Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl7b |
T |
C |
4: 56,740,224 (GRCm39) |
E378G |
probably damaging |
Het |
Adam17 |
A |
T |
12: 21,403,949 (GRCm39) |
V99E |
probably damaging |
Het |
Alkal2 |
G |
A |
12: 30,937,057 (GRCm39) |
R90Q |
probably damaging |
Het |
Amy1 |
C |
T |
3: 113,355,549 (GRCm39) |
V309M |
probably damaging |
Het |
Apob |
T |
C |
12: 8,061,883 (GRCm39) |
L3455P |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,892,436 (GRCm39) |
H1438Q |
probably damaging |
Het |
BC024139 |
A |
G |
15: 76,003,996 (GRCm39) |
S757P |
probably benign |
Het |
Btd |
G |
A |
14: 31,363,065 (GRCm39) |
|
probably benign |
Het |
C2cd3 |
T |
A |
7: 100,090,283 (GRCm39) |
F462Y |
probably damaging |
Het |
C4bp |
T |
A |
1: 130,566,809 (GRCm39) |
K177* |
probably null |
Het |
Cacna1h |
G |
T |
17: 25,610,250 (GRCm39) |
P752Q |
probably benign |
Het |
Cd34 |
G |
A |
1: 194,631,877 (GRCm39) |
|
probably null |
Het |
Cimap1a |
G |
T |
7: 140,428,554 (GRCm39) |
R73L |
possibly damaging |
Het |
Clptm1 |
G |
A |
7: 19,367,731 (GRCm39) |
|
probably benign |
Het |
Dip2c |
T |
C |
13: 9,673,802 (GRCm39) |
S1081P |
probably damaging |
Het |
Dnm3 |
CAGCCTTCGTTGGGTG |
C |
1: 161,838,637 (GRCm39) |
|
probably benign |
Het |
Efcab6 |
T |
G |
15: 83,763,835 (GRCm39) |
M1166L |
possibly damaging |
Het |
Fam151a |
G |
A |
4: 106,605,395 (GRCm39) |
V586M |
probably damaging |
Het |
Fap |
T |
G |
2: 62,385,114 (GRCm39) |
Y54S |
possibly damaging |
Het |
Grhl1 |
A |
G |
12: 24,630,746 (GRCm39) |
|
probably null |
Het |
Hcrtr2 |
T |
C |
9: 76,167,064 (GRCm39) |
Y91C |
probably damaging |
Het |
Ift70b |
T |
C |
2: 75,768,144 (GRCm39) |
Y203C |
probably damaging |
Het |
Kat6b |
C |
T |
14: 21,720,555 (GRCm39) |
R1745C |
probably damaging |
Het |
Kdm5a |
T |
C |
6: 120,389,267 (GRCm39) |
L898P |
probably damaging |
Het |
Lipo5 |
T |
C |
19: 33,445,317 (GRCm39) |
Q84R |
unknown |
Het |
Mptx2 |
G |
A |
1: 173,102,414 (GRCm39) |
L92F |
probably benign |
Het |
Mtfmt |
T |
C |
9: 65,354,586 (GRCm39) |
|
probably null |
Het |
Nsun2 |
C |
G |
13: 69,775,767 (GRCm39) |
Q404E |
probably benign |
Het |
Or1j17 |
T |
C |
2: 36,578,559 (GRCm39) |
S182P |
probably benign |
Het |
Or2at4 |
C |
T |
7: 99,384,377 (GRCm39) |
S9L |
possibly damaging |
Het |
Or52d1 |
A |
G |
7: 103,755,779 (GRCm39) |
M98V |
probably damaging |
Het |
Or5b123 |
C |
T |
19: 13,597,249 (GRCm39) |
A241V |
probably benign |
Het |
Or5j3 |
T |
A |
2: 86,129,019 (GRCm39) |
N286K |
probably damaging |
Het |
Or5p70 |
G |
T |
7: 107,995,035 (GRCm39) |
S236I |
possibly damaging |
Het |
Or6c215 |
G |
A |
10: 129,637,689 (GRCm39) |
A235V |
probably damaging |
Het |
Or6c215 |
C |
A |
10: 129,637,690 (GRCm39) |
A235S |
probably damaging |
Het |
Parp9 |
A |
G |
16: 35,773,996 (GRCm39) |
I90V |
possibly damaging |
Het |
Pate7 |
A |
T |
9: 35,688,442 (GRCm39) |
S48T |
possibly damaging |
Het |
Pax2 |
T |
A |
19: 44,779,175 (GRCm39) |
S183T |
probably damaging |
Het |
Pcdha11 |
T |
C |
18: 37,144,509 (GRCm39) |
L200P |
probably damaging |
Het |
Pcdhb4 |
T |
C |
18: 37,441,482 (GRCm39) |
V264A |
possibly damaging |
Het |
Plch1 |
G |
T |
3: 63,606,279 (GRCm39) |
N1199K |
possibly damaging |
Het |
Ptpn22 |
A |
G |
3: 103,819,331 (GRCm39) |
N795S |
probably damaging |
Het |
Qars1 |
T |
C |
9: 108,385,297 (GRCm39) |
S6P |
probably benign |
Het |
Sema3a |
T |
C |
5: 13,630,969 (GRCm39) |
Y502H |
probably damaging |
Het |
Sema4f |
A |
G |
6: 82,914,085 (GRCm39) |
I91T |
probably damaging |
Het |
Setx |
T |
G |
2: 29,030,302 (GRCm39) |
I247S |
probably damaging |
Het |
Slc9c1 |
T |
C |
16: 45,395,731 (GRCm39) |
L594P |
probably damaging |
Het |
Tnfrsf19 |
A |
T |
14: 61,208,588 (GRCm39) |
M311K |
probably benign |
Het |
Tubgcp4 |
T |
C |
2: 121,024,589 (GRCm39) |
I588T |
probably benign |
Het |
Tyro3 |
T |
C |
2: 119,643,304 (GRCm39) |
V655A |
probably damaging |
Het |
Uba7 |
T |
A |
9: 107,856,138 (GRCm39) |
D504E |
probably benign |
Het |
Vav3 |
C |
T |
3: 109,571,681 (GRCm39) |
T201M |
probably damaging |
Het |
Vldlr |
A |
G |
19: 27,215,477 (GRCm39) |
E117G |
possibly damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,381,005 (GRCm39) |
I296K |
probably damaging |
Het |
Vmn2r80 |
T |
A |
10: 79,017,837 (GRCm39) |
C521S |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,949,958 (GRCm39) |
|
probably benign |
Het |
Xpo1 |
T |
C |
11: 23,237,434 (GRCm39) |
S766P |
probably damaging |
Het |
Zcchc4 |
A |
G |
5: 52,953,486 (GRCm39) |
N165S |
possibly damaging |
Het |
|
Other mutations in Mfn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01155:Mfn1
|
APN |
3 |
32,596,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01687:Mfn1
|
APN |
3 |
32,617,515 (GRCm39) |
splice site |
probably benign |
|
IGL02743:Mfn1
|
APN |
3 |
32,628,439 (GRCm39) |
missense |
probably benign |
0.10 |
PIT4520001:Mfn1
|
UTSW |
3 |
32,615,695 (GRCm39) |
missense |
probably benign |
|
R0039:Mfn1
|
UTSW |
3 |
32,592,416 (GRCm39) |
splice site |
probably benign |
|
R0571:Mfn1
|
UTSW |
3 |
32,615,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Mfn1
|
UTSW |
3 |
32,588,385 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1661:Mfn1
|
UTSW |
3 |
32,588,471 (GRCm39) |
missense |
probably benign |
0.00 |
R1665:Mfn1
|
UTSW |
3 |
32,588,471 (GRCm39) |
missense |
probably benign |
0.00 |
R2153:Mfn1
|
UTSW |
3 |
32,596,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Mfn1
|
UTSW |
3 |
32,588,400 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2260:Mfn1
|
UTSW |
3 |
32,617,575 (GRCm39) |
nonsense |
probably null |
|
R2420:Mfn1
|
UTSW |
3 |
32,623,664 (GRCm39) |
missense |
probably benign |
0.21 |
R3864:Mfn1
|
UTSW |
3 |
32,617,241 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4079:Mfn1
|
UTSW |
3 |
32,596,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R4162:Mfn1
|
UTSW |
3 |
32,617,147 (GRCm39) |
splice site |
probably benign |
|
R4897:Mfn1
|
UTSW |
3 |
32,600,711 (GRCm39) |
intron |
probably benign |
|
R5115:Mfn1
|
UTSW |
3 |
32,618,456 (GRCm39) |
critical splice donor site |
probably null |
|
R5276:Mfn1
|
UTSW |
3 |
32,618,354 (GRCm39) |
missense |
probably benign |
0.39 |
R5590:Mfn1
|
UTSW |
3 |
32,617,996 (GRCm39) |
missense |
probably benign |
0.00 |
R5629:Mfn1
|
UTSW |
3 |
32,615,659 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6114:Mfn1
|
UTSW |
3 |
32,617,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6560:Mfn1
|
UTSW |
3 |
32,623,665 (GRCm39) |
missense |
probably damaging |
0.96 |
R6891:Mfn1
|
UTSW |
3 |
32,631,252 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7053:Mfn1
|
UTSW |
3 |
32,586,114 (GRCm39) |
missense |
probably benign |
0.00 |
R7071:Mfn1
|
UTSW |
3 |
32,622,544 (GRCm39) |
missense |
probably benign |
0.00 |
R7182:Mfn1
|
UTSW |
3 |
32,618,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Mfn1
|
UTSW |
3 |
32,622,538 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8998:Mfn1
|
UTSW |
3 |
32,623,683 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8999:Mfn1
|
UTSW |
3 |
32,623,683 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9255:Mfn1
|
UTSW |
3 |
32,598,287 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9619:Mfn1
|
UTSW |
3 |
32,628,478 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1177:Mfn1
|
UTSW |
3 |
32,618,440 (GRCm39) |
nonsense |
probably null |
|
|