Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
A |
11: 109,870,711 (GRCm39) |
S147L |
probably benign |
Het |
Abraxas1 |
A |
G |
5: 100,957,649 (GRCm39) |
V190A |
probably benign |
Het |
Aoc1l2 |
A |
T |
6: 48,907,298 (GRCm39) |
K99N |
probably benign |
Het |
Aox1 |
T |
A |
1: 58,104,501 (GRCm39) |
H559Q |
possibly damaging |
Het |
Arhgap31 |
C |
T |
16: 38,422,988 (GRCm39) |
G1026D |
probably benign |
Het |
C1ra |
T |
C |
6: 124,490,819 (GRCm39) |
F71L |
probably benign |
Het |
C530025M09Rik |
T |
C |
2: 149,672,640 (GRCm39) |
H165R |
unknown |
Het |
Celf2 |
A |
T |
2: 6,726,404 (GRCm39) |
M43K |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,706,961 (GRCm39) |
V1148A |
possibly damaging |
Het |
Cmya5 |
T |
G |
13: 93,229,884 (GRCm39) |
K1735Q |
probably benign |
Het |
Cntln |
A |
C |
4: 84,968,318 (GRCm39) |
M846L |
probably benign |
Het |
Cntn5 |
T |
C |
9: 9,673,817 (GRCm39) |
T762A |
probably benign |
Het |
Col11a1 |
T |
A |
3: 113,899,046 (GRCm39) |
L525Q |
unknown |
Het |
Col12a1 |
T |
C |
9: 79,589,364 (GRCm39) |
T1064A |
probably benign |
Het |
Cyc1 |
T |
C |
15: 76,229,273 (GRCm39) |
V211A |
possibly damaging |
Het |
Ddx56 |
A |
G |
11: 6,215,516 (GRCm39) |
S296P |
probably damaging |
Het |
Ezh1 |
C |
T |
11: 101,094,265 (GRCm39) |
R409H |
possibly damaging |
Het |
Fam228b |
T |
A |
12: 4,798,147 (GRCm39) |
E190V |
probably damaging |
Het |
Fkbp15 |
A |
T |
4: 62,237,210 (GRCm39) |
L635H |
probably damaging |
Het |
Frem1 |
G |
A |
4: 82,901,622 (GRCm39) |
L969F |
possibly damaging |
Het |
Gabrg2 |
T |
C |
11: 41,858,433 (GRCm39) |
R232G |
probably benign |
Het |
Gpr26 |
G |
A |
7: 131,568,963 (GRCm39) |
D103N |
probably damaging |
Het |
Grid2ip |
T |
G |
5: 143,361,103 (GRCm39) |
|
probably null |
Het |
Ints7 |
T |
C |
1: 191,351,793 (GRCm39) |
V834A |
probably damaging |
Het |
Kcnh7 |
T |
A |
2: 62,667,612 (GRCm39) |
H309L |
probably benign |
Het |
Mael |
T |
C |
1: 166,053,282 (GRCm39) |
E241G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,122,277 (GRCm39) |
E584V |
|
Het |
Nexn |
C |
T |
3: 151,959,401 (GRCm39) |
V23M |
probably damaging |
Het |
Npas1 |
T |
C |
7: 16,190,231 (GRCm39) |
|
probably null |
Het |
Or51f1 |
T |
C |
7: 102,506,014 (GRCm39) |
I158M |
probably benign |
Het |
Pcdh17 |
T |
G |
14: 84,685,522 (GRCm39) |
V663G |
probably damaging |
Het |
Pga5 |
C |
T |
19: 10,646,897 (GRCm39) |
G303S |
probably damaging |
Het |
Poln |
T |
A |
5: 34,164,842 (GRCm39) |
K844N |
probably damaging |
Het |
Prkar1b |
C |
T |
5: 139,036,442 (GRCm39) |
D227N |
probably damaging |
Het |
Proc |
T |
A |
18: 32,256,336 (GRCm39) |
I444F |
probably damaging |
Het |
Ptprn |
G |
T |
1: 75,229,135 (GRCm39) |
H791N |
probably benign |
Het |
Ror1 |
T |
C |
4: 100,191,709 (GRCm39) |
S160P |
probably benign |
Het |
Satb2 |
T |
A |
1: 56,870,797 (GRCm39) |
|
probably null |
Het |
Slc43a3 |
C |
T |
2: 84,780,771 (GRCm39) |
A332V |
probably benign |
Het |
Sp100 |
G |
A |
1: 85,627,336 (GRCm39) |
V410M |
probably damaging |
Het |
Srgap2 |
T |
C |
1: 131,217,346 (GRCm39) |
T989A |
probably benign |
Het |
Ssc5d |
T |
C |
7: 4,930,283 (GRCm39) |
|
probably null |
Het |
Tll2 |
A |
G |
19: 41,116,997 (GRCm39) |
Y273H |
probably benign |
Het |
Tub |
T |
C |
7: 108,626,211 (GRCm39) |
V295A |
possibly damaging |
Het |
Unc13b |
T |
A |
4: 43,172,512 (GRCm39) |
D1113E |
unknown |
Het |
Usp9y |
C |
A |
Y: 1,364,776 (GRCm39) |
M1012I |
probably benign |
Het |
Vmn1r238 |
A |
G |
18: 3,122,676 (GRCm39) |
V246A |
probably damaging |
Het |
Vmn2r88 |
T |
G |
14: 51,656,197 (GRCm39) |
V802G |
|
Het |
Wnt7b |
T |
C |
15: 85,443,175 (GRCm39) |
Q76R |
probably damaging |
Het |
Zan |
T |
C |
5: 137,389,917 (GRCm39) |
R4852G |
unknown |
Het |
Zfp618 |
A |
T |
4: 63,051,258 (GRCm39) |
T680S |
probably damaging |
Het |
Zfp784 |
T |
A |
7: 5,041,338 (GRCm39) |
D25V |
unknown |
Het |
|
Other mutations in Deptor |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01666:Deptor
|
APN |
15 |
55,012,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02374:Deptor
|
APN |
15 |
55,044,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R1199:Deptor
|
UTSW |
15 |
55,115,406 (GRCm39) |
missense |
probably benign |
0.00 |
R1659:Deptor
|
UTSW |
15 |
55,081,670 (GRCm39) |
critical splice donor site |
probably null |
|
R4061:Deptor
|
UTSW |
15 |
55,072,177 (GRCm39) |
missense |
probably benign |
|
R4688:Deptor
|
UTSW |
15 |
55,072,177 (GRCm39) |
missense |
probably benign |
0.01 |
R4731:Deptor
|
UTSW |
15 |
55,044,406 (GRCm39) |
missense |
probably benign |
0.00 |
R4732:Deptor
|
UTSW |
15 |
55,044,406 (GRCm39) |
missense |
probably benign |
0.00 |
R4733:Deptor
|
UTSW |
15 |
55,044,406 (GRCm39) |
missense |
probably benign |
0.00 |
R4757:Deptor
|
UTSW |
15 |
55,075,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Deptor
|
UTSW |
15 |
55,044,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7940:Deptor
|
UTSW |
15 |
55,072,244 (GRCm39) |
missense |
probably benign |
0.03 |
R8691:Deptor
|
UTSW |
15 |
55,083,596 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8752:Deptor
|
UTSW |
15 |
55,044,280 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Deptor
|
UTSW |
15 |
54,996,855 (GRCm39) |
start gained |
probably benign |
|
|