Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas2 |
A |
T |
7: 132,476,685 (GRCm39) |
I142F |
probably damaging |
Het |
Adamts16 |
A |
G |
13: 70,984,496 (GRCm39) |
Y56H |
probably damaging |
Het |
Alms1 |
A |
G |
6: 85,618,357 (GRCm39) |
D2801G |
probably damaging |
Het |
Anpep |
A |
G |
7: 79,489,269 (GRCm39) |
I301T |
probably benign |
Het |
Atxn7l2 |
G |
A |
3: 108,114,285 (GRCm39) |
T159M |
probably benign |
Het |
B130006D01Rik |
C |
T |
11: 95,617,175 (GRCm39) |
|
probably benign |
Het |
Btf3l4b |
C |
A |
13: 96,217,432 (GRCm39) |
D136Y |
possibly damaging |
Het |
Ccdc175 |
T |
C |
12: 72,202,392 (GRCm39) |
K301R |
probably damaging |
Het |
Cecr2 |
A |
T |
6: 120,733,894 (GRCm39) |
Q627L |
probably benign |
Het |
Cerkl |
C |
A |
2: 79,172,751 (GRCm39) |
M307I |
probably benign |
Het |
Eif2ak4 |
A |
G |
2: 118,293,207 (GRCm39) |
I1254M |
probably damaging |
Het |
Epha3 |
T |
C |
16: 63,664,510 (GRCm39) |
T37A |
probably benign |
Het |
Fancm |
T |
C |
12: 65,171,931 (GRCm39) |
V1857A |
probably damaging |
Het |
Il1r2 |
T |
C |
1: 40,162,416 (GRCm39) |
V353A |
probably damaging |
Het |
Irgq |
A |
T |
7: 24,233,715 (GRCm39) |
R519W |
probably damaging |
Het |
Map1b |
T |
A |
13: 99,652,950 (GRCm39) |
S16C |
probably damaging |
Het |
Myo9a |
T |
G |
9: 59,739,573 (GRCm39) |
C762G |
probably damaging |
Het |
Nup107 |
A |
T |
10: 117,606,374 (GRCm39) |
V454E |
probably damaging |
Het |
Or10h5 |
A |
G |
17: 33,434,868 (GRCm39) |
V150A |
probably benign |
Het |
Or4p20 |
A |
T |
2: 88,254,228 (GRCm39) |
I47N |
probably damaging |
Het |
Or7g35 |
T |
G |
9: 19,496,265 (GRCm39) |
L144R |
probably damaging |
Het |
Pcdha11 |
A |
G |
18: 37,145,937 (GRCm39) |
K676R |
probably benign |
Het |
Pknox2 |
C |
T |
9: 36,834,986 (GRCm39) |
R161H |
probably damaging |
Het |
Prr5l |
T |
C |
2: 101,547,430 (GRCm39) |
N365S |
probably benign |
Het |
Prrg4 |
A |
G |
2: 104,679,501 (GRCm39) |
L8P |
probably damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,453,595 (GRCm39) |
|
probably null |
Het |
Rtp4 |
A |
T |
16: 23,428,827 (GRCm39) |
H30L |
probably benign |
Het |
Rxfp2 |
T |
G |
5: 149,993,834 (GRCm39) |
I632S |
possibly damaging |
Het |
Spata31h1 |
A |
C |
10: 82,126,314 (GRCm39) |
F2232C |
probably damaging |
Het |
Sptbn1 |
C |
A |
11: 30,070,758 (GRCm39) |
E1533D |
possibly damaging |
Het |
Ssbp1 |
A |
G |
6: 40,454,941 (GRCm39) |
I133M |
probably damaging |
Het |
Stap1 |
A |
G |
5: 86,242,602 (GRCm39) |
I188V |
possibly damaging |
Het |
Topaz1 |
T |
C |
9: 122,603,173 (GRCm39) |
M1040T |
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,887,501 (GRCm39) |
F877L |
possibly damaging |
Het |
Ush1c |
A |
G |
7: 45,858,674 (GRCm39) |
L538P |
probably damaging |
Het |
Zfp518a |
G |
A |
19: 40,904,162 (GRCm39) |
A1364T |
probably benign |
Het |
|
Other mutations in Gm3486 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0227:Gm3486
|
UTSW |
14 |
41,206,518 (GRCm39) |
missense |
probably benign |
0.23 |
R1731:Gm3486
|
UTSW |
14 |
41,206,492 (GRCm39) |
missense |
probably benign |
0.00 |
R4157:Gm3486
|
UTSW |
14 |
41,208,343 (GRCm39) |
missense |
probably benign |
0.24 |
R6248:Gm3486
|
UTSW |
14 |
41,206,472 (GRCm39) |
makesense |
probably null |
|
R6397:Gm3486
|
UTSW |
14 |
41,208,343 (GRCm39) |
missense |
probably benign |
0.24 |
R6858:Gm3486
|
UTSW |
14 |
41,210,322 (GRCm39) |
missense |
probably damaging |
0.98 |
R6945:Gm3486
|
UTSW |
14 |
41,206,518 (GRCm39) |
missense |
probably benign |
0.03 |
R8554:Gm3486
|
UTSW |
14 |
41,209,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R9283:Gm3486
|
UTSW |
14 |
41,210,268 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9352:Gm3486
|
UTSW |
14 |
41,208,318 (GRCm39) |
missense |
possibly damaging |
0.66 |
|