Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
A |
G |
4: 53,086,039 (GRCm39) |
F488S |
probably damaging |
Het |
Acap3 |
C |
T |
4: 155,983,881 (GRCm39) |
R116W |
probably damaging |
Het |
Adamts10 |
C |
A |
17: 33,764,364 (GRCm39) |
P663T |
possibly damaging |
Het |
Akap12 |
G |
A |
10: 4,303,333 (GRCm39) |
G48S |
probably damaging |
Het |
Ankrd7 |
T |
A |
6: 18,870,030 (GRCm39) |
M261K |
probably benign |
Het |
Ankzf1 |
C |
A |
1: 75,174,948 (GRCm39) |
D599E |
possibly damaging |
Het |
Aox1 |
T |
C |
1: 58,144,173 (GRCm39) |
I1278T |
possibly damaging |
Het |
Apcdd1 |
T |
C |
18: 63,083,150 (GRCm39) |
Y327H |
probably benign |
Het |
Asxl3 |
T |
A |
18: 22,544,553 (GRCm39) |
|
probably benign |
Het |
Birc6 |
C |
A |
17: 74,969,827 (GRCm39) |
|
probably benign |
Het |
Btaf1 |
T |
A |
19: 36,987,048 (GRCm39) |
L1714* |
probably null |
Het |
Cacng6 |
T |
A |
7: 3,473,520 (GRCm39) |
|
probably benign |
Het |
Cdc20b |
A |
G |
13: 113,215,146 (GRCm39) |
D238G |
probably damaging |
Het |
Celf5 |
T |
A |
10: 81,306,532 (GRCm39) |
R113W |
probably null |
Het |
Cfap251 |
T |
C |
5: 123,421,510 (GRCm39) |
V182A |
probably damaging |
Het |
Cfap70 |
C |
A |
14: 20,462,415 (GRCm39) |
E659D |
probably damaging |
Het |
Clspn |
T |
A |
4: 126,484,391 (GRCm39) |
M1183K |
possibly damaging |
Het |
Dpy19l1 |
G |
A |
9: 24,365,187 (GRCm39) |
R275C |
probably damaging |
Het |
Dst |
C |
T |
1: 34,226,016 (GRCm39) |
S1721L |
probably benign |
Het |
Fam168b |
T |
C |
1: 34,858,769 (GRCm39) |
M133V |
probably damaging |
Het |
Farp2 |
T |
C |
1: 93,496,809 (GRCm39) |
I172T |
probably damaging |
Het |
Fer |
T |
G |
17: 64,203,273 (GRCm39) |
S68A |
probably damaging |
Het |
Fmo5 |
A |
G |
3: 97,552,997 (GRCm39) |
E315G |
probably damaging |
Het |
Gpr89 |
A |
T |
3: 96,778,796 (GRCm39) |
F426I |
probably damaging |
Het |
Hinfp |
T |
C |
9: 44,207,624 (GRCm39) |
I461V |
possibly damaging |
Het |
Hsd11b1 |
A |
T |
1: 192,922,556 (GRCm39) |
V167D |
probably damaging |
Het |
Htt |
A |
G |
5: 35,054,252 (GRCm39) |
K2574E |
probably benign |
Het |
I830077J02Rik |
A |
G |
3: 105,833,821 (GRCm39) |
S112P |
probably benign |
Het |
Igf2bp3 |
T |
A |
6: 49,082,551 (GRCm39) |
M344L |
probably benign |
Het |
Itch |
A |
T |
2: 155,044,177 (GRCm39) |
Q494L |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,598,321 (GRCm39) |
|
probably benign |
Het |
Jaml |
T |
A |
9: 45,005,065 (GRCm39) |
D152E |
probably benign |
Het |
Kif22 |
A |
C |
7: 126,641,572 (GRCm39) |
M1R |
probably null |
Het |
Kifap3 |
T |
C |
1: 163,710,955 (GRCm39) |
Y663H |
probably benign |
Het |
Letm2 |
T |
A |
8: 26,068,786 (GRCm39) |
N472I |
probably damaging |
Het |
Mthfr |
T |
G |
4: 148,136,681 (GRCm39) |
V446G |
probably damaging |
Het |
Myh11 |
T |
C |
16: 14,029,124 (GRCm39) |
E1206G |
possibly damaging |
Het |
Myo6 |
G |
A |
9: 80,195,338 (GRCm39) |
V903I |
probably damaging |
Het |
Myo9b |
C |
T |
8: 71,807,869 (GRCm39) |
|
probably benign |
Het |
Nr2f2 |
G |
C |
7: 70,009,923 (GRCm39) |
P52R |
probably damaging |
Het |
Nsd3 |
A |
G |
8: 26,173,273 (GRCm39) |
N859S |
probably benign |
Het |
Nucb2 |
C |
A |
7: 116,135,245 (GRCm39) |
A384E |
probably damaging |
Het |
Ogdhl |
C |
A |
14: 32,063,994 (GRCm39) |
|
probably null |
Het |
Or10al3 |
C |
A |
17: 38,011,949 (GRCm39) |
C129* |
probably null |
Het |
Or1e22 |
A |
T |
11: 73,377,401 (GRCm39) |
L83Q |
probably benign |
Het |
Or1i2 |
T |
C |
10: 78,447,705 (GRCm39) |
T257A |
probably benign |
Het |
Or4a74 |
G |
A |
2: 89,440,207 (GRCm39) |
L80F |
probably damaging |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Parp10 |
C |
T |
15: 76,126,833 (GRCm39) |
S145N |
probably benign |
Het |
Pigh |
A |
G |
12: 79,130,483 (GRCm39) |
|
probably benign |
Het |
Pigo |
A |
G |
4: 43,023,824 (GRCm39) |
|
probably benign |
Het |
Pkp4 |
T |
A |
2: 59,135,832 (GRCm39) |
V199D |
possibly damaging |
Het |
Polr1e |
C |
A |
4: 45,025,143 (GRCm39) |
|
probably null |
Het |
Ppfia3 |
C |
A |
7: 44,997,958 (GRCm39) |
R723L |
probably damaging |
Het |
Prex1 |
C |
A |
2: 166,427,818 (GRCm39) |
A945S |
possibly damaging |
Het |
Prrt3 |
A |
T |
6: 113,472,801 (GRCm39) |
V457E |
probably damaging |
Het |
Rab39 |
A |
G |
9: 53,617,271 (GRCm39) |
F49L |
possibly damaging |
Het |
Rrs1 |
C |
A |
1: 9,615,987 (GRCm39) |
|
probably null |
Het |
Rrs1 |
G |
A |
1: 9,615,992 (GRCm39) |
E82K |
probably damaging |
Het |
Serpinb3c |
T |
C |
1: 107,204,722 (GRCm39) |
D8G |
probably benign |
Het |
Slc17a6 |
A |
G |
7: 51,295,928 (GRCm39) |
|
probably benign |
Het |
Slc24a4 |
T |
A |
12: 102,195,210 (GRCm39) |
|
probably null |
Het |
Smc1b |
C |
T |
15: 85,007,960 (GRCm39) |
M272I |
probably benign |
Het |
Smc6 |
T |
C |
12: 11,333,179 (GRCm39) |
|
probably benign |
Het |
Tcf20 |
T |
C |
15: 82,739,286 (GRCm39) |
T722A |
probably benign |
Het |
Tesmin |
A |
T |
19: 3,454,088 (GRCm39) |
M141L |
probably benign |
Het |
Tmprss5 |
T |
A |
9: 49,024,460 (GRCm39) |
H274Q |
possibly damaging |
Het |
Tns1 |
C |
T |
1: 73,976,477 (GRCm39) |
|
probably null |
Het |
Tpr |
T |
C |
1: 150,293,178 (GRCm39) |
S868P |
possibly damaging |
Het |
Trank1 |
C |
T |
9: 111,195,321 (GRCm39) |
T1115I |
probably damaging |
Het |
Trmt44 |
A |
T |
5: 35,730,261 (GRCm39) |
I203K |
possibly damaging |
Het |
Ulk2 |
A |
T |
11: 61,668,611 (GRCm39) |
V1037E |
probably benign |
Het |
Usp43 |
A |
G |
11: 67,767,325 (GRCm39) |
Y682H |
probably damaging |
Het |
Vipr2 |
A |
T |
12: 116,106,502 (GRCm39) |
Q366L |
probably damaging |
Het |
Vmn1r185 |
C |
A |
7: 26,311,014 (GRCm39) |
V164L |
possibly damaging |
Het |
Vmn2r120 |
C |
T |
17: 57,832,052 (GRCm39) |
V246I |
probably benign |
Het |
Wiz |
C |
T |
17: 32,576,007 (GRCm39) |
G790R |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,929,694 (GRCm39) |
S1016R |
probably damaging |
Het |
Zc3hav1 |
A |
G |
6: 38,288,109 (GRCm39) |
L909S |
probably benign |
Het |
Zfp236 |
T |
A |
18: 82,658,352 (GRCm39) |
I637F |
probably damaging |
Het |
Zfp788 |
G |
A |
7: 41,299,020 (GRCm39) |
G532D |
probably damaging |
Het |
Zranb1 |
T |
C |
7: 132,552,114 (GRCm39) |
I255T |
probably damaging |
Het |
|
Other mutations in Faap100 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Faap100
|
APN |
11 |
120,262,958 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02954:Faap100
|
APN |
11 |
120,262,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Faap100
|
UTSW |
11 |
120,261,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R0034:Faap100
|
UTSW |
11 |
120,262,973 (GRCm39) |
missense |
probably benign |
0.34 |
R0432:Faap100
|
UTSW |
11 |
120,264,702 (GRCm39) |
splice site |
probably benign |
|
R0570:Faap100
|
UTSW |
11 |
120,265,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0748:Faap100
|
UTSW |
11 |
120,262,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R0782:Faap100
|
UTSW |
11 |
120,267,530 (GRCm39) |
critical splice donor site |
probably null |
|
R1218:Faap100
|
UTSW |
11 |
120,269,166 (GRCm39) |
missense |
probably benign |
0.06 |
R1612:Faap100
|
UTSW |
11 |
120,267,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Faap100
|
UTSW |
11 |
120,265,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Faap100
|
UTSW |
11 |
120,268,059 (GRCm39) |
missense |
probably damaging |
0.99 |
R2881:Faap100
|
UTSW |
11 |
120,265,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R2893:Faap100
|
UTSW |
11 |
120,265,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R3969:Faap100
|
UTSW |
11 |
120,269,531 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4824:Faap100
|
UTSW |
11 |
120,266,412 (GRCm39) |
splice site |
probably null |
|
R4911:Faap100
|
UTSW |
11 |
120,262,939 (GRCm39) |
missense |
probably benign |
0.37 |
R5152:Faap100
|
UTSW |
11 |
120,268,458 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5155:Faap100
|
UTSW |
11 |
120,268,458 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5327:Faap100
|
UTSW |
11 |
120,268,458 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5328:Faap100
|
UTSW |
11 |
120,268,458 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5386:Faap100
|
UTSW |
11 |
120,268,458 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5480:Faap100
|
UTSW |
11 |
120,267,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Faap100
|
UTSW |
11 |
120,268,458 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5629:Faap100
|
UTSW |
11 |
120,267,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R5911:Faap100
|
UTSW |
11 |
120,267,958 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6285:Faap100
|
UTSW |
11 |
120,267,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R6350:Faap100
|
UTSW |
11 |
120,265,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R6525:Faap100
|
UTSW |
11 |
120,269,590 (GRCm39) |
splice site |
probably null |
|
R7046:Faap100
|
UTSW |
11 |
120,268,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7539:Faap100
|
UTSW |
11 |
120,268,464 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7781:Faap100
|
UTSW |
11 |
120,265,089 (GRCm39) |
missense |
probably benign |
0.00 |
R8345:Faap100
|
UTSW |
11 |
120,267,856 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8679:Faap100
|
UTSW |
11 |
120,263,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R8715:Faap100
|
UTSW |
11 |
120,265,299 (GRCm39) |
missense |
probably benign |
0.13 |
R8942:Faap100
|
UTSW |
11 |
120,267,856 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8956:Faap100
|
UTSW |
11 |
120,268,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Faap100
|
UTSW |
11 |
120,267,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R9590:Faap100
|
UTSW |
11 |
120,269,545 (GRCm39) |
unclassified |
probably benign |
|
|