Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503E14Rik |
T |
C |
14: 44,407,796 (GRCm39) |
E79G |
probably damaging |
Het |
4930583I09Rik |
T |
A |
17: 65,141,288 (GRCm39) |
Q78L |
unknown |
Het |
9330159F19Rik |
G |
T |
10: 29,103,344 (GRCm39) |
V642F |
probably benign |
Het |
Abca9 |
T |
A |
11: 110,006,280 (GRCm39) |
Q1275L |
probably benign |
Het |
Abca9 |
G |
T |
11: 110,006,281 (GRCm39) |
Q1275K |
probably benign |
Het |
Ager |
C |
T |
17: 34,819,090 (GRCm39) |
P313S |
probably benign |
Het |
Ap4m1 |
T |
A |
5: 138,171,273 (GRCm39) |
N98K |
probably benign |
Het |
Arhgef12 |
T |
G |
9: 42,929,650 (GRCm39) |
K215T |
possibly damaging |
Het |
Arhgef4 |
T |
C |
1: 34,849,518 (GRCm39) |
Y370H |
probably benign |
Het |
Bcat1 |
T |
G |
6: 144,994,488 (GRCm39) |
H3P |
probably benign |
Het |
Btnl6 |
T |
A |
17: 34,732,635 (GRCm39) |
Q313L |
probably benign |
Het |
Cad |
T |
C |
5: 31,229,703 (GRCm39) |
S1458P |
probably benign |
Het |
Cfap161 |
A |
G |
7: 83,442,579 (GRCm39) |
V78A |
probably benign |
Het |
Chd2 |
C |
A |
7: 73,079,555 (GRCm39) |
A1782S |
probably benign |
Het |
Cimip2b |
T |
A |
4: 43,427,554 (GRCm39) |
R257* |
probably null |
Het |
Col4a3 |
A |
T |
1: 82,668,301 (GRCm39) |
T1042S |
unknown |
Het |
Cramp1 |
A |
T |
17: 25,196,545 (GRCm39) |
N856K |
probably damaging |
Het |
Crispld2 |
G |
A |
8: 120,760,316 (GRCm39) |
R414H |
probably benign |
Het |
Ctsb |
T |
A |
14: 63,370,917 (GRCm39) |
|
probably null |
Het |
Cyp2c69 |
T |
C |
19: 39,839,504 (GRCm39) |
D373G |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,644,981 (GRCm39) |
V1100A |
probably benign |
Het |
Dnajb6 |
A |
T |
5: 29,971,374 (GRCm39) |
L225F |
probably damaging |
Het |
Dscc1 |
A |
T |
15: 54,946,837 (GRCm39) |
I296K |
unknown |
Het |
Epb41l2 |
A |
G |
10: 25,317,798 (GRCm39) |
D105G |
probably benign |
Het |
Evpl |
G |
A |
11: 116,123,497 (GRCm39) |
R292C |
probably damaging |
Het |
Flnc |
T |
C |
6: 29,455,447 (GRCm39) |
I2032T |
probably damaging |
Het |
Fryl |
T |
A |
5: 73,222,299 (GRCm39) |
D2094V |
probably damaging |
Het |
Gigyf2 |
A |
G |
1: 87,331,457 (GRCm39) |
S202G |
unknown |
Het |
Hdgfl1 |
A |
T |
13: 26,953,812 (GRCm39) |
M87K |
probably benign |
Het |
Htra3 |
T |
A |
5: 35,836,654 (GRCm39) |
I13F |
unknown |
Het |
Igf2r |
T |
C |
17: 12,913,027 (GRCm39) |
N1774D |
probably benign |
Het |
Ighj1 |
A |
T |
12: 113,393,446 (GRCm39) |
Y3N |
|
Het |
Incenp |
T |
C |
19: 9,871,329 (GRCm39) |
H100R |
unknown |
Het |
Klrb1c |
A |
G |
6: 128,760,625 (GRCm39) |
|
probably null |
Het |
Lmbrd1 |
T |
A |
1: 24,732,065 (GRCm39) |
V94D |
probably damaging |
Het |
Lmna |
A |
T |
3: 88,389,793 (GRCm39) |
S611T |
probably benign |
Het |
Lsp1 |
A |
C |
7: 142,044,142 (GRCm39) |
I296L |
probably benign |
Het |
Mdga1 |
A |
T |
17: 30,051,991 (GRCm39) |
I892N |
probably damaging |
Het |
Micu3 |
A |
G |
8: 40,828,666 (GRCm39) |
E351G |
probably benign |
Het |
Mrpl35 |
A |
G |
6: 71,795,704 (GRCm39) |
V61A |
probably benign |
Het |
Nhsl1 |
A |
G |
10: 18,401,599 (GRCm39) |
K908E |
possibly damaging |
Het |
Nlk |
A |
G |
11: 78,481,753 (GRCm39) |
L236P |
|
Het |
Nwd1 |
T |
A |
8: 73,401,106 (GRCm39) |
H735Q |
probably damaging |
Het |
Or1e1b-ps1 |
A |
T |
11: 73,845,656 (GRCm39) |
I47F |
probably benign |
Het |
Or5d47 |
A |
G |
2: 87,804,596 (GRCm39) |
S138P |
possibly damaging |
Het |
Or5w17 |
A |
T |
2: 87,583,671 (GRCm39) |
I222N |
probably damaging |
Het |
Or7h8 |
T |
A |
9: 20,124,402 (GRCm39) |
Y252* |
probably null |
Het |
Otof |
T |
A |
5: 30,584,895 (GRCm39) |
S70C |
probably benign |
Het |
Pcdh20 |
A |
T |
14: 88,707,162 (GRCm39) |
V46D |
probably benign |
Het |
Pjvk |
A |
G |
2: 76,487,827 (GRCm39) |
T240A |
probably benign |
Het |
Pou2f1 |
A |
G |
1: 165,703,600 (GRCm39) |
S697P |
probably damaging |
Het |
Prkn |
T |
A |
17: 11,286,062 (GRCm39) |
D18E |
possibly damaging |
Het |
Prmt9 |
G |
A |
8: 78,307,267 (GRCm39) |
V739I |
probably benign |
Het |
Prr14 |
A |
G |
7: 127,073,091 (GRCm39) |
D146G |
probably benign |
Het |
Rai14 |
T |
G |
15: 10,574,803 (GRCm39) |
E747D |
probably damaging |
Het |
Rapgef4 |
A |
T |
2: 72,036,018 (GRCm39) |
T504S |
probably benign |
Het |
Rilpl2 |
C |
A |
5: 124,616,240 (GRCm39) |
|
probably benign |
Het |
Ror2 |
A |
T |
13: 53,439,561 (GRCm39) |
M1K |
probably null |
Het |
Shisa9 |
A |
G |
16: 12,085,446 (GRCm39) |
T352A |
probably benign |
Het |
Slc35a4 |
A |
G |
18: 36,813,651 (GRCm39) |
N33S |
probably benign |
Het |
Slx4 |
G |
T |
16: 3,806,890 (GRCm39) |
L518I |
probably benign |
Het |
Speer1i |
A |
G |
5: 11,092,852 (GRCm39) |
K132R |
|
Het |
Spon2 |
T |
C |
5: 33,374,702 (GRCm39) |
T35A |
probably benign |
Het |
Syne3 |
A |
C |
12: 104,924,247 (GRCm39) |
L471R |
probably benign |
Het |
Tas2r115 |
A |
G |
6: 132,714,390 (GRCm39) |
L187S |
probably benign |
Het |
Tbc1d30 |
G |
T |
10: 121,102,886 (GRCm39) |
S715R |
possibly damaging |
Het |
Tdrd1 |
A |
G |
19: 56,819,572 (GRCm39) |
E24G |
probably benign |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,962,644 (GRCm39) |
S1178P |
probably benign |
Het |
Upf2 |
A |
G |
2: 6,051,715 (GRCm39) |
S1126G |
unknown |
Het |
Vmn1r128 |
G |
T |
7: 21,083,362 (GRCm39) |
C22F |
probably damaging |
Het |
Vmn2r95 |
G |
T |
17: 18,660,607 (GRCm39) |
V340F |
probably damaging |
Het |
Vps13c |
A |
T |
9: 67,863,025 (GRCm39) |
K3014* |
probably null |
Het |
Wdr75 |
T |
C |
1: 45,843,013 (GRCm39) |
V126A |
unknown |
Het |
Yeats4 |
A |
T |
10: 117,053,343 (GRCm39) |
Y139* |
probably null |
Het |
Zc3h13 |
A |
G |
14: 75,567,989 (GRCm39) |
D1094G |
probably damaging |
Het |
Zfp772 |
A |
T |
7: 7,212,793 (GRCm39) |
M1K |
probably null |
Het |
Zfp827 |
A |
G |
8: 79,906,756 (GRCm39) |
M923V |
possibly damaging |
Het |
|
Other mutations in Zfp143 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Zfp143
|
APN |
7 |
109,690,979 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01610:Zfp143
|
APN |
7 |
109,673,333 (GRCm39) |
nonsense |
probably null |
|
IGL01678:Zfp143
|
APN |
7 |
109,679,558 (GRCm39) |
splice site |
probably benign |
|
IGL01734:Zfp143
|
APN |
7 |
109,671,416 (GRCm39) |
splice site |
probably benign |
|
IGL02505:Zfp143
|
APN |
7 |
109,690,993 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02577:Zfp143
|
APN |
7 |
109,691,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03084:Zfp143
|
APN |
7 |
109,668,818 (GRCm39) |
splice site |
probably benign |
|
H8786:Zfp143
|
UTSW |
7 |
109,693,575 (GRCm39) |
missense |
probably damaging |
1.00 |
P0015:Zfp143
|
UTSW |
7 |
109,685,318 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0324:Zfp143
|
UTSW |
7 |
109,676,354 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0445:Zfp143
|
UTSW |
7 |
109,660,324 (GRCm39) |
unclassified |
probably benign |
|
R0668:Zfp143
|
UTSW |
7 |
109,660,481 (GRCm39) |
unclassified |
probably benign |
|
R1178:Zfp143
|
UTSW |
7 |
109,674,928 (GRCm39) |
splice site |
probably benign |
|
R1587:Zfp143
|
UTSW |
7 |
109,673,275 (GRCm39) |
missense |
probably benign |
0.06 |
R1992:Zfp143
|
UTSW |
7 |
109,660,489 (GRCm39) |
unclassified |
probably benign |
|
R2110:Zfp143
|
UTSW |
7 |
109,685,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Zfp143
|
UTSW |
7 |
109,682,449 (GRCm39) |
missense |
probably damaging |
0.97 |
R2417:Zfp143
|
UTSW |
7 |
109,668,803 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2899:Zfp143
|
UTSW |
7 |
109,671,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Zfp143
|
UTSW |
7 |
109,673,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R4117:Zfp143
|
UTSW |
7 |
109,691,120 (GRCm39) |
missense |
probably damaging |
0.97 |
R4804:Zfp143
|
UTSW |
7 |
109,687,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Zfp143
|
UTSW |
7 |
109,673,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R5097:Zfp143
|
UTSW |
7 |
109,687,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Zfp143
|
UTSW |
7 |
109,693,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Zfp143
|
UTSW |
7 |
109,669,687 (GRCm39) |
missense |
probably benign |
0.02 |
R5543:Zfp143
|
UTSW |
7 |
109,682,522 (GRCm39) |
nonsense |
probably null |
|
R5630:Zfp143
|
UTSW |
7 |
109,687,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5806:Zfp143
|
UTSW |
7 |
109,685,442 (GRCm39) |
nonsense |
probably null |
|
R6334:Zfp143
|
UTSW |
7 |
109,685,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Zfp143
|
UTSW |
7 |
109,691,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Zfp143
|
UTSW |
7 |
109,692,287 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7448:Zfp143
|
UTSW |
7 |
109,669,705 (GRCm39) |
missense |
probably benign |
0.00 |
R7635:Zfp143
|
UTSW |
7 |
109,688,025 (GRCm39) |
missense |
probably benign |
0.37 |
R7717:Zfp143
|
UTSW |
7 |
109,685,427 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7943:Zfp143
|
UTSW |
7 |
109,671,681 (GRCm39) |
splice site |
probably null |
|
R8191:Zfp143
|
UTSW |
7 |
109,676,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R8268:Zfp143
|
UTSW |
7 |
109,690,991 (GRCm39) |
missense |
probably benign |
0.27 |
R8368:Zfp143
|
UTSW |
7 |
109,682,455 (GRCm39) |
missense |
probably damaging |
0.96 |
R8724:Zfp143
|
UTSW |
7 |
109,681,110 (GRCm39) |
missense |
probably benign |
0.00 |
R8935:Zfp143
|
UTSW |
7 |
109,669,736 (GRCm39) |
missense |
probably damaging |
1.00 |
|