Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 138,067,635 |
S862G |
probably benign |
Het |
2410089E03Rik |
T |
C |
15: 8,270,803 |
V3198A |
unknown |
Het |
Adgrf1 |
G |
A |
17: 43,291,005 |
|
probably benign |
Het |
Adss |
T |
G |
1: 177,796,388 |
I3L |
probably benign |
Het |
Anapc7 |
T |
A |
5: 122,438,217 |
D302E |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,953,476 |
|
probably null |
Het |
Astn2 |
A |
C |
4: 65,397,005 |
V1145G |
probably damaging |
Het |
Babam2 |
C |
T |
5: 32,007,230 |
|
probably benign |
Het |
Blvrb |
A |
G |
7: 27,465,846 |
H238R |
possibly damaging |
Het |
Cacna1b |
C |
T |
2: 24,706,216 |
V488I |
probably damaging |
Het |
Ccdc88a |
C |
T |
11: 29,463,409 |
T649M |
possibly damaging |
Het |
Cdh12 |
A |
C |
15: 21,583,912 |
S613R |
probably damaging |
Het |
Cisd2 |
A |
G |
3: 135,408,835 |
V125A |
probably benign |
Het |
Clcn2 |
C |
A |
16: 20,709,669 |
G478W |
possibly damaging |
Het |
Cntnap2 |
T |
A |
6: 47,107,969 |
H1121Q |
probably benign |
Het |
Corin |
A |
T |
5: 72,304,953 |
C876S |
probably damaging |
Het |
Cox7c |
T |
C |
13: 86,046,620 |
Y19C |
probably benign |
Het |
Cspp1 |
T |
G |
1: 10,134,126 |
L1038R |
probably damaging |
Het |
Cwc15 |
A |
G |
9: 14,504,938 |
K147E |
possibly damaging |
Het |
Dlgap2 |
A |
G |
8: 14,823,614 |
D739G |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,369,189 |
|
probably benign |
Het |
Dock5 |
A |
G |
14: 67,805,756 |
V864A |
possibly damaging |
Het |
Dock7 |
A |
G |
4: 98,989,038 |
F1088L |
possibly damaging |
Het |
Dpysl3 |
T |
C |
18: 43,361,036 |
Y193C |
probably damaging |
Het |
Dtna |
T |
C |
18: 23,651,613 |
Y730H |
probably damaging |
Het |
Dusp3 |
A |
G |
11: 101,984,625 |
Y38H |
possibly damaging |
Het |
Eif3m |
A |
T |
2: 105,012,932 |
I151N |
probably damaging |
Het |
Entpd2 |
C |
T |
2: 25,399,726 |
T380I |
probably damaging |
Het |
Epb41l3 |
C |
A |
17: 69,286,800 |
H810N |
probably damaging |
Het |
Fcrl5 |
A |
G |
3: 87,446,391 |
T348A |
probably benign |
Het |
Ginm1 |
A |
G |
10: 7,779,314 |
S55P |
probably damaging |
Het |
Glt1d1 |
C |
A |
5: 127,657,084 |
|
probably null |
Het |
Gm15433 |
T |
A |
1: 84,964,112 |
|
noncoding transcript |
Het |
Gm8221 |
A |
G |
15: 77,626,152 |
|
noncoding transcript |
Het |
Gramd1c |
A |
G |
16: 43,983,241 |
V603A |
probably benign |
Het |
Grm1 |
A |
G |
10: 11,080,442 |
S33P |
probably benign |
Het |
Gstp3 |
T |
C |
19: 4,057,922 |
N137S |
possibly damaging |
Het |
Kdm5d |
C |
T |
Y: 927,995 |
P756S |
probably benign |
Het |
Ly75 |
A |
T |
2: 60,311,771 |
L1332M |
possibly damaging |
Het |
Med1 |
T |
A |
11: 98,163,963 |
K378N |
probably damaging |
Het |
Mn1 |
A |
G |
5: 111,421,886 |
|
probably null |
Het |
Mpo |
T |
C |
11: 87,803,611 |
|
probably null |
Het |
Nom1 |
C |
G |
5: 29,441,379 |
R555G |
probably damaging |
Het |
Nsmce4a |
C |
T |
7: 130,538,170 |
R276Q |
probably benign |
Het |
Nt5c |
G |
A |
11: 115,490,817 |
|
probably null |
Het |
Olfr472 |
T |
C |
7: 107,903,491 |
I258T |
possibly damaging |
Het |
Olfr670 |
G |
T |
7: 104,959,996 |
H245Q |
probably damaging |
Het |
Olfr908 |
CACAACAACA |
CACAACA |
9: 38,516,138 |
|
probably benign |
Het |
Pcdhga4 |
T |
C |
18: 37,685,596 |
V66A |
probably damaging |
Het |
Pik3c3 |
T |
C |
18: 30,312,561 |
S534P |
probably benign |
Het |
Pla2g4e |
A |
T |
2: 120,186,395 |
C222S |
probably benign |
Het |
Plch1 |
A |
C |
3: 63,698,078 |
H1468Q |
probably benign |
Het |
Psd2 |
T |
A |
18: 36,007,503 |
W610R |
probably damaging |
Het |
Ptgs1 |
A |
T |
2: 36,251,186 |
K548N |
probably damaging |
Het |
Ptprz1 |
T |
A |
6: 23,007,355 |
V1639E |
probably damaging |
Het |
Rangap1 |
A |
T |
15: 81,706,494 |
S466T |
probably benign |
Het |
Rgsl1 |
C |
T |
1: 153,790,307 |
V986I |
probably benign |
Het |
Rhobtb3 |
T |
C |
13: 75,878,895 |
Y453C |
probably damaging |
Het |
Rspry1 |
T |
C |
8: 94,623,008 |
V8A |
probably benign |
Het |
Rspry1 |
C |
A |
8: 94,654,264 |
R399S |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,147,663 |
C537R |
probably damaging |
Het |
Rxfp2 |
A |
G |
5: 150,070,260 |
T596A |
probably benign |
Het |
Sap18b |
G |
A |
8: 95,825,370 |
A3T |
unknown |
Het |
Serpina3j |
A |
G |
12: 104,314,727 |
D53G |
probably damaging |
Het |
Skint3 |
T |
A |
4: 112,298,189 |
D381E |
possibly damaging |
Het |
Slirp |
T |
C |
12: 87,449,422 |
S96P |
possibly damaging |
Het |
Snx6 |
T |
C |
12: 54,770,728 |
E128G |
probably damaging |
Het |
Stap1 |
A |
G |
5: 86,090,928 |
T152A |
possibly damaging |
Het |
Tcf20 |
A |
T |
15: 82,851,957 |
N1764K |
probably damaging |
Het |
Thap2 |
A |
T |
10: 115,372,839 |
Y125* |
probably null |
Het |
Ticrr |
T |
G |
7: 79,690,942 |
Y1031* |
probably null |
Het |
Tnrc18 |
G |
A |
5: 142,740,156 |
R1793C |
unknown |
Het |
Trpm3 |
C |
T |
19: 22,926,184 |
R945* |
probably null |
Het |
Ugt1a10 |
T |
A |
1: 88,055,910 |
D143E |
probably damaging |
Het |
Ush2a |
C |
T |
1: 188,755,206 |
T3057M |
probably benign |
Het |
Zfp518a |
T |
C |
19: 40,913,510 |
S628P |
probably benign |
Het |
Zufsp |
T |
C |
10: 33,927,466 |
N541D |
possibly damaging |
Het |
|