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 |
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 |
Zfat |
G |
A |
15: 67,956,250 (GRCm39) |
S1212L |
probably damaging |
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 Cpd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Cpd
|
APN |
11 |
76,688,615 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00698:Cpd
|
APN |
11 |
76,731,270 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01025:Cpd
|
APN |
11 |
76,686,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01292:Cpd
|
APN |
11 |
76,737,071 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01571:Cpd
|
APN |
11 |
76,673,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01606:Cpd
|
APN |
11 |
76,703,466 (GRCm39) |
missense |
probably benign |
|
IGL02283:Cpd
|
APN |
11 |
76,731,251 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02895:Cpd
|
APN |
11 |
76,676,029 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02965:Cpd
|
APN |
11 |
76,681,814 (GRCm39) |
splice site |
probably benign |
|
IGL03116:Cpd
|
APN |
11 |
76,702,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03178:Cpd
|
APN |
11 |
76,696,877 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4280001:Cpd
|
UTSW |
11 |
76,681,850 (GRCm39) |
missense |
probably benign |
0.23 |
PIT4382001:Cpd
|
UTSW |
11 |
76,688,614 (GRCm39) |
missense |
probably benign |
|
R0050:Cpd
|
UTSW |
11 |
76,683,685 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0054:Cpd
|
UTSW |
11 |
76,681,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Cpd
|
UTSW |
11 |
76,681,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Cpd
|
UTSW |
11 |
76,731,273 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0416:Cpd
|
UTSW |
11 |
76,676,030 (GRCm39) |
missense |
probably benign |
0.13 |
R0556:Cpd
|
UTSW |
11 |
76,693,171 (GRCm39) |
splice site |
probably benign |
|
R0666:Cpd
|
UTSW |
11 |
76,673,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R0668:Cpd
|
UTSW |
11 |
76,675,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R1180:Cpd
|
UTSW |
11 |
76,692,579 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1472:Cpd
|
UTSW |
11 |
76,675,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R1518:Cpd
|
UTSW |
11 |
76,731,212 (GRCm39) |
critical splice donor site |
probably null |
|
R1617:Cpd
|
UTSW |
11 |
76,737,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Cpd
|
UTSW |
11 |
76,683,624 (GRCm39) |
missense |
probably benign |
0.00 |
R1854:Cpd
|
UTSW |
11 |
76,677,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Cpd
|
UTSW |
11 |
76,675,208 (GRCm39) |
splice site |
probably benign |
|
R2159:Cpd
|
UTSW |
11 |
76,688,467 (GRCm39) |
missense |
probably damaging |
0.96 |
R2205:Cpd
|
UTSW |
11 |
76,693,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R2281:Cpd
|
UTSW |
11 |
76,688,627 (GRCm39) |
missense |
probably benign |
0.00 |
R2680:Cpd
|
UTSW |
11 |
76,681,825 (GRCm39) |
missense |
probably benign |
|
R2928:Cpd
|
UTSW |
11 |
76,737,200 (GRCm39) |
missense |
probably benign |
|
R2937:Cpd
|
UTSW |
11 |
76,702,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Cpd
|
UTSW |
11 |
76,705,644 (GRCm39) |
nonsense |
probably null |
|
R4241:Cpd
|
UTSW |
11 |
76,737,611 (GRCm39) |
missense |
probably benign |
0.03 |
R4369:Cpd
|
UTSW |
11 |
76,688,537 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4538:Cpd
|
UTSW |
11 |
76,681,825 (GRCm39) |
missense |
probably benign |
|
R4551:Cpd
|
UTSW |
11 |
76,702,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R4617:Cpd
|
UTSW |
11 |
76,731,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Cpd
|
UTSW |
11 |
76,702,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R4733:Cpd
|
UTSW |
11 |
76,702,620 (GRCm39) |
missense |
probably damaging |
0.99 |
R4821:Cpd
|
UTSW |
11 |
76,737,063 (GRCm39) |
missense |
probably benign |
0.38 |
R4852:Cpd
|
UTSW |
11 |
76,675,976 (GRCm39) |
missense |
probably benign |
0.32 |
R4901:Cpd
|
UTSW |
11 |
76,681,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Cpd
|
UTSW |
11 |
76,705,656 (GRCm39) |
missense |
probably damaging |
0.98 |
R4999:Cpd
|
UTSW |
11 |
76,737,048 (GRCm39) |
critical splice donor site |
probably null |
|
R5005:Cpd
|
UTSW |
11 |
76,704,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Cpd
|
UTSW |
11 |
76,702,530 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5438:Cpd
|
UTSW |
11 |
76,682,792 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5524:Cpd
|
UTSW |
11 |
76,688,727 (GRCm39) |
nonsense |
probably null |
|
R5677:Cpd
|
UTSW |
11 |
76,690,651 (GRCm39) |
missense |
probably benign |
|
R5826:Cpd
|
UTSW |
11 |
76,675,242 (GRCm39) |
nonsense |
probably null |
|
R6031:Cpd
|
UTSW |
11 |
76,681,714 (GRCm39) |
missense |
probably benign |
0.00 |
R6031:Cpd
|
UTSW |
11 |
76,681,714 (GRCm39) |
missense |
probably benign |
0.00 |
R6103:Cpd
|
UTSW |
11 |
76,690,625 (GRCm39) |
missense |
probably benign |
0.00 |
R6257:Cpd
|
UTSW |
11 |
76,703,496 (GRCm39) |
missense |
probably benign |
0.37 |
R6263:Cpd
|
UTSW |
11 |
76,737,097 (GRCm39) |
missense |
probably benign |
0.00 |
R6485:Cpd
|
UTSW |
11 |
76,699,533 (GRCm39) |
splice site |
probably null |
|
R6671:Cpd
|
UTSW |
11 |
76,686,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Cpd
|
UTSW |
11 |
76,675,881 (GRCm39) |
missense |
probably benign |
0.02 |
R7074:Cpd
|
UTSW |
11 |
76,704,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7192:Cpd
|
UTSW |
11 |
76,705,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R7341:Cpd
|
UTSW |
11 |
76,737,779 (GRCm39) |
missense |
unknown |
|
R7371:Cpd
|
UTSW |
11 |
76,737,437 (GRCm39) |
missense |
probably benign |
0.25 |
R7380:Cpd
|
UTSW |
11 |
76,693,151 (GRCm39) |
nonsense |
probably null |
|
R7392:Cpd
|
UTSW |
11 |
76,692,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7410:Cpd
|
UTSW |
11 |
76,673,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R7509:Cpd
|
UTSW |
11 |
76,688,702 (GRCm39) |
missense |
probably benign |
0.17 |
R7767:Cpd
|
UTSW |
11 |
76,704,385 (GRCm39) |
missense |
probably benign |
0.03 |
R8935:Cpd
|
UTSW |
11 |
76,731,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R9151:Cpd
|
UTSW |
11 |
76,675,275 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9172:Cpd
|
UTSW |
11 |
76,675,252 (GRCm39) |
missense |
probably benign |
0.21 |
R9173:Cpd
|
UTSW |
11 |
76,699,649 (GRCm39) |
missense |
probably damaging |
0.97 |
R9666:Cpd
|
UTSW |
11 |
76,693,133 (GRCm39) |
missense |
probably benign |
0.02 |
Z1088:Cpd
|
UTSW |
11 |
76,692,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|