Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
C |
5: 124,211,665 (GRCm39) |
Y628C |
probably damaging |
Het |
Alpk2 |
C |
T |
18: 65,482,901 (GRCm39) |
C369Y |
probably damaging |
Het |
Atl1 |
T |
C |
12: 70,005,989 (GRCm39) |
Y432H |
probably damaging |
Het |
Cacnb4 |
C |
T |
2: 52,355,663 (GRCm39) |
V215M |
probably damaging |
Het |
Cep170 |
C |
T |
1: 176,596,808 (GRCm39) |
M516I |
probably damaging |
Het |
Cep83 |
A |
C |
10: 94,573,804 (GRCm39) |
N231T |
probably damaging |
Het |
Cfap44 |
G |
A |
16: 44,234,054 (GRCm39) |
G338D |
probably benign |
Het |
Col6a6 |
A |
T |
9: 105,576,219 (GRCm39) |
V2047E |
probably damaging |
Het |
Coro1c |
C |
T |
5: 114,003,820 (GRCm39) |
|
silent |
Het |
Csf1r |
G |
C |
18: 61,257,947 (GRCm39) |
G639R |
probably damaging |
Het |
Epha5 |
A |
G |
5: 84,381,513 (GRCm39) |
V446A |
probably benign |
Het |
Esam |
T |
C |
9: 37,448,317 (GRCm39) |
V252A |
probably damaging |
Het |
F13b |
T |
G |
1: 139,450,186 (GRCm39) |
M616R |
probably benign |
Het |
Fbxw21 |
T |
C |
9: 108,975,694 (GRCm39) |
Y234C |
probably benign |
Het |
Fshr |
C |
T |
17: 89,293,818 (GRCm39) |
E287K |
probably benign |
Het |
Fstl4 |
T |
C |
11: 52,891,050 (GRCm39) |
S63P |
probably benign |
Het |
Glra1 |
G |
A |
11: 55,424,688 (GRCm39) |
P174L |
probably damaging |
Het |
Golga7 |
A |
T |
8: 23,746,731 (GRCm39) |
C24S |
possibly damaging |
Het |
Gpr3 |
G |
A |
4: 132,938,271 (GRCm39) |
R134C |
probably damaging |
Het |
Greb1 |
T |
C |
12: 16,761,790 (GRCm39) |
E530G |
probably damaging |
Het |
Hmgcs2 |
C |
T |
3: 98,198,444 (GRCm39) |
R116C |
probably damaging |
Het |
Kcnj9 |
C |
A |
1: 172,153,623 (GRCm39) |
R167L |
probably damaging |
Het |
Kcnq5 |
T |
A |
1: 21,549,644 (GRCm39) |
Q361L |
probably damaging |
Het |
Lrrc40 |
T |
C |
3: 157,769,397 (GRCm39) |
S532P |
possibly damaging |
Het |
Mob3a |
A |
T |
10: 80,525,846 (GRCm39) |
I155N |
probably damaging |
Het |
Mpi |
A |
T |
9: 57,457,881 (GRCm39) |
L107Q |
probably damaging |
Het |
Npffr2 |
G |
A |
5: 89,730,513 (GRCm39) |
V148I |
probably benign |
Het |
Nrp1 |
G |
T |
8: 129,158,504 (GRCm39) |
V264L |
probably benign |
Het |
Oas1a |
T |
C |
5: 121,035,080 (GRCm39) |
E360G |
probably benign |
Het |
Or4k15c |
A |
T |
14: 50,321,367 (GRCm39) |
I257N |
possibly damaging |
Het |
Or52e8 |
A |
T |
7: 104,625,080 (GRCm39) |
Y41* |
probably null |
Het |
Or5b96 |
A |
C |
19: 12,867,095 (GRCm39) |
V282G |
probably damaging |
Het |
Pcdha2 |
A |
G |
18: 37,072,579 (GRCm39) |
D70G |
probably benign |
Het |
Pcsk2 |
A |
T |
2: 143,655,450 (GRCm39) |
K545* |
probably null |
Het |
Phf11b |
T |
C |
14: 59,568,722 (GRCm39) |
S64G |
probably benign |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Pygo2 |
T |
C |
3: 89,340,235 (GRCm39) |
L211P |
possibly damaging |
Het |
Rbbp6 |
C |
T |
7: 122,584,468 (GRCm39) |
T161I |
probably damaging |
Het |
Rcsd1 |
A |
T |
1: 165,482,911 (GRCm39) |
I390N |
probably benign |
Het |
Rpl21 |
T |
C |
5: 146,772,702 (GRCm39) |
V141A |
probably benign |
Het |
Rufy3 |
C |
A |
5: 88,790,851 (GRCm39) |
D517E |
probably benign |
Het |
Ryr3 |
A |
T |
2: 112,606,009 (GRCm39) |
L2417Q |
probably damaging |
Het |
Ryr3 |
C |
T |
2: 112,705,422 (GRCm39) |
E831K |
probably damaging |
Het |
Sipa1l1 |
A |
C |
12: 82,496,700 (GRCm39) |
Q1744P |
probably damaging |
Het |
Sirt6 |
A |
G |
10: 81,458,240 (GRCm39) |
|
probably null |
Het |
Slain1 |
C |
A |
14: 103,925,782 (GRCm39) |
Q377K |
possibly damaging |
Het |
Slc30a6 |
T |
G |
17: 74,730,018 (GRCm39) |
S303A |
probably damaging |
Het |
Sorcs3 |
T |
A |
19: 48,752,734 (GRCm39) |
L843Q |
possibly damaging |
Het |
Usp45 |
G |
A |
4: 21,824,543 (GRCm39) |
A432T |
probably benign |
Het |
Vmn1r91 |
T |
A |
7: 19,835,218 (GRCm39) |
S46T |
possibly damaging |
Het |
Ybx3 |
T |
C |
6: 131,361,469 (GRCm39) |
N100S |
probably benign |
Het |
Zfp747 |
A |
G |
7: 126,973,225 (GRCm39) |
L315P |
probably benign |
Het |
Zfp750 |
T |
C |
11: 121,402,706 (GRCm39) |
T681A |
probably benign |
Het |
|
Other mutations in Cplx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00755:Cplx4
|
APN |
18 |
66,090,166 (GRCm39) |
splice site |
probably benign |
|
IGL01577:Cplx4
|
APN |
18 |
66,103,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02124:Cplx4
|
APN |
18 |
66,103,123 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02137:Cplx4
|
APN |
18 |
66,090,125 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02885:Cplx4
|
APN |
18 |
66,089,984 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03263:Cplx4
|
APN |
18 |
66,100,559 (GRCm39) |
missense |
probably benign |
0.04 |
R0894:Cplx4
|
UTSW |
18 |
66,090,116 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2107:Cplx4
|
UTSW |
18 |
66,089,964 (GRCm39) |
missense |
probably benign |
0.05 |
R3767:Cplx4
|
UTSW |
18 |
66,102,998 (GRCm39) |
missense |
probably benign |
0.39 |
R3768:Cplx4
|
UTSW |
18 |
66,102,998 (GRCm39) |
missense |
probably benign |
0.39 |
R3769:Cplx4
|
UTSW |
18 |
66,102,998 (GRCm39) |
missense |
probably benign |
0.39 |
R4772:Cplx4
|
UTSW |
18 |
66,103,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5347:Cplx4
|
UTSW |
18 |
66,103,157 (GRCm39) |
start gained |
probably benign |
|
R7081:Cplx4
|
UTSW |
18 |
66,100,538 (GRCm39) |
critical splice donor site |
probably null |
|
R7231:Cplx4
|
UTSW |
18 |
66,090,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7953:Cplx4
|
UTSW |
18 |
66,090,190 (GRCm39) |
splice site |
probably null |
|
R8469:Cplx4
|
UTSW |
18 |
66,090,083 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9041:Cplx4
|
UTSW |
18 |
66,103,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|