Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts1 |
A |
C |
16: 85,595,404 (GRCm39) |
V258G |
possibly damaging |
Het |
Adcy1 |
A |
G |
11: 7,094,804 (GRCm39) |
T577A |
probably benign |
Het |
Adgb |
T |
C |
10: 10,274,695 (GRCm39) |
N728S |
probably benign |
Het |
Alpk1 |
A |
G |
3: 127,473,175 (GRCm39) |
S943P |
probably damaging |
Het |
Ankdd1a |
T |
C |
9: 65,410,791 (GRCm39) |
D398G |
probably damaging |
Het |
Asah1 |
A |
G |
8: 41,796,761 (GRCm39) |
|
probably null |
Het |
Atp13a1 |
T |
C |
8: 70,251,329 (GRCm39) |
S495P |
probably damaging |
Het |
Camta2 |
T |
C |
11: 70,571,766 (GRCm39) |
D510G |
probably damaging |
Het |
Cdh8 |
T |
A |
8: 100,143,321 (GRCm39) |
|
probably benign |
Het |
Cul9 |
C |
T |
17: 46,849,262 (GRCm39) |
A628T |
probably benign |
Het |
Ddx19a |
A |
G |
8: 111,703,111 (GRCm39) |
V442A |
probably benign |
Het |
Ddx41 |
G |
A |
13: 55,682,293 (GRCm39) |
R205W |
possibly damaging |
Het |
Dnah7c |
T |
A |
1: 46,787,795 (GRCm39) |
S3283T |
possibly damaging |
Het |
Fmo9 |
T |
A |
1: 166,507,799 (GRCm39) |
I19F |
probably damaging |
Het |
Gmeb2 |
A |
T |
2: 180,906,938 (GRCm39) |
|
probably null |
Het |
H2-K2 |
G |
A |
17: 34,219,035 (GRCm39) |
R23C |
probably benign |
Het |
Icam5 |
T |
A |
9: 20,946,802 (GRCm39) |
C443* |
probably null |
Het |
Il16 |
A |
G |
7: 83,300,046 (GRCm39) |
|
probably benign |
Het |
Kcnj3 |
A |
T |
2: 55,327,877 (GRCm39) |
H222L |
probably damaging |
Het |
Lpin3 |
A |
G |
2: 160,737,354 (GRCm39) |
T134A |
probably benign |
Het |
Man1b1 |
C |
G |
2: 25,222,867 (GRCm39) |
|
probably benign |
Het |
Msc |
G |
C |
1: 14,825,902 (GRCm39) |
P24R |
probably damaging |
Het |
Mylk |
A |
G |
16: 34,732,522 (GRCm39) |
K601E |
probably benign |
Het |
Myzap |
A |
G |
9: 71,499,563 (GRCm39) |
|
probably benign |
Het |
Ncor2 |
A |
T |
5: 125,179,705 (GRCm39) |
|
probably null |
Het |
Nrxn3 |
T |
C |
12: 90,171,515 (GRCm39) |
S276P |
probably damaging |
Het |
Or1j16 |
T |
C |
2: 36,530,233 (GRCm39) |
F61L |
probably damaging |
Het |
Or4c114 |
T |
C |
2: 88,905,382 (GRCm39) |
N18D |
probably benign |
Het |
Or4d6 |
T |
C |
19: 12,086,547 (GRCm39) |
|
probably null |
Het |
Or51b4 |
G |
A |
7: 103,530,956 (GRCm39) |
P165S |
probably benign |
Het |
Or6c202 |
G |
A |
10: 128,996,383 (GRCm39) |
L157F |
probably benign |
Het |
Or8c13 |
A |
G |
9: 38,091,666 (GRCm39) |
M151T |
probably damaging |
Het |
Or8d1 |
T |
C |
9: 38,766,927 (GRCm39) |
S190P |
probably damaging |
Het |
Pramel5 |
T |
C |
4: 143,997,915 (GRCm39) |
K443E |
possibly damaging |
Het |
Rock2 |
C |
T |
12: 17,021,276 (GRCm39) |
Q1019* |
probably null |
Het |
Rps18-ps3 |
T |
A |
8: 107,989,762 (GRCm39) |
|
noncoding transcript |
Het |
Sis |
T |
C |
3: 72,835,492 (GRCm39) |
|
probably null |
Het |
Slc22a21 |
T |
A |
11: 53,846,839 (GRCm39) |
I345F |
probably benign |
Het |
Sox5 |
A |
G |
6: 143,790,491 (GRCm39) |
M523T |
possibly damaging |
Het |
Taf1c |
T |
C |
8: 120,326,361 (GRCm39) |
K526R |
probably benign |
Het |
Taf2 |
T |
C |
15: 54,922,276 (GRCm39) |
D337G |
possibly damaging |
Het |
Tbx4 |
A |
G |
11: 85,802,948 (GRCm39) |
I275V |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Tmem9 |
A |
G |
1: 135,955,234 (GRCm39) |
T123A |
probably benign |
Het |
Trim69 |
A |
G |
2: 122,009,080 (GRCm39) |
Y380C |
probably damaging |
Het |
Vldlr |
G |
T |
19: 27,212,219 (GRCm39) |
V78L |
probably damaging |
Het |
Vmn1r68 |
A |
T |
7: 10,261,275 (GRCm39) |
N274K |
probably benign |
Het |
Vmn2r104 |
G |
T |
17: 20,262,503 (GRCm39) |
S209Y |
probably damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,682,990 (GRCm39) |
N738I |
probably damaging |
Het |
Wnt3 |
A |
G |
11: 103,703,450 (GRCm39) |
D311G |
probably damaging |
Het |
Yme1l1 |
T |
C |
2: 23,076,344 (GRCm39) |
|
probably null |
Het |
Zcchc14 |
C |
T |
8: 122,378,498 (GRCm39) |
|
probably benign |
Het |
Zfp148 |
T |
C |
16: 33,316,602 (GRCm39) |
Y383H |
probably damaging |
Het |
Zfp41 |
A |
G |
15: 75,490,368 (GRCm39) |
R107G |
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 |
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 |
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 |
|
|