Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas1 |
C |
T |
5: 100,960,040 (GRCm39) |
R104H |
possibly damaging |
Het |
Adamts3 |
A |
G |
5: 89,831,034 (GRCm39) |
S1007P |
probably damaging |
Het |
Adcy10 |
T |
A |
1: 165,386,166 (GRCm39) |
L1118Q |
probably damaging |
Het |
Adgre4 |
A |
G |
17: 56,085,872 (GRCm39) |
E57G |
probably benign |
Het |
Alpk2 |
T |
C |
18: 65,439,687 (GRCm39) |
S1036G |
probably benign |
Het |
Ank3 |
T |
C |
10: 69,818,034 (GRCm39) |
|
probably benign |
Het |
Ankfy1 |
T |
A |
11: 72,646,722 (GRCm39) |
|
probably benign |
Het |
Antxrl |
A |
G |
14: 33,793,646 (GRCm39) |
|
probably benign |
Het |
Apaf1 |
A |
T |
10: 90,856,585 (GRCm39) |
V874D |
probably damaging |
Het |
Arhgap39 |
T |
A |
15: 76,609,346 (GRCm39) |
T1025S |
probably damaging |
Het |
Arhgef12 |
A |
T |
9: 42,912,302 (GRCm39) |
C519S |
probably damaging |
Het |
Aspm |
G |
A |
1: 139,416,225 (GRCm39) |
V1512M |
possibly damaging |
Het |
Atp13a3 |
T |
C |
16: 30,168,643 (GRCm39) |
T449A |
probably benign |
Het |
Atxn2 |
A |
T |
5: 121,940,142 (GRCm39) |
|
probably null |
Het |
Birc6 |
T |
A |
17: 74,967,609 (GRCm39) |
L301Q |
probably damaging |
Het |
Camk2d |
A |
G |
3: 126,574,064 (GRCm39) |
D157G |
probably damaging |
Het |
Ccdc122 |
T |
C |
14: 77,329,103 (GRCm39) |
|
probably benign |
Het |
Ccdc137 |
G |
A |
11: 120,353,090 (GRCm39) |
|
probably null |
Het |
Ccdc18 |
A |
C |
5: 108,376,454 (GRCm39) |
E1298D |
probably damaging |
Het |
Coq10b |
G |
A |
1: 55,092,136 (GRCm39) |
A35T |
probably benign |
Het |
Cracdl |
C |
A |
1: 37,652,556 (GRCm39) |
V1084L |
probably benign |
Het |
Creb3l3 |
T |
C |
10: 80,927,652 (GRCm39) |
I47V |
probably benign |
Het |
Csgalnact1 |
A |
T |
8: 68,914,160 (GRCm39) |
I15N |
probably benign |
Het |
Dcp1b |
A |
G |
6: 119,192,227 (GRCm39) |
Q381R |
probably benign |
Het |
Dnajc21 |
A |
G |
15: 10,462,021 (GRCm39) |
S127P |
probably benign |
Het |
Dnal1 |
C |
T |
12: 84,183,480 (GRCm39) |
Q80* |
probably null |
Het |
Dtd2 |
A |
G |
12: 52,046,638 (GRCm39) |
V67A |
probably benign |
Het |
Gart |
A |
G |
16: 91,439,928 (GRCm39) |
|
probably null |
Het |
Gm17421 |
T |
A |
12: 113,333,107 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
T |
C |
16: 12,577,958 (GRCm39) |
|
noncoding transcript |
Het |
Gm8674 |
T |
C |
13: 50,054,699 (GRCm39) |
|
noncoding transcript |
Het |
Gpr107 |
G |
A |
2: 31,075,541 (GRCm39) |
G351S |
probably damaging |
Het |
H2-M10.5 |
A |
G |
17: 37,085,891 (GRCm39) |
I308V |
probably benign |
Het |
Krt13 |
A |
T |
11: 100,010,877 (GRCm39) |
L159Q |
probably benign |
Het |
Krt78 |
T |
C |
15: 101,855,699 (GRCm39) |
E704G |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,057,548 (GRCm39) |
M541L |
probably benign |
Het |
Lenep |
G |
A |
3: 89,309,881 (GRCm39) |
|
probably null |
Het |
Lrp1b |
T |
C |
2: 40,772,145 (GRCm39) |
|
probably benign |
Het |
Ly6g6e |
G |
A |
17: 35,297,122 (GRCm39) |
R121Q |
probably benign |
Het |
Lyn |
C |
T |
4: 3,748,787 (GRCm39) |
A255V |
possibly damaging |
Het |
Mdn1 |
T |
A |
4: 32,723,621 (GRCm39) |
I2519K |
probably damaging |
Het |
Mmaa |
T |
A |
8: 80,008,061 (GRCm39) |
R59W |
probably damaging |
Het |
Ms4a4b |
A |
G |
19: 11,432,061 (GRCm39) |
I61V |
possibly damaging |
Het |
Ndufaf1 |
T |
C |
2: 119,486,218 (GRCm39) |
E298G |
probably damaging |
Het |
Or10d5 |
A |
G |
9: 39,861,824 (GRCm39) |
L81P |
possibly damaging |
Het |
Or13a1 |
T |
A |
6: 116,470,674 (GRCm39) |
C35S |
probably benign |
Het |
Or4c114 |
T |
C |
2: 88,905,336 (GRCm39) |
Y33C |
possibly damaging |
Het |
Or5k15 |
T |
C |
16: 58,710,328 (GRCm39) |
E85G |
probably benign |
Het |
Or5k8 |
T |
C |
16: 58,644,709 (GRCm39) |
D121G |
probably damaging |
Het |
Pef1 |
C |
A |
4: 130,021,110 (GRCm39) |
C221* |
probably null |
Het |
Plekhg1 |
G |
A |
10: 3,908,048 (GRCm39) |
M988I |
probably benign |
Het |
Pnliprp1 |
T |
A |
19: 58,732,517 (GRCm39) |
I460N |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,255,138 (GRCm39) |
N239S |
probably benign |
Het |
Ppp4r3a |
A |
G |
12: 101,008,912 (GRCm39) |
|
probably benign |
Het |
Prlr |
T |
A |
15: 10,319,343 (GRCm39) |
W91R |
probably damaging |
Het |
Psmd2 |
T |
A |
16: 20,478,856 (GRCm39) |
|
probably null |
Het |
Ptprt |
T |
A |
2: 162,119,960 (GRCm39) |
|
probably benign |
Het |
Pttg1ip2 |
T |
C |
5: 5,505,912 (GRCm39) |
Y123C |
probably benign |
Het |
Rbm12b2 |
T |
C |
4: 12,095,127 (GRCm39) |
F662S |
possibly damaging |
Het |
Rgs6 |
C |
A |
12: 83,163,057 (GRCm39) |
T421K |
possibly damaging |
Het |
Ryr2 |
T |
G |
13: 11,606,123 (GRCm39) |
Q4486H |
probably damaging |
Het |
Scn7a |
A |
T |
2: 66,556,646 (GRCm39) |
|
probably benign |
Het |
Smc1a |
A |
G |
X: 150,830,971 (GRCm39) |
|
probably benign |
Het |
Synrg |
A |
G |
11: 83,900,050 (GRCm39) |
E674G |
probably damaging |
Het |
Syt9 |
G |
A |
7: 107,035,988 (GRCm39) |
R335K |
probably benign |
Het |
Taar7a |
T |
C |
10: 23,868,415 (GRCm39) |
N322S |
probably damaging |
Het |
Tfb2m |
C |
A |
1: 179,361,231 (GRCm39) |
W252C |
possibly damaging |
Het |
Tmub2 |
T |
A |
11: 102,178,581 (GRCm39) |
D161E |
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,537,652 (GRCm39) |
S206L |
probably benign |
Het |
Tyw1 |
A |
T |
5: 130,298,101 (GRCm39) |
H214L |
probably damaging |
Het |
Tyw5 |
A |
G |
1: 57,435,907 (GRCm39) |
I82T |
possibly damaging |
Het |
Uba6 |
A |
G |
5: 86,280,475 (GRCm39) |
|
probably null |
Het |
Unc13c |
T |
C |
9: 73,838,829 (GRCm39) |
Y674C |
probably damaging |
Het |
Vangl2 |
T |
C |
1: 171,835,526 (GRCm39) |
Y382C |
probably damaging |
Het |
Vmn2r105 |
T |
A |
17: 20,448,097 (GRCm39) |
R242S |
probably benign |
Het |
Vmn2r12 |
A |
G |
5: 109,234,398 (GRCm39) |
Y605H |
probably benign |
Het |
Vps13a |
T |
G |
19: 16,737,035 (GRCm39) |
I101L |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,415,385 (GRCm39) |
F792I |
probably damaging |
Het |
Wdhd1 |
G |
A |
14: 47,496,041 (GRCm39) |
H608Y |
probably benign |
Het |
Wdr48 |
T |
A |
9: 119,731,470 (GRCm39) |
I56K |
probably damaging |
Het |
Xpo4 |
T |
C |
14: 57,866,960 (GRCm39) |
D194G |
probably benign |
Het |
Zfp644 |
A |
G |
5: 106,785,110 (GRCm39) |
M479T |
possibly damaging |
Het |
Zfp821 |
T |
A |
8: 110,436,165 (GRCm39) |
|
probably null |
Het |
Zswim8 |
A |
G |
14: 20,769,525 (GRCm39) |
Y1237C |
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 |
|
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 |
|
|