Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adra1d |
A |
T |
2: 131,403,289 (GRCm39) |
M267K |
probably damaging |
Het |
Aen |
T |
C |
7: 78,555,793 (GRCm39) |
|
probably null |
Het |
Ano2 |
A |
G |
6: 125,992,502 (GRCm39) |
D825G |
probably damaging |
Het |
Bdh2 |
T |
C |
3: 135,001,025 (GRCm39) |
S142P |
probably damaging |
Het |
Celsr1 |
A |
G |
15: 85,800,924 (GRCm39) |
L2507P |
possibly damaging |
Het |
Ces3a |
T |
C |
8: 105,782,212 (GRCm39) |
F308S |
probably benign |
Het |
Cfap47 |
C |
T |
X: 78,454,218 (GRCm39) |
R1646Q |
probably damaging |
Het |
Chd4 |
T |
A |
6: 125,082,320 (GRCm39) |
M603K |
probably damaging |
Het |
Cit |
T |
C |
5: 116,106,068 (GRCm39) |
V984A |
probably benign |
Het |
Clstn3 |
A |
T |
6: 124,436,166 (GRCm39) |
D194E |
probably damaging |
Het |
Ctdp1 |
T |
C |
18: 80,492,696 (GRCm39) |
R600G |
probably benign |
Het |
Ctnnd1 |
C |
T |
2: 84,439,907 (GRCm39) |
G801D |
probably damaging |
Het |
Dgkg |
A |
G |
16: 22,407,049 (GRCm39) |
F179L |
probably damaging |
Het |
Dlg3 |
G |
A |
X: 99,817,827 (GRCm39) |
D379N |
probably damaging |
Het |
Drd2 |
G |
T |
9: 49,314,571 (GRCm39) |
R267S |
probably benign |
Het |
Dsg1b |
T |
C |
18: 20,542,675 (GRCm39) |
*1061Q |
probably null |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Edc3 |
T |
C |
9: 57,620,826 (GRCm39) |
V49A |
probably damaging |
Het |
Ern1 |
G |
A |
11: 106,300,750 (GRCm39) |
T548I |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,838,192 (GRCm39) |
D2684G |
possibly damaging |
Het |
Fam20a |
A |
G |
11: 109,565,449 (GRCm39) |
M454T |
probably benign |
Het |
Frmd4b |
A |
T |
6: 97,464,577 (GRCm39) |
C47S |
probably damaging |
Het |
Gtf2h1 |
T |
A |
7: 46,464,747 (GRCm39) |
I388N |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,453,206 (GRCm39) |
V571A |
possibly damaging |
Het |
Helz2 |
T |
A |
2: 180,870,841 (GRCm39) |
K2832* |
probably null |
Het |
Herc1 |
T |
A |
9: 66,372,688 (GRCm39) |
D3081E |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,591,566 (GRCm39) |
S1878T |
probably damaging |
Het |
Iars1 |
A |
G |
13: 49,841,605 (GRCm39) |
|
probably null |
Het |
Il17rd |
A |
T |
14: 26,816,835 (GRCm39) |
K180M |
probably damaging |
Het |
Ints6l |
T |
A |
X: 55,550,110 (GRCm39) |
H678Q |
probably benign |
Het |
Khdrbs1 |
A |
G |
4: 129,613,830 (GRCm39) |
|
probably null |
Het |
Lce3a |
A |
C |
3: 92,832,837 (GRCm39) |
S88A |
unknown |
Het |
Lgals12 |
C |
T |
19: 7,578,606 (GRCm39) |
|
probably null |
Het |
Lnpk |
T |
C |
2: 74,399,373 (GRCm39) |
T57A |
probably benign |
Het |
Lrp2bp |
C |
T |
8: 46,466,206 (GRCm39) |
T105I |
probably benign |
Het |
Lrrc4c |
C |
G |
2: 97,459,657 (GRCm39) |
N94K |
possibly damaging |
Het |
Mag |
A |
T |
7: 30,600,066 (GRCm39) |
Y571* |
probably null |
Het |
Mbd1 |
T |
A |
18: 74,410,449 (GRCm39) |
D583E |
probably damaging |
Het |
Mill1 |
T |
A |
7: 17,998,544 (GRCm39) |
Y251* |
probably null |
Het |
Mllt10 |
T |
C |
2: 18,211,871 (GRCm39) |
I928T |
probably benign |
Het |
Ms4a18 |
T |
C |
19: 10,991,029 (GRCm39) |
T22A |
probably benign |
Het |
Mtmr14 |
T |
C |
6: 113,257,700 (GRCm39) |
F250L |
probably damaging |
Het |
Mtmr3 |
A |
T |
11: 4,449,032 (GRCm39) |
W244R |
probably damaging |
Het |
Myorg |
A |
G |
4: 41,497,704 (GRCm39) |
I642T |
probably damaging |
Het |
Nat10 |
C |
A |
2: 103,556,522 (GRCm39) |
E885D |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,321,054 (GRCm39) |
L2055H |
probably damaging |
Het |
Necab3 |
T |
A |
2: 154,388,999 (GRCm39) |
I192F |
possibly damaging |
Het |
Nedd4 |
T |
A |
9: 72,650,000 (GRCm39) |
N783K |
probably damaging |
Het |
Nf2 |
A |
T |
11: 4,749,899 (GRCm39) |
W61R |
probably damaging |
Het |
Nox4 |
T |
A |
7: 87,023,588 (GRCm39) |
F491L |
probably benign |
Het |
Omt2b |
G |
A |
9: 78,235,457 (GRCm39) |
|
probably benign |
Het |
Or4c125 |
A |
T |
2: 89,170,009 (GRCm39) |
Y212* |
probably null |
Het |
Or4c127 |
T |
A |
2: 89,832,774 (GRCm39) |
I8N |
probably damaging |
Het |
Or8i2 |
A |
G |
2: 86,852,855 (GRCm39) |
V11A |
probably benign |
Het |
Osbpl5 |
A |
T |
7: 143,247,596 (GRCm39) |
Y723* |
probably null |
Het |
Otop2 |
T |
C |
11: 115,217,757 (GRCm39) |
S198P |
possibly damaging |
Het |
Pgam5 |
T |
G |
5: 110,413,785 (GRCm39) |
H126P |
probably damaging |
Het |
Phip |
A |
T |
9: 82,753,868 (GRCm39) |
N1625K |
probably damaging |
Het |
Phospho2 |
T |
A |
2: 69,626,451 (GRCm39) |
Y202* |
probably null |
Het |
Pkd1l3 |
T |
A |
8: 110,347,156 (GRCm39) |
H176Q |
unknown |
Het |
Plxdc2 |
A |
G |
2: 16,570,147 (GRCm39) |
R109G |
probably damaging |
Het |
Prorsd1 |
T |
C |
11: 29,463,592 (GRCm39) |
K57E |
probably benign |
Het |
Rnf150 |
A |
T |
8: 83,591,020 (GRCm39) |
R128W |
probably damaging |
Het |
Samm50 |
G |
A |
15: 84,084,625 (GRCm39) |
|
probably null |
Het |
Skint6 |
A |
T |
4: 112,722,909 (GRCm39) |
Y889* |
probably null |
Het |
Slc35b1 |
T |
C |
11: 95,276,640 (GRCm39) |
Y40H |
probably damaging |
Het |
Speg |
A |
G |
1: 75,394,371 (GRCm39) |
H1722R |
probably damaging |
Het |
Suz12 |
T |
C |
11: 79,913,024 (GRCm39) |
L356P |
probably damaging |
Het |
Tln2 |
T |
G |
9: 67,262,503 (GRCm39) |
I585L |
probably damaging |
Het |
Trim2 |
G |
A |
3: 84,098,225 (GRCm39) |
Q359* |
probably null |
Het |
Ttc28 |
T |
C |
5: 111,371,362 (GRCm39) |
Y635H |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,543,549 (GRCm39) |
E33146K |
probably damaging |
Het |
Vcp |
G |
T |
4: 42,982,547 (GRCm39) |
T715K |
probably benign |
Het |
Vmn1r230 |
T |
A |
17: 21,067,355 (GRCm39) |
N181K |
probably benign |
Het |
Vmn2r17 |
T |
A |
5: 109,582,144 (GRCm39) |
M511K |
possibly damaging |
Het |
Wdfy3 |
C |
T |
5: 102,055,408 (GRCm39) |
R1554Q |
possibly damaging |
Het |
Zfp112 |
A |
T |
7: 23,824,863 (GRCm39) |
Q277L |
probably damaging |
Het |
Zfp850 |
T |
C |
7: 27,684,620 (GRCm39) |
E42G |
probably damaging |
Het |
Zfp976 |
G |
A |
7: 42,262,695 (GRCm39) |
P381S |
probably damaging |
Het |
Zzef1 |
A |
T |
11: 72,800,982 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Fbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00510:Fbp2
|
APN |
13 |
62,989,698 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01284:Fbp2
|
APN |
13 |
62,988,099 (GRCm39) |
missense |
probably benign |
0.32 |
R0020:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0218:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Fbp2
|
UTSW |
13 |
63,001,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R1530:Fbp2
|
UTSW |
13 |
62,984,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Fbp2
|
UTSW |
13 |
63,001,875 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2091:Fbp2
|
UTSW |
13 |
63,006,021 (GRCm39) |
missense |
probably damaging |
0.99 |
R3943:Fbp2
|
UTSW |
13 |
62,989,607 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4092:Fbp2
|
UTSW |
13 |
62,988,174 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4124:Fbp2
|
UTSW |
13 |
63,002,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R4508:Fbp2
|
UTSW |
13 |
62,989,679 (GRCm39) |
missense |
probably damaging |
0.96 |
R4841:Fbp2
|
UTSW |
13 |
63,002,727 (GRCm39) |
missense |
probably benign |
0.29 |
R5576:Fbp2
|
UTSW |
13 |
62,985,005 (GRCm39) |
missense |
probably benign |
0.00 |
R5893:Fbp2
|
UTSW |
13 |
62,984,916 (GRCm39) |
missense |
probably benign |
0.03 |
R6989:Fbp2
|
UTSW |
13 |
63,005,991 (GRCm39) |
missense |
probably damaging |
0.99 |
R7156:Fbp2
|
UTSW |
13 |
62,989,675 (GRCm39) |
missense |
probably benign |
0.02 |
R7340:Fbp2
|
UTSW |
13 |
62,985,061 (GRCm39) |
missense |
probably damaging |
0.98 |
R7366:Fbp2
|
UTSW |
13 |
62,985,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7413:Fbp2
|
UTSW |
13 |
62,985,067 (GRCm39) |
missense |
probably benign |
0.00 |
R8855:Fbp2
|
UTSW |
13 |
62,989,709 (GRCm39) |
missense |
probably benign |
0.00 |
R8866:Fbp2
|
UTSW |
13 |
62,989,709 (GRCm39) |
missense |
probably benign |
0.00 |
R9136:Fbp2
|
UTSW |
13 |
63,002,840 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9233:Fbp2
|
UTSW |
13 |
62,989,622 (GRCm39) |
missense |
possibly damaging |
0.77 |
|