Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap21 |
T |
C |
2: 20,885,117 (GRCm39) |
S526G |
probably benign |
Het |
Atad2b |
A |
T |
12: 5,068,056 (GRCm39) |
N1018I |
possibly damaging |
Het |
Baz1b |
A |
G |
5: 135,237,951 (GRCm39) |
E209G |
probably benign |
Het |
Bltp1 |
A |
G |
3: 36,960,884 (GRCm39) |
T445A |
probably damaging |
Het |
Capn11 |
T |
A |
17: 45,950,782 (GRCm39) |
T264S |
probably benign |
Het |
Cdh1 |
A |
G |
8: 107,380,418 (GRCm39) |
E187G |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,196,923 (GRCm39) |
I325V |
probably benign |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,687,152 (GRCm39) |
|
probably benign |
Het |
Dnaaf3 |
T |
C |
7: 4,530,496 (GRCm39) |
D203G |
probably damaging |
Het |
Eif2ak3 |
A |
G |
6: 70,878,441 (GRCm39) |
Y1045C |
probably benign |
Het |
Fam13a |
T |
A |
6: 58,912,586 (GRCm39) |
D689V |
possibly damaging |
Het |
Fnip1 |
T |
A |
11: 54,384,200 (GRCm39) |
L342I |
probably damaging |
Het |
Frk |
T |
A |
10: 34,360,330 (GRCm39) |
N110K |
probably damaging |
Het |
Gm5134 |
T |
C |
10: 75,790,536 (GRCm39) |
|
probably null |
Het |
Gm53 |
T |
C |
11: 96,142,549 (GRCm39) |
|
noncoding transcript |
Het |
Gm9312 |
A |
T |
12: 24,302,163 (GRCm39) |
|
noncoding transcript |
Het |
Gm9936 |
A |
G |
5: 114,995,152 (GRCm39) |
|
probably benign |
Het |
Hk3 |
A |
G |
13: 55,162,281 (GRCm39) |
F108L |
probably damaging |
Het |
Homer2 |
A |
T |
7: 81,260,147 (GRCm39) |
S296T |
probably benign |
Het |
Itga2b |
T |
A |
11: 102,357,145 (GRCm39) |
H245L |
probably benign |
Het |
Ky |
T |
C |
9: 102,414,985 (GRCm39) |
F299S |
possibly damaging |
Het |
Lama5 |
A |
G |
2: 179,849,012 (GRCm39) |
Y224H |
possibly damaging |
Het |
Leng9 |
G |
T |
7: 4,151,723 (GRCm39) |
L318I |
probably damaging |
Het |
Lpin1 |
A |
G |
12: 16,608,408 (GRCm39) |
|
probably null |
Het |
Lrp2 |
T |
C |
2: 69,297,224 (GRCm39) |
I3246V |
probably benign |
Het |
Map2k3 |
A |
G |
11: 60,837,590 (GRCm39) |
Y230C |
probably damaging |
Het |
Myef2 |
T |
C |
2: 124,955,959 (GRCm39) |
|
probably null |
Het |
Myh3 |
A |
T |
11: 66,989,409 (GRCm39) |
I1510L |
probably benign |
Het |
Mypn |
T |
C |
10: 62,959,057 (GRCm39) |
D1088G |
possibly damaging |
Het |
Nek9 |
C |
A |
12: 85,354,704 (GRCm39) |
V745L |
probably null |
Het |
Neu1 |
T |
A |
17: 35,153,641 (GRCm39) |
V355D |
possibly damaging |
Het |
Nlrp4a |
G |
T |
7: 26,148,703 (GRCm39) |
K103N |
possibly damaging |
Het |
Or4c107 |
A |
G |
2: 88,789,028 (GRCm39) |
T73A |
probably benign |
Het |
Or6e1 |
T |
C |
14: 54,519,409 (GRCm39) |
*314W |
probably null |
Het |
Papola |
A |
T |
12: 105,795,442 (GRCm39) |
N631I |
possibly damaging |
Het |
Pcnx1 |
T |
C |
12: 81,965,878 (GRCm39) |
S682P |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,039,925 (GRCm39) |
S2071P |
possibly damaging |
Het |
Pga5 |
A |
G |
19: 10,649,277 (GRCm39) |
|
probably benign |
Het |
Phlda1 |
T |
A |
10: 111,343,014 (GRCm39) |
M250K |
probably damaging |
Het |
Phox2b |
A |
G |
5: 67,253,869 (GRCm39) |
|
probably benign |
Het |
Pkdrej |
A |
G |
15: 85,699,994 (GRCm39) |
Y1981H |
possibly damaging |
Het |
Pold1 |
G |
A |
7: 44,191,663 (GRCm39) |
P108S |
probably benign |
Het |
Ptprg |
T |
G |
14: 12,220,613 (GRCm38) |
F442V |
probably damaging |
Het |
Rab36 |
A |
G |
10: 74,887,874 (GRCm39) |
I248M |
probably damaging |
Het |
Scnn1b |
G |
A |
7: 121,502,113 (GRCm39) |
R257Q |
probably null |
Het |
Sdc1 |
A |
G |
12: 8,840,835 (GRCm39) |
Q200R |
possibly damaging |
Het |
Slc10a7 |
A |
G |
8: 79,242,292 (GRCm39) |
T60A |
probably damaging |
Het |
Snx13 |
A |
G |
12: 35,156,800 (GRCm39) |
D484G |
probably damaging |
Het |
Tlr1 |
G |
A |
5: 65,083,797 (GRCm39) |
T260M |
probably damaging |
Het |
Tpcn1 |
A |
G |
5: 120,691,596 (GRCm39) |
V286A |
probably damaging |
Het |
Traip |
T |
G |
9: 107,845,936 (GRCm39) |
L343R |
possibly damaging |
Het |
Unc13b |
A |
G |
4: 43,165,828 (GRCm39) |
H204R |
probably damaging |
Het |
Unc80 |
A |
G |
1: 66,569,224 (GRCm39) |
S960G |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,930,202 (GRCm39) |
F3980I |
probably benign |
Het |
Vps13d |
T |
C |
4: 144,854,879 (GRCm39) |
N2248S |
probably benign |
Het |
Vps26c |
G |
T |
16: 94,302,549 (GRCm39) |
|
probably benign |
Het |
Wnk4 |
T |
C |
11: 101,154,783 (GRCm39) |
L324P |
probably damaging |
Het |
|
Other mutations in V1ra8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02572:V1ra8
|
APN |
6 |
90,180,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0368:V1ra8
|
UTSW |
6 |
90,179,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0395:V1ra8
|
UTSW |
6 |
90,179,991 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1476:V1ra8
|
UTSW |
6 |
90,180,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:V1ra8
|
UTSW |
6 |
90,180,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R2189:V1ra8
|
UTSW |
6 |
90,179,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2288:V1ra8
|
UTSW |
6 |
90,180,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R3962:V1ra8
|
UTSW |
6 |
90,180,466 (GRCm39) |
missense |
probably benign |
0.02 |
R5380:V1ra8
|
UTSW |
6 |
90,180,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R5469:V1ra8
|
UTSW |
6 |
90,180,186 (GRCm39) |
missense |
probably benign |
0.00 |
R5521:V1ra8
|
UTSW |
6 |
90,180,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R5651:V1ra8
|
UTSW |
6 |
90,180,508 (GRCm39) |
missense |
probably benign |
0.18 |
R6088:V1ra8
|
UTSW |
6 |
90,180,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R6527:V1ra8
|
UTSW |
6 |
90,180,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R7804:V1ra8
|
UTSW |
6 |
90,180,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:V1ra8
|
UTSW |
6 |
90,180,246 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8355:V1ra8
|
UTSW |
6 |
90,180,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:V1ra8
|
UTSW |
6 |
90,180,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R8455:V1ra8
|
UTSW |
6 |
90,180,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8483:V1ra8
|
UTSW |
6 |
90,179,916 (GRCm39) |
missense |
probably benign |
0.09 |
R8834:V1ra8
|
UTSW |
6 |
90,180,622 (GRCm39) |
missense |
unknown |
|
R8909:V1ra8
|
UTSW |
6 |
90,179,938 (GRCm39) |
missense |
possibly damaging |
0.70 |
RF008:V1ra8
|
UTSW |
6 |
90,180,591 (GRCm39) |
missense |
probably benign |
|
|