Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449I24Rik |
T |
C |
5: 146,441,506 (GRCm39) |
S218P |
probably benign |
Het |
Ahctf1 |
A |
C |
1: 179,596,615 (GRCm39) |
S121A |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,491,479 (GRCm39) |
R174H |
probably benign |
Het |
Arhgef18 |
T |
C |
8: 3,435,010 (GRCm39) |
|
probably null |
Het |
Becn1 |
A |
G |
11: 101,179,629 (GRCm39) |
|
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,561,549 (GRCm39) |
Y984C |
probably damaging |
Het |
Cacna2d4 |
G |
T |
6: 119,324,213 (GRCm39) |
|
probably null |
Het |
Ccdc14 |
T |
G |
16: 34,543,542 (GRCm39) |
N633K |
probably damaging |
Het |
Cdk5rap1 |
T |
A |
2: 154,177,489 (GRCm39) |
T577S |
possibly damaging |
Het |
Clca4b |
T |
C |
3: 144,630,940 (GRCm39) |
R307G |
possibly damaging |
Het |
Colgalt2 |
A |
G |
1: 152,360,620 (GRCm39) |
Q219R |
possibly damaging |
Het |
Cops3 |
A |
T |
11: 59,718,762 (GRCm39) |
D177E |
possibly damaging |
Het |
Cyp2d9 |
T |
C |
15: 82,338,256 (GRCm39) |
Y127H |
probably damaging |
Het |
Dnajc11 |
A |
G |
4: 152,052,983 (GRCm39) |
T98A |
probably damaging |
Het |
Dst |
T |
C |
1: 34,265,058 (GRCm39) |
S4757P |
possibly damaging |
Het |
Dvl2 |
C |
T |
11: 69,898,957 (GRCm39) |
T448I |
possibly damaging |
Het |
E230016K23Rik |
T |
G |
11: 83,512,496 (GRCm39) |
|
noncoding transcript |
Het |
Efl1 |
G |
T |
7: 82,323,714 (GRCm39) |
D219Y |
probably damaging |
Het |
Epha10 |
T |
A |
4: 124,807,793 (GRCm39) |
|
probably benign |
Het |
Folr1 |
T |
A |
7: 101,513,184 (GRCm39) |
D37V |
probably damaging |
Het |
Fshb |
T |
A |
2: 106,889,224 (GRCm39) |
I27F |
probably damaging |
Het |
Gm8521 |
A |
T |
Y: 3,859,335 (GRCm39) |
|
noncoding transcript |
Het |
Gpr45 |
T |
C |
1: 43,071,998 (GRCm39) |
S214P |
probably damaging |
Het |
Hgf |
G |
A |
5: 16,771,860 (GRCm39) |
|
probably null |
Het |
Hs6st1 |
T |
C |
1: 36,143,259 (GRCm39) |
V398A |
probably benign |
Het |
Ighmbp2 |
A |
G |
19: 3,321,646 (GRCm39) |
V371A |
probably damaging |
Het |
Kif18a |
T |
A |
2: 109,148,370 (GRCm39) |
N621K |
probably benign |
Het |
Lama5 |
A |
G |
2: 179,822,911 (GRCm39) |
F2785S |
probably damaging |
Het |
Lcor |
G |
A |
19: 41,574,791 (GRCm39) |
G1182D |
probably damaging |
Het |
Lrriq3 |
T |
C |
3: 154,835,108 (GRCm39) |
I281T |
possibly damaging |
Het |
Macf1 |
C |
T |
4: 123,367,229 (GRCm39) |
A2511T |
probably damaging |
Het |
Mark4 |
T |
C |
7: 19,170,886 (GRCm39) |
D328G |
possibly damaging |
Het |
Myo1c |
G |
A |
11: 75,552,852 (GRCm39) |
E434K |
possibly damaging |
Het |
Nfe2l1 |
A |
G |
11: 96,710,205 (GRCm39) |
S387P |
probably damaging |
Het |
Nr1d2 |
A |
G |
14: 18,215,197 (GRCm38) |
S272P |
probably benign |
Het |
Nsrp1 |
T |
C |
11: 76,940,293 (GRCm39) |
H104R |
probably damaging |
Het |
Odf1 |
T |
A |
15: 38,219,863 (GRCm39) |
S64T |
probably benign |
Het |
Or2aa1 |
A |
T |
11: 59,480,477 (GRCm39) |
V146E |
probably damaging |
Het |
Or4c106 |
T |
A |
2: 88,683,122 (GRCm39) |
I276K |
probably damaging |
Het |
Or7g25 |
C |
T |
9: 19,160,329 (GRCm39) |
R122H |
possibly damaging |
Het |
Pde4b |
C |
A |
4: 102,278,985 (GRCm39) |
|
probably benign |
Het |
Phox2a |
C |
T |
7: 101,470,057 (GRCm39) |
T96M |
probably damaging |
Het |
Plg |
A |
G |
17: 12,622,114 (GRCm39) |
E478G |
possibly damaging |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Ppp1r12c |
T |
A |
7: 4,486,983 (GRCm39) |
T517S |
probably benign |
Het |
Ptk7 |
C |
T |
17: 46,883,603 (GRCm39) |
V821M |
probably damaging |
Het |
Ptpn6 |
C |
T |
6: 124,709,913 (GRCm39) |
V2M |
probably benign |
Het |
Rgl2 |
T |
C |
17: 34,152,529 (GRCm39) |
V380A |
probably benign |
Het |
Rpl13a-ps1 |
A |
G |
19: 50,018,591 (GRCm39) |
V195A |
possibly damaging |
Het |
Rsph1 |
C |
A |
17: 31,492,351 (GRCm39) |
V72F |
probably benign |
Het |
Sh3bp4 |
T |
C |
1: 89,073,072 (GRCm39) |
V640A |
probably benign |
Het |
Simc1 |
T |
A |
13: 54,672,795 (GRCm39) |
V381E |
probably benign |
Het |
Slc15a3 |
A |
T |
19: 10,833,296 (GRCm39) |
T438S |
probably damaging |
Het |
Slc5a4b |
C |
T |
10: 75,898,233 (GRCm39) |
V494M |
probably benign |
Het |
Sos2 |
C |
A |
12: 69,674,058 (GRCm39) |
R335L |
probably benign |
Het |
Trp53i13 |
A |
T |
11: 77,399,566 (GRCm39) |
N254K |
probably damaging |
Het |
Trpc6 |
A |
G |
9: 8,609,922 (GRCm39) |
Y130C |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,130,415 (GRCm39) |
I174V |
probably damaging |
Het |
Tsnax |
T |
A |
8: 125,742,458 (GRCm39) |
D62E |
probably damaging |
Het |
Vezt |
T |
A |
10: 93,806,193 (GRCm39) |
E739D |
probably benign |
Het |
Vmn1r59 |
T |
A |
7: 5,457,209 (GRCm39) |
I184F |
probably damaging |
Het |
Yeats2 |
T |
C |
16: 20,005,175 (GRCm39) |
V385A |
probably benign |
Het |
|
Other mutations in Fbxw22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00592:Fbxw22
|
APN |
9 |
109,213,108 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00655:Fbxw22
|
APN |
9 |
109,211,312 (GRCm39) |
splice site |
probably benign |
|
IGL01122:Fbxw22
|
APN |
9 |
109,215,739 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01419:Fbxw22
|
APN |
9 |
109,210,790 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01455:Fbxw22
|
APN |
9 |
109,214,062 (GRCm39) |
missense |
probably benign |
|
IGL01486:Fbxw22
|
APN |
9 |
109,207,941 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01734:Fbxw22
|
APN |
9 |
109,212,993 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02106:Fbxw22
|
APN |
9 |
109,231,087 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02255:Fbxw22
|
APN |
9 |
109,215,619 (GRCm39) |
splice site |
probably benign |
|
IGL02466:Fbxw22
|
APN |
9 |
109,214,160 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02820:Fbxw22
|
APN |
9 |
109,215,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R0395:Fbxw22
|
UTSW |
9 |
109,210,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R0705:Fbxw22
|
UTSW |
9 |
109,232,164 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0741:Fbxw22
|
UTSW |
9 |
109,211,287 (GRCm39) |
missense |
probably benign |
0.01 |
R1603:Fbxw22
|
UTSW |
9 |
109,207,915 (GRCm39) |
missense |
probably benign |
0.00 |
R1673:Fbxw22
|
UTSW |
9 |
109,211,196 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1874:Fbxw22
|
UTSW |
9 |
109,214,179 (GRCm39) |
nonsense |
probably null |
|
R2265:Fbxw22
|
UTSW |
9 |
109,213,062 (GRCm39) |
missense |
probably benign |
0.02 |
R2269:Fbxw22
|
UTSW |
9 |
109,213,062 (GRCm39) |
missense |
probably benign |
0.02 |
R2385:Fbxw22
|
UTSW |
9 |
109,211,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4329:Fbxw22
|
UTSW |
9 |
109,213,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R4695:Fbxw22
|
UTSW |
9 |
109,207,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Fbxw22
|
UTSW |
9 |
109,207,937 (GRCm39) |
missense |
probably benign |
0.02 |
R4915:Fbxw22
|
UTSW |
9 |
109,213,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5010:Fbxw22
|
UTSW |
9 |
109,232,492 (GRCm39) |
missense |
probably benign |
0.40 |
R5070:Fbxw22
|
UTSW |
9 |
109,214,183 (GRCm39) |
missense |
probably benign |
|
R5571:Fbxw22
|
UTSW |
9 |
109,232,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R5765:Fbxw22
|
UTSW |
9 |
109,214,064 (GRCm39) |
missense |
probably benign |
0.00 |
R5846:Fbxw22
|
UTSW |
9 |
109,215,829 (GRCm39) |
missense |
probably benign |
|
R6002:Fbxw22
|
UTSW |
9 |
109,210,750 (GRCm39) |
nonsense |
probably null |
|
R6180:Fbxw22
|
UTSW |
9 |
109,215,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6313:Fbxw22
|
UTSW |
9 |
109,232,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R6860:Fbxw22
|
UTSW |
9 |
109,213,030 (GRCm39) |
missense |
probably benign |
0.01 |
R6949:Fbxw22
|
UTSW |
9 |
109,211,144 (GRCm39) |
missense |
probably benign |
0.06 |
R7084:Fbxw22
|
UTSW |
9 |
109,233,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Fbxw22
|
UTSW |
9 |
109,211,143 (GRCm39) |
missense |
probably benign |
|
R8499:Fbxw22
|
UTSW |
9 |
109,214,068 (GRCm39) |
missense |
probably benign |
0.00 |
R9088:Fbxw22
|
UTSW |
9 |
109,207,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Fbxw22
|
UTSW |
9 |
109,215,653 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9501:Fbxw22
|
UTSW |
9 |
109,207,920 (GRCm39) |
missense |
probably benign |
0.01 |
R9600:Fbxw22
|
UTSW |
9 |
109,212,986 (GRCm39) |
missense |
probably damaging |
1.00 |
|