Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
A |
T |
19: 57,057,346 (GRCm39) |
S292R |
probably damaging |
Het |
Adamts19 |
A |
G |
18: 59,105,851 (GRCm39) |
T749A |
probably damaging |
Het |
Agap2 |
A |
T |
10: 126,923,865 (GRCm39) |
I747F |
unknown |
Het |
Arhgap35 |
T |
A |
7: 16,298,399 (GRCm39) |
N222I |
probably damaging |
Het |
Atp10b |
A |
G |
11: 43,125,256 (GRCm39) |
E1074G |
probably damaging |
Het |
Brd3 |
T |
C |
2: 27,354,101 (GRCm39) |
T4A |
possibly damaging |
Het |
Col6a6 |
A |
G |
9: 105,660,865 (GRCm39) |
S415P |
probably damaging |
Het |
Dennd2a |
A |
G |
6: 39,500,070 (GRCm39) |
V165A |
probably damaging |
Het |
Dnm1l |
T |
A |
16: 16,159,317 (GRCm39) |
E95V |
probably damaging |
Het |
Dock9 |
A |
G |
14: 121,817,995 (GRCm39) |
Y1609H |
possibly damaging |
Het |
Esm1 |
A |
C |
13: 113,353,216 (GRCm39) |
E166A |
possibly damaging |
Het |
F2rl2 |
A |
C |
13: 95,837,836 (GRCm39) |
I294L |
probably benign |
Het |
Gstt3 |
A |
G |
10: 75,610,822 (GRCm39) |
S187P |
probably benign |
Het |
Katna1 |
T |
C |
10: 7,628,574 (GRCm39) |
C268R |
probably damaging |
Het |
Mbd5 |
T |
A |
2: 49,140,233 (GRCm39) |
C66S |
possibly damaging |
Het |
Naa35 |
G |
A |
13: 59,748,880 (GRCm39) |
E167K |
probably damaging |
Het |
Or10ak16 |
T |
C |
4: 118,750,748 (GRCm39) |
L156S |
probably benign |
Het |
Osbpl2 |
A |
G |
2: 179,778,873 (GRCm39) |
N2S |
probably benign |
Het |
Parp6 |
T |
C |
9: 59,537,895 (GRCm39) |
|
probably benign |
Het |
Pcnx4 |
T |
C |
12: 72,620,520 (GRCm39) |
L780P |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,935,276 (GRCm39) |
D851E |
probably benign |
Het |
Ppfia2 |
A |
G |
10: 106,749,560 (GRCm39) |
S1149G |
probably damaging |
Het |
Prkca |
A |
G |
11: 107,869,178 (GRCm39) |
V469A |
probably damaging |
Het |
Ryr1 |
A |
T |
7: 28,756,410 (GRCm39) |
V3468D |
probably damaging |
Het |
Spmip3 |
G |
A |
1: 177,568,640 (GRCm39) |
G46R |
probably benign |
Het |
Stxbp4 |
A |
G |
11: 90,431,074 (GRCm39) |
V412A |
possibly damaging |
Het |
Vmn1r238 |
G |
T |
18: 3,122,770 (GRCm39) |
Q215K |
possibly damaging |
Het |
Wdr11 |
A |
G |
7: 129,209,637 (GRCm39) |
M482V |
probably benign |
Het |
Wdr72 |
T |
C |
9: 74,086,788 (GRCm39) |
|
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,340,021 (GRCm39) |
L754P |
probably damaging |
Het |
Zmym6 |
G |
A |
4: 127,017,899 (GRCm39) |
G1135S |
probably benign |
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 |
|
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 |
IGL01962:Pcdhb5
|
APN |
18 |
37,454,093 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|