Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,592,103 (GRCm39) |
|
probably benign |
Het |
Acadl |
A |
T |
1: 66,896,712 (GRCm39) |
C27S |
probably benign |
Het |
Adgrb3 |
C |
T |
1: 25,598,931 (GRCm39) |
G258E |
probably damaging |
Het |
Akna |
T |
C |
4: 63,299,962 (GRCm39) |
|
probably null |
Het |
Angpt2 |
T |
C |
8: 18,791,233 (GRCm39) |
N21S |
probably benign |
Het |
Ano6 |
A |
G |
15: 95,847,447 (GRCm39) |
Y585C |
probably damaging |
Het |
Ascc3 |
A |
T |
10: 50,518,615 (GRCm39) |
|
probably benign |
Het |
Clec10a |
T |
A |
11: 70,060,567 (GRCm39) |
S103T |
possibly damaging |
Het |
Clstn2 |
T |
C |
9: 97,339,662 (GRCm39) |
R770G |
probably benign |
Het |
Cndp2 |
C |
A |
18: 84,696,916 (GRCm39) |
C95F |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,527,371 (GRCm39) |
V2653A |
probably benign |
Het |
Daam1 |
A |
G |
12: 72,022,085 (GRCm39) |
|
probably benign |
Het |
H2-M9 |
A |
G |
17: 36,953,484 (GRCm39) |
V18A |
probably benign |
Het |
Heatr1 |
T |
A |
13: 12,439,491 (GRCm39) |
|
probably benign |
Het |
Impg1 |
T |
C |
9: 80,221,675 (GRCm39) |
D715G |
probably benign |
Het |
Incenp |
T |
C |
19: 9,861,379 (GRCm39) |
K425E |
unknown |
Het |
Kif13b |
T |
C |
14: 65,013,681 (GRCm39) |
|
probably benign |
Het |
Msh2 |
T |
A |
17: 88,014,607 (GRCm39) |
|
probably null |
Het |
Myh2 |
A |
G |
11: 67,071,604 (GRCm39) |
N474D |
probably damaging |
Het |
Myo18b |
T |
C |
5: 112,978,185 (GRCm39) |
T1246A |
probably benign |
Het |
Nob1 |
T |
C |
8: 108,148,136 (GRCm39) |
H102R |
probably damaging |
Het |
Or4z4 |
G |
T |
19: 12,076,198 (GRCm39) |
D268E |
probably benign |
Het |
Pard3b |
A |
T |
1: 62,203,316 (GRCm39) |
I415F |
probably damaging |
Het |
Pfkl |
T |
G |
10: 77,829,250 (GRCm39) |
K386T |
possibly damaging |
Het |
Plekhs1 |
T |
C |
19: 56,474,195 (GRCm39) |
V447A |
probably benign |
Het |
Poli |
C |
T |
18: 70,650,574 (GRCm39) |
V266I |
probably benign |
Het |
Rapgef4 |
A |
T |
2: 71,861,449 (GRCm39) |
K46N |
possibly damaging |
Het |
Shisa6 |
T |
C |
11: 66,265,975 (GRCm39) |
|
probably benign |
Het |
Six3 |
T |
A |
17: 85,929,285 (GRCm39) |
D206E |
probably damaging |
Het |
Slc12a1 |
A |
T |
2: 125,060,158 (GRCm39) |
E944D |
possibly damaging |
Het |
Sptb |
A |
G |
12: 76,659,381 (GRCm39) |
F1173S |
probably damaging |
Het |
Tfdp1 |
C |
A |
8: 13,423,837 (GRCm39) |
|
probably benign |
Het |
Trrap |
A |
G |
5: 144,726,409 (GRCm39) |
|
probably benign |
Het |
Wbp11 |
A |
G |
6: 136,791,513 (GRCm39) |
|
probably benign |
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 |
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 |
|
R6583:Col4a3
|
UTSW |
1 |
82,619,197 (GRCm39) |
missense |
unknown |
|
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 |
|
|