Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arfgef2 |
A |
G |
2: 166,710,971 (GRCm39) |
|
probably benign |
Het |
Btbd7 |
A |
G |
12: 102,803,921 (GRCm39) |
L373P |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,322,382 (GRCm39) |
N414S |
possibly damaging |
Het |
Ccdc186 |
A |
T |
19: 56,781,920 (GRCm39) |
I753N |
probably benign |
Het |
Ccser2 |
G |
A |
14: 36,662,716 (GRCm39) |
T156I |
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,915,927 (GRCm39) |
M682T |
probably damaging |
Het |
Cep97 |
C |
A |
16: 55,738,903 (GRCm39) |
S267I |
probably damaging |
Het |
Dhx35 |
A |
G |
2: 158,643,370 (GRCm39) |
Y39C |
probably damaging |
Het |
Dscam |
A |
T |
16: 96,510,447 (GRCm39) |
D937E |
probably damaging |
Het |
Elmod2 |
A |
G |
8: 84,043,562 (GRCm39) |
Y202H |
probably damaging |
Het |
Fyco1 |
T |
C |
9: 123,659,396 (GRCm39) |
N260S |
possibly damaging |
Het |
Gm5591 |
A |
G |
7: 38,218,842 (GRCm39) |
L677P |
probably damaging |
Het |
Gmppa |
A |
G |
1: 75,418,474 (GRCm39) |
|
probably null |
Het |
Hltf |
C |
T |
3: 20,153,981 (GRCm39) |
T639I |
probably damaging |
Het |
Inhca |
C |
A |
9: 103,154,773 (GRCm39) |
V173L |
probably damaging |
Het |
Kpnb1 |
T |
C |
11: 97,066,612 (GRCm39) |
Y321C |
probably damaging |
Het |
Lgr4 |
G |
A |
2: 109,748,598 (GRCm39) |
G45R |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,179,547 (GRCm39) |
D1538G |
probably benign |
Het |
Maf1 |
T |
A |
15: 76,237,220 (GRCm39) |
|
probably benign |
Het |
Ncan |
C |
T |
8: 70,567,698 (GRCm39) |
R138H |
possibly damaging |
Het |
Or10ak7 |
A |
T |
4: 118,791,859 (GRCm39) |
M62K |
probably damaging |
Het |
Or5ac21 |
G |
T |
16: 59,123,649 (GRCm39) |
L44F |
probably damaging |
Het |
Parg |
T |
C |
14: 31,960,531 (GRCm39) |
L82S |
probably damaging |
Het |
Ppp2r2b |
A |
T |
18: 42,778,874 (GRCm39) |
H417Q |
probably damaging |
Het |
Rb1cc1 |
T |
C |
1: 6,334,807 (GRCm39) |
L98P |
probably damaging |
Het |
Ryr1 |
C |
A |
7: 28,748,220 (GRCm39) |
V3752L |
possibly damaging |
Het |
Slc25a12 |
A |
G |
2: 71,109,979 (GRCm39) |
L489P |
probably damaging |
Het |
Slc38a8 |
C |
T |
8: 120,212,282 (GRCm39) |
V354M |
probably benign |
Het |
Slf2 |
A |
G |
19: 44,930,459 (GRCm39) |
E512G |
probably benign |
Het |
Tarbp1 |
A |
G |
8: 127,180,583 (GRCm39) |
M597T |
probably damaging |
Het |
Tgfb3 |
G |
A |
12: 86,116,550 (GRCm39) |
R163C |
probably damaging |
Het |
Tmco5b |
A |
G |
2: 113,127,265 (GRCm39) |
M279V |
probably benign |
Het |
Ttll9 |
G |
A |
2: 152,844,871 (GRCm39) |
G413D |
probably damaging |
Het |
Tut1 |
A |
G |
19: 8,939,751 (GRCm39) |
D245G |
probably damaging |
Het |
Usf3 |
T |
A |
16: 44,041,589 (GRCm39) |
V2023E |
probably damaging |
Het |
Vps33a |
C |
T |
5: 123,669,239 (GRCm39) |
G554D |
probably damaging |
Het |
Zfp27 |
C |
A |
7: 29,595,680 (GRCm39) |
R95M |
possibly damaging |
Het |
|
Other mutations in Morn5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02158:Morn5
|
APN |
2 |
35,947,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02190:Morn5
|
APN |
2 |
35,969,527 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02441:Morn5
|
APN |
2 |
35,945,038 (GRCm39) |
nonsense |
probably null |
|
R0306:Morn5
|
UTSW |
2 |
35,944,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R1449:Morn5
|
UTSW |
2 |
35,947,092 (GRCm39) |
nonsense |
probably null |
|
R1803:Morn5
|
UTSW |
2 |
35,943,089 (GRCm39) |
missense |
probably benign |
0.03 |
R1819:Morn5
|
UTSW |
2 |
35,942,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Morn5
|
UTSW |
2 |
35,942,950 (GRCm39) |
missense |
probably benign |
0.03 |
R3932:Morn5
|
UTSW |
2 |
35,943,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R7078:Morn5
|
UTSW |
2 |
35,944,990 (GRCm39) |
missense |
probably benign |
|
R7681:Morn5
|
UTSW |
2 |
35,947,156 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7938:Morn5
|
UTSW |
2 |
35,947,082 (GRCm39) |
missense |
probably benign |
0.03 |
R8438:Morn5
|
UTSW |
2 |
35,945,076 (GRCm39) |
missense |
probably benign |
0.03 |
R8805:Morn5
|
UTSW |
2 |
35,969,533 (GRCm39) |
missense |
probably benign |
0.28 |
R9153:Morn5
|
UTSW |
2 |
35,942,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:Morn5
|
UTSW |
2 |
35,945,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9256:Morn5
|
UTSW |
2 |
35,939,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R9447:Morn5
|
UTSW |
2 |
35,969,525 (GRCm39) |
critical splice acceptor site |
probably null |
|
|