|
UTSW |
10 |
38,943,948 (GRCm39) |
missense |
probably benign |
|
R6532:Lama4
|
UTSW |
10 |
38,924,073 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6547:Lama4
|
UTSW |
10 |
38,949,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Lama4
|
UTSW |
10 |
38,893,361 (GRCm39) |
missense |
probably benign |
0.01 |
R6737:Lama4
|
UTSW |
10 |
38,970,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R6987:Lama4
|
UTSW |
10 |
38,950,275 (GRCm39) |
missense |
probably benign |
0.00 |
R7040:Lama4
|
UTSW |
10 |
38,936,158 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7139:Lama4
|
UTSW |
10 |
38,951,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7188:Lama4
|
UTSW |
10 |
38,841,729 (GRCm39) |
start gained |
probably benign |
|
R7189:Lama4
|
UTSW |
10 |
38,841,729 (GRCm39) |
start gained |
probably benign |
|
R7199:Lama4
|
UTSW |
10 |
38,956,536 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7211:Lama4
|
UTSW |
10 |
38,881,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R7262:Lama4
|
UTSW |
10 |
38,970,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Lama4
|
UTSW |
10 |
38,968,295 (GRCm39) |
missense |
probably benign |
0.00 |
R7311:Lama4
|
UTSW |
10 |
38,902,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Lama4
|
UTSW |
10 |
38,963,383 (GRCm39) |
critical splice donor site |
probably null |
|
R7399:Lama4
|
UTSW |
10 |
38,923,944 (GRCm39) |
missense |
probably damaging |
0.98 |
R7426:Lama4
|
UTSW |
10 |
38,921,751 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7472:Lama4
|
UTSW |
10 |
38,963,369 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7635:Lama4
|
UTSW |
10 |
38,968,184 (GRCm39) |
missense |
probably benign |
|
R7775:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7805:Lama4
|
UTSW |
10 |
38,902,747 (GRCm39) |
critical splice donor site |
probably null |
|
R7885:Lama4
|
UTSW |
10 |
38,964,840 (GRCm39) |
missense |
probably benign |
0.01 |
R7895:Lama4
|
UTSW |
10 |
38,964,325 (GRCm39) |
missense |
probably damaging |
0.96 |
R7910:Lama4
|
UTSW |
10 |
38,946,005 (GRCm39) |
missense |
probably damaging |
0.99 |
R7929:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7952:Lama4
|
UTSW |
10 |
38,906,486 (GRCm39) |
missense |
probably benign |
0.39 |
R7991:Lama4
|
UTSW |
10 |
38,921,805 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8059:Lama4
|
UTSW |
10 |
38,842,057 (GRCm39) |
missense |
probably benign |
0.00 |
R8194:Lama4
|
UTSW |
10 |
38,954,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Lama4
|
UTSW |
10 |
38,937,375 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8252:Lama4
|
UTSW |
10 |
38,936,142 (GRCm39) |
missense |
probably benign |
0.00 |
R8265:Lama4
|
UTSW |
10 |
38,981,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8275:Lama4
|
UTSW |
10 |
38,948,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R8426:Lama4
|
UTSW |
10 |
38,979,487 (GRCm39) |
missense |
probably damaging |
0.98 |
R8434:Lama4
|
UTSW |
10 |
38,902,703 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8720:Lama4
|
UTSW |
10 |
38,971,079 (GRCm39) |
missense |
probably damaging |
0.97 |
R8792:Lama4
|
UTSW |
10 |
38,924,048 (GRCm39) |
missense |
probably benign |
0.00 |
R8836:Lama4
|
UTSW |
10 |
38,902,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Lama4
|
UTSW |
10 |
38,923,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R8892:Lama4
|
UTSW |
10 |
38,973,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Lama4
|
UTSW |
10 |
38,982,039 (GRCm39) |
missense |
probably benign |
0.10 |
R9129:Lama4
|
UTSW |
10 |
38,932,887 (GRCm39) |
missense |
probably benign |
|
R9177:Lama4
|
UTSW |
10 |
38,950,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R9187:Lama4
|
UTSW |
10 |
38,924,124 (GRCm39) |
critical splice donor site |
probably null |
|
R9193:Lama4
|
UTSW |
10 |
38,951,444 (GRCm39) |
missense |
probably benign |
0.03 |
R9268:Lama4
|
UTSW |
10 |
38,950,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R9287:Lama4
|
UTSW |
10 |
38,981,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Lama4
|
UTSW |
10 |
38,948,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9303:Lama4
|
UTSW |
10 |
38,973,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R9330:Lama4
|
UTSW |
10 |
38,954,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R9430:Lama4
|
UTSW |
10 |
38,921,802 (GRCm39) |
missense |
probably null |
|
R9572:Lama4
|
UTSW |
10 |
38,959,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9636:Lama4
|
UTSW |
10 |
38,956,500 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9663:Lama4
|
UTSW |
10 |
38,923,944 (GRCm39) |
missense |
probably damaging |
0.98 |
R9777:Lama4
|
UTSW |
10 |
38,924,101 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Lama4
|
UTSW |
10 |
38,921,688 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Lama4
|
UTSW |
10 |
38,881,421 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lama4
|
UTSW |
10 |
38,881,420 (GRCm39) |
nonsense |
probably null |
|
|