Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4632415L05Rik |
A |
G |
3: 19,949,276 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl4fm4 |
T |
C |
4: 144,400,349 (GRCm39) |
D143G |
probably benign |
Het |
Adcy1 |
A |
C |
11: 7,087,385 (GRCm39) |
N420H |
probably damaging |
Het |
Avp |
T |
C |
2: 130,422,593 (GRCm39) |
|
probably benign |
Het |
B3galnt2 |
A |
T |
13: 14,155,270 (GRCm39) |
I216F |
probably benign |
Het |
Cdc42bpa |
T |
C |
1: 179,902,137 (GRCm39) |
S465P |
probably damaging |
Het |
Cdc42bpg |
T |
A |
19: 6,362,235 (GRCm39) |
|
probably benign |
Het |
Cdcp2 |
T |
C |
4: 106,964,308 (GRCm39) |
F386S |
probably benign |
Het |
Cdh4 |
A |
G |
2: 179,515,937 (GRCm39) |
T372A |
probably damaging |
Het |
Clspn |
T |
G |
4: 126,466,971 (GRCm39) |
M612R |
probably damaging |
Het |
Dll4 |
T |
C |
2: 119,161,590 (GRCm39) |
C391R |
probably damaging |
Het |
Dll4 |
T |
C |
2: 119,163,226 (GRCm39) |
Y616H |
probably damaging |
Het |
Exoc1 |
A |
G |
5: 76,690,091 (GRCm39) |
|
probably benign |
Het |
F830045P16Rik |
A |
G |
2: 129,302,232 (GRCm39) |
|
probably null |
Het |
Fhod1 |
A |
G |
8: 106,074,439 (GRCm39) |
|
probably benign |
Het |
Fign |
T |
C |
2: 63,810,104 (GRCm39) |
R389G |
possibly damaging |
Het |
Kit |
C |
T |
5: 75,771,536 (GRCm39) |
T231M |
probably damaging |
Het |
Neu3 |
T |
C |
7: 99,463,087 (GRCm39) |
H212R |
probably benign |
Het |
Nup214 |
G |
T |
2: 31,924,712 (GRCm39) |
S1747I |
probably damaging |
Het |
Or4f4b |
T |
C |
2: 111,314,446 (GRCm39) |
S224P |
probably damaging |
Het |
Or4q3 |
G |
T |
14: 50,583,071 (GRCm39) |
A276E |
probably damaging |
Het |
Or8b12i |
G |
T |
9: 20,082,826 (GRCm39) |
L14I |
probably damaging |
Het |
Secisbp2 |
T |
C |
13: 51,830,491 (GRCm39) |
|
probably null |
Het |
Slc26a10 |
G |
A |
10: 127,010,046 (GRCm39) |
|
probably benign |
Het |
Slc7a6 |
T |
C |
8: 106,906,232 (GRCm39) |
S155P |
probably damaging |
Het |
Slf1 |
A |
T |
13: 77,260,767 (GRCm39) |
I173N |
probably damaging |
Het |
Tedc1 |
C |
T |
12: 113,126,808 (GRCm39) |
R357* |
probably null |
Het |
Tkfc |
A |
G |
19: 10,578,015 (GRCm39) |
L38P |
probably damaging |
Het |
Tubgcp4 |
A |
G |
2: 121,015,264 (GRCm39) |
D324G |
probably null |
Het |
Zfyve16 |
T |
C |
13: 92,644,791 (GRCm39) |
H1137R |
probably damaging |
Het |
|
Other mutations in Gm13941 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Gm13941
|
APN |
2 |
110,935,198 (GRCm39) |
missense |
unknown |
|
IGL00420:Gm13941
|
APN |
2 |
110,922,193 (GRCm39) |
splice site |
probably benign |
|
IGL01319:Gm13941
|
APN |
2 |
110,925,150 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02557:Gm13941
|
APN |
2 |
110,931,501 (GRCm39) |
missense |
unknown |
|
IGL03163:Gm13941
|
APN |
2 |
110,928,761 (GRCm39) |
missense |
unknown |
|
R0067:Gm13941
|
UTSW |
2 |
110,889,761 (GRCm39) |
unclassified |
noncoding transcript |
|
R0918:Gm13941
|
UTSW |
2 |
110,930,945 (GRCm39) |
missense |
unknown |
|
R2315:Gm13941
|
UTSW |
2 |
110,935,162 (GRCm39) |
missense |
unknown |
|
R3847:Gm13941
|
UTSW |
2 |
110,935,198 (GRCm39) |
missense |
unknown |
|
R3848:Gm13941
|
UTSW |
2 |
110,935,198 (GRCm39) |
missense |
unknown |
|
R5416:Gm13941
|
UTSW |
2 |
110,925,079 (GRCm39) |
missense |
unknown |
|
R5574:Gm13941
|
UTSW |
2 |
110,930,951 (GRCm39) |
missense |
unknown |
|
R6389:Gm13941
|
UTSW |
2 |
110,928,734 (GRCm39) |
missense |
unknown |
|
R6616:Gm13941
|
UTSW |
2 |
110,931,520 (GRCm39) |
missense |
unknown |
|
R7056:Gm13941
|
UTSW |
2 |
110,927,147 (GRCm39) |
missense |
unknown |
|
R7455:Gm13941
|
UTSW |
2 |
110,925,085 (GRCm39) |
missense |
unknown |
|
R8197:Gm13941
|
UTSW |
2 |
110,926,921 (GRCm39) |
splice site |
probably null |
|
R9116:Gm13941
|
UTSW |
2 |
110,935,146 (GRCm39) |
missense |
unknown |
|
R9164:Gm13941
|
UTSW |
2 |
110,936,324 (GRCm39) |
missense |
unknown |
|
R9536:Gm13941
|
UTSW |
2 |
110,918,861 (GRCm39) |
missense |
unknown |
|
R9763:Gm13941
|
UTSW |
2 |
110,931,518 (GRCm39) |
missense |
unknown |
|
Z1177:Gm13941
|
UTSW |
2 |
110,925,123 (GRCm39) |
missense |
unknown |
|
|