Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap2 |
A |
T |
16: 30,958,459 (GRCm39) |
F102I |
probably damaging |
Het |
Acp7 |
A |
T |
7: 28,314,152 (GRCm39) |
Y348N |
probably damaging |
Het |
Adgre4 |
A |
T |
17: 56,099,016 (GRCm39) |
D174V |
probably benign |
Het |
Ahdc1 |
A |
G |
4: 132,791,161 (GRCm39) |
T801A |
possibly damaging |
Het |
Aldh1a7 |
A |
C |
19: 20,693,343 (GRCm39) |
V192G |
possibly damaging |
Het |
Anp32b |
T |
G |
4: 46,451,301 (GRCm39) |
D2E |
probably benign |
Het |
Arhgef11 |
A |
T |
3: 87,591,808 (GRCm39) |
D53V |
probably damaging |
Het |
Arid5b |
T |
C |
10: 67,964,771 (GRCm39) |
N300S |
probably benign |
Het |
Ascc2 |
A |
G |
11: 4,618,389 (GRCm39) |
N328S |
probably benign |
Het |
Aspm |
A |
T |
1: 139,382,872 (GRCm39) |
Q68L |
probably benign |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Ccser1 |
A |
T |
6: 61,288,932 (GRCm39) |
H365L |
probably benign |
Het |
Col1a2 |
T |
A |
6: 4,518,500 (GRCm39) |
N213K |
unknown |
Het |
Col7a1 |
T |
C |
9: 108,787,763 (GRCm39) |
V681A |
unknown |
Het |
Cplane1 |
A |
G |
15: 8,239,446 (GRCm39) |
I1216V |
probably benign |
Het |
Dock9 |
A |
T |
14: 121,863,396 (GRCm39) |
Y792* |
probably null |
Het |
Fam241b |
A |
T |
10: 61,970,271 (GRCm39) |
S10R |
|
Het |
Gab1 |
C |
T |
8: 81,515,395 (GRCm39) |
D308N |
probably damaging |
Het |
Gdf11 |
C |
T |
10: 128,722,210 (GRCm39) |
R215H |
probably benign |
Het |
Gpc1 |
T |
C |
1: 92,782,970 (GRCm39) |
|
probably null |
Het |
Hnf4a |
G |
T |
2: 163,400,980 (GRCm39) |
E200* |
probably null |
Het |
Ints2 |
T |
C |
11: 86,103,888 (GRCm39) |
T1086A |
probably damaging |
Het |
Kbtbd7 |
A |
G |
14: 79,664,806 (GRCm39) |
T213A |
probably benign |
Het |
Kcnt2 |
A |
G |
1: 140,501,385 (GRCm39) |
D917G |
probably damaging |
Het |
Kdm5a |
C |
A |
6: 120,375,979 (GRCm39) |
Y578* |
probably null |
Het |
Lrrtm4 |
A |
T |
6: 79,999,343 (GRCm39) |
T252S |
possibly damaging |
Het |
Mamdc4 |
C |
T |
2: 25,458,677 (GRCm39) |
W305* |
probably null |
Het |
Mzb1 |
A |
G |
18: 35,780,913 (GRCm39) |
I125T |
possibly damaging |
Het |
Nfrkb |
A |
G |
9: 31,321,450 (GRCm39) |
T716A |
possibly damaging |
Het |
Or2ad1 |
T |
A |
13: 21,327,093 (GRCm39) |
I45F |
probably damaging |
Het |
Or4f6 |
A |
G |
2: 111,839,192 (GRCm39) |
V113A |
probably benign |
Het |
Or52r1b |
A |
G |
7: 102,691,060 (GRCm39) |
M120V |
probably damaging |
Het |
Or8k16 |
G |
A |
2: 85,519,838 (GRCm39) |
E22K |
probably benign |
Het |
Poteg |
C |
T |
8: 27,939,942 (GRCm39) |
P95L |
probably benign |
Het |
Prdm9 |
A |
T |
17: 15,773,804 (GRCm39) |
Y322* |
probably null |
Het |
Rab11fip2 |
G |
C |
19: 59,925,655 (GRCm39) |
I187M |
possibly damaging |
Het |
Ranbp2 |
G |
T |
10: 58,314,277 (GRCm39) |
E1666* |
probably null |
Het |
Rin3 |
T |
C |
12: 102,335,735 (GRCm39) |
S549P |
probably damaging |
Het |
Scn10a |
C |
T |
9: 119,464,508 (GRCm39) |
|
probably null |
Het |
Scn3a |
A |
G |
2: 65,327,826 (GRCm39) |
F888S |
probably damaging |
Het |
Sik3 |
T |
A |
9: 46,034,528 (GRCm39) |
I96N |
probably damaging |
Het |
Slc12a7 |
T |
A |
13: 73,936,723 (GRCm39) |
C128S |
possibly damaging |
Het |
Spata31h1 |
T |
C |
10: 82,123,456 (GRCm39) |
S3185G |
possibly damaging |
Het |
Syde2 |
A |
G |
3: 145,726,020 (GRCm39) |
E1304G |
probably damaging |
Het |
Tagln |
T |
C |
9: 45,841,680 (GRCm39) |
I199V |
probably damaging |
Het |
Tars3 |
T |
A |
7: 65,327,899 (GRCm39) |
V536E |
probably benign |
Het |
Tas2r140 |
A |
G |
6: 40,469,097 (GRCm39) |
K309R |
probably damaging |
Het |
Thra |
A |
T |
11: 98,659,257 (GRCm39) |
D462V |
probably damaging |
Het |
Topaz1 |
A |
G |
9: 122,578,652 (GRCm39) |
T521A |
possibly damaging |
Het |
Uhrf1 |
A |
G |
17: 56,619,884 (GRCm39) |
N265S |
possibly damaging |
Het |
Upk3b |
A |
T |
5: 136,069,057 (GRCm39) |
Y142F |
probably benign |
Het |
Vmn1r219 |
T |
C |
13: 23,347,363 (GRCm39) |
V184A |
possibly damaging |
Het |
Vmn1r58 |
T |
C |
7: 5,413,753 (GRCm39) |
D159G |
probably damaging |
Het |
Vnn3 |
C |
A |
10: 23,743,146 (GRCm39) |
A452D |
possibly damaging |
Het |
Wscd1 |
T |
A |
11: 71,679,560 (GRCm39) |
Y478N |
probably damaging |
Het |
Xrcc5 |
C |
T |
1: 72,369,090 (GRCm39) |
R315C |
probably damaging |
Het |
Zkscan5 |
A |
C |
5: 145,157,676 (GRCm39) |
H726P |
probably damaging |
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 |
R7821:Plcxd2
|
UTSW |
16 |
45,785,524 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|