Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030J22Rik |
T |
C |
8: 117,698,859 (GRCm39) |
I83V |
possibly damaging |
Het |
Abcf1 |
G |
A |
17: 36,272,621 (GRCm39) |
A288V |
probably null |
Het |
Acer1 |
A |
T |
17: 57,262,598 (GRCm39) |
V184D |
probably damaging |
Het |
Apoh |
T |
C |
11: 108,298,307 (GRCm39) |
|
probably null |
Het |
Arid1a |
T |
C |
4: 133,413,625 (GRCm39) |
Y959C |
unknown |
Het |
Asb3 |
A |
T |
11: 30,978,962 (GRCm39) |
H84L |
probably benign |
Het |
Atxn1 |
A |
C |
13: 45,721,494 (GRCm39) |
Y134D |
probably damaging |
Het |
Btbd1 |
T |
C |
7: 81,478,985 (GRCm39) |
Y52C |
probably damaging |
Het |
Cabp2 |
A |
G |
19: 4,136,464 (GRCm39) |
D170G |
probably damaging |
Het |
Cacna1a |
C |
A |
8: 85,263,046 (GRCm39) |
A407E |
probably damaging |
Het |
Cacna2d4 |
T |
A |
6: 119,248,914 (GRCm39) |
|
probably null |
Het |
Cc2d2a |
T |
C |
5: 43,852,488 (GRCm39) |
F404S |
probably damaging |
Het |
Cdh20 |
T |
C |
1: 104,875,061 (GRCm39) |
M281T |
probably damaging |
Het |
Cfap54 |
A |
T |
10: 92,798,177 (GRCm39) |
M1694K |
unknown |
Het |
Chd6 |
G |
T |
2: 160,881,181 (GRCm39) |
T261K |
probably damaging |
Het |
Cnksr1 |
T |
C |
4: 133,956,330 (GRCm39) |
S585G |
probably damaging |
Het |
Cntnap2 |
A |
T |
6: 45,978,281 (GRCm39) |
Y312F |
probably damaging |
Het |
Coa7 |
T |
A |
4: 108,195,510 (GRCm39) |
Y146* |
probably null |
Het |
Col28a1 |
T |
C |
6: 8,175,414 (GRCm39) |
K145E |
unknown |
Het |
Coq8b |
T |
A |
7: 26,941,486 (GRCm39) |
I221N |
probably damaging |
Het |
Cpd |
A |
T |
11: 76,705,607 (GRCm39) |
L375* |
probably null |
Het |
Dnah5 |
T |
C |
15: 28,448,579 (GRCm39) |
F4214S |
probably damaging |
Het |
Dnai3 |
C |
T |
3: 145,802,895 (GRCm39) |
|
probably null |
Het |
Dock2 |
A |
G |
11: 34,244,139 (GRCm39) |
F1067S |
possibly damaging |
Het |
Dpp6 |
G |
A |
5: 27,836,439 (GRCm39) |
A310T |
probably damaging |
Het |
Dpp6 |
C |
A |
5: 27,930,642 (GRCm39) |
L825I |
probably benign |
Het |
Efcab5 |
A |
G |
11: 77,004,531 (GRCm39) |
V929A |
probably benign |
Het |
Ephx3 |
C |
G |
17: 32,408,290 (GRCm39) |
D45H |
probably benign |
Het |
Espl1 |
G |
A |
15: 102,205,285 (GRCm39) |
|
probably null |
Het |
Firrm |
A |
G |
1: 163,792,089 (GRCm39) |
C610R |
probably damaging |
Het |
Gm4847 |
T |
C |
1: 166,460,281 (GRCm39) |
R402G |
probably benign |
Het |
Grid1 |
T |
C |
14: 34,748,762 (GRCm39) |
L194S |
probably damaging |
Het |
Heatr1 |
A |
T |
13: 12,453,491 (GRCm39) |
H2122L |
probably benign |
Het |
Il17b |
T |
A |
18: 61,825,334 (GRCm39) |
C123* |
probably null |
Het |
Il17rc |
T |
C |
6: 113,451,210 (GRCm39) |
L181P |
probably damaging |
Het |
Inpp5e |
T |
A |
2: 26,287,940 (GRCm39) |
I619L |
probably benign |
Het |
Itgax |
C |
A |
7: 127,741,432 (GRCm39) |
Y814* |
probably null |
Het |
Marcks |
C |
T |
10: 37,012,487 (GRCm39) |
E183K |
unknown |
Het |
Mefv |
T |
C |
16: 3,533,252 (GRCm39) |
T340A |
probably benign |
Het |
Mical2 |
A |
G |
7: 111,950,920 (GRCm39) |
K958R |
probably benign |
Het |
Mrtfb |
T |
A |
16: 13,218,954 (GRCm39) |
D533E |
probably benign |
Het |
Mtor |
T |
A |
4: 148,553,834 (GRCm39) |
L811Q |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,145,570 (GRCm39) |
Y1351C |
probably damaging |
Het |
Neb |
T |
C |
2: 52,153,708 (GRCm39) |
M2406V |
probably benign |
Het |
Nebl |
T |
C |
2: 17,353,678 (GRCm39) |
T214A |
probably benign |
Het |
Nlrx1 |
A |
T |
9: 44,164,705 (GRCm39) |
I913N |
probably damaging |
Het |
Npr2 |
G |
T |
4: 43,632,404 (GRCm39) |
A74S |
probably benign |
Het |
Or4c115 |
T |
A |
2: 88,928,257 (GRCm39) |
S5C |
probably damaging |
Het |
Or6b6 |
C |
A |
7: 106,570,678 (GRCm39) |
C291F |
probably damaging |
Het |
Or6c88 |
T |
A |
10: 129,406,687 (GRCm39) |
N54K |
probably benign |
Het |
Pard3b |
G |
T |
1: 62,205,528 (GRCm39) |
V441F |
probably damaging |
Het |
Pcsk1 |
G |
A |
13: 75,238,191 (GRCm39) |
R4K |
probably benign |
Het |
Pisd |
G |
T |
5: 32,894,784 (GRCm39) |
N337K |
possibly damaging |
Het |
Pml |
T |
C |
9: 58,156,945 (GRCm39) |
K10R |
probably benign |
Het |
Prkci |
T |
C |
3: 31,083,664 (GRCm39) |
W132R |
probably damaging |
Het |
Prrc2a |
A |
T |
17: 35,374,975 (GRCm39) |
M1225K |
probably benign |
Het |
Prss23 |
T |
C |
7: 89,159,142 (GRCm39) |
D309G |
probably damaging |
Het |
Pxdn |
G |
A |
12: 30,052,051 (GRCm39) |
G743S |
probably damaging |
Het |
Rab29 |
A |
T |
1: 131,799,860 (GRCm39) |
E145V |
probably damaging |
Het |
Rasef |
C |
T |
4: 73,653,956 (GRCm39) |
|
probably null |
Het |
Rcbtb1 |
T |
G |
14: 59,472,699 (GRCm39) |
I496S |
probably benign |
Het |
Rcor1 |
T |
C |
12: 111,066,393 (GRCm39) |
Y228H |
|
Het |
Reep5 |
C |
T |
18: 34,490,222 (GRCm39) |
V92I |
probably damaging |
Het |
Rfx3 |
T |
C |
19: 27,827,329 (GRCm39) |
S86G |
probably benign |
Het |
Rptn |
T |
A |
3: 93,304,384 (GRCm39) |
D572E |
probably benign |
Het |
Rsl1 |
A |
T |
13: 67,324,510 (GRCm39) |
|
probably null |
Het |
Sbf2 |
T |
C |
7: 109,914,292 (GRCm39) |
E1630G |
possibly damaging |
Het |
Sele |
G |
A |
1: 163,876,975 (GRCm39) |
V84I |
probably benign |
Het |
Serpina1b |
T |
C |
12: 103,698,756 (GRCm39) |
D31G |
probably benign |
Het |
Serpina3c |
T |
C |
12: 104,115,813 (GRCm39) |
I244V |
probably benign |
Het |
Serpinb6e |
A |
G |
13: 34,017,204 (GRCm39) |
V272A |
probably benign |
Het |
Serpinb9b |
A |
G |
13: 33,219,523 (GRCm39) |
D150G |
probably benign |
Het |
Sgpp1 |
T |
C |
12: 75,769,374 (GRCm39) |
T265A |
probably benign |
Het |
Slc9a1 |
T |
A |
4: 133,143,681 (GRCm39) |
M389K |
probably damaging |
Het |
Slco3a1 |
A |
T |
7: 74,204,236 (GRCm39) |
C35S |
probably damaging |
Het |
Slco6d1 |
T |
A |
1: 98,427,619 (GRCm39) |
V650E |
possibly damaging |
Het |
Slit2 |
T |
C |
5: 48,349,568 (GRCm39) |
V274A |
possibly damaging |
Het |
Snd1 |
A |
G |
6: 28,795,936 (GRCm39) |
E593G |
probably null |
Het |
Spata2l |
C |
T |
8: 123,960,873 (GRCm39) |
V139M |
probably benign |
Het |
Suco |
T |
C |
1: 161,684,427 (GRCm39) |
K231R |
probably damaging |
Het |
Tenm3 |
C |
A |
8: 49,008,935 (GRCm39) |
|
probably benign |
Het |
Tg |
T |
C |
15: 66,699,118 (GRCm39) |
S2415P |
possibly damaging |
Het |
Traf6 |
C |
A |
2: 101,527,072 (GRCm39) |
A274D |
possibly damaging |
Het |
Usp14 |
A |
G |
18: 9,996,239 (GRCm39) |
I447T |
possibly damaging |
Het |
Usp32 |
G |
A |
11: 84,942,028 (GRCm39) |
L355F |
probably benign |
Het |
Vcpip1 |
T |
C |
1: 9,817,927 (GRCm39) |
N152S |
possibly damaging |
Het |
Vgf |
A |
G |
5: 137,061,110 (GRCm39) |
Q424R |
probably benign |
Het |
Vmn2r84 |
A |
T |
10: 130,227,993 (GRCm39) |
M81K |
possibly damaging |
Het |
Washc5 |
G |
A |
15: 59,218,067 (GRCm39) |
A732V |
possibly damaging |
Het |
Xrcc3 |
T |
G |
12: 111,771,485 (GRCm39) |
D213A |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 44,886,988 (GRCm39) |
T690A |
probably benign |
Het |
Zfp623 |
C |
T |
15: 75,819,949 (GRCm39) |
L302F |
probably damaging |
Het |
Zfp799 |
A |
C |
17: 33,039,733 (GRCm39) |
C178G |
possibly damaging |
Het |
Zfy1 |
T |
C |
Y: 727,634 (GRCm39) |
E348G |
unknown |
Het |
Zhx3 |
A |
G |
2: 160,621,393 (GRCm39) |
W925R |
possibly damaging |
Het |
|
Other mutations in Zfat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00542:Zfat
|
APN |
15 |
68,042,071 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00862:Zfat
|
APN |
15 |
68,130,512 (GRCm39) |
splice site |
probably null |
|
IGL01021:Zfat
|
APN |
15 |
68,042,015 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01152:Zfat
|
APN |
15 |
67,982,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01733:Zfat
|
APN |
15 |
68,052,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01873:Zfat
|
APN |
15 |
68,096,744 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01990:Zfat
|
APN |
15 |
68,096,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Zfat
|
APN |
15 |
68,052,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Zfat
|
APN |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02955:Zfat
|
APN |
15 |
68,052,963 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03201:Zfat
|
APN |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R0145:Zfat
|
UTSW |
15 |
68,058,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0408:Zfat
|
UTSW |
15 |
68,052,141 (GRCm39) |
missense |
probably benign |
0.10 |
R0633:Zfat
|
UTSW |
15 |
68,052,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Zfat
|
UTSW |
15 |
68,084,432 (GRCm39) |
splice site |
probably benign |
|
R1508:Zfat
|
UTSW |
15 |
68,050,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Zfat
|
UTSW |
15 |
68,084,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R1641:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.19 |
R1889:Zfat
|
UTSW |
15 |
67,973,388 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Zfat
|
UTSW |
15 |
68,018,392 (GRCm39) |
missense |
probably benign |
0.32 |
R2030:Zfat
|
UTSW |
15 |
67,990,783 (GRCm39) |
critical splice donor site |
probably null |
|
R2202:Zfat
|
UTSW |
15 |
68,051,709 (GRCm39) |
missense |
probably benign |
0.36 |
R2340:Zfat
|
UTSW |
15 |
67,973,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R3440:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R3442:Zfat
|
UTSW |
15 |
67,973,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Zfat
|
UTSW |
15 |
67,956,402 (GRCm39) |
missense |
probably benign |
0.00 |
R4406:Zfat
|
UTSW |
15 |
68,052,040 (GRCm39) |
missense |
probably benign |
0.00 |
R4649:Zfat
|
UTSW |
15 |
68,056,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Zfat
|
UTSW |
15 |
68,052,131 (GRCm39) |
missense |
probably benign |
|
R4712:Zfat
|
UTSW |
15 |
67,982,324 (GRCm39) |
critical splice donor site |
probably null |
|
R4745:Zfat
|
UTSW |
15 |
68,052,223 (GRCm39) |
missense |
probably benign |
0.09 |
R4862:Zfat
|
UTSW |
15 |
68,051,959 (GRCm39) |
missense |
probably benign |
0.02 |
R5015:Zfat
|
UTSW |
15 |
68,050,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Zfat
|
UTSW |
15 |
68,052,079 (GRCm39) |
missense |
probably benign |
|
R5208:Zfat
|
UTSW |
15 |
68,052,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Zfat
|
UTSW |
15 |
68,037,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Zfat
|
UTSW |
15 |
67,982,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Zfat
|
UTSW |
15 |
68,052,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Zfat
|
UTSW |
15 |
67,990,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Zfat
|
UTSW |
15 |
68,051,806 (GRCm39) |
missense |
probably benign |
|
R6046:Zfat
|
UTSW |
15 |
68,052,626 (GRCm39) |
missense |
probably damaging |
0.99 |
R6315:Zfat
|
UTSW |
15 |
67,956,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Zfat
|
UTSW |
15 |
68,052,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Zfat
|
UTSW |
15 |
68,037,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R6789:Zfat
|
UTSW |
15 |
67,956,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Zfat
|
UTSW |
15 |
68,052,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7033:Zfat
|
UTSW |
15 |
68,052,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Zfat
|
UTSW |
15 |
68,052,211 (GRCm39) |
missense |
probably benign |
|
R7065:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Zfat
|
UTSW |
15 |
68,050,631 (GRCm39) |
missense |
probably benign |
0.12 |
R7208:Zfat
|
UTSW |
15 |
68,051,856 (GRCm39) |
missense |
probably benign |
0.39 |
R7330:Zfat
|
UTSW |
15 |
68,084,600 (GRCm39) |
missense |
probably benign |
0.00 |
R7345:Zfat
|
UTSW |
15 |
67,976,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R7378:Zfat
|
UTSW |
15 |
68,052,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R7405:Zfat
|
UTSW |
15 |
68,056,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Zfat
|
UTSW |
15 |
68,050,715 (GRCm39) |
nonsense |
probably null |
|
R7672:Zfat
|
UTSW |
15 |
68,130,535 (GRCm39) |
start codon destroyed |
probably null |
0.39 |
R7676:Zfat
|
UTSW |
15 |
68,096,693 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7701:Zfat
|
UTSW |
15 |
68,052,757 (GRCm39) |
nonsense |
probably null |
|
R7825:Zfat
|
UTSW |
15 |
68,051,769 (GRCm39) |
missense |
probably benign |
0.01 |
R8152:Zfat
|
UTSW |
15 |
67,973,355 (GRCm39) |
missense |
probably benign |
0.23 |
R8404:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8405:Zfat
|
UTSW |
15 |
68,018,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8502:Zfat
|
UTSW |
15 |
67,976,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8534:Zfat
|
UTSW |
15 |
68,037,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Zfat
|
UTSW |
15 |
67,956,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8887:Zfat
|
UTSW |
15 |
68,056,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Zfat
|
UTSW |
15 |
68,052,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Zfat
|
UTSW |
15 |
67,956,404 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9117:Zfat
|
UTSW |
15 |
68,058,918 (GRCm39) |
missense |
probably damaging |
0.98 |
R9137:Zfat
|
UTSW |
15 |
68,051,794 (GRCm39) |
missense |
probably benign |
0.00 |
R9482:Zfat
|
UTSW |
15 |
68,084,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9611:Zfat
|
UTSW |
15 |
68,051,655 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9630:Zfat
|
UTSW |
15 |
67,990,793 (GRCm39) |
missense |
probably benign |
0.37 |
Z1088:Zfat
|
UTSW |
15 |
68,058,950 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfat
|
UTSW |
15 |
68,051,677 (GRCm39) |
missense |
probably damaging |
0.99 |
|