Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
A |
T |
18: 70,601,134 (GRCm39) |
S249R |
possibly damaging |
Het |
Acadvl |
T |
A |
11: 69,901,181 (GRCm39) |
I638F |
probably damaging |
Het |
Acnat2 |
T |
A |
4: 49,380,587 (GRCm39) |
T264S |
probably benign |
Het |
Acrv1 |
C |
T |
9: 36,605,551 (GRCm39) |
Q33* |
probably null |
Het |
Actrt3 |
T |
A |
3: 30,653,901 (GRCm39) |
N33I |
probably damaging |
Het |
Alyref2 |
T |
C |
1: 171,331,168 (GRCm39) |
|
probably benign |
Het |
Ank2 |
C |
A |
3: 126,726,709 (GRCm39) |
E3712* |
probably null |
Het |
Ano7 |
C |
A |
1: 93,313,346 (GRCm39) |
H161Q |
probably benign |
Het |
Arhgap10 |
C |
A |
8: 78,085,216 (GRCm39) |
E451* |
probably null |
Het |
Arhgap29 |
T |
A |
3: 121,801,729 (GRCm39) |
Y748N |
probably damaging |
Het |
Arhgap45 |
C |
T |
10: 79,853,932 (GRCm39) |
Q149* |
probably null |
Het |
Asap2 |
C |
T |
12: 21,274,393 (GRCm39) |
H371Y |
probably damaging |
Het |
Atp6v1b1 |
T |
C |
6: 83,735,372 (GRCm39) |
I480T |
probably benign |
Het |
BC034090 |
T |
C |
1: 155,101,610 (GRCm39) |
D218G |
possibly damaging |
Het |
Brdt |
A |
T |
5: 107,491,450 (GRCm39) |
D74V |
probably damaging |
Het |
C4b |
A |
G |
17: 34,962,638 (GRCm39) |
|
probably benign |
Het |
Card11 |
T |
A |
5: 140,888,660 (GRCm39) |
K233* |
probably null |
Het |
Catip |
T |
G |
1: 74,401,929 (GRCm39) |
F35V |
possibly damaging |
Het |
Ccdc13 |
C |
T |
9: 121,648,647 (GRCm39) |
G247R |
probably damaging |
Het |
Cep97 |
T |
A |
16: 55,735,385 (GRCm39) |
D471V |
probably damaging |
Het |
Col17a1 |
A |
T |
19: 47,659,370 (GRCm39) |
L403Q |
probably damaging |
Het |
Crbn |
A |
G |
6: 106,767,906 (GRCm39) |
S194P |
possibly damaging |
Het |
Degs1l |
A |
G |
1: 180,878,884 (GRCm39) |
M1V |
probably null |
Het |
Dennd10 |
A |
G |
19: 60,806,021 (GRCm39) |
Y102C |
probably damaging |
Het |
Dhx58 |
T |
A |
11: 100,594,400 (GRCm39) |
H97L |
probably benign |
Het |
Dnah8 |
T |
C |
17: 31,073,914 (GRCm39) |
I4528T |
probably damaging |
Het |
Dpyd |
A |
G |
3: 118,404,092 (GRCm39) |
|
probably null |
Het |
Entpd1 |
A |
T |
19: 40,714,680 (GRCm39) |
Q263L |
probably benign |
Het |
Entrep1 |
A |
T |
19: 23,957,059 (GRCm39) |
I317N |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,218,244 (GRCm39) |
I130M |
probably benign |
Het |
Etv1 |
T |
C |
12: 38,902,261 (GRCm39) |
F264S |
probably benign |
Het |
Fat1 |
T |
C |
8: 45,463,519 (GRCm39) |
S1354P |
probably benign |
Het |
Fat4 |
C |
A |
3: 39,005,304 (GRCm39) |
T1901N |
probably damaging |
Het |
Fmo3 |
A |
G |
1: 162,795,356 (GRCm39) |
F160L |
possibly damaging |
Het |
Fyb2 |
T |
A |
4: 104,861,113 (GRCm39) |
D592E |
probably damaging |
Het |
Gjb4 |
T |
C |
4: 127,245,663 (GRCm39) |
M93V |
possibly damaging |
Het |
Gm5089 |
C |
A |
14: 122,673,566 (GRCm39) |
G52* |
probably null |
Het |
Gm6401 |
G |
T |
14: 41,788,840 (GRCm39) |
N76K |
probably benign |
Het |
Gm6871 |
A |
G |
7: 41,195,901 (GRCm39) |
S279P |
probably damaging |
Het |
Gtf2ird2 |
T |
G |
5: 134,240,081 (GRCm39) |
V301G |
probably benign |
Het |
H2bw2 |
A |
C |
X: 135,828,216 (GRCm39) |
D35A |
unknown |
Het |
Hfm1 |
A |
G |
5: 107,028,380 (GRCm39) |
F817L |
probably damaging |
Het |
Hfm1 |
T |
C |
5: 107,043,869 (GRCm39) |
E589G |
probably damaging |
Het |
Hivep2 |
A |
T |
10: 14,005,249 (GRCm39) |
K616* |
probably null |
Het |
Hmcn1 |
A |
T |
1: 150,551,735 (GRCm39) |
I2623N |
probably damaging |
Het |
Igf2bp3 |
G |
T |
6: 49,082,565 (GRCm39) |
A339E |
probably damaging |
Het |
Insyn2b |
T |
A |
11: 34,354,263 (GRCm39) |
|
probably null |
Het |
Irx4 |
T |
C |
13: 73,415,757 (GRCm39) |
I182T |
possibly damaging |
Het |
Jcad |
T |
C |
18: 4,674,511 (GRCm39) |
S758P |
probably damaging |
Het |
Klhdc4 |
A |
T |
8: 122,526,226 (GRCm39) |
Y304* |
probably null |
Het |
Lama1 |
A |
G |
17: 68,060,786 (GRCm39) |
I705V |
probably benign |
Het |
Mbd5 |
A |
G |
2: 49,147,044 (GRCm39) |
N418S |
probably benign |
Het |
Mmp21 |
C |
T |
7: 133,279,014 (GRCm39) |
V279I |
probably damaging |
Het |
Morc4 |
A |
C |
X: 138,755,279 (GRCm39) |
C272W |
probably damaging |
Het |
Mrm1 |
A |
T |
11: 84,709,518 (GRCm39) |
C180S |
probably damaging |
Het |
Ncor1 |
T |
C |
11: 62,313,831 (GRCm39) |
D103G |
probably damaging |
Het |
Ndrg4 |
A |
G |
8: 96,437,314 (GRCm39) |
D251G |
probably damaging |
Het |
Ndufaf5 |
T |
C |
2: 140,035,522 (GRCm39) |
V246A |
possibly damaging |
Het |
Noa1 |
T |
C |
5: 77,457,572 (GRCm39) |
E111G |
possibly damaging |
Het |
Nod1 |
C |
A |
6: 54,921,044 (GRCm39) |
V425F |
probably damaging |
Het |
Nos1 |
A |
T |
5: 118,033,984 (GRCm39) |
I369F |
probably damaging |
Het |
Nsun5 |
C |
T |
5: 135,400,170 (GRCm39) |
H98Y |
probably damaging |
Het |
Optn |
G |
A |
2: 5,057,941 (GRCm39) |
T76I |
possibly damaging |
Het |
Or14c39 |
G |
A |
7: 86,344,318 (GRCm39) |
R218H |
probably benign |
Het |
Or4k15c |
C |
G |
14: 50,321,827 (GRCm39) |
V104L |
probably benign |
Het |
Or5k1b |
A |
G |
16: 58,581,504 (GRCm39) |
F12L |
probably benign |
Het |
Or8d1b |
A |
G |
9: 38,887,202 (GRCm39) |
I77V |
probably damaging |
Het |
Or8g28 |
T |
C |
9: 39,169,867 (GRCm39) |
I37V |
probably benign |
Het |
Or9g19 |
C |
T |
2: 85,600,199 (GRCm39) |
T18I |
probably benign |
Het |
Oscar |
C |
T |
7: 3,614,855 (GRCm39) |
W22* |
probably null |
Het |
Palmd |
T |
A |
3: 116,717,306 (GRCm39) |
Y397F |
probably damaging |
Het |
Plk1 |
A |
G |
7: 121,768,121 (GRCm39) |
D447G |
probably damaging |
Het |
Plscr5 |
T |
A |
9: 92,087,581 (GRCm39) |
N183K |
probably damaging |
Het |
Polk |
T |
G |
13: 96,625,712 (GRCm39) |
D364A |
probably damaging |
Het |
Polr3d |
T |
C |
14: 70,680,450 (GRCm39) |
T36A |
probably benign |
Het |
Ppp1r10 |
A |
T |
17: 36,237,428 (GRCm39) |
R199S |
probably damaging |
Het |
Prkcz |
C |
T |
4: 155,346,969 (GRCm39) |
D388N |
probably damaging |
Het |
Prrc2b |
T |
C |
2: 32,102,234 (GRCm39) |
L769P |
probably damaging |
Het |
Psg26 |
A |
G |
7: 18,213,966 (GRCm39) |
V232A |
probably damaging |
Het |
Pth2r |
T |
C |
1: 65,375,997 (GRCm39) |
V85A |
possibly damaging |
Het |
Rbpms2 |
T |
C |
9: 65,566,494 (GRCm39) |
|
probably benign |
Het |
Reps1 |
A |
T |
10: 17,994,698 (GRCm39) |
D514V |
possibly damaging |
Het |
Riok3 |
G |
T |
18: 12,276,018 (GRCm39) |
R238L |
probably benign |
Het |
Rnf19a |
T |
C |
15: 36,244,353 (GRCm39) |
Q569R |
probably damaging |
Het |
Rorb |
G |
A |
19: 18,937,865 (GRCm39) |
T267I |
probably damaging |
Het |
Rrm2b |
A |
T |
15: 37,929,340 (GRCm39) |
M70K |
probably damaging |
Het |
Rsf1 |
A |
T |
7: 97,311,556 (GRCm39) |
E762V |
possibly damaging |
Het |
S100a2 |
G |
A |
3: 90,498,699 (GRCm39) |
V67I |
probably benign |
Het |
Skp1 |
T |
A |
11: 52,133,442 (GRCm39) |
D42E |
probably benign |
Het |
Slc22a4 |
A |
T |
11: 53,918,801 (GRCm39) |
M1K |
probably null |
Het |
Slc2a9 |
T |
A |
5: 38,539,387 (GRCm39) |
Q371L |
probably damaging |
Het |
Slc4a9 |
A |
G |
18: 36,665,075 (GRCm39) |
T475A |
probably benign |
Het |
Slc8b1 |
A |
G |
5: 120,657,717 (GRCm39) |
N60S |
probably damaging |
Het |
Slx4 |
A |
C |
16: 3,817,022 (GRCm39) |
D66E |
probably benign |
Het |
Smg8 |
A |
T |
11: 86,977,113 (GRCm39) |
I156N |
probably damaging |
Het |
Snx25 |
A |
T |
8: 46,569,244 (GRCm39) |
C218S |
possibly damaging |
Het |
Sulf2 |
T |
C |
2: 165,920,992 (GRCm39) |
I784V |
probably benign |
Het |
Tatdn2 |
G |
T |
6: 113,674,888 (GRCm39) |
R72L |
possibly damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,445,918 (GRCm39) |
D91G |
possibly damaging |
Het |
Tifab |
C |
A |
13: 56,324,433 (GRCm39) |
R3S |
probably benign |
Het |
Tm4sf1 |
A |
T |
3: 57,200,304 (GRCm39) |
S104T |
probably damaging |
Het |
Tmem132e |
T |
A |
11: 82,334,343 (GRCm39) |
I618N |
probably damaging |
Het |
Ttc7b |
A |
T |
12: 100,369,667 (GRCm39) |
D367E |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,719,203 (GRCm39) |
D678G |
possibly damaging |
Het |
Vgll4 |
A |
G |
6: 114,934,895 (GRCm39) |
|
probably null |
Het |
Vmn2r124 |
A |
T |
17: 18,282,187 (GRCm39) |
|
probably benign |
Het |
Vmn2r2 |
T |
C |
3: 64,024,820 (GRCm39) |
D587G |
probably benign |
Het |
Vmn2r84 |
G |
A |
10: 130,226,968 (GRCm39) |
A290V |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,818,811 (GRCm39) |
S1077R |
probably benign |
Het |
Vsig10 |
C |
T |
5: 117,489,719 (GRCm39) |
A495V |
probably benign |
Het |
Vwa3a |
A |
T |
7: 120,403,254 (GRCm39) |
|
probably null |
Het |
Zfhx2 |
C |
A |
14: 55,303,455 (GRCm39) |
A1510S |
possibly damaging |
Het |
Zfp142 |
T |
A |
1: 74,611,389 (GRCm39) |
D601V |
probably damaging |
Het |
Zfp62 |
T |
C |
11: 49,108,510 (GRCm39) |
I867T |
probably benign |
Het |
|
Other mutations in Fbxw13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02033:Fbxw13
|
APN |
9 |
109,010,484 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02455:Fbxw13
|
APN |
9 |
109,012,255 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03154:Fbxw13
|
APN |
9 |
109,010,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R0304:Fbxw13
|
UTSW |
9 |
109,023,789 (GRCm39) |
missense |
probably benign |
0.02 |
R1259:Fbxw13
|
UTSW |
9 |
109,014,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R1912:Fbxw13
|
UTSW |
9 |
109,010,611 (GRCm39) |
missense |
probably benign |
0.10 |
R2877:Fbxw13
|
UTSW |
9 |
109,010,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R2878:Fbxw13
|
UTSW |
9 |
109,010,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R3085:Fbxw13
|
UTSW |
9 |
109,013,299 (GRCm39) |
nonsense |
probably null |
|
R4321:Fbxw13
|
UTSW |
9 |
109,010,503 (GRCm39) |
missense |
probably benign |
0.10 |
R4969:Fbxw13
|
UTSW |
9 |
109,010,592 (GRCm39) |
splice site |
probably null |
|
R5024:Fbxw13
|
UTSW |
9 |
109,008,403 (GRCm39) |
missense |
probably benign |
0.00 |
R5450:Fbxw13
|
UTSW |
9 |
109,013,225 (GRCm39) |
missense |
probably benign |
0.41 |
R5957:Fbxw13
|
UTSW |
9 |
109,021,734 (GRCm39) |
critical splice donor site |
probably null |
|
R6801:Fbxw13
|
UTSW |
9 |
109,023,795 (GRCm39) |
missense |
probably null |
1.00 |
R7448:Fbxw13
|
UTSW |
9 |
109,014,471 (GRCm39) |
missense |
unknown |
|
R7710:Fbxw13
|
UTSW |
9 |
109,024,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R8163:Fbxw13
|
UTSW |
9 |
109,012,122 (GRCm39) |
missense |
probably benign |
0.45 |
R8320:Fbxw13
|
UTSW |
9 |
109,012,134 (GRCm39) |
missense |
probably benign |
0.02 |
R8714:Fbxw13
|
UTSW |
9 |
109,023,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8845:Fbxw13
|
UTSW |
9 |
109,023,833 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8884:Fbxw13
|
UTSW |
9 |
109,010,469 (GRCm39) |
missense |
probably benign |
0.00 |
R8979:Fbxw13
|
UTSW |
9 |
109,013,197 (GRCm39) |
missense |
probably damaging |
0.96 |
R9223:Fbxw13
|
UTSW |
9 |
109,024,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Fbxw13
|
UTSW |
9 |
109,008,382 (GRCm39) |
missense |
probably benign |
0.17 |
X0065:Fbxw13
|
UTSW |
9 |
109,021,776 (GRCm39) |
missense |
probably damaging |
0.96 |
|