Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,247,527 (GRCm39) |
F2425L |
probably benign |
Het |
Adgre4 |
A |
T |
17: 56,121,188 (GRCm39) |
Y418F |
probably benign |
Het |
Adra1a |
G |
T |
14: 66,875,322 (GRCm39) |
C99F |
probably damaging |
Het |
Aox3 |
C |
A |
1: 58,197,431 (GRCm39) |
H592Q |
probably benign |
Het |
Cacna1f |
A |
G |
X: 7,495,644 (GRCm39) |
|
probably null |
Het |
Cacna2d2 |
T |
A |
9: 107,342,753 (GRCm39) |
I100N |
probably damaging |
Het |
Cblif |
A |
T |
19: 11,729,596 (GRCm39) |
N185I |
probably damaging |
Het |
Ccr9 |
T |
A |
9: 123,608,911 (GRCm39) |
C198S |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Csnk2a2 |
T |
C |
8: 96,203,859 (GRCm39) |
D100G |
possibly damaging |
Het |
Cstf2t |
G |
A |
19: 31,061,277 (GRCm39) |
G271E |
possibly damaging |
Het |
Fbxw22 |
T |
C |
9: 109,214,160 (GRCm39) |
R219G |
probably damaging |
Het |
Homez |
A |
G |
14: 55,095,559 (GRCm39) |
F50L |
probably damaging |
Het |
Hspa4l |
C |
T |
3: 40,707,657 (GRCm39) |
Q81* |
probably null |
Het |
Ifi202b |
T |
C |
1: 173,799,875 (GRCm39) |
D202G |
possibly damaging |
Het |
Inava |
T |
C |
1: 136,144,173 (GRCm39) |
|
probably null |
Het |
Mansc1 |
T |
A |
6: 134,587,814 (GRCm39) |
D121V |
probably damaging |
Het |
Or13a24 |
A |
G |
7: 140,154,684 (GRCm39) |
Y206C |
probably benign |
Het |
Or4a27 |
T |
G |
2: 88,559,739 (GRCm39) |
D68A |
probably damaging |
Het |
Or51h5 |
T |
A |
7: 102,577,723 (GRCm39) |
V296E |
possibly damaging |
Het |
P2rx1 |
A |
T |
11: 72,900,410 (GRCm39) |
|
probably null |
Het |
Phactr4 |
A |
G |
4: 132,104,483 (GRCm39) |
|
probably benign |
Het |
Pus10 |
C |
T |
11: 23,675,574 (GRCm39) |
T482I |
probably damaging |
Het |
Scyl2 |
G |
T |
10: 89,488,871 (GRCm39) |
Y206* |
probably null |
Het |
Sell |
G |
A |
1: 163,896,632 (GRCm39) |
|
probably null |
Het |
Slfn10-ps |
C |
T |
11: 82,921,090 (GRCm39) |
|
noncoding transcript |
Het |
Ssh2 |
T |
C |
11: 77,307,233 (GRCm39) |
|
probably benign |
Het |
Tas2r117 |
A |
G |
6: 132,779,963 (GRCm39) |
M34V |
probably benign |
Het |
Vmn2r103 |
A |
T |
17: 19,993,631 (GRCm39) |
T3S |
probably benign |
Het |
Vmn2r73 |
A |
T |
7: 85,522,084 (GRCm39) |
I85K |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,770,887 (GRCm39) |
V2110A |
possibly damaging |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
Zfp592 |
G |
A |
7: 80,673,746 (GRCm39) |
G237R |
probably damaging |
Het |
Zkscan7 |
A |
G |
9: 122,717,950 (GRCm39) |
E115G |
probably damaging |
Het |
Zranb3 |
G |
A |
1: 127,943,829 (GRCm39) |
T306M |
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 |
|
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 |
|
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 |
|
|