Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A4gnt |
A |
G |
9: 99,502,284 (GRCm39) |
H148R |
probably damaging |
Het |
Acrbp |
A |
G |
6: 125,037,885 (GRCm39) |
D394G |
probably damaging |
Het |
Adam18 |
T |
C |
8: 25,115,868 (GRCm39) |
T609A |
probably benign |
Het |
Adam25 |
T |
A |
8: 41,208,991 (GRCm39) |
N752K |
probably benign |
Het |
Ano6 |
A |
C |
15: 95,811,469 (GRCm39) |
S176R |
probably benign |
Het |
Ano7 |
T |
C |
1: 93,302,918 (GRCm39) |
S19P |
probably benign |
Het |
Ap1b1 |
A |
G |
11: 4,976,364 (GRCm39) |
E437G |
probably damaging |
Het |
Arfgap2 |
T |
A |
2: 91,095,982 (GRCm39) |
C46* |
probably null |
Het |
Arhgef26 |
T |
A |
3: 62,247,981 (GRCm39) |
L355Q |
probably damaging |
Het |
B4galnt4 |
C |
T |
7: 140,644,983 (GRCm39) |
T219I |
probably damaging |
Het |
Bap1 |
C |
T |
14: 30,979,243 (GRCm39) |
|
probably benign |
Het |
Catip |
T |
G |
1: 74,401,954 (GRCm39) |
L43R |
probably damaging |
Het |
Ccdc177 |
G |
A |
12: 80,805,282 (GRCm39) |
R331C |
unknown |
Het |
Cep85l |
T |
C |
10: 53,195,690 (GRCm39) |
|
probably null |
Het |
Cfap206 |
T |
A |
4: 34,714,502 (GRCm39) |
Q398L |
probably benign |
Het |
Clec18a |
A |
G |
8: 111,800,368 (GRCm39) |
C352R |
probably damaging |
Het |
Clic6 |
A |
T |
16: 92,336,339 (GRCm39) |
Y549F |
probably damaging |
Het |
Cpne9 |
C |
T |
6: 113,270,034 (GRCm39) |
|
probably benign |
Het |
Cyb5r3 |
A |
C |
15: 83,042,836 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,090,471 (GRCm39) |
R2293K |
probably damaging |
Het |
Dnmbp |
C |
A |
19: 43,890,879 (GRCm39) |
R296L |
probably damaging |
Het |
Dtwd1 |
C |
A |
2: 125,996,694 (GRCm39) |
Q60K |
probably benign |
Het |
Esyt1 |
C |
A |
10: 128,352,443 (GRCm39) |
V723L |
probably benign |
Het |
Fbxo42 |
T |
C |
4: 140,926,335 (GRCm39) |
L339P |
probably damaging |
Het |
Furin |
A |
T |
7: 80,043,169 (GRCm39) |
N347K |
probably damaging |
Het |
Fzd7 |
T |
C |
1: 59,522,522 (GRCm39) |
M135T |
probably damaging |
Het |
Garin1b |
A |
G |
6: 29,323,896 (GRCm39) |
D207G |
probably damaging |
Het |
Hlf |
A |
G |
11: 90,278,632 (GRCm39) |
M144T |
probably benign |
Het |
Hyal5 |
C |
T |
6: 24,876,648 (GRCm39) |
Q174* |
probably null |
Het |
Kcnb1 |
T |
A |
2: 166,947,103 (GRCm39) |
M582L |
possibly damaging |
Het |
Kdm5d |
T |
C |
Y: 916,692 (GRCm39) |
Y391H |
probably damaging |
Het |
Khdc4 |
T |
A |
3: 88,604,032 (GRCm39) |
I283N |
probably damaging |
Het |
Kif21b |
C |
T |
1: 136,096,966 (GRCm39) |
T1297M |
probably damaging |
Het |
Krt8 |
T |
G |
15: 101,906,875 (GRCm39) |
N317T |
possibly damaging |
Het |
Lctl |
G |
T |
9: 64,045,196 (GRCm39) |
V372L |
probably benign |
Het |
Lig1 |
C |
T |
7: 13,042,432 (GRCm39) |
H822Y |
possibly damaging |
Het |
Lrrc4b |
A |
G |
7: 44,111,988 (GRCm39) |
D620G |
possibly damaging |
Het |
Mboat4 |
C |
T |
8: 34,582,275 (GRCm39) |
H10Y |
probably benign |
Het |
Med1 |
A |
T |
11: 98,048,066 (GRCm39) |
M910K |
probably benign |
Het |
Mia2 |
A |
T |
12: 59,154,911 (GRCm39) |
D209V |
probably damaging |
Het |
Mpp4 |
C |
T |
1: 59,184,017 (GRCm39) |
|
probably benign |
Het |
Mrgprb1 |
A |
T |
7: 48,097,225 (GRCm39) |
V229E |
possibly damaging |
Het |
Mtor |
T |
A |
4: 148,548,189 (GRCm39) |
C485S |
probably damaging |
Het |
Mx1 |
T |
C |
16: 97,258,628 (GRCm39) |
D23G |
probably damaging |
Het |
Myrfl |
T |
C |
10: 116,619,138 (GRCm39) |
D740G |
probably benign |
Het |
Myt1l |
G |
A |
12: 29,882,331 (GRCm39) |
G509R |
unknown |
Het |
Nav2 |
G |
A |
7: 49,185,661 (GRCm39) |
V874I |
probably damaging |
Het |
Ntrk3 |
A |
T |
7: 78,110,914 (GRCm39) |
N262K |
possibly damaging |
Het |
Opa1 |
A |
T |
16: 29,437,077 (GRCm39) |
D699V |
probably damaging |
Het |
Or10u4 |
C |
T |
10: 129,802,078 (GRCm39) |
A164T |
probably benign |
Het |
Or8b51 |
A |
G |
9: 38,569,374 (GRCm39) |
C105R |
possibly damaging |
Het |
Otud7a |
A |
G |
7: 63,407,181 (GRCm39) |
N495D |
possibly damaging |
Het |
Pcsk9 |
T |
C |
4: 106,320,950 (GRCm39) |
D53G |
probably benign |
Het |
Pdcd5 |
A |
G |
7: 35,346,421 (GRCm39) |
|
probably benign |
Het |
Phf21a |
C |
T |
2: 92,058,822 (GRCm39) |
P28L |
probably damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,158,130 (GRCm39) |
D573E |
probably damaging |
Het |
Ppp1r35 |
C |
T |
5: 137,777,406 (GRCm39) |
|
probably benign |
Het |
Ptprq |
T |
C |
10: 107,535,496 (GRCm39) |
Q423R |
probably damaging |
Het |
Pum1 |
A |
T |
4: 130,490,125 (GRCm39) |
Y699F |
probably benign |
Het |
Rabgef1 |
A |
G |
5: 130,241,841 (GRCm39) |
D415G |
probably benign |
Het |
Rapgef6 |
A |
G |
11: 54,413,943 (GRCm39) |
E23G |
probably benign |
Het |
Rpia |
G |
T |
6: 70,760,563 (GRCm39) |
C121* |
probably null |
Het |
Sanbr |
A |
G |
11: 23,525,483 (GRCm39) |
*719Q |
probably null |
Het |
Serpinb13 |
T |
A |
1: 106,926,427 (GRCm39) |
W201R |
probably damaging |
Het |
Sh3bp4 |
T |
C |
1: 89,065,456 (GRCm39) |
C17R |
probably damaging |
Het |
Sh3d21 |
A |
G |
4: 126,055,858 (GRCm39) |
|
probably benign |
Het |
Slamf6 |
A |
C |
1: 171,764,249 (GRCm39) |
N214T |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,361,130 (GRCm39) |
Y365H |
possibly damaging |
Het |
Sox18 |
T |
C |
2: 181,312,971 (GRCm39) |
|
probably null |
Het |
Spink7 |
A |
T |
18: 62,725,507 (GRCm39) |
F79I |
possibly damaging |
Het |
Srpk3 |
C |
T |
X: 72,818,555 (GRCm39) |
R82* |
probably null |
Het |
Sspo |
A |
T |
6: 48,470,244 (GRCm39) |
H4561L |
probably damaging |
Het |
Tcaf1 |
T |
C |
6: 42,653,793 (GRCm39) |
K700R |
probably benign |
Het |
Tcf25 |
G |
T |
8: 124,115,372 (GRCm39) |
R203L |
probably damaging |
Het |
Tcp11 |
T |
C |
17: 28,290,757 (GRCm39) |
I201V |
possibly damaging |
Het |
Tex2 |
T |
C |
11: 106,437,615 (GRCm39) |
D685G |
unknown |
Het |
Themis |
G |
T |
10: 28,637,195 (GRCm39) |
E100* |
probably null |
Het |
Tmem52b |
G |
A |
6: 129,491,221 (GRCm39) |
|
probably null |
Het |
Tnr |
C |
T |
1: 159,512,226 (GRCm39) |
|
probably benign |
Het |
Tpm2 |
T |
A |
4: 43,514,828 (GRCm39) |
E269V |
probably benign |
Het |
Tulp1 |
C |
T |
17: 28,581,651 (GRCm39) |
|
probably benign |
Het |
Tymp |
GC |
GCC |
15: 89,258,567 (GRCm39) |
|
probably null |
Het |
Ube2j2 |
A |
C |
4: 156,033,515 (GRCm39) |
K30Q |
possibly damaging |
Het |
Usp19 |
T |
A |
9: 108,369,807 (GRCm39) |
M1K |
probably null |
Het |
Vmn2r52 |
C |
A |
7: 9,910,197 (GRCm39) |
R6L |
probably benign |
Het |
Zbed4 |
G |
A |
15: 88,665,290 (GRCm39) |
V453M |
probably benign |
Het |
Zfp319 |
T |
C |
8: 96,055,099 (GRCm39) |
E368G |
probably benign |
Het |
Zfp366 |
A |
C |
13: 99,366,117 (GRCm39) |
E426A |
probably damaging |
Het |
Zfp687 |
A |
T |
3: 94,916,777 (GRCm39) |
I783N |
probably damaging |
Het |
|
Other mutations in Tox3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00948:Tox3
|
APN |
8 |
90,997,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02417:Tox3
|
APN |
8 |
90,984,759 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL02447:Tox3
|
APN |
8 |
90,984,781 (GRCm39) |
splice site |
probably benign |
|
R1139:Tox3
|
UTSW |
8 |
90,975,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Tox3
|
UTSW |
8 |
90,980,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Tox3
|
UTSW |
8 |
90,996,869 (GRCm39) |
missense |
probably benign |
0.31 |
R1906:Tox3
|
UTSW |
8 |
90,975,057 (GRCm39) |
unclassified |
probably benign |
|
R2847:Tox3
|
UTSW |
8 |
90,975,018 (GRCm39) |
nonsense |
probably null |
|
R2849:Tox3
|
UTSW |
8 |
90,975,018 (GRCm39) |
nonsense |
probably null |
|
R3703:Tox3
|
UTSW |
8 |
90,975,533 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3705:Tox3
|
UTSW |
8 |
90,975,533 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4984:Tox3
|
UTSW |
8 |
90,975,270 (GRCm39) |
unclassified |
probably benign |
|
R5722:Tox3
|
UTSW |
8 |
91,074,489 (GRCm39) |
critical splice donor site |
probably null |
|
R6291:Tox3
|
UTSW |
8 |
90,975,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6451:Tox3
|
UTSW |
8 |
90,984,687 (GRCm39) |
missense |
probably benign |
0.31 |
R7653:Tox3
|
UTSW |
8 |
90,975,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Tox3
|
UTSW |
8 |
90,975,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R8220:Tox3
|
UTSW |
8 |
90,984,708 (GRCm39) |
missense |
probably damaging |
0.97 |
R8337:Tox3
|
UTSW |
8 |
91,074,507 (GRCm39) |
missense |
probably damaging |
0.99 |
R8387:Tox3
|
UTSW |
8 |
90,984,595 (GRCm39) |
missense |
probably benign |
|
R8525:Tox3
|
UTSW |
8 |
91,001,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R8951:Tox3
|
UTSW |
8 |
91,074,543 (GRCm39) |
missense |
probably benign |
0.28 |
R9029:Tox3
|
UTSW |
8 |
90,996,864 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9182:Tox3
|
UTSW |
8 |
90,984,507 (GRCm39) |
missense |
probably benign |
0.03 |
R9645:Tox3
|
UTSW |
8 |
90,984,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R9790:Tox3
|
UTSW |
8 |
90,975,206 (GRCm39) |
missense |
unknown |
|
R9791:Tox3
|
UTSW |
8 |
90,975,206 (GRCm39) |
missense |
unknown |
|
|