Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
C |
T |
1: 130,670,635 (GRCm39) |
P286S |
possibly damaging |
Het |
Aagab |
T |
A |
9: 63,526,444 (GRCm39) |
S156T |
probably damaging |
Het |
Abca14 |
T |
G |
7: 119,823,642 (GRCm39) |
Y390D |
probably damaging |
Het |
Abcc2 |
T |
A |
19: 43,814,386 (GRCm39) |
I1122N |
possibly damaging |
Het |
Adamts16 |
T |
C |
13: 70,927,730 (GRCm39) |
E503G |
possibly damaging |
Het |
Adamts9 |
A |
T |
6: 92,835,038 (GRCm39) |
C697* |
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,623,112 (GRCm39) |
D3837G |
possibly damaging |
Het |
Ahcyl |
T |
A |
16: 45,974,246 (GRCm39) |
D377V |
probably benign |
Het |
Aire |
T |
A |
10: 77,878,433 (GRCm39) |
R128S |
probably damaging |
Het |
Alkbh2 |
A |
C |
5: 114,262,011 (GRCm39) |
*240E |
probably null |
Het |
Als2 |
T |
C |
1: 59,219,742 (GRCm39) |
Y1191C |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,952,667 (GRCm39) |
V186E |
probably benign |
Het |
Apob |
C |
T |
12: 8,040,307 (GRCm39) |
A548V |
probably damaging |
Het |
B3galt4 |
A |
T |
17: 34,169,722 (GRCm39) |
V172E |
probably damaging |
Het |
Bbs7 |
A |
C |
3: 36,646,525 (GRCm39) |
C432G |
possibly damaging |
Het |
Cacna2d3 |
T |
A |
14: 28,767,601 (GRCm39) |
E758V |
probably damaging |
Het |
Cactin |
T |
G |
10: 81,158,496 (GRCm39) |
L154R |
probably benign |
Het |
Ccdc88a |
A |
C |
11: 29,411,021 (GRCm39) |
R502S |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,450,784 (GRCm39) |
I398N |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,988,828 (GRCm39) |
D1527V |
probably damaging |
Het |
Chd1 |
A |
T |
17: 15,988,830 (GRCm39) |
M1528L |
probably benign |
Het |
Chrac1 |
G |
A |
15: 72,964,675 (GRCm39) |
|
probably null |
Het |
Cln3 |
T |
G |
7: 126,182,217 (GRCm39) |
M1L |
probably damaging |
Het |
Cnot6 |
T |
C |
11: 49,568,263 (GRCm39) |
Y442C |
probably damaging |
Het |
Col19a1 |
A |
T |
1: 24,324,132 (GRCm39) |
|
probably null |
Het |
Col1a2 |
T |
C |
6: 4,537,838 (GRCm39) |
F1116L |
unknown |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cops4 |
T |
G |
5: 100,676,408 (GRCm39) |
V53G |
probably damaging |
Het |
Crnkl1 |
A |
G |
2: 145,761,875 (GRCm39) |
S561P |
probably benign |
Het |
Ctnnb1 |
C |
A |
9: 120,780,778 (GRCm39) |
Q99K |
probably benign |
Het |
Cxcr5 |
T |
C |
9: 44,424,578 (GRCm39) |
S360G |
probably benign |
Het |
Dab2 |
G |
A |
15: 6,447,797 (GRCm39) |
V60M |
probably damaging |
Het |
Ddx3y |
A |
T |
Y: 1,263,321 (GRCm39) |
Y648* |
probably null |
Het |
Dennd2a |
T |
A |
6: 39,474,044 (GRCm39) |
D430V |
probably damaging |
Het |
Dsp |
G |
T |
13: 38,376,846 (GRCm39) |
E1544* |
probably null |
Het |
Efcab7 |
A |
T |
4: 99,719,631 (GRCm39) |
M38L |
possibly damaging |
Het |
Fto |
A |
G |
8: 92,136,155 (GRCm39) |
N141S |
probably damaging |
Het |
Gabrp |
A |
G |
11: 33,504,362 (GRCm39) |
F318L |
probably damaging |
Het |
Gmeb1 |
A |
C |
4: 131,969,663 (GRCm39) |
C103W |
probably damaging |
Het |
Heatr9 |
T |
C |
11: 83,405,365 (GRCm39) |
D365G |
probably damaging |
Het |
Hif3a |
G |
A |
7: 16,778,325 (GRCm39) |
R436W |
probably benign |
Het |
Hint2 |
A |
G |
4: 43,654,378 (GRCm39) |
V145A |
probably damaging |
Het |
Hmcn2 |
T |
A |
2: 31,313,237 (GRCm39) |
L3482* |
probably null |
Het |
Hsd3b1 |
A |
T |
3: 98,760,590 (GRCm39) |
Y134N |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,080,848 (GRCm39) |
V775E |
probably damaging |
Het |
Ipo5 |
A |
G |
14: 121,159,635 (GRCm39) |
I154M |
probably benign |
Het |
Itgad |
T |
A |
7: 127,797,550 (GRCm39) |
F893Y |
probably benign |
Het |
Itprid1 |
A |
T |
6: 55,875,228 (GRCm39) |
M393L |
possibly damaging |
Het |
Kdm4a |
T |
C |
4: 118,018,903 (GRCm39) |
R438G |
probably benign |
Het |
Klk1b11 |
T |
A |
7: 43,425,943 (GRCm39) |
M1K |
probably null |
Het |
Lama5 |
A |
T |
2: 179,824,219 (GRCm39) |
V2602D |
possibly damaging |
Het |
Lrch3 |
T |
C |
16: 32,799,870 (GRCm39) |
S35P |
probably damaging |
Het |
Mgat4c |
A |
T |
10: 102,224,565 (GRCm39) |
I260F |
probably damaging |
Het |
Mon1b |
T |
A |
8: 114,364,375 (GRCm39) |
S51T |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,036,744 (GRCm39) |
D993G |
probably benign |
Het |
Myo1a |
A |
G |
10: 127,552,166 (GRCm39) |
N762D |
probably benign |
Het |
Nacc2 |
A |
T |
2: 25,950,345 (GRCm39) |
Y464N |
probably damaging |
Het |
Nckap1 |
A |
G |
2: 80,383,714 (GRCm39) |
I150T |
probably benign |
Het |
Ndufv2 |
G |
T |
17: 66,387,816 (GRCm39) |
P119T |
probably damaging |
Het |
Noc4l |
G |
A |
5: 110,800,241 (GRCm39) |
R95* |
probably null |
Het |
Ntng1 |
A |
T |
3: 110,042,819 (GRCm39) |
Y2* |
probably null |
Het |
Oog4 |
T |
C |
4: 143,165,773 (GRCm39) |
N53D |
probably benign |
Het |
Or10ak11 |
A |
T |
4: 118,687,022 (GRCm39) |
V205D |
possibly damaging |
Het |
Or4d11 |
C |
T |
19: 12,013,525 (GRCm39) |
V194I |
probably benign |
Het |
Or6c6c |
A |
G |
10: 129,541,638 (GRCm39) |
E297G |
possibly damaging |
Het |
Or9i1b |
C |
T |
19: 13,896,873 (GRCm39) |
T163I |
probably benign |
Het |
Phkg2 |
T |
G |
7: 127,173,075 (GRCm39) |
L11R |
probably damaging |
Het |
Pogz |
A |
G |
3: 94,777,424 (GRCm39) |
D368G |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,355,289 (GRCm39) |
L1530Q |
probably damaging |
Het |
Prmt1 |
C |
T |
7: 44,628,878 (GRCm39) |
E144K |
probably damaging |
Het |
Prss8 |
T |
A |
7: 127,526,348 (GRCm39) |
I121F |
probably benign |
Het |
Psmd13 |
T |
C |
7: 140,477,624 (GRCm39) |
L314P |
probably damaging |
Het |
Ptch2 |
G |
A |
4: 116,966,081 (GRCm39) |
G467D |
probably damaging |
Het |
Rbm20 |
C |
A |
19: 53,852,596 (GRCm39) |
P1192Q |
probably damaging |
Het |
Rpl19 |
T |
A |
11: 97,919,200 (GRCm39) |
D45E |
probably benign |
Het |
Rsph10b |
C |
T |
5: 143,903,946 (GRCm39) |
A219V |
probably damaging |
Het |
Rtraf |
C |
T |
14: 19,864,600 (GRCm39) |
|
probably null |
Het |
Scaf1 |
T |
A |
7: 44,658,175 (GRCm39) |
T235S |
probably damaging |
Het |
Shank1 |
T |
A |
7: 43,968,594 (GRCm39) |
C296S |
unknown |
Het |
Slc39a7 |
A |
T |
17: 34,247,924 (GRCm39) |
V426D |
probably damaging |
Het |
Slc41a2 |
A |
T |
10: 83,119,610 (GRCm39) |
V384D |
probably damaging |
Het |
Slco1c1 |
T |
C |
6: 141,505,499 (GRCm39) |
L475P |
probably benign |
Het |
Slco6d1 |
A |
C |
1: 98,418,359 (GRCm39) |
K515T |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,682,459 (GRCm39) |
E253G |
probably damaging |
Het |
Sp6 |
G |
T |
11: 96,912,361 (GRCm39) |
D25Y |
possibly damaging |
Het |
Syt11 |
A |
C |
3: 88,669,855 (GRCm39) |
D12E |
possibly damaging |
Het |
Taf2 |
A |
G |
15: 54,910,856 (GRCm39) |
L606P |
probably damaging |
Het |
Tbc1d5 |
A |
G |
17: 51,273,764 (GRCm39) |
Y116H |
probably damaging |
Het |
Tnfrsf8 |
A |
G |
4: 145,015,029 (GRCm39) |
I243T |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,917,153 (GRCm39) |
S2183G |
probably benign |
Het |
Trim66 |
T |
C |
7: 109,059,379 (GRCm39) |
Y853C |
probably benign |
Het |
Ttn |
T |
A |
2: 76,567,839 (GRCm39) |
T27685S |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,573,466 (GRCm39) |
E25809G |
probably damaging |
Het |
Uvssa |
G |
A |
5: 33,566,191 (GRCm39) |
G445S |
probably benign |
Het |
Zfp326 |
T |
C |
5: 106,058,141 (GRCm39) |
S427P |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 80,674,637 (GRCm39) |
T534A |
possibly damaging |
Het |
Zfp672 |
A |
G |
11: 58,207,173 (GRCm39) |
S383P |
possibly damaging |
Het |
Zfp799 |
A |
G |
17: 33,039,700 (GRCm39) |
S188P |
possibly damaging |
Het |
Zyg11b |
A |
C |
4: 108,129,450 (GRCm39) |
V54G |
possibly damaging |
Het |
|
Other mutations in Mfn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02313:Mfn2
|
APN |
4 |
147,969,947 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03236:Mfn2
|
APN |
4 |
147,966,562 (GRCm39) |
missense |
probably damaging |
1.00 |
milkshake
|
UTSW |
4 |
147,971,909 (GRCm39) |
missense |
probably benign |
0.12 |
R0066:Mfn2
|
UTSW |
4 |
147,969,902 (GRCm39) |
unclassified |
probably benign |
|
R0066:Mfn2
|
UTSW |
4 |
147,969,902 (GRCm39) |
unclassified |
probably benign |
|
R0376:Mfn2
|
UTSW |
4 |
147,969,983 (GRCm39) |
missense |
probably benign |
0.24 |
R0564:Mfn2
|
UTSW |
4 |
147,967,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R0962:Mfn2
|
UTSW |
4 |
147,966,658 (GRCm39) |
missense |
probably benign |
|
R1595:Mfn2
|
UTSW |
4 |
147,979,153 (GRCm39) |
missense |
probably benign |
0.08 |
R2105:Mfn2
|
UTSW |
4 |
147,973,162 (GRCm39) |
nonsense |
probably null |
|
R2260:Mfn2
|
UTSW |
4 |
147,979,063 (GRCm39) |
nonsense |
probably null |
|
R4544:Mfn2
|
UTSW |
4 |
147,971,909 (GRCm39) |
missense |
probably benign |
0.12 |
R4546:Mfn2
|
UTSW |
4 |
147,971,909 (GRCm39) |
missense |
probably benign |
0.12 |
R4561:Mfn2
|
UTSW |
4 |
147,961,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Mfn2
|
UTSW |
4 |
147,970,785 (GRCm39) |
missense |
probably benign |
0.10 |
R5355:Mfn2
|
UTSW |
4 |
147,979,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Mfn2
|
UTSW |
4 |
147,979,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Mfn2
|
UTSW |
4 |
147,974,693 (GRCm39) |
missense |
probably benign |
0.03 |
R9345:Mfn2
|
UTSW |
4 |
147,966,649 (GRCm39) |
missense |
probably benign |
0.38 |
|