Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg1 |
T |
C |
17: 31,324,514 (GRCm39) |
F253S |
probably benign |
Het |
AI429214 |
T |
A |
8: 37,461,383 (GRCm39) |
I177N |
probably damaging |
Het |
Astn1 |
C |
A |
1: 158,496,201 (GRCm39) |
T1077K |
probably damaging |
Het |
Asxl3 |
A |
T |
18: 22,655,502 (GRCm39) |
I1171L |
probably benign |
Het |
Cdca2 |
A |
T |
14: 67,943,172 (GRCm39) |
S206T |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,248,319 (GRCm39) |
M858V |
possibly damaging |
Het |
Cyp2j12 |
C |
T |
4: 95,987,999 (GRCm39) |
A464T |
probably benign |
Het |
Fryl |
A |
T |
5: 73,190,134 (GRCm39) |
D2787E |
possibly damaging |
Het |
Hmx3 |
G |
A |
7: 131,146,000 (GRCm39) |
R236H |
probably damaging |
Het |
Il1rap |
T |
A |
16: 26,529,318 (GRCm39) |
C330* |
probably null |
Het |
Klrc1 |
A |
T |
6: 129,655,865 (GRCm39) |
N3K |
probably damaging |
Het |
Nars1 |
A |
G |
18: 64,643,554 (GRCm39) |
F142L |
probably benign |
Het |
Nipal1 |
A |
G |
5: 72,825,401 (GRCm39) |
S365G |
possibly damaging |
Het |
Or1n1 |
T |
A |
2: 36,749,787 (GRCm39) |
H191L |
probably benign |
Het |
Or2ag15 |
G |
A |
7: 106,340,991 (GRCm39) |
T50I |
probably benign |
Het |
Or51s1 |
T |
G |
7: 102,559,054 (GRCm39) |
|
probably benign |
Het |
Or8k17 |
C |
A |
2: 86,066,456 (GRCm39) |
R234M |
probably damaging |
Het |
Pcdhb4 |
A |
G |
18: 37,442,057 (GRCm39) |
T456A |
possibly damaging |
Het |
Pcsk2 |
C |
T |
2: 143,655,552 (GRCm39) |
Q579* |
probably null |
Het |
Phactr4 |
G |
A |
4: 132,091,086 (GRCm39) |
R577W |
probably damaging |
Het |
Rbms3 |
T |
C |
9: 116,524,879 (GRCm39) |
|
probably benign |
Het |
Rxfp1 |
T |
G |
3: 79,594,175 (GRCm39) |
D73A |
probably damaging |
Het |
Scmh1 |
A |
T |
4: 120,340,781 (GRCm39) |
|
probably benign |
Het |
Syk |
T |
G |
13: 52,764,993 (GRCm39) |
L40R |
probably damaging |
Het |
Tcn2 |
T |
C |
11: 3,875,072 (GRCm39) |
N153S |
probably benign |
Het |
Tnks |
A |
G |
8: 35,336,678 (GRCm39) |
L502P |
probably damaging |
Het |
Vmn2r111 |
A |
G |
17: 22,767,265 (GRCm39) |
V744A |
possibly damaging |
Het |
|
Other mutations in Pcdhb5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Pcdhb5
|
APN |
18 |
37,455,162 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00895:Pcdhb5
|
APN |
18 |
37,454,036 (GRCm39) |
missense |
probably benign |
0.42 |
IGL00896:Pcdhb5
|
APN |
18 |
37,455,838 (GRCm39) |
splice site |
probably null |
|
IGL01385:Pcdhb5
|
APN |
18 |
37,455,267 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01619:Pcdhb5
|
APN |
18 |
37,455,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01712:Pcdhb5
|
APN |
18 |
37,454,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01716:Pcdhb5
|
APN |
18 |
37,454,075 (GRCm39) |
missense |
probably benign |
|
IGL01719:Pcdhb5
|
APN |
18 |
37,454,075 (GRCm39) |
missense |
probably benign |
|
IGL01720:Pcdhb5
|
APN |
18 |
37,454,075 (GRCm39) |
missense |
probably benign |
|
IGL01723:Pcdhb5
|
APN |
18 |
37,454,075 (GRCm39) |
missense |
probably benign |
|
IGL01724:Pcdhb5
|
APN |
18 |
37,454,075 (GRCm39) |
missense |
probably benign |
|
IGL01839:Pcdhb5
|
APN |
18 |
37,454,502 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01884:Pcdhb5
|
APN |
18 |
37,454,387 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02088:Pcdhb5
|
APN |
18 |
37,455,012 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02299:Pcdhb5
|
APN |
18 |
37,453,943 (GRCm39) |
missense |
probably benign |
|
IGL02444:Pcdhb5
|
APN |
18 |
37,454,103 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03372:Pcdhb5
|
APN |
18 |
37,453,713 (GRCm39) |
missense |
probably benign |
0.22 |
R0034:Pcdhb5
|
UTSW |
18 |
37,455,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Pcdhb5
|
UTSW |
18 |
37,454,321 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0179:Pcdhb5
|
UTSW |
18 |
37,455,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0466:Pcdhb5
|
UTSW |
18 |
37,455,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0471:Pcdhb5
|
UTSW |
18 |
37,454,359 (GRCm39) |
nonsense |
probably null |
|
R0565:Pcdhb5
|
UTSW |
18 |
37,453,820 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0646:Pcdhb5
|
UTSW |
18 |
37,454,675 (GRCm39) |
missense |
probably benign |
|
R1014:Pcdhb5
|
UTSW |
18 |
37,455,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R1617:Pcdhb5
|
UTSW |
18 |
37,454,455 (GRCm39) |
nonsense |
probably null |
|
R1676:Pcdhb5
|
UTSW |
18 |
37,453,805 (GRCm39) |
missense |
probably benign |
0.01 |
R1774:Pcdhb5
|
UTSW |
18 |
37,455,725 (GRCm39) |
missense |
probably damaging |
0.99 |
R1826:Pcdhb5
|
UTSW |
18 |
37,454,522 (GRCm39) |
nonsense |
probably null |
|
R1854:Pcdhb5
|
UTSW |
18 |
37,455,393 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2355:Pcdhb5
|
UTSW |
18 |
37,455,169 (GRCm39) |
missense |
probably benign |
|
R4290:Pcdhb5
|
UTSW |
18 |
37,455,734 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4292:Pcdhb5
|
UTSW |
18 |
37,455,734 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4293:Pcdhb5
|
UTSW |
18 |
37,455,734 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4294:Pcdhb5
|
UTSW |
18 |
37,455,734 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4295:Pcdhb5
|
UTSW |
18 |
37,455,734 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4391:Pcdhb5
|
UTSW |
18 |
37,455,789 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4411:Pcdhb5
|
UTSW |
18 |
37,455,050 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4480:Pcdhb5
|
UTSW |
18 |
37,453,805 (GRCm39) |
missense |
probably benign |
0.43 |
R4852:Pcdhb5
|
UTSW |
18 |
37,455,524 (GRCm39) |
missense |
probably benign |
0.04 |
R5121:Pcdhb5
|
UTSW |
18 |
37,454,170 (GRCm39) |
missense |
probably benign |
0.11 |
R5133:Pcdhb5
|
UTSW |
18 |
37,453,943 (GRCm39) |
missense |
probably benign |
|
R5630:Pcdhb5
|
UTSW |
18 |
37,454,208 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5833:Pcdhb5
|
UTSW |
18 |
37,454,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R5896:Pcdhb5
|
UTSW |
18 |
37,455,732 (GRCm39) |
nonsense |
probably null |
|
R5942:Pcdhb5
|
UTSW |
18 |
37,453,838 (GRCm39) |
nonsense |
probably null |
|
R5945:Pcdhb5
|
UTSW |
18 |
37,454,523 (GRCm39) |
missense |
probably benign |
0.08 |
R5970:Pcdhb5
|
UTSW |
18 |
37,454,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R6045:Pcdhb5
|
UTSW |
18 |
37,454,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6054:Pcdhb5
|
UTSW |
18 |
37,454,133 (GRCm39) |
missense |
probably damaging |
0.98 |
R6147:Pcdhb5
|
UTSW |
18 |
37,453,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R6152:Pcdhb5
|
UTSW |
18 |
37,455,886 (GRCm39) |
nonsense |
probably null |
|
R6193:Pcdhb5
|
UTSW |
18 |
37,455,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Pcdhb5
|
UTSW |
18 |
37,454,558 (GRCm39) |
missense |
probably benign |
0.08 |
R6505:Pcdhb5
|
UTSW |
18 |
37,453,933 (GRCm39) |
missense |
probably benign |
0.00 |
R6608:Pcdhb5
|
UTSW |
18 |
37,454,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R6737:Pcdhb5
|
UTSW |
18 |
37,455,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7146:Pcdhb5
|
UTSW |
18 |
37,454,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Pcdhb5
|
UTSW |
18 |
37,454,739 (GRCm39) |
missense |
probably benign |
0.16 |
R7584:Pcdhb5
|
UTSW |
18 |
37,455,425 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8214:Pcdhb5
|
UTSW |
18 |
37,454,636 (GRCm39) |
missense |
probably benign |
0.37 |
R8327:Pcdhb5
|
UTSW |
18 |
37,453,953 (GRCm39) |
missense |
probably benign |
0.00 |
R8676:Pcdhb5
|
UTSW |
18 |
37,454,129 (GRCm39) |
missense |
probably benign |
0.01 |
R9234:Pcdhb5
|
UTSW |
18 |
37,453,695 (GRCm39) |
missense |
probably benign |
|
R9424:Pcdhb5
|
UTSW |
18 |
37,454,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R9505:Pcdhb5
|
UTSW |
18 |
37,454,664 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9635:Pcdhb5
|
UTSW |
18 |
37,454,510 (GRCm39) |
missense |
probably benign |
0.06 |
|