Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
G |
A |
7: 28,315,920 (GRCm39) |
A222V |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,979,883 (GRCm39) |
D389G |
probably benign |
Het |
Aldh1l2 |
A |
T |
10: 83,337,789 (GRCm39) |
S559T |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,576,877 (GRCm39) |
N144K |
possibly damaging |
Het |
Anp32b |
T |
A |
4: 46,469,868 (GRCm39) |
|
probably null |
Het |
Atf7 |
C |
T |
15: 102,459,944 (GRCm39) |
R57H |
probably damaging |
Het |
Atp10b |
A |
T |
11: 43,092,000 (GRCm39) |
H345L |
probably benign |
Het |
Cacna2d1 |
A |
T |
5: 16,563,950 (GRCm39) |
I859F |
probably damaging |
Het |
Calcr |
T |
A |
6: 3,714,730 (GRCm39) |
|
probably null |
Het |
Cd248 |
A |
G |
19: 5,119,963 (GRCm39) |
T604A |
probably benign |
Het |
Cemip |
C |
T |
7: 83,610,849 (GRCm39) |
V702M |
probably damaging |
Het |
Cep295 |
G |
T |
9: 15,243,282 (GRCm39) |
Q469K |
probably damaging |
Het |
Cntn5 |
A |
G |
9: 9,748,427 (GRCm39) |
W485R |
probably damaging |
Het |
Cpe |
T |
C |
8: 65,062,189 (GRCm39) |
N289S |
possibly damaging |
Het |
Cyp2j11 |
G |
A |
4: 96,233,358 (GRCm39) |
R113C |
probably damaging |
Het |
Dcp1b |
T |
C |
6: 119,194,872 (GRCm39) |
S531P |
probably benign |
Het |
Defb7 |
T |
G |
8: 19,545,167 (GRCm39) |
L15R |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Ednrb |
T |
C |
14: 104,060,831 (GRCm39) |
D198G |
probably damaging |
Het |
Engase |
A |
C |
11: 118,378,146 (GRCm39) |
E312A |
possibly damaging |
Het |
Evl |
G |
A |
12: 108,639,612 (GRCm39) |
|
probably null |
Het |
Garre1 |
T |
A |
7: 33,953,416 (GRCm39) |
T449S |
possibly damaging |
Het |
Garre1 |
T |
G |
7: 33,984,134 (GRCm39) |
D163A |
probably damaging |
Het |
Gm5460 |
C |
A |
14: 33,767,752 (GRCm39) |
N453K |
possibly damaging |
Het |
Gm7356 |
T |
A |
17: 14,220,869 (GRCm39) |
I387F |
possibly damaging |
Het |
H1f2 |
A |
G |
13: 23,923,148 (GRCm39) |
K106R |
probably damaging |
Het |
Hagh |
T |
C |
17: 25,069,568 (GRCm39) |
M1T |
probably null |
Het |
Hars1 |
A |
T |
18: 36,905,369 (GRCm39) |
V155E |
probably damaging |
Het |
Lca5 |
C |
A |
9: 83,280,619 (GRCm39) |
D394Y |
probably benign |
Het |
Lmtk3 |
T |
C |
7: 45,440,834 (GRCm39) |
L280P |
probably damaging |
Het |
Lrit1 |
C |
T |
14: 36,784,385 (GRCm39) |
A571V |
possibly damaging |
Het |
Map4k2 |
C |
A |
19: 6,396,836 (GRCm39) |
P584H |
probably damaging |
Het |
Mgst1 |
T |
C |
6: 138,118,798 (GRCm39) |
|
probably benign |
Het |
Mtrex |
A |
T |
13: 113,009,590 (GRCm39) |
C936* |
probably null |
Het |
Neb |
C |
T |
2: 52,086,339 (GRCm39) |
V5245I |
probably damaging |
Het |
Oas3 |
T |
C |
5: 120,896,867 (GRCm39) |
N918S |
probably benign |
Het |
Or4c106 |
C |
T |
2: 88,683,023 (GRCm39) |
T243I |
probably benign |
Het |
Or5d16 |
T |
A |
2: 87,773,552 (GRCm39) |
Q140L |
probably benign |
Het |
Or8b8 |
A |
C |
9: 37,809,359 (GRCm39) |
I220L |
possibly damaging |
Het |
Ovch2 |
A |
G |
7: 107,393,201 (GRCm39) |
L224P |
probably damaging |
Het |
Patj |
A |
T |
4: 98,409,047 (GRCm39) |
K34* |
probably null |
Het |
Pcf11 |
T |
A |
7: 92,308,016 (GRCm39) |
R717S |
possibly damaging |
Het |
Plcb1 |
A |
T |
2: 135,177,400 (GRCm39) |
E577D |
probably benign |
Het |
Plxnb2 |
T |
C |
15: 89,042,899 (GRCm39) |
K1497E |
probably damaging |
Het |
Pyroxd1 |
C |
A |
6: 142,299,266 (GRCm39) |
L141I |
probably damaging |
Het |
Rhobtb3 |
G |
T |
13: 76,020,537 (GRCm39) |
N588K |
probably benign |
Het |
Rnasel |
G |
A |
1: 153,629,452 (GRCm39) |
|
probably benign |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Shank1 |
A |
T |
7: 44,003,911 (GRCm39) |
I1868F |
possibly damaging |
Het |
Slc28a3 |
A |
T |
13: 58,706,463 (GRCm39) |
S593T |
probably damaging |
Het |
Slc29a4 |
T |
C |
5: 142,699,853 (GRCm39) |
I168T |
possibly damaging |
Het |
Slc35f5 |
C |
T |
1: 125,518,775 (GRCm39) |
P502L |
probably benign |
Het |
Slco6d1 |
T |
C |
1: 98,408,493 (GRCm39) |
I463T |
probably damaging |
Het |
Slk |
A |
G |
19: 47,608,451 (GRCm39) |
D468G |
probably benign |
Het |
Spata31d1d |
G |
T |
13: 59,874,322 (GRCm39) |
P1071Q |
probably damaging |
Het |
Tert |
G |
A |
13: 73,787,275 (GRCm39) |
V754I |
probably damaging |
Het |
Thada |
T |
C |
17: 84,759,155 (GRCm39) |
T235A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,564,472 (GRCm39) |
D28555G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,710,328 (GRCm39) |
|
probably null |
Het |
Ubqln4 |
T |
C |
3: 88,472,575 (GRCm39) |
L464P |
probably damaging |
Het |
Unc45b |
A |
T |
11: 82,813,643 (GRCm39) |
N350I |
possibly damaging |
Het |
Vmn2r65 |
T |
C |
7: 84,589,900 (GRCm39) |
D672G |
probably benign |
Het |
Zfp947 |
T |
A |
17: 22,365,066 (GRCm39) |
I203L |
probably benign |
Het |
Zfp964 |
T |
A |
8: 70,116,766 (GRCm39) |
H454Q |
probably benign |
Het |
|
Other mutations in Faf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Faf1
|
APN |
4 |
109,697,578 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00569:Faf1
|
APN |
4 |
109,819,077 (GRCm39) |
makesense |
probably null |
|
IGL01398:Faf1
|
APN |
4 |
109,593,793 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01640:Faf1
|
APN |
4 |
109,697,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01739:Faf1
|
APN |
4 |
109,534,278 (GRCm39) |
splice site |
probably benign |
|
IGL02265:Faf1
|
APN |
4 |
109,600,101 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02372:Faf1
|
APN |
4 |
109,792,779 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02999:Faf1
|
APN |
4 |
109,719,090 (GRCm39) |
missense |
probably benign |
0.01 |
R0058:Faf1
|
UTSW |
4 |
109,593,821 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Faf1
|
UTSW |
4 |
109,593,821 (GRCm39) |
missense |
probably benign |
0.00 |
R0098:Faf1
|
UTSW |
4 |
109,792,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0098:Faf1
|
UTSW |
4 |
109,792,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0183:Faf1
|
UTSW |
4 |
109,792,807 (GRCm39) |
missense |
probably benign |
|
R0463:Faf1
|
UTSW |
4 |
109,748,138 (GRCm39) |
missense |
probably benign |
0.02 |
R0505:Faf1
|
UTSW |
4 |
109,697,600 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0755:Faf1
|
UTSW |
4 |
109,819,036 (GRCm39) |
missense |
probably benign |
0.00 |
R1705:Faf1
|
UTSW |
4 |
109,534,199 (GRCm39) |
start gained |
probably benign |
|
R2061:Faf1
|
UTSW |
4 |
109,568,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Faf1
|
UTSW |
4 |
109,568,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Faf1
|
UTSW |
4 |
109,568,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R2696:Faf1
|
UTSW |
4 |
109,698,525 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3937:Faf1
|
UTSW |
4 |
109,614,889 (GRCm39) |
splice site |
probably benign |
|
R3939:Faf1
|
UTSW |
4 |
109,719,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4602:Faf1
|
UTSW |
4 |
109,584,625 (GRCm39) |
missense |
probably benign |
|
R4727:Faf1
|
UTSW |
4 |
109,697,564 (GRCm39) |
missense |
probably damaging |
0.96 |
R4860:Faf1
|
UTSW |
4 |
109,600,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R4860:Faf1
|
UTSW |
4 |
109,600,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R4896:Faf1
|
UTSW |
4 |
109,699,496 (GRCm39) |
missense |
probably benign |
0.02 |
R4913:Faf1
|
UTSW |
4 |
109,792,746 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5721:Faf1
|
UTSW |
4 |
109,792,863 (GRCm39) |
missense |
probably benign |
0.34 |
R5905:Faf1
|
UTSW |
4 |
109,748,126 (GRCm39) |
missense |
probably benign |
0.03 |
R6190:Faf1
|
UTSW |
4 |
109,719,012 (GRCm39) |
missense |
probably damaging |
0.97 |
R6364:Faf1
|
UTSW |
4 |
109,818,997 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6454:Faf1
|
UTSW |
4 |
109,699,531 (GRCm39) |
missense |
probably benign |
0.27 |
R6805:Faf1
|
UTSW |
4 |
109,719,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7101:Faf1
|
UTSW |
4 |
109,783,153 (GRCm39) |
missense |
probably benign |
0.12 |
R7381:Faf1
|
UTSW |
4 |
109,719,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R7392:Faf1
|
UTSW |
4 |
109,652,040 (GRCm39) |
missense |
probably benign |
0.01 |
R7584:Faf1
|
UTSW |
4 |
109,783,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R7660:Faf1
|
UTSW |
4 |
109,719,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R7678:Faf1
|
UTSW |
4 |
109,687,061 (GRCm39) |
missense |
probably benign |
0.00 |
R7715:Faf1
|
UTSW |
4 |
109,568,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R7721:Faf1
|
UTSW |
4 |
109,593,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R8773:Faf1
|
UTSW |
4 |
109,699,507 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9004:Faf1
|
UTSW |
4 |
109,698,550 (GRCm39) |
missense |
probably benign |
0.01 |
R9028:Faf1
|
UTSW |
4 |
109,748,105 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9646:Faf1
|
UTSW |
4 |
109,652,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9700:Faf1
|
UTSW |
4 |
109,748,179 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Faf1
|
UTSW |
4 |
109,697,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|