Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap5z1 |
A |
G |
5: 142,453,442 (GRCm39) |
K137E |
possibly damaging |
Het |
Atm |
A |
C |
9: 53,429,923 (GRCm39) |
V371G |
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 29,068,987 (GRCm39) |
Y247H |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,917,556 (GRCm39) |
V927A |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Edar |
G |
A |
10: 58,443,257 (GRCm39) |
P290S |
possibly damaging |
Het |
Ext2 |
T |
C |
2: 93,526,606 (GRCm39) |
I677V |
probably benign |
Het |
Fam53a |
A |
G |
5: 33,765,080 (GRCm39) |
S209P |
probably damaging |
Het |
Fshr |
A |
T |
17: 89,318,441 (GRCm39) |
|
probably null |
Het |
Gfm2 |
G |
A |
13: 97,299,659 (GRCm39) |
A406T |
probably damaging |
Het |
Gm14295 |
A |
T |
2: 176,502,465 (GRCm39) |
I652L |
probably benign |
Het |
Gm5431 |
T |
A |
11: 48,779,716 (GRCm39) |
E402V |
probably damaging |
Het |
Gm6899 |
GGAGGCCGCCCAGTGGCAGAGGCCGCCCAGTGGCAGAGGC |
GGAGGCCGCCCAGTGGCAGAGGC |
11: 26,543,725 (GRCm39) |
|
probably null |
Het |
Itih2 |
T |
C |
2: 10,115,346 (GRCm39) |
D342G |
probably benign |
Het |
Lgi2 |
A |
T |
5: 52,711,827 (GRCm39) |
D164E |
probably damaging |
Het |
Lrriq1 |
A |
G |
10: 103,050,448 (GRCm39) |
I768T |
probably damaging |
Het |
Map1a |
C |
A |
2: 121,132,868 (GRCm39) |
A990E |
probably damaging |
Het |
Mdh1b |
A |
G |
1: 63,759,163 (GRCm39) |
V143A |
probably benign |
Het |
Mrgprb3 |
C |
T |
7: 48,293,059 (GRCm39) |
C164Y |
probably damaging |
Het |
Mtpap |
T |
A |
18: 4,386,328 (GRCm39) |
V316E |
probably damaging |
Het |
Mybpc3 |
T |
A |
2: 90,959,023 (GRCm39) |
C655* |
probably null |
Het |
Myh15 |
A |
G |
16: 48,986,204 (GRCm39) |
E1558G |
possibly damaging |
Het |
Mylk |
A |
G |
16: 34,742,127 (GRCm39) |
T880A |
probably benign |
Het |
Nckap1 |
T |
A |
2: 80,370,466 (GRCm39) |
D408V |
probably damaging |
Het |
Nos3 |
A |
T |
5: 24,582,343 (GRCm39) |
H605L |
probably benign |
Het |
Nrxn2 |
C |
A |
19: 6,581,428 (GRCm39) |
D411E |
probably benign |
Het |
Or1af1 |
T |
C |
2: 37,109,633 (GRCm39) |
V44A |
probably benign |
Het |
Or8j3b |
T |
A |
2: 86,205,094 (GRCm39) |
I221L |
possibly damaging |
Het |
Pde4d |
C |
A |
13: 109,769,398 (GRCm39) |
P29T |
probably benign |
Het |
Pde4d |
C |
T |
13: 109,769,399 (GRCm39) |
P29L |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,636,094 (GRCm39) |
V412A |
possibly damaging |
Het |
Rev1 |
T |
A |
1: 38,118,474 (GRCm39) |
I480L |
probably benign |
Het |
Rimbp3 |
A |
G |
16: 17,028,708 (GRCm39) |
T711A |
probably benign |
Het |
RP23-191E1.1 |
T |
A |
3: 106,204,784 (GRCm39) |
|
noncoding transcript |
Het |
Serpina11 |
A |
T |
12: 103,952,221 (GRCm39) |
I183N |
probably damaging |
Het |
Siglec1 |
T |
C |
2: 130,921,236 (GRCm39) |
H645R |
probably damaging |
Het |
Skint7 |
G |
A |
4: 111,837,501 (GRCm39) |
R93H |
probably damaging |
Het |
Slfn8 |
T |
C |
11: 82,894,910 (GRCm39) |
E632G |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,673,992 (GRCm39) |
V208I |
probably benign |
Het |
Trps1 |
G |
A |
15: 50,528,156 (GRCm39) |
T658I |
probably damaging |
Het |
Ubash3a |
A |
G |
17: 31,438,691 (GRCm39) |
T287A |
probably damaging |
Het |
Ugt2b35 |
G |
A |
5: 87,159,139 (GRCm39) |
W444* |
probably null |
Het |
Vmn1r219 |
T |
A |
13: 23,347,063 (GRCm39) |
V84D |
probably damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,154,121 (GRCm39) |
Y61C |
probably damaging |
Het |
Vmn2r104 |
G |
A |
17: 20,250,163 (GRCm39) |
P703S |
probably damaging |
Het |
Wdsub1 |
T |
A |
2: 59,708,873 (GRCm39) |
|
probably benign |
Het |
Zfp667 |
A |
G |
7: 6,308,715 (GRCm39) |
Q461R |
probably benign |
Het |
Zfp941 |
C |
A |
7: 140,391,872 (GRCm39) |
G496* |
probably null |
Het |
|
Other mutations in Gm14403 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01835:Gm14403
|
APN |
2 |
177,199,049 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02660:Gm14403
|
APN |
2 |
177,201,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Gm14403
|
UTSW |
2 |
177,200,359 (GRCm39) |
missense |
probably benign |
0.09 |
R0932:Gm14403
|
UTSW |
2 |
177,198,810 (GRCm39) |
missense |
probably benign |
0.01 |
R0975:Gm14403
|
UTSW |
2 |
177,201,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Gm14403
|
UTSW |
2 |
177,199,024 (GRCm39) |
splice site |
probably benign |
|
R1853:Gm14403
|
UTSW |
2 |
177,200,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Gm14403
|
UTSW |
2 |
177,200,786 (GRCm39) |
missense |
probably benign |
|
R3803:Gm14403
|
UTSW |
2 |
177,200,569 (GRCm39) |
missense |
probably benign |
0.04 |
R4589:Gm14403
|
UTSW |
2 |
177,200,428 (GRCm39) |
missense |
probably benign |
0.29 |
R4805:Gm14403
|
UTSW |
2 |
177,200,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R5085:Gm14403
|
UTSW |
2 |
177,200,282 (GRCm39) |
missense |
probably benign |
0.04 |
R5425:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R5643:Gm14403
|
UTSW |
2 |
177,199,054 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5644:Gm14403
|
UTSW |
2 |
177,199,054 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5739:Gm14403
|
UTSW |
2 |
177,201,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Gm14403
|
UTSW |
2 |
177,200,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R6197:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R6198:Gm14403
|
UTSW |
2 |
177,201,448 (GRCm39) |
unclassified |
probably benign |
|
R6892:Gm14403
|
UTSW |
2 |
177,201,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Gm14403
|
UTSW |
2 |
177,201,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7168:Gm14403
|
UTSW |
2 |
177,201,318 (GRCm39) |
missense |
probably damaging |
0.96 |
R7510:Gm14403
|
UTSW |
2 |
177,200,403 (GRCm39) |
missense |
probably benign |
0.01 |
R7623:Gm14403
|
UTSW |
2 |
177,200,405 (GRCm39) |
missense |
probably benign |
|
R8049:Gm14403
|
UTSW |
2 |
177,200,311 (GRCm39) |
missense |
probably benign |
0.00 |
R8557:Gm14403
|
UTSW |
2 |
177,201,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R9224:Gm14403
|
UTSW |
2 |
177,200,336 (GRCm39) |
missense |
probably benign |
|
R9333:Gm14403
|
UTSW |
2 |
177,200,919 (GRCm39) |
missense |
probably benign |
0.42 |
R9632:Gm14403
|
UTSW |
2 |
177,201,421 (GRCm39) |
missense |
probably benign |
0.00 |
|