Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
T |
A |
8: 44,022,669 (GRCm39) |
M274L |
probably benign |
Het |
Adarb1 |
T |
A |
10: 77,158,267 (GRCm39) |
N60I |
possibly damaging |
Het |
Adgrv1 |
T |
A |
13: 81,654,274 (GRCm39) |
N2919I |
probably damaging |
Het |
Adora3 |
C |
T |
3: 105,814,613 (GRCm39) |
T121M |
possibly damaging |
Het |
Aoc1l3 |
A |
T |
6: 48,965,260 (GRCm39) |
N423Y |
probably damaging |
Het |
Arhgap19 |
A |
T |
19: 41,761,566 (GRCm39) |
F466Y |
probably benign |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Atxn7l1 |
C |
T |
12: 33,417,315 (GRCm39) |
T492I |
probably benign |
Het |
B3galnt2 |
T |
C |
13: 14,170,393 (GRCm39) |
S248P |
probably damaging |
Het |
Casp2 |
T |
C |
6: 42,246,332 (GRCm39) |
V230A |
probably benign |
Het |
Creb3l1 |
C |
T |
2: 91,822,231 (GRCm39) |
|
probably null |
Het |
Ctnnbl1 |
G |
A |
2: 157,651,445 (GRCm39) |
G240E |
possibly damaging |
Het |
Dhx16 |
T |
A |
17: 36,200,203 (GRCm39) |
F874Y |
probably damaging |
Het |
Dnah14 |
A |
T |
1: 181,562,369 (GRCm39) |
Y2643F |
possibly damaging |
Het |
Dnah2 |
C |
A |
11: 69,384,073 (GRCm39) |
V1048L |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,436,307 (GRCm39) |
I4012V |
probably benign |
Het |
Duox2 |
G |
A |
2: 122,115,729 (GRCm39) |
R1002* |
probably null |
Het |
Ears2 |
T |
A |
7: 121,643,786 (GRCm39) |
K391* |
probably null |
Het |
Eif4e |
T |
C |
3: 138,259,470 (GRCm39) |
V176A |
probably benign |
Het |
Erbb4 |
T |
A |
1: 68,329,638 (GRCm39) |
I626L |
probably benign |
Het |
Fam171a1 |
C |
T |
2: 3,226,037 (GRCm39) |
T390I |
probably benign |
Het |
Fam187b |
A |
G |
7: 30,677,037 (GRCm39) |
E182G |
possibly damaging |
Het |
Fam204a |
A |
G |
19: 60,209,685 (GRCm39) |
V15A |
probably benign |
Het |
Fscn3 |
C |
T |
6: 28,430,432 (GRCm39) |
R201* |
probably null |
Het |
Fzd6 |
A |
G |
15: 38,895,043 (GRCm39) |
D403G |
probably damaging |
Het |
Gars1 |
G |
A |
6: 55,029,249 (GRCm39) |
A210T |
probably null |
Het |
Gmcl1 |
A |
T |
6: 86,677,569 (GRCm39) |
I428N |
probably damaging |
Het |
Gmip |
T |
A |
8: 70,263,832 (GRCm39) |
I92N |
probably damaging |
Het |
Il17rc |
G |
A |
6: 113,456,048 (GRCm39) |
V298I |
probably damaging |
Het |
Kifap3 |
A |
G |
1: 163,610,630 (GRCm39) |
I37V |
probably benign |
Het |
Marf1 |
T |
C |
16: 13,963,789 (GRCm39) |
K505E |
probably damaging |
Het |
Masp2 |
A |
T |
4: 148,692,396 (GRCm39) |
|
probably null |
Het |
Mmp15 |
G |
A |
8: 96,093,002 (GRCm39) |
R127H |
probably damaging |
Het |
Nrdc |
A |
G |
4: 108,889,658 (GRCm39) |
T402A |
possibly damaging |
Het |
Or10d1c |
A |
T |
9: 38,894,081 (GRCm39) |
N86K |
probably benign |
Het |
Or4k6 |
T |
A |
14: 50,475,407 (GRCm39) |
I312L |
probably benign |
Het |
Papln |
A |
T |
12: 83,833,638 (GRCm39) |
I1185F |
probably damaging |
Het |
Pcdhgb1 |
A |
G |
18: 37,814,705 (GRCm39) |
N399D |
probably benign |
Het |
Pcdhgb6 |
T |
A |
18: 37,876,872 (GRCm39) |
S527T |
probably benign |
Het |
Phkb |
T |
A |
8: 86,743,493 (GRCm39) |
Y530* |
probably null |
Het |
Pira2 |
A |
G |
7: 3,844,030 (GRCm39) |
S581P |
probably benign |
Het |
Pou4f3 |
A |
T |
18: 42,528,329 (GRCm39) |
T91S |
probably benign |
Het |
Prpf38a |
A |
G |
4: 108,424,112 (GRCm39) |
S296P |
unknown |
Het |
Rnf213 |
T |
C |
11: 119,332,975 (GRCm39) |
V2729A |
|
Het |
Rtl1 |
G |
A |
12: 109,557,226 (GRCm39) |
Q1538* |
probably null |
Het |
Sars2 |
T |
C |
7: 28,447,273 (GRCm39) |
S224P |
probably damaging |
Het |
Senp8 |
A |
G |
9: 59,645,105 (GRCm39) |
V17A |
probably benign |
Het |
Serpinb13 |
T |
A |
1: 106,923,562 (GRCm39) |
L89* |
probably null |
Het |
Sh3bp2 |
T |
A |
5: 34,718,453 (GRCm39) |
|
probably null |
Het |
Shank2 |
A |
G |
7: 143,960,945 (GRCm39) |
T254A |
probably benign |
Het |
Smdt1 |
A |
T |
15: 82,231,504 (GRCm39) |
E12D |
probably benign |
Het |
Sp110 |
G |
A |
1: 85,506,813 (GRCm39) |
R417C |
probably benign |
Het |
Taar2 |
A |
G |
10: 23,817,345 (GRCm39) |
N295S |
probably damaging |
Het |
Trim24 |
A |
G |
6: 37,892,208 (GRCm39) |
Q247R |
probably damaging |
Het |
Trpc4 |
T |
A |
3: 54,209,610 (GRCm39) |
N658K |
probably damaging |
Het |
Ube2e1 |
T |
C |
14: 18,284,348 (GRCm38) |
D137G |
probably damaging |
Het |
Ubn1 |
T |
A |
16: 4,899,422 (GRCm39) |
H1055Q |
probably benign |
Het |
Vmn1r235 |
A |
G |
17: 21,482,190 (GRCm39) |
T172A |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,882,333 (GRCm39) |
F1087L |
|
Het |
Xirp2 |
T |
C |
2: 67,349,653 (GRCm39) |
S3283P |
probably damaging |
Het |
Zeb2 |
C |
A |
2: 44,887,158 (GRCm39) |
S633I |
possibly damaging |
Het |
|
Other mutations in Dennd2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01763:Dennd2c
|
APN |
3 |
103,064,224 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01791:Dennd2c
|
APN |
3 |
103,073,741 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02100:Dennd2c
|
APN |
3 |
103,060,991 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02119:Dennd2c
|
APN |
3 |
103,044,559 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02395:Dennd2c
|
APN |
3 |
103,065,081 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02631:Dennd2c
|
APN |
3 |
103,063,387 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02895:Dennd2c
|
APN |
3 |
103,044,519 (GRCm39) |
missense |
possibly damaging |
0.76 |
convolution
|
UTSW |
3 |
103,063,423 (GRCm39) |
missense |
probably damaging |
1.00 |
Resolution
|
UTSW |
3 |
103,040,661 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1749:Dennd2c
|
UTSW |
3 |
103,039,352 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1931:Dennd2c
|
UTSW |
3 |
103,040,568 (GRCm39) |
missense |
probably benign |
0.32 |
R1964:Dennd2c
|
UTSW |
3 |
103,073,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Dennd2c
|
UTSW |
3 |
103,039,014 (GRCm39) |
missense |
probably benign |
0.01 |
R1973:Dennd2c
|
UTSW |
3 |
103,039,014 (GRCm39) |
missense |
probably benign |
0.01 |
R2025:Dennd2c
|
UTSW |
3 |
103,039,005 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2350:Dennd2c
|
UTSW |
3 |
103,039,317 (GRCm39) |
missense |
probably benign |
0.00 |
R2373:Dennd2c
|
UTSW |
3 |
103,064,158 (GRCm39) |
missense |
probably damaging |
0.99 |
R4555:Dennd2c
|
UTSW |
3 |
103,039,202 (GRCm39) |
missense |
probably benign |
0.00 |
R4916:Dennd2c
|
UTSW |
3 |
103,039,140 (GRCm39) |
missense |
probably benign |
0.00 |
R5560:Dennd2c
|
UTSW |
3 |
103,068,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Dennd2c
|
UTSW |
3 |
103,038,925 (GRCm39) |
nonsense |
probably null |
|
R6395:Dennd2c
|
UTSW |
3 |
103,056,540 (GRCm39) |
critical splice donor site |
probably null |
|
R6567:Dennd2c
|
UTSW |
3 |
103,039,335 (GRCm39) |
missense |
probably benign |
0.02 |
R6681:Dennd2c
|
UTSW |
3 |
103,038,977 (GRCm39) |
missense |
probably benign |
0.01 |
R7106:Dennd2c
|
UTSW |
3 |
103,038,893 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7162:Dennd2c
|
UTSW |
3 |
103,063,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7514:Dennd2c
|
UTSW |
3 |
103,070,378 (GRCm39) |
missense |
probably benign |
0.00 |
R7591:Dennd2c
|
UTSW |
3 |
103,040,661 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7698:Dennd2c
|
UTSW |
3 |
103,072,359 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8069:Dennd2c
|
UTSW |
3 |
103,072,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R8086:Dennd2c
|
UTSW |
3 |
103,040,661 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8247:Dennd2c
|
UTSW |
3 |
103,059,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R8347:Dennd2c
|
UTSW |
3 |
103,065,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R8829:Dennd2c
|
UTSW |
3 |
103,059,720 (GRCm39) |
critical splice donor site |
probably null |
|
R8832:Dennd2c
|
UTSW |
3 |
103,059,720 (GRCm39) |
critical splice donor site |
probably null |
|
R9131:Dennd2c
|
UTSW |
3 |
103,065,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R9332:Dennd2c
|
UTSW |
3 |
103,038,877 (GRCm39) |
missense |
probably benign |
0.01 |
R9520:Dennd2c
|
UTSW |
3 |
103,044,484 (GRCm39) |
missense |
probably benign |
|
|