Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 109,997,415 (GRCm39) |
M1551T |
possibly damaging |
Het |
Abcc9 |
A |
G |
6: 142,539,733 (GRCm39) |
*1547Q |
probably null |
Het |
Adamts20 |
A |
C |
15: 94,249,641 (GRCm39) |
C459G |
probably damaging |
Het |
Adamts5 |
C |
T |
16: 85,674,808 (GRCm39) |
W452* |
probably null |
Het |
Adcy8 |
G |
T |
15: 64,792,054 (GRCm39) |
Q301K |
possibly damaging |
Het |
Adgrv1 |
A |
C |
13: 81,715,570 (GRCm39) |
C873G |
probably benign |
Het |
Ak9 |
A |
G |
10: 41,296,535 (GRCm39) |
D1427G |
unknown |
Het |
Amy2a1 |
T |
A |
3: 113,324,190 (GRCm39) |
M117L |
possibly damaging |
Het |
Ap5z1 |
G |
T |
5: 142,452,039 (GRCm39) |
R23L |
probably benign |
Het |
Ap5z1 |
C |
T |
5: 142,456,191 (GRCm39) |
Q337* |
probably null |
Het |
Astn1 |
C |
A |
1: 158,429,508 (GRCm39) |
Q759K |
probably damaging |
Het |
Cd276 |
T |
A |
9: 58,444,762 (GRCm39) |
T70S |
possibly damaging |
Het |
Cd38 |
C |
T |
5: 44,057,746 (GRCm39) |
T106I |
probably damaging |
Het |
Cdon |
C |
G |
9: 35,388,244 (GRCm39) |
R740G |
probably damaging |
Het |
Clk2 |
C |
T |
3: 89,076,201 (GRCm39) |
R124W |
possibly damaging |
Het |
Cyp1b1 |
C |
T |
17: 80,021,644 (GRCm39) |
V33M |
possibly damaging |
Het |
Dab1 |
T |
A |
4: 104,589,335 (GRCm39) |
D547E |
probably benign |
Het |
Degs1 |
A |
T |
1: 182,104,416 (GRCm39) |
Y290N |
probably damaging |
Het |
Degs1 |
G |
C |
1: 182,104,417 (GRCm39) |
H289Q |
probably benign |
Het |
Dop1b |
T |
A |
16: 93,607,092 (GRCm39) |
C2249S |
probably benign |
Het |
Ecpas |
T |
C |
4: 58,853,708 (GRCm39) |
N361S |
probably damaging |
Het |
Ehd4 |
A |
C |
2: 119,932,909 (GRCm39) |
Y172* |
probably null |
Het |
Erc2 |
A |
G |
14: 27,499,165 (GRCm39) |
D347G |
probably damaging |
Het |
Espl1 |
T |
G |
15: 102,212,460 (GRCm39) |
V522G |
probably damaging |
Het |
Fabp9 |
T |
A |
3: 10,262,227 (GRCm39) |
T10S |
probably benign |
Het |
Fhod1 |
T |
C |
8: 106,057,789 (GRCm39) |
E912G |
probably damaging |
Het |
Gja1 |
T |
C |
10: 56,264,645 (GRCm39) |
F335L |
possibly damaging |
Het |
Gm29106 |
A |
G |
1: 118,127,265 (GRCm39) |
H319R |
probably damaging |
Het |
Hunk |
C |
T |
16: 90,269,353 (GRCm39) |
S299F |
probably damaging |
Het |
Hydin |
C |
T |
8: 111,239,642 (GRCm39) |
T1974M |
possibly damaging |
Het |
Ighv10-1 |
T |
A |
12: 114,442,650 (GRCm39) |
T112S |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,789,620 (GRCm39) |
V98E |
probably damaging |
Het |
Irf4 |
A |
C |
13: 30,937,435 (GRCm39) |
H167P |
probably benign |
Het |
Irf6 |
C |
T |
1: 192,845,021 (GRCm39) |
P164L |
probably benign |
Het |
Josd1 |
A |
G |
15: 79,561,451 (GRCm39) |
I119T |
probably damaging |
Het |
Kcna5 |
G |
T |
6: 126,512,011 (GRCm39) |
T39K |
probably damaging |
Het |
Klhl24 |
A |
G |
16: 19,941,750 (GRCm39) |
D566G |
probably damaging |
Het |
Kmt2a |
T |
A |
9: 44,761,154 (GRCm39) |
K232* |
probably null |
Het |
Krt36 |
A |
G |
11: 99,996,061 (GRCm39) |
L121P |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,595,864 (GRCm39) |
H931L |
probably benign |
Het |
Lamp3 |
A |
T |
16: 19,474,141 (GRCm39) |
I411N |
probably damaging |
Het |
Lingo3 |
C |
T |
10: 80,670,610 (GRCm39) |
W440* |
probably null |
Het |
Mia2 |
T |
C |
12: 59,236,433 (GRCm39) |
Y712H |
probably damaging |
Het |
Mlh1 |
T |
A |
9: 111,059,145 (GRCm39) |
|
probably null |
Het |
Mta3 |
T |
A |
17: 84,070,363 (GRCm39) |
S174T |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,381,963 (GRCm39) |
T347A |
|
Het |
Naaladl2 |
C |
T |
3: 23,900,718 (GRCm39) |
R704H |
possibly damaging |
Het |
Nfib |
T |
C |
4: 82,246,030 (GRCm39) |
N394S |
probably benign |
Het |
Nr2f2 |
A |
G |
7: 70,009,681 (GRCm39) |
Y133H |
probably damaging |
Het |
Or2ak7 |
C |
T |
11: 58,575,500 (GRCm39) |
S267F |
possibly damaging |
Het |
Or2i1 |
C |
T |
17: 37,508,047 (GRCm39) |
E196K |
probably damaging |
Het |
Or4c115 |
A |
G |
2: 88,927,932 (GRCm39) |
V113A |
possibly damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,822 (GRCm39) |
C75S |
probably benign |
Het |
Or5p62 |
T |
A |
7: 107,771,391 (GRCm39) |
M187L |
probably benign |
Het |
Phgdh |
C |
A |
3: 98,247,124 (GRCm39) |
V9L |
probably damaging |
Het |
Pkd2 |
T |
A |
5: 104,628,103 (GRCm39) |
D392E |
probably damaging |
Het |
Plekhm3 |
A |
G |
1: 64,960,874 (GRCm39) |
S461P |
probably benign |
Het |
Prss39 |
A |
G |
1: 34,539,308 (GRCm39) |
T183A |
probably benign |
Het |
Pter |
T |
A |
2: 12,999,566 (GRCm39) |
I235K |
probably damaging |
Het |
Ptp4a3 |
T |
C |
15: 73,628,756 (GRCm39) |
V172A |
probably benign |
Het |
Rasa2 |
T |
C |
9: 96,484,780 (GRCm39) |
N145D |
probably benign |
Het |
Rasal2 |
A |
T |
1: 157,071,218 (GRCm39) |
H45Q |
probably benign |
Het |
Rbm43 |
A |
G |
2: 51,815,909 (GRCm39) |
V104A |
probably damaging |
Het |
Rhbdd2 |
C |
A |
5: 135,667,969 (GRCm39) |
|
probably null |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rimbp2 |
T |
A |
5: 128,838,528 (GRCm39) |
N1023I |
probably damaging |
Het |
Rtl1 |
A |
T |
12: 109,561,031 (GRCm39) |
D269E |
possibly damaging |
Het |
Sbp |
A |
G |
17: 24,161,163 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,316,020 (GRCm39) |
T374S |
probably benign |
Het |
Tgs1 |
A |
T |
4: 3,598,652 (GRCm39) |
K655I |
probably benign |
Het |
Thsd1 |
A |
C |
8: 22,749,585 (GRCm39) |
T819P |
probably damaging |
Het |
Tmprss11c |
C |
T |
5: 86,379,655 (GRCm39) |
V418M |
probably damaging |
Het |
Top2a |
A |
T |
11: 98,900,431 (GRCm39) |
D645E |
probably damaging |
Het |
Top2b |
G |
A |
14: 16,413,081 (GRCm38) |
V997I |
possibly damaging |
Het |
Ttc34 |
A |
G |
4: 154,943,840 (GRCm39) |
D118G |
probably damaging |
Het |
Ttll5 |
A |
G |
12: 85,935,948 (GRCm39) |
D353G |
probably damaging |
Het |
Uba6 |
A |
T |
5: 86,265,924 (GRCm39) |
Y994* |
probably null |
Het |
Vinac1 |
A |
C |
2: 128,879,049 (GRCm39) |
V959G |
unknown |
Het |
Vmn1r189 |
A |
T |
13: 22,285,906 (GRCm39) |
Y310* |
probably null |
Het |
Vps13c |
T |
A |
9: 67,834,265 (GRCm39) |
I1644N |
probably damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,821 (GRCm39) |
D73G |
possibly damaging |
Het |
Zfp951 |
A |
T |
5: 104,962,838 (GRCm39) |
C243S |
probably benign |
Het |
|
Other mutations in Fam193a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01981:Fam193a
|
APN |
5 |
34,588,537 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02111:Fam193a
|
APN |
5 |
34,568,001 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02139:Fam193a
|
APN |
5 |
34,602,081 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02218:Fam193a
|
APN |
5 |
34,600,932 (GRCm39) |
missense |
possibly damaging |
0.68 |
BB010:Fam193a
|
UTSW |
5 |
34,623,539 (GRCm39) |
missense |
possibly damaging |
0.53 |
BB020:Fam193a
|
UTSW |
5 |
34,623,539 (GRCm39) |
missense |
possibly damaging |
0.53 |
P0017:Fam193a
|
UTSW |
5 |
34,597,807 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4418001:Fam193a
|
UTSW |
5 |
34,597,879 (GRCm39) |
missense |
probably damaging |
0.97 |
R0172:Fam193a
|
UTSW |
5 |
34,622,957 (GRCm39) |
missense |
probably damaging |
0.97 |
R0413:Fam193a
|
UTSW |
5 |
34,623,552 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0512:Fam193a
|
UTSW |
5 |
34,583,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R0735:Fam193a
|
UTSW |
5 |
34,596,722 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0764:Fam193a
|
UTSW |
5 |
34,600,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R0904:Fam193a
|
UTSW |
5 |
34,619,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Fam193a
|
UTSW |
5 |
34,623,636 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1765:Fam193a
|
UTSW |
5 |
34,593,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1766:Fam193a
|
UTSW |
5 |
34,619,475 (GRCm39) |
missense |
probably damaging |
0.99 |
R1845:Fam193a
|
UTSW |
5 |
34,600,716 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2051:Fam193a
|
UTSW |
5 |
34,619,494 (GRCm39) |
missense |
probably benign |
0.19 |
R2483:Fam193a
|
UTSW |
5 |
34,623,102 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3014:Fam193a
|
UTSW |
5 |
34,623,016 (GRCm39) |
missense |
probably benign |
0.33 |
R4523:Fam193a
|
UTSW |
5 |
34,600,715 (GRCm39) |
missense |
probably benign |
0.07 |
R4723:Fam193a
|
UTSW |
5 |
34,578,130 (GRCm39) |
missense |
probably benign |
0.04 |
R4823:Fam193a
|
UTSW |
5 |
34,616,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R4826:Fam193a
|
UTSW |
5 |
34,593,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Fam193a
|
UTSW |
5 |
34,623,549 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5331:Fam193a
|
UTSW |
5 |
34,622,915 (GRCm39) |
splice site |
probably null |
|
R5364:Fam193a
|
UTSW |
5 |
34,623,597 (GRCm39) |
missense |
probably benign |
0.01 |
R5564:Fam193a
|
UTSW |
5 |
34,578,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R5580:Fam193a
|
UTSW |
5 |
34,578,132 (GRCm39) |
missense |
probably benign |
0.33 |
R5784:Fam193a
|
UTSW |
5 |
34,623,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R5933:Fam193a
|
UTSW |
5 |
34,623,024 (GRCm39) |
missense |
probably damaging |
0.98 |
R5949:Fam193a
|
UTSW |
5 |
34,597,816 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6106:Fam193a
|
UTSW |
5 |
34,616,374 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6181:Fam193a
|
UTSW |
5 |
34,600,884 (GRCm39) |
splice site |
probably null |
|
R7095:Fam193a
|
UTSW |
5 |
34,615,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R7109:Fam193a
|
UTSW |
5 |
34,623,165 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7344:Fam193a
|
UTSW |
5 |
34,643,074 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7401:Fam193a
|
UTSW |
5 |
34,622,979 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7453:Fam193a
|
UTSW |
5 |
34,621,460 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7456:Fam193a
|
UTSW |
5 |
34,578,132 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7648:Fam193a
|
UTSW |
5 |
34,588,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R7768:Fam193a
|
UTSW |
5 |
34,623,135 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7783:Fam193a
|
UTSW |
5 |
34,588,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R7818:Fam193a
|
UTSW |
5 |
34,622,997 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7852:Fam193a
|
UTSW |
5 |
34,568,161 (GRCm39) |
missense |
probably benign |
0.01 |
R7853:Fam193a
|
UTSW |
5 |
34,597,473 (GRCm39) |
missense |
probably benign |
0.12 |
R7933:Fam193a
|
UTSW |
5 |
34,623,539 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7957:Fam193a
|
UTSW |
5 |
34,619,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Fam193a
|
UTSW |
5 |
34,597,917 (GRCm39) |
missense |
probably damaging |
0.96 |
R8281:Fam193a
|
UTSW |
5 |
34,600,780 (GRCm39) |
missense |
unknown |
|
R8554:Fam193a
|
UTSW |
5 |
34,633,115 (GRCm39) |
missense |
probably benign |
0.05 |
R8743:Fam193a
|
UTSW |
5 |
34,577,501 (GRCm39) |
critical splice donor site |
probably null |
|
R8821:Fam193a
|
UTSW |
5 |
34,616,374 (GRCm39) |
missense |
probably benign |
0.01 |
R8831:Fam193a
|
UTSW |
5 |
34,616,374 (GRCm39) |
missense |
probably benign |
0.01 |
R8896:Fam193a
|
UTSW |
5 |
34,583,828 (GRCm39) |
missense |
probably benign |
0.03 |
R8943:Fam193a
|
UTSW |
5 |
34,597,796 (GRCm39) |
missense |
probably benign |
0.01 |
R9026:Fam193a
|
UTSW |
5 |
34,616,536 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9182:Fam193a
|
UTSW |
5 |
34,623,361 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9210:Fam193a
|
UTSW |
5 |
34,597,481 (GRCm39) |
missense |
probably benign |
0.01 |
R9212:Fam193a
|
UTSW |
5 |
34,597,481 (GRCm39) |
missense |
probably benign |
0.01 |
R9291:Fam193a
|
UTSW |
5 |
34,593,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R9515:Fam193a
|
UTSW |
5 |
34,615,371 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1088:Fam193a
|
UTSW |
5 |
34,578,239 (GRCm39) |
missense |
probably benign |
|
|