Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam28 |
C |
A |
14: 68,870,668 (GRCm39) |
R335L |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,716,862 (GRCm39) |
|
probably benign |
Het |
Calcrl |
A |
G |
2: 84,205,668 (GRCm39) |
C8R |
probably benign |
Het |
Cntn4 |
T |
A |
6: 106,632,490 (GRCm39) |
S505T |
probably benign |
Het |
Cyp3a16 |
T |
C |
5: 145,378,758 (GRCm39) |
|
probably benign |
Het |
Dync2i2 |
A |
G |
2: 29,928,402 (GRCm39) |
S75P |
probably benign |
Het |
Fhip1a |
G |
T |
3: 85,629,752 (GRCm39) |
P280T |
probably damaging |
Het |
Gpatch11 |
A |
G |
17: 79,149,593 (GRCm39) |
T198A |
probably benign |
Het |
H2-T15 |
G |
T |
17: 36,367,222 (GRCm39) |
N333K |
possibly damaging |
Het |
Heatr5a |
C |
A |
12: 51,962,941 (GRCm39) |
L986F |
probably damaging |
Het |
Ift172 |
A |
G |
5: 31,443,948 (GRCm39) |
I90T |
probably benign |
Het |
Igkv3-9 |
A |
G |
6: 70,565,445 (GRCm39) |
|
probably benign |
Het |
Iqsec1 |
G |
A |
6: 90,667,331 (GRCm39) |
P369S |
probably benign |
Het |
Myh1 |
C |
A |
11: 67,111,382 (GRCm39) |
T1607K |
probably benign |
Het |
Myo18b |
T |
C |
5: 113,022,838 (GRCm39) |
|
probably benign |
Het |
Nobox |
A |
G |
6: 43,284,472 (GRCm39) |
L58P |
probably damaging |
Het |
Nwd2 |
T |
A |
5: 63,962,042 (GRCm39) |
I542N |
possibly damaging |
Het |
Or4k51 |
A |
G |
2: 111,584,824 (GRCm39) |
T77A |
probably damaging |
Het |
Or5p54 |
A |
G |
7: 107,553,953 (GRCm39) |
Y35C |
probably damaging |
Het |
Osm |
C |
T |
11: 4,189,470 (GRCm39) |
R85W |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,397,129 (GRCm39) |
|
probably benign |
Het |
Sec14l2 |
A |
G |
11: 4,061,114 (GRCm39) |
S116P |
probably benign |
Het |
Selenbp2 |
A |
C |
3: 94,605,461 (GRCm39) |
N96H |
possibly damaging |
Het |
Smarcal1 |
T |
C |
1: 72,635,099 (GRCm39) |
S393P |
probably damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,414,335 (GRCm39) |
Q103R |
probably damaging |
Het |
Tmem63c |
T |
C |
12: 87,119,647 (GRCm39) |
Y314H |
probably damaging |
Het |
Zfp663 |
A |
C |
2: 165,200,993 (GRCm39) |
S14A |
probably benign |
Het |
Zmynd10 |
A |
G |
9: 107,427,731 (GRCm39) |
N345S |
probably damaging |
Het |
|
Other mutations in Pcdh20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00566:Pcdh20
|
APN |
14 |
88,705,317 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01112:Pcdh20
|
APN |
14 |
88,704,636 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01586:Pcdh20
|
APN |
14 |
88,708,344 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02545:Pcdh20
|
APN |
14 |
88,706,280 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02935:Pcdh20
|
APN |
14 |
88,704,438 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4362001:Pcdh20
|
UTSW |
14 |
88,704,462 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4403001:Pcdh20
|
UTSW |
14 |
88,704,462 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4453001:Pcdh20
|
UTSW |
14 |
88,704,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R0322:Pcdh20
|
UTSW |
14 |
88,706,383 (GRCm39) |
missense |
probably benign |
0.24 |
R0372:Pcdh20
|
UTSW |
14 |
88,706,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R0391:Pcdh20
|
UTSW |
14 |
88,706,104 (GRCm39) |
missense |
probably benign |
|
R0575:Pcdh20
|
UTSW |
14 |
88,705,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0789:Pcdh20
|
UTSW |
14 |
88,706,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R1370:Pcdh20
|
UTSW |
14 |
88,705,737 (GRCm39) |
missense |
probably benign |
0.00 |
R1465:Pcdh20
|
UTSW |
14 |
88,706,673 (GRCm39) |
missense |
probably benign |
0.00 |
R1465:Pcdh20
|
UTSW |
14 |
88,706,673 (GRCm39) |
missense |
probably benign |
0.00 |
R1664:Pcdh20
|
UTSW |
14 |
88,705,758 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1677:Pcdh20
|
UTSW |
14 |
88,705,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Pcdh20
|
UTSW |
14 |
88,706,620 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1907:Pcdh20
|
UTSW |
14 |
88,706,140 (GRCm39) |
missense |
probably benign |
0.01 |
R2043:Pcdh20
|
UTSW |
14 |
88,704,591 (GRCm39) |
missense |
probably benign |
0.01 |
R2430:Pcdh20
|
UTSW |
14 |
88,704,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R2471:Pcdh20
|
UTSW |
14 |
88,704,672 (GRCm39) |
missense |
probably benign |
0.00 |
R3838:Pcdh20
|
UTSW |
14 |
88,705,899 (GRCm39) |
missense |
probably benign |
0.00 |
R4163:Pcdh20
|
UTSW |
14 |
88,705,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Pcdh20
|
UTSW |
14 |
88,706,434 (GRCm39) |
missense |
probably benign |
0.21 |
R4602:Pcdh20
|
UTSW |
14 |
88,705,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4681:Pcdh20
|
UTSW |
14 |
88,705,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Pcdh20
|
UTSW |
14 |
88,705,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Pcdh20
|
UTSW |
14 |
88,707,162 (GRCm39) |
missense |
probably benign |
0.01 |
R5204:Pcdh20
|
UTSW |
14 |
88,706,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Pcdh20
|
UTSW |
14 |
88,705,813 (GRCm39) |
missense |
probably benign |
|
R5652:Pcdh20
|
UTSW |
14 |
88,704,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R5815:Pcdh20
|
UTSW |
14 |
88,708,312 (GRCm39) |
missense |
probably benign |
0.03 |
R6195:Pcdh20
|
UTSW |
14 |
88,705,488 (GRCm39) |
missense |
probably benign |
0.39 |
R6233:Pcdh20
|
UTSW |
14 |
88,705,488 (GRCm39) |
missense |
probably benign |
0.39 |
R6848:Pcdh20
|
UTSW |
14 |
88,704,690 (GRCm39) |
missense |
probably benign |
0.03 |
R6913:Pcdh20
|
UTSW |
14 |
88,706,038 (GRCm39) |
missense |
probably benign |
|
R7044:Pcdh20
|
UTSW |
14 |
88,706,607 (GRCm39) |
missense |
probably damaging |
0.98 |
R7224:Pcdh20
|
UTSW |
14 |
88,706,511 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7388:Pcdh20
|
UTSW |
14 |
88,706,103 (GRCm39) |
missense |
probably benign |
0.33 |
R7486:Pcdh20
|
UTSW |
14 |
88,706,050 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7651:Pcdh20
|
UTSW |
14 |
88,706,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:Pcdh20
|
UTSW |
14 |
88,706,803 (GRCm39) |
missense |
probably benign |
|
R7706:Pcdh20
|
UTSW |
14 |
88,704,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Pcdh20
|
UTSW |
14 |
88,707,143 (GRCm39) |
missense |
probably null |
0.02 |
R7892:Pcdh20
|
UTSW |
14 |
88,704,867 (GRCm39) |
nonsense |
probably null |
|
R8218:Pcdh20
|
UTSW |
14 |
88,706,047 (GRCm39) |
missense |
probably damaging |
0.96 |
R8545:Pcdh20
|
UTSW |
14 |
88,706,601 (GRCm39) |
missense |
probably damaging |
0.96 |
R8701:Pcdh20
|
UTSW |
14 |
88,705,849 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9219:Pcdh20
|
UTSW |
14 |
88,706,255 (GRCm39) |
missense |
probably benign |
0.01 |
R9238:Pcdh20
|
UTSW |
14 |
88,706,190 (GRCm39) |
missense |
probably benign |
0.43 |
R9418:Pcdh20
|
UTSW |
14 |
88,705,455 (GRCm39) |
missense |
probably benign |
|
R9665:Pcdh20
|
UTSW |
14 |
88,707,162 (GRCm39) |
missense |
probably benign |
0.44 |
X0028:Pcdh20
|
UTSW |
14 |
88,705,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|