Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
A |
6: 23,120,929 (GRCm39) |
T112S |
probably damaging |
Het |
Abca12 |
G |
T |
1: 71,298,950 (GRCm39) |
S2320R |
probably benign |
Het |
Abca7 |
TGGTGCGTGAG |
TG |
10: 79,838,424 (GRCm39) |
|
probably benign |
Het |
Adh7 |
T |
A |
3: 137,932,136 (GRCm39) |
I250N |
probably damaging |
Het |
Albfm1 |
T |
C |
5: 90,740,747 (GRCm39) |
V560A |
possibly damaging |
Het |
Aoc1 |
T |
A |
6: 48,882,745 (GRCm39) |
I229N |
probably damaging |
Het |
C2cd6 |
A |
T |
1: 59,106,951 (GRCm39) |
Y291* |
probably null |
Het |
Cacnb4 |
T |
C |
2: 52,324,520 (GRCm39) |
D514G |
possibly damaging |
Het |
Ccdc202 |
A |
G |
14: 96,119,486 (GRCm39) |
Q81R |
possibly damaging |
Het |
Clec2g |
A |
G |
6: 128,925,740 (GRCm39) |
T50A |
probably benign |
Het |
Col6a5 |
T |
C |
9: 105,741,458 (GRCm39) |
E2487G |
probably damaging |
Het |
D130040H23Rik |
A |
T |
8: 69,752,887 (GRCm39) |
|
probably null |
Het |
D6Ertd527e |
G |
A |
6: 87,087,879 (GRCm39) |
S14N |
unknown |
Het |
Dchs1 |
G |
A |
7: 105,414,352 (GRCm39) |
T821I |
probably benign |
Het |
Dhcr24 |
T |
C |
4: 106,428,633 (GRCm39) |
S138P |
possibly damaging |
Het |
Dhrs9 |
G |
A |
2: 69,224,782 (GRCm39) |
G157R |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,411,678 (GRCm39) |
D3682E |
possibly damaging |
Het |
Dst |
T |
C |
1: 34,314,443 (GRCm39) |
|
probably null |
Het |
Fat1 |
A |
T |
8: 45,403,261 (GRCm39) |
H4L |
probably benign |
Het |
Flnb |
A |
G |
14: 7,939,113 (GRCm38) |
I2319V |
probably benign |
Het |
Foxe1 |
T |
C |
4: 46,344,578 (GRCm39) |
W129R |
probably damaging |
Het |
Foxred2 |
G |
A |
15: 77,827,550 (GRCm39) |
P603L |
probably benign |
Het |
Fshr |
A |
G |
17: 89,293,641 (GRCm39) |
S346P |
probably damaging |
Het |
Galnt2 |
T |
A |
8: 125,070,134 (GRCm39) |
S550R |
possibly damaging |
Het |
Gpc2 |
A |
G |
5: 138,274,559 (GRCm39) |
S312P |
probably benign |
Het |
Gpr150 |
C |
A |
13: 76,204,511 (GRCm39) |
A145S |
probably benign |
Het |
Grk4 |
T |
A |
5: 34,867,553 (GRCm39) |
W173R |
probably damaging |
Het |
Hoxb9 |
C |
G |
11: 96,162,537 (GRCm39) |
P57R |
probably damaging |
Het |
Hsf5 |
A |
G |
11: 87,528,954 (GRCm39) |
Q563R |
probably benign |
Het |
Ighv1-58 |
A |
G |
12: 115,275,796 (GRCm39) |
F114S |
possibly damaging |
Het |
Klra9 |
T |
A |
6: 130,162,563 (GRCm39) |
I158F |
probably damaging |
Het |
Lrrc8d |
T |
C |
5: 105,960,210 (GRCm39) |
S207P |
probably damaging |
Het |
Nbeal2 |
T |
C |
9: 110,459,320 (GRCm39) |
E1929G |
probably damaging |
Het |
Ncoa1 |
A |
G |
12: 4,346,221 (GRCm39) |
M89T |
probably benign |
Het |
Nkx2-4 |
T |
C |
2: 146,927,208 (GRCm39) |
I20V |
probably benign |
Het |
Nup214 |
T |
C |
2: 31,916,917 (GRCm39) |
S1191P |
possibly damaging |
Het |
Or2n1d |
A |
G |
17: 38,646,855 (GRCm39) |
D269G |
probably benign |
Het |
Pfkp |
T |
A |
13: 6,647,908 (GRCm39) |
N556I |
probably damaging |
Het |
Pidd1 |
A |
T |
7: 141,022,193 (GRCm39) |
S199T |
probably benign |
Het |
Pik3r2 |
T |
A |
8: 71,222,408 (GRCm39) |
I515F |
probably damaging |
Het |
Prmt6 |
C |
A |
3: 110,158,303 (GRCm39) |
|
probably benign |
Het |
Prpf8 |
A |
G |
11: 75,385,300 (GRCm39) |
I812V |
probably benign |
Het |
Rasa2 |
T |
C |
9: 96,462,537 (GRCm39) |
|
probably null |
Het |
Rsad1 |
A |
C |
11: 94,435,288 (GRCm39) |
D266E |
probably benign |
Het |
Rsf1 |
GGCG |
GGCGACGGCTGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Shroom3 |
T |
A |
5: 93,088,705 (GRCm39) |
V485E |
probably damaging |
Het |
Siae |
T |
A |
9: 37,556,196 (GRCm39) |
Y451N |
probably damaging |
Het |
Slc7a11 |
A |
T |
3: 50,335,476 (GRCm39) |
I354N |
probably damaging |
Het |
Spryd7 |
A |
T |
14: 61,783,129 (GRCm39) |
|
probably null |
Het |
Srcap |
A |
G |
7: 127,129,499 (GRCm39) |
|
probably benign |
Het |
Svep1 |
T |
A |
4: 58,179,601 (GRCm39) |
D214V |
probably damaging |
Het |
Tmtc4 |
T |
C |
14: 123,209,289 (GRCm39) |
I119V |
probably benign |
Het |
Trim5 |
G |
A |
7: 103,927,633 (GRCm39) |
T169I |
probably benign |
Het |
Ttc33 |
T |
C |
15: 5,241,506 (GRCm39) |
F83S |
probably benign |
Het |
Ubr5 |
A |
T |
15: 37,997,431 (GRCm39) |
S1741T |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Wdcp |
A |
G |
12: 4,907,975 (GRCm39) |
N694S |
probably benign |
Het |
Zfp174 |
T |
A |
16: 3,666,041 (GRCm39) |
I102N |
probably damaging |
Het |
Zfp354a |
T |
C |
11: 50,960,539 (GRCm39) |
F248S |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,302,098 (GRCm39) |
C404S |
probably damaging |
Het |
Zmynd8 |
A |
T |
2: 165,723,000 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Plcxd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01658:Plcxd2
|
APN |
16 |
45,785,424 (GRCm39) |
missense |
probably benign |
|
IGL02011:Plcxd2
|
APN |
16 |
45,785,454 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02079:Plcxd2
|
APN |
16 |
45,792,706 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02658:Plcxd2
|
APN |
16 |
45,792,689 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03082:Plcxd2
|
APN |
16 |
45,785,473 (GRCm39) |
missense |
probably damaging |
1.00 |
G1patch:Plcxd2
|
UTSW |
16 |
45,792,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R0137:Plcxd2
|
UTSW |
16 |
45,800,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R0173:Plcxd2
|
UTSW |
16 |
45,785,542 (GRCm39) |
splice site |
probably null |
|
R0276:Plcxd2
|
UTSW |
16 |
45,830,070 (GRCm39) |
missense |
probably benign |
0.12 |
R0453:Plcxd2
|
UTSW |
16 |
45,800,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R3848:Plcxd2
|
UTSW |
16 |
45,792,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Plcxd2
|
UTSW |
16 |
45,800,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Plcxd2
|
UTSW |
16 |
45,800,700 (GRCm39) |
missense |
probably benign |
0.00 |
R4915:Plcxd2
|
UTSW |
16 |
45,800,941 (GRCm39) |
nonsense |
probably null |
|
R5293:Plcxd2
|
UTSW |
16 |
45,800,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R6477:Plcxd2
|
UTSW |
16 |
45,801,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R6629:Plcxd2
|
UTSW |
16 |
45,785,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R6725:Plcxd2
|
UTSW |
16 |
45,792,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R6845:Plcxd2
|
UTSW |
16 |
45,830,223 (GRCm39) |
start gained |
probably benign |
|
R6953:Plcxd2
|
UTSW |
16 |
45,800,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Plcxd2
|
UTSW |
16 |
45,800,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R7711:Plcxd2
|
UTSW |
16 |
45,800,693 (GRCm39) |
missense |
probably benign |
0.04 |
R7875:Plcxd2
|
UTSW |
16 |
45,830,065 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8500:Plcxd2
|
UTSW |
16 |
45,800,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9781:Plcxd2
|
UTSW |
16 |
45,830,117 (GRCm39) |
missense |
probably benign |
0.25 |
|