Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank2 |
A |
C |
3: 126,810,613 (GRCm39) |
I491S |
probably damaging |
Het |
Armc12 |
A |
T |
17: 28,757,588 (GRCm39) |
Q240L |
probably null |
Het |
Cntnap5c |
C |
T |
17: 58,637,272 (GRCm39) |
P1050S |
probably damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,062,436 (GRCm39) |
V28A |
probably damaging |
Het |
Dbf4 |
A |
G |
5: 8,448,143 (GRCm39) |
S355P |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,150,516 (GRCm39) |
V749A |
probably benign |
Het |
Exoc4 |
T |
C |
6: 33,792,688 (GRCm39) |
L606P |
probably damaging |
Het |
Fggy |
T |
C |
4: 95,489,210 (GRCm39) |
S109P |
probably benign |
Het |
Gdf7 |
T |
A |
12: 8,351,758 (GRCm39) |
Q59L |
unknown |
Het |
M6pr |
T |
C |
6: 122,290,349 (GRCm39) |
V104A |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,364,739 (GRCm39) |
|
probably null |
Het |
Micu2 |
T |
C |
14: 58,181,127 (GRCm39) |
K169R |
probably damaging |
Het |
Mthfd1l |
A |
G |
10: 3,997,937 (GRCm39) |
D636G |
probably damaging |
Het |
Myo1c |
C |
T |
11: 75,562,461 (GRCm39) |
P918S |
probably benign |
Het |
Nfib |
T |
G |
4: 82,416,708 (GRCm39) |
D125A |
probably damaging |
Het |
Nuf2 |
T |
C |
1: 169,332,117 (GRCm39) |
T393A |
probably benign |
Het |
Or8b49 |
G |
A |
9: 38,506,260 (GRCm39) |
V248I |
possibly damaging |
Het |
Paox |
T |
A |
7: 139,706,291 (GRCm39) |
N70K |
probably damaging |
Het |
Pnma8b |
A |
G |
7: 16,679,844 (GRCm39) |
N276S |
probably damaging |
Het |
Ralgds |
G |
A |
2: 28,423,656 (GRCm39) |
A32T |
probably damaging |
Het |
Samd11 |
T |
A |
4: 156,332,591 (GRCm39) |
N446I |
possibly damaging |
Het |
Soat1 |
T |
C |
1: 156,294,062 (GRCm39) |
|
probably null |
Het |
Tmem87a |
A |
T |
2: 120,205,958 (GRCm39) |
V339E |
possibly damaging |
Het |
Tmprss13 |
G |
T |
9: 45,256,603 (GRCm39) |
C516F |
probably damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,059,017 (GRCm39) |
T515A |
probably benign |
Het |
Xrcc5 |
T |
C |
1: 72,351,752 (GRCm39) |
|
probably null |
Het |
Ywhaz |
T |
C |
15: 36,791,166 (GRCm39) |
Y19C |
probably damaging |
Het |
Zfp964 |
G |
T |
8: 70,115,633 (GRCm39) |
D78Y |
probably damaging |
Het |
|
Other mutations in Col4a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00693:Col4a3
|
APN |
1 |
82,675,475 (GRCm39) |
missense |
unknown |
|
IGL00847:Col4a3
|
APN |
1 |
82,695,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Col4a3
|
APN |
1 |
82,660,022 (GRCm39) |
missense |
unknown |
|
IGL01102:Col4a3
|
APN |
1 |
82,647,976 (GRCm39) |
missense |
unknown |
|
IGL01102:Col4a3
|
APN |
1 |
82,647,441 (GRCm39) |
missense |
unknown |
|
IGL02071:Col4a3
|
APN |
1 |
82,638,608 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02244:Col4a3
|
APN |
1 |
82,647,492 (GRCm39) |
splice site |
probably benign |
|
IGL02380:Col4a3
|
APN |
1 |
82,650,509 (GRCm39) |
splice site |
probably benign |
|
IGL02431:Col4a3
|
APN |
1 |
82,657,344 (GRCm39) |
nonsense |
probably null |
|
IGL02466:Col4a3
|
APN |
1 |
82,647,913 (GRCm39) |
missense |
unknown |
|
IGL02694:Col4a3
|
APN |
1 |
82,688,515 (GRCm39) |
unclassified |
probably benign |
|
IGL02709:Col4a3
|
APN |
1 |
82,656,833 (GRCm39) |
missense |
unknown |
|
IGL02752:Col4a3
|
APN |
1 |
82,637,946 (GRCm39) |
missense |
unknown |
|
IGL02792:Col4a3
|
APN |
1 |
82,696,524 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03203:Col4a3
|
APN |
1 |
82,650,360 (GRCm39) |
nonsense |
probably null |
|
IGL03218:Col4a3
|
APN |
1 |
82,620,927 (GRCm39) |
splice site |
probably benign |
|
FR4976:Col4a3
|
UTSW |
1 |
82,696,627 (GRCm39) |
frame shift |
probably null |
|
PIT4260001:Col4a3
|
UTSW |
1 |
82,660,482 (GRCm39) |
missense |
unknown |
|
PIT4515001:Col4a3
|
UTSW |
1 |
82,660,024 (GRCm39) |
missense |
unknown |
|
R0035:Col4a3
|
UTSW |
1 |
82,650,474 (GRCm39) |
missense |
unknown |
|
R0099:Col4a3
|
UTSW |
1 |
82,695,714 (GRCm39) |
missense |
probably benign |
0.41 |
R0433:Col4a3
|
UTSW |
1 |
82,647,940 (GRCm39) |
missense |
unknown |
|
R0573:Col4a3
|
UTSW |
1 |
82,694,084 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0606:Col4a3
|
UTSW |
1 |
82,650,307 (GRCm39) |
splice site |
probably benign |
|
R0715:Col4a3
|
UTSW |
1 |
82,629,879 (GRCm39) |
splice site |
probably benign |
|
R0961:Col4a3
|
UTSW |
1 |
82,686,297 (GRCm39) |
splice site |
probably benign |
|
R1257:Col4a3
|
UTSW |
1 |
82,694,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Col4a3
|
UTSW |
1 |
82,621,022 (GRCm39) |
splice site |
probably benign |
|
R1373:Col4a3
|
UTSW |
1 |
82,667,808 (GRCm39) |
splice site |
probably benign |
|
R1694:Col4a3
|
UTSW |
1 |
82,668,384 (GRCm39) |
splice site |
probably null |
|
R1895:Col4a3
|
UTSW |
1 |
82,656,829 (GRCm39) |
missense |
unknown |
|
R1925:Col4a3
|
UTSW |
1 |
82,689,595 (GRCm39) |
unclassified |
probably benign |
|
R1925:Col4a3
|
UTSW |
1 |
82,678,094 (GRCm39) |
missense |
unknown |
|
R2033:Col4a3
|
UTSW |
1 |
82,695,732 (GRCm39) |
intron |
probably benign |
|
R2044:Col4a3
|
UTSW |
1 |
82,674,040 (GRCm39) |
missense |
unknown |
|
R2122:Col4a3
|
UTSW |
1 |
82,632,678 (GRCm39) |
missense |
unknown |
|
R2282:Col4a3
|
UTSW |
1 |
82,686,359 (GRCm39) |
missense |
unknown |
|
R2318:Col4a3
|
UTSW |
1 |
82,626,290 (GRCm39) |
splice site |
probably null |
|
R2421:Col4a3
|
UTSW |
1 |
82,647,996 (GRCm39) |
splice site |
probably benign |
|
R2517:Col4a3
|
UTSW |
1 |
82,658,431 (GRCm39) |
missense |
unknown |
|
R2965:Col4a3
|
UTSW |
1 |
82,626,321 (GRCm39) |
missense |
unknown |
|
R3085:Col4a3
|
UTSW |
1 |
82,628,979 (GRCm39) |
missense |
unknown |
|
R3150:Col4a3
|
UTSW |
1 |
82,634,858 (GRCm39) |
splice site |
probably null |
|
R3947:Col4a3
|
UTSW |
1 |
82,693,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R4756:Col4a3
|
UTSW |
1 |
82,694,018 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4910:Col4a3
|
UTSW |
1 |
82,650,400 (GRCm39) |
missense |
unknown |
|
R4928:Col4a3
|
UTSW |
1 |
82,688,698 (GRCm39) |
unclassified |
probably benign |
|
R5044:Col4a3
|
UTSW |
1 |
82,644,267 (GRCm39) |
missense |
unknown |
|
R5557:Col4a3
|
UTSW |
1 |
82,692,968 (GRCm39) |
unclassified |
probably benign |
|
R5761:Col4a3
|
UTSW |
1 |
82,693,778 (GRCm39) |
nonsense |
probably null |
|
R5970:Col4a3
|
UTSW |
1 |
82,694,050 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6576:Col4a3
|
UTSW |
1 |
82,686,295 (GRCm39) |
splice site |
probably null |
|
R6675:Col4a3
|
UTSW |
1 |
82,646,646 (GRCm39) |
missense |
unknown |
|
R7170:Col4a3
|
UTSW |
1 |
82,693,630 (GRCm39) |
splice site |
probably null |
|
R7592:Col4a3
|
UTSW |
1 |
82,626,338 (GRCm39) |
missense |
unknown |
|
R7624:Col4a3
|
UTSW |
1 |
82,696,605 (GRCm39) |
missense |
probably benign |
|
R7994:Col4a3
|
UTSW |
1 |
82,640,627 (GRCm39) |
missense |
unknown |
|
R8127:Col4a3
|
UTSW |
1 |
82,627,481 (GRCm39) |
missense |
unknown |
|
R8702:Col4a3
|
UTSW |
1 |
82,688,700 (GRCm39) |
missense |
unknown |
|
R8865:Col4a3
|
UTSW |
1 |
82,647,483 (GRCm39) |
critical splice donor site |
probably null |
|
R8973:Col4a3
|
UTSW |
1 |
82,693,052 (GRCm39) |
missense |
probably benign |
0.11 |
R9611:Col4a3
|
UTSW |
1 |
82,678,018 (GRCm39) |
missense |
unknown |
|
R9665:Col4a3
|
UTSW |
1 |
82,668,301 (GRCm39) |
missense |
unknown |
|
R9765:Col4a3
|
UTSW |
1 |
82,646,678 (GRCm39) |
nonsense |
probably null |
|
X0067:Col4a3
|
UTSW |
1 |
82,693,880 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Col4a3
|
UTSW |
1 |
82,667,760 (GRCm39) |
missense |
unknown |
|
|