Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005K14Rik |
T |
A |
1: 83,036,678 (GRCm39) |
K118* |
probably null |
Het |
Actr2 |
A |
G |
11: 20,050,933 (GRCm39) |
F17L |
probably damaging |
Het |
Adam26b |
T |
C |
8: 43,974,818 (GRCm39) |
I61M |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,746,829 (GRCm39) |
|
probably benign |
Het |
Angptl3 |
T |
C |
4: 98,919,675 (GRCm39) |
L145P |
probably damaging |
Het |
Ank2 |
T |
C |
3: 126,726,871 (GRCm39) |
T808A |
probably damaging |
Het |
Ark2c |
T |
A |
18: 77,650,931 (GRCm39) |
|
probably benign |
Het |
Cadm3 |
A |
G |
1: 173,194,977 (GRCm39) |
|
probably null |
Het |
Cog7 |
C |
T |
7: 121,534,966 (GRCm39) |
R573Q |
probably damaging |
Het |
Dchs1 |
T |
A |
7: 105,407,385 (GRCm39) |
I2110F |
probably damaging |
Het |
Fbxo47 |
G |
A |
11: 97,747,089 (GRCm39) |
R326C |
probably damaging |
Het |
Frmpd1 |
A |
T |
4: 45,279,024 (GRCm39) |
D583V |
probably damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,321 (GRCm39) |
L911Q |
probably damaging |
Het |
Gprin1 |
G |
A |
13: 54,888,124 (GRCm39) |
A50V |
possibly damaging |
Het |
Grik4 |
A |
T |
9: 42,459,024 (GRCm39) |
Y571* |
probably null |
Het |
Gucy2e |
A |
G |
11: 69,126,483 (GRCm39) |
V299A |
probably benign |
Het |
Hectd2 |
C |
T |
19: 36,589,728 (GRCm39) |
L618F |
probably damaging |
Het |
Lactbl1 |
A |
T |
4: 136,360,300 (GRCm39) |
I160F |
possibly damaging |
Het |
Lats1 |
T |
A |
10: 7,577,434 (GRCm39) |
V186D |
possibly damaging |
Het |
Lmtk2 |
A |
G |
5: 144,110,624 (GRCm39) |
H448R |
possibly damaging |
Het |
Map10 |
T |
C |
8: 126,398,113 (GRCm39) |
I502T |
probably benign |
Het |
Mok |
A |
G |
12: 110,777,189 (GRCm39) |
F239S |
probably damaging |
Het |
Mprip |
G |
A |
11: 59,648,552 (GRCm39) |
G752D |
probably benign |
Het |
Naip5 |
C |
A |
13: 100,359,652 (GRCm39) |
G528V |
possibly damaging |
Het |
Neu2 |
T |
C |
1: 87,524,464 (GRCm39) |
W150R |
probably damaging |
Het |
Or1ak2 |
T |
A |
2: 36,827,539 (GRCm39) |
M136K |
possibly damaging |
Het |
Or5an1 |
T |
C |
19: 12,260,519 (GRCm39) |
Y36H |
probably damaging |
Het |
Or5as1 |
T |
A |
2: 86,980,207 (GRCm39) |
Y266F |
probably damaging |
Het |
Or5l13 |
T |
A |
2: 87,780,335 (GRCm39) |
M81L |
probably benign |
Het |
Pip5k1c |
T |
A |
10: 81,144,830 (GRCm39) |
Y224N |
probably damaging |
Het |
Plch1 |
T |
C |
3: 63,758,399 (GRCm39) |
E5G |
probably damaging |
Het |
Pspc1 |
T |
C |
14: 57,001,660 (GRCm39) |
*59W |
probably null |
Het |
Ptprq |
T |
C |
10: 107,444,102 (GRCm39) |
T1501A |
probably damaging |
Het |
Rorb |
G |
T |
19: 18,929,614 (GRCm39) |
P304T |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,514,444 (GRCm39) |
L1110Q |
probably damaging |
Het |
Serpine2 |
C |
T |
1: 79,780,847 (GRCm39) |
|
probably null |
Het |
Slco1c1 |
A |
G |
6: 141,477,170 (GRCm39) |
|
probably null |
Het |
Smarca2 |
T |
A |
19: 26,608,331 (GRCm39) |
V130D |
probably damaging |
Het |
Sox17 |
G |
T |
1: 4,562,655 (GRCm39) |
P117T |
possibly damaging |
Het |
Sparcl1 |
A |
T |
5: 104,240,310 (GRCm39) |
Y371* |
probably null |
Het |
Tdpoz2 |
T |
C |
3: 93,559,267 (GRCm39) |
D235G |
possibly damaging |
Het |
Tns2 |
A |
C |
15: 102,022,269 (GRCm39) |
K1182N |
possibly damaging |
Het |
Tpte |
G |
T |
8: 22,805,121 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,799,503 (GRCm39) |
I459K |
possibly damaging |
Het |
Wdr97 |
T |
C |
15: 76,242,478 (GRCm39) |
Y823H |
probably benign |
Het |
Zc3h15 |
G |
A |
2: 83,491,492 (GRCm39) |
R240H |
probably benign |
Het |
Zfp455 |
C |
A |
13: 67,355,121 (GRCm39) |
L130I |
probably benign |
Het |
Zfp777 |
A |
T |
6: 48,021,419 (GRCm39) |
S68T |
probably damaging |
Het |
|
Other mutations in Ahcyl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02173:Ahcyl
|
APN |
16 |
45,974,441 (GRCm39) |
missense |
probably benign |
|
IGL03347:Ahcyl
|
APN |
16 |
45,974,852 (GRCm39) |
missense |
probably benign |
0.01 |
R0326:Ahcyl
|
UTSW |
16 |
45,974,246 (GRCm39) |
missense |
probably benign |
0.03 |
R0552:Ahcyl
|
UTSW |
16 |
45,974,955 (GRCm39) |
missense |
probably benign |
|
R0610:Ahcyl
|
UTSW |
16 |
45,974,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Ahcyl
|
UTSW |
16 |
45,974,211 (GRCm39) |
missense |
probably benign |
0.01 |
R1465:Ahcyl
|
UTSW |
16 |
45,974,211 (GRCm39) |
missense |
probably benign |
0.01 |
R1473:Ahcyl
|
UTSW |
16 |
45,975,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R2997:Ahcyl
|
UTSW |
16 |
45,974,288 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4546:Ahcyl
|
UTSW |
16 |
45,974,330 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4818:Ahcyl
|
UTSW |
16 |
45,974,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Ahcyl
|
UTSW |
16 |
45,974,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R7689:Ahcyl
|
UTSW |
16 |
45,974,970 (GRCm39) |
missense |
probably benign |
0.12 |
R8260:Ahcyl
|
UTSW |
16 |
45,974,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Ahcyl
|
UTSW |
16 |
45,974,468 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9048:Ahcyl
|
UTSW |
16 |
45,974,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Ahcyl
|
UTSW |
16 |
45,975,035 (GRCm39) |
missense |
probably benign |
0.40 |
R9655:Ahcyl
|
UTSW |
16 |
45,974,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Ahcyl
|
UTSW |
16 |
45,974,342 (GRCm39) |
missense |
probably benign |
0.17 |
Z1176:Ahcyl
|
UTSW |
16 |
45,974,592 (GRCm39) |
missense |
probably benign |
0.14 |
|