Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap1 |
A |
G |
7: 101,043,980 (GRCm39) |
T680A |
probably damaging |
Het |
Asb3 |
C |
A |
11: 31,031,554 (GRCm39) |
Y391* |
probably null |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Ccdc80 |
A |
G |
16: 44,943,238 (GRCm39) |
I783V |
probably damaging |
Het |
Ccnf |
A |
G |
17: 24,450,805 (GRCm39) |
V391A |
probably damaging |
Het |
Chmp2b |
A |
T |
16: 65,343,769 (GRCm39) |
M96K |
probably benign |
Het |
Cspg4b |
A |
T |
13: 113,479,045 (GRCm39) |
I1530F |
|
Het |
Dennd4a |
T |
C |
9: 64,795,850 (GRCm39) |
S725P |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,106,208 (GRCm39) |
N1843S |
probably damaging |
Het |
Dpy19l3 |
A |
G |
7: 35,449,281 (GRCm39) |
F41L |
probably benign |
Het |
Eif3e |
A |
T |
15: 43,135,703 (GRCm39) |
M112K |
probably benign |
Het |
Faim |
T |
C |
9: 98,874,786 (GRCm39) |
V111A |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,404,728 (GRCm39) |
E493G |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,819,699 (GRCm39) |
D5144G |
possibly damaging |
Het |
Fuz |
T |
C |
7: 44,545,684 (GRCm39) |
M1T |
probably null |
Het |
Ggcx |
T |
C |
6: 72,405,587 (GRCm39) |
V529A |
possibly damaging |
Het |
Gm7145 |
A |
T |
1: 117,913,894 (GRCm39) |
T259S |
probably benign |
Het |
Gria2 |
T |
G |
3: 80,709,006 (GRCm39) |
T59P |
probably damaging |
Het |
H2-Q10 |
A |
T |
17: 35,781,338 (GRCm39) |
I47F |
probably damaging |
Het |
Heatr6 |
A |
G |
11: 83,644,735 (GRCm39) |
N63D |
probably benign |
Het |
Ints7 |
CCGGATCG |
CCGGATCGGATCG |
1: 191,345,180 (GRCm39) |
|
probably null |
Het |
Ints7 |
GATCG |
GATCGTATCG |
1: 191,345,183 (GRCm39) |
|
probably null |
Het |
Lcn6 |
T |
A |
2: 25,566,883 (GRCm39) |
L19* |
probably null |
Het |
Lhcgr |
T |
C |
17: 89,049,784 (GRCm39) |
T581A |
probably damaging |
Het |
Map4k1 |
T |
C |
7: 28,687,573 (GRCm39) |
I203T |
probably damaging |
Het |
Mctp1 |
G |
C |
13: 77,039,670 (GRCm39) |
L783F |
probably damaging |
Het |
Mlf1 |
A |
T |
3: 67,291,921 (GRCm39) |
M29L |
probably damaging |
Het |
Npas3 |
T |
A |
12: 53,687,312 (GRCm39) |
I159N |
probably damaging |
Het |
Nup98 |
T |
C |
7: 101,794,930 (GRCm39) |
|
probably null |
Het |
Or4a39 |
A |
G |
2: 89,237,081 (GRCm39) |
V114A |
probably benign |
Het |
Or4m1 |
T |
C |
14: 50,558,023 (GRCm39) |
K90E |
probably damaging |
Het |
Or51h5 |
A |
T |
7: 102,577,773 (GRCm39) |
K313* |
probably null |
Het |
Or5b110-ps1 |
A |
G |
19: 13,260,215 (GRCm39) |
F69S |
probably damaging |
Het |
Or7d11 |
A |
G |
9: 19,966,301 (GRCm39) |
F35L |
probably benign |
Het |
Or8b41 |
T |
C |
9: 38,054,973 (GRCm39) |
Y176H |
probably damaging |
Het |
Otud3 |
T |
C |
4: 138,623,111 (GRCm39) |
S377G |
probably benign |
Het |
Pclo |
T |
A |
5: 14,571,214 (GRCm39) |
S200T |
probably damaging |
Het |
Pex6 |
G |
C |
17: 47,033,325 (GRCm39) |
G616A |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,451,662 (GRCm39) |
H2211L |
possibly damaging |
Het |
Sec13 |
T |
C |
6: 113,712,050 (GRCm39) |
K95R |
probably benign |
Het |
Sema3c |
T |
C |
5: 17,932,480 (GRCm39) |
V661A |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,574,987 (GRCm39) |
Y365C |
probably damaging |
Het |
Sp140l2 |
T |
A |
1: 85,231,881 (GRCm39) |
T180S |
probably benign |
Het |
Sprr2h |
A |
T |
3: 92,294,120 (GRCm39) |
E61V |
unknown |
Het |
Tead3 |
A |
C |
17: 28,552,203 (GRCm39) |
V365G |
probably damaging |
Het |
Trpm7 |
T |
A |
2: 126,688,119 (GRCm39) |
N236I |
probably damaging |
Het |
Ubxn2b |
A |
G |
4: 6,191,167 (GRCm39) |
E13G |
probably benign |
Het |
Zfp639 |
C |
A |
3: 32,574,215 (GRCm39) |
A280E |
probably damaging |
Het |
|
Other mutations in Cd5l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01992:Cd5l
|
APN |
3 |
87,275,118 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02301:Cd5l
|
APN |
3 |
87,273,300 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02639:Cd5l
|
APN |
3 |
87,275,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R1104:Cd5l
|
UTSW |
3 |
87,268,206 (GRCm39) |
missense |
probably benign |
0.06 |
R1763:Cd5l
|
UTSW |
3 |
87,275,187 (GRCm39) |
critical splice donor site |
probably null |
|
R1775:Cd5l
|
UTSW |
3 |
87,275,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R4614:Cd5l
|
UTSW |
3 |
87,275,926 (GRCm39) |
missense |
probably benign |
|
R4618:Cd5l
|
UTSW |
3 |
87,275,926 (GRCm39) |
missense |
probably benign |
|
R4838:Cd5l
|
UTSW |
3 |
87,273,258 (GRCm39) |
missense |
probably benign |
0.41 |
R4871:Cd5l
|
UTSW |
3 |
87,274,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4980:Cd5l
|
UTSW |
3 |
87,274,908 (GRCm39) |
missense |
probably benign |
0.33 |
R5611:Cd5l
|
UTSW |
3 |
87,275,082 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5632:Cd5l
|
UTSW |
3 |
87,273,414 (GRCm39) |
nonsense |
probably null |
|
R6261:Cd5l
|
UTSW |
3 |
87,275,915 (GRCm39) |
missense |
probably benign |
0.35 |
R7017:Cd5l
|
UTSW |
3 |
87,273,368 (GRCm39) |
nonsense |
probably null |
|
R7727:Cd5l
|
UTSW |
3 |
87,275,162 (GRCm39) |
nonsense |
probably null |
|
R8900:Cd5l
|
UTSW |
3 |
87,274,882 (GRCm39) |
missense |
probably benign |
|
R9008:Cd5l
|
UTSW |
3 |
87,275,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Cd5l
|
UTSW |
3 |
87,274,932 (GRCm39) |
missense |
probably benign |
0.19 |
R9546:Cd5l
|
UTSW |
3 |
87,268,201 (GRCm39) |
missense |
probably benign |
0.00 |
R9747:Cd5l
|
UTSW |
3 |
87,275,104 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Cd5l
|
UTSW |
3 |
87,276,068 (GRCm39) |
missense |
probably damaging |
0.96 |
|