Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
T |
C |
14: 29,706,030 (GRCm39) |
V113A |
possibly damaging |
Het |
Adcy7 |
A |
G |
8: 89,037,666 (GRCm39) |
M245V |
possibly damaging |
Het |
Adgra1 |
G |
T |
7: 139,456,034 (GRCm39) |
R554L |
probably benign |
Het |
Agfg2 |
T |
A |
5: 137,653,664 (GRCm39) |
M351L |
probably benign |
Het |
Ahnak |
G |
A |
19: 8,979,619 (GRCm39) |
G301D |
probably benign |
Het |
Ambra1 |
C |
T |
2: 91,602,697 (GRCm39) |
A227V |
possibly damaging |
Het |
Ankrd24 |
T |
A |
10: 81,474,152 (GRCm39) |
D166E |
unknown |
Het |
Anks1 |
C |
T |
17: 28,205,778 (GRCm39) |
P341S |
probably benign |
Het |
Ano4 |
C |
T |
10: 88,808,607 (GRCm39) |
D766N |
probably benign |
Het |
Apol7e |
A |
T |
15: 77,602,007 (GRCm39) |
T202S |
possibly damaging |
Het |
Arhgap44 |
C |
A |
11: 64,929,479 (GRCm39) |
C275F |
probably damaging |
Het |
Arl6ip4 |
A |
C |
5: 124,255,095 (GRCm39) |
K95T |
probably damaging |
Het |
Bbs9 |
T |
C |
9: 22,590,284 (GRCm39) |
L674P |
probably damaging |
Het |
Bmp4 |
T |
A |
14: 46,621,972 (GRCm39) |
M191L |
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,787,090 (GRCm39) |
L2753P |
probably damaging |
Het |
Cerkl |
T |
A |
2: 79,163,901 (GRCm39) |
H473L |
probably benign |
Het |
Cfap99 |
A |
T |
5: 34,482,502 (GRCm39) |
T538S |
possibly damaging |
Het |
Clock |
A |
T |
5: 76,375,051 (GRCm39) |
V706E |
probably damaging |
Het |
Cpne6 |
T |
C |
14: 55,749,485 (GRCm39) |
M15T |
probably benign |
Het |
Deaf1 |
T |
C |
7: 140,894,324 (GRCm39) |
D351G |
probably damaging |
Het |
Dnajb8 |
C |
T |
6: 88,199,940 (GRCm39) |
R159C |
possibly damaging |
Het |
Eif3j1 |
A |
T |
2: 121,877,969 (GRCm39) |
D119V |
probably damaging |
Het |
Eps8l1 |
C |
A |
7: 4,474,297 (GRCm39) |
S195Y |
probably benign |
Het |
Exosc5 |
T |
C |
7: 25,365,769 (GRCm39) |
|
probably null |
Het |
Fabp2 |
A |
T |
3: 122,690,419 (GRCm39) |
H34L |
probably benign |
Het |
Fbln5 |
T |
A |
12: 101,723,555 (GRCm39) |
Q382L |
probably damaging |
Het |
Fndc8 |
T |
G |
11: 82,788,686 (GRCm39) |
V172G |
probably damaging |
Het |
Frs2 |
C |
T |
10: 116,910,784 (GRCm39) |
V193I |
possibly damaging |
Het |
Gadd45a |
A |
G |
6: 67,013,813 (GRCm39) |
I44T |
possibly damaging |
Het |
Gprin3 |
A |
G |
6: 59,331,456 (GRCm39) |
S284P |
possibly damaging |
Het |
Gsta4 |
T |
C |
9: 78,105,654 (GRCm39) |
V28A |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,325,733 (GRCm39) |
D1402E |
probably benign |
Het |
Hipk2 |
A |
T |
6: 38,795,728 (GRCm39) |
S180R |
possibly damaging |
Het |
Hrg |
A |
T |
16: 22,779,793 (GRCm39) |
H357L |
unknown |
Het |
Htr4 |
A |
G |
18: 62,570,971 (GRCm39) |
Q342R |
possibly damaging |
Het |
Impa1 |
A |
G |
3: 10,386,688 (GRCm39) |
S184P |
possibly damaging |
Het |
Iqgap3 |
A |
T |
3: 87,998,086 (GRCm39) |
Q281L |
probably damaging |
Het |
Kcnh8 |
C |
T |
17: 53,263,936 (GRCm39) |
P811L |
probably damaging |
Het |
Lpin1 |
T |
C |
12: 16,599,003 (GRCm39) |
I628V |
|
Het |
Lrrc38 |
G |
A |
4: 143,077,303 (GRCm39) |
G189R |
probably damaging |
Het |
Mfn1 |
A |
T |
3: 32,622,538 (GRCm39) |
I599F |
possibly damaging |
Het |
Nalcn |
T |
A |
14: 123,837,351 (GRCm39) |
R4S |
possibly damaging |
Het |
Nbeal2 |
C |
T |
9: 110,455,158 (GRCm39) |
R2580Q |
probably benign |
Het |
Nlrp4b |
A |
G |
7: 10,448,319 (GRCm39) |
N174S |
probably damaging |
Het |
Or3a4 |
T |
A |
11: 73,945,305 (GRCm39) |
R93S |
probably benign |
Het |
Or4q3 |
A |
T |
14: 50,583,179 (GRCm39) |
V240D |
probably damaging |
Het |
Or52a5 |
A |
T |
7: 103,426,802 (GRCm39) |
V250D |
probably damaging |
Het |
Or5p63 |
A |
G |
7: 107,811,014 (GRCm39) |
F241L |
possibly damaging |
Het |
Pabpc2 |
G |
A |
18: 39,908,520 (GRCm39) |
R595Q |
probably benign |
Het |
Pak6 |
C |
T |
2: 118,520,578 (GRCm39) |
Q190* |
probably null |
Het |
Pds5a |
A |
T |
5: 65,781,341 (GRCm39) |
H1046Q |
probably damaging |
Het |
Plin1 |
A |
G |
7: 79,373,028 (GRCm39) |
S314P |
probably benign |
Het |
Pramel20 |
T |
G |
4: 143,298,530 (GRCm39) |
Y158D |
probably benign |
Het |
Ptpra |
G |
A |
2: 30,328,351 (GRCm39) |
S224N |
probably damaging |
Het |
Rbp1 |
T |
G |
9: 98,326,709 (GRCm39) |
W107G |
probably damaging |
Het |
Rgs7bp |
T |
C |
13: 105,189,617 (GRCm39) |
N61D |
probably damaging |
Het |
Slc1a6 |
A |
G |
10: 78,627,067 (GRCm39) |
T135A |
probably damaging |
Het |
Smarcc1 |
T |
A |
9: 110,031,602 (GRCm39) |
D783E |
probably benign |
Het |
Sufu |
G |
T |
19: 46,389,636 (GRCm39) |
E86* |
probably null |
Het |
Synm |
A |
T |
7: 67,383,654 (GRCm39) |
M1336K |
probably benign |
Het |
Tgm1 |
C |
T |
14: 55,942,341 (GRCm39) |
G670D |
probably damaging |
Het |
Tmc8 |
T |
G |
11: 117,682,186 (GRCm39) |
|
probably null |
Het |
Togaram1 |
T |
C |
12: 65,053,686 (GRCm39) |
V1322A |
probably damaging |
Het |
Uxs1 |
A |
T |
1: 43,810,911 (GRCm39) |
I225K |
possibly damaging |
Het |
Vil1 |
G |
T |
1: 74,474,052 (GRCm39) |
E796* |
probably null |
Het |
Vmn1r174 |
T |
C |
7: 23,453,568 (GRCm39) |
F78S |
probably damaging |
Het |
Vps13d |
T |
A |
4: 144,879,321 (GRCm39) |
I1501F |
|
Het |
Vps8 |
A |
T |
16: 21,393,780 (GRCm39) |
T1216S |
possibly damaging |
Het |
Yipf4 |
G |
T |
17: 74,800,967 (GRCm39) |
R95L |
probably damaging |
Het |
Zan |
T |
A |
5: 137,465,346 (GRCm39) |
T470S |
probably damaging |
Het |
Zfp113 |
G |
T |
5: 138,143,258 (GRCm39) |
H331N |
probably damaging |
Het |
Zfp62 |
A |
G |
11: 49,106,902 (GRCm39) |
Y331C |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,327,610 (GRCm39) |
H580R |
probably benign |
Het |
|
Other mutations in Fbxo34 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Fbxo34
|
APN |
14 |
47,766,931 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01337:Fbxo34
|
APN |
14 |
47,767,674 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01418:Fbxo34
|
APN |
14 |
47,768,241 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02069:Fbxo34
|
APN |
14 |
47,767,070 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02829:Fbxo34
|
APN |
14 |
47,767,146 (GRCm39) |
missense |
probably benign |
0.00 |
R0601:Fbxo34
|
UTSW |
14 |
47,767,714 (GRCm39) |
missense |
probably benign |
|
R0714:Fbxo34
|
UTSW |
14 |
47,767,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R1186:Fbxo34
|
UTSW |
14 |
47,768,043 (GRCm39) |
missense |
probably damaging |
0.99 |
R1714:Fbxo34
|
UTSW |
14 |
47,766,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R1842:Fbxo34
|
UTSW |
14 |
47,768,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R2127:Fbxo34
|
UTSW |
14 |
47,767,563 (GRCm39) |
missense |
probably damaging |
0.98 |
R4199:Fbxo34
|
UTSW |
14 |
47,768,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Fbxo34
|
UTSW |
14 |
47,767,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Fbxo34
|
UTSW |
14 |
47,768,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Fbxo34
|
UTSW |
14 |
47,768,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Fbxo34
|
UTSW |
14 |
47,766,911 (GRCm39) |
missense |
probably benign |
0.26 |
R5475:Fbxo34
|
UTSW |
14 |
47,766,802 (GRCm39) |
missense |
probably benign |
0.01 |
R5888:Fbxo34
|
UTSW |
14 |
47,767,176 (GRCm39) |
missense |
probably damaging |
0.98 |
R6573:Fbxo34
|
UTSW |
14 |
47,767,124 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7236:Fbxo34
|
UTSW |
14 |
47,767,841 (GRCm39) |
missense |
probably benign |
0.00 |
R7257:Fbxo34
|
UTSW |
14 |
47,738,329 (GRCm39) |
critical splice donor site |
probably null |
|
R7381:Fbxo34
|
UTSW |
14 |
47,767,992 (GRCm39) |
missense |
probably benign |
0.02 |
R7515:Fbxo34
|
UTSW |
14 |
47,767,798 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7562:Fbxo34
|
UTSW |
14 |
47,767,135 (GRCm39) |
missense |
probably benign |
0.00 |
R9094:Fbxo34
|
UTSW |
14 |
47,767,928 (GRCm39) |
missense |
probably benign |
0.00 |
R9620:Fbxo34
|
UTSW |
14 |
47,768,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Fbxo34
|
UTSW |
14 |
47,768,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9710:Fbxo34
|
UTSW |
14 |
47,768,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|