Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,241,118 (GRCm39) |
I994V |
probably benign |
Het |
Acan |
T |
G |
7: 78,738,055 (GRCm39) |
|
probably null |
Het |
Adamts12 |
G |
A |
15: 11,277,425 (GRCm39) |
V680I |
possibly damaging |
Het |
Adgrg7 |
T |
C |
16: 56,545,342 (GRCm39) |
I712V |
probably damaging |
Het |
Adgrl3 |
A |
G |
5: 81,942,597 (GRCm39) |
H1477R |
probably damaging |
Het |
Adgrv1 |
T |
A |
13: 81,666,245 (GRCm39) |
D1937V |
probably damaging |
Het |
Alms1 |
T |
C |
6: 85,599,088 (GRCm39) |
S1305P |
probably benign |
Het |
Banp |
T |
A |
8: 122,701,236 (GRCm39) |
M39K |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,135,111 (GRCm39) |
T75A |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
Bltp3b |
G |
A |
10: 89,645,518 (GRCm39) |
G1197D |
probably damaging |
Het |
Brinp2 |
C |
T |
1: 158,078,938 (GRCm39) |
C295Y |
probably damaging |
Het |
Card11 |
C |
T |
5: 140,883,993 (GRCm39) |
V429I |
probably benign |
Het |
Cdca3 |
G |
A |
6: 124,809,538 (GRCm39) |
R184H |
probably benign |
Het |
Cep104 |
A |
G |
4: 154,067,509 (GRCm39) |
|
probably null |
Het |
Clspn |
A |
G |
4: 126,484,430 (GRCm39) |
K1196R |
possibly damaging |
Het |
Cntnap5b |
A |
G |
1: 99,894,994 (GRCm39) |
T89A |
possibly damaging |
Het |
Cpne9 |
A |
T |
6: 113,266,974 (GRCm39) |
I136L |
probably damaging |
Het |
Crat |
T |
A |
2: 30,296,477 (GRCm39) |
I330F |
probably damaging |
Het |
Ctbp2 |
G |
T |
7: 132,615,697 (GRCm39) |
Q413K |
possibly damaging |
Het |
D630045J12Rik |
T |
C |
6: 38,151,238 (GRCm39) |
E1220G |
probably damaging |
Het |
Dap |
A |
G |
15: 31,235,985 (GRCm39) |
D41G |
probably damaging |
Het |
Dnah14 |
A |
G |
1: 181,590,967 (GRCm39) |
I3287V |
probably benign |
Het |
Dsp |
A |
G |
13: 38,356,819 (GRCm39) |
H233R |
probably damaging |
Het |
Dst |
T |
C |
1: 34,231,770 (GRCm39) |
I3121T |
probably benign |
Het |
Espnl |
T |
G |
1: 91,250,036 (GRCm39) |
L61R |
probably damaging |
Het |
Evc2 |
T |
C |
5: 37,527,983 (GRCm39) |
S331P |
possibly damaging |
Het |
Gars1 |
A |
G |
6: 55,050,344 (GRCm39) |
E535G |
probably benign |
Het |
Hfm1 |
A |
G |
5: 107,043,084 (GRCm39) |
I650T |
possibly damaging |
Het |
Iyd |
T |
A |
10: 3,495,690 (GRCm39) |
I116N |
probably damaging |
Het |
Kif16b |
A |
G |
2: 142,553,792 (GRCm39) |
L1002S |
probably damaging |
Het |
Kifbp |
C |
T |
10: 62,394,843 (GRCm39) |
V600I |
possibly damaging |
Het |
Lgi1 |
G |
A |
19: 38,272,468 (GRCm39) |
G113D |
probably damaging |
Het |
Lgi2 |
G |
A |
5: 52,695,604 (GRCm39) |
R452C |
probably damaging |
Het |
Man2b2 |
T |
G |
5: 36,970,722 (GRCm39) |
N764T |
probably damaging |
Het |
Mrps18b |
A |
G |
17: 36,221,587 (GRCm39) |
I246T |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,426,287 (GRCm39) |
T4795A |
possibly damaging |
Het |
Mybl2 |
G |
A |
2: 162,924,513 (GRCm39) |
G627D |
possibly damaging |
Het |
Ndufb8 |
C |
T |
19: 44,543,794 (GRCm39) |
R16K |
probably benign |
Het |
Or5k17 |
A |
T |
16: 58,746,121 (GRCm39) |
V271E |
possibly damaging |
Het |
P4htm |
C |
T |
9: 108,457,991 (GRCm39) |
V335M |
probably damaging |
Het |
Plod3 |
G |
T |
5: 137,019,335 (GRCm39) |
V360L |
probably benign |
Het |
Podxl2 |
C |
T |
6: 88,826,632 (GRCm39) |
D161N |
probably benign |
Het |
Polr1b |
G |
T |
2: 128,960,993 (GRCm39) |
V651L |
probably benign |
Het |
Prr14 |
T |
C |
7: 127,075,749 (GRCm39) |
S586P |
probably benign |
Het |
Pum3 |
C |
T |
19: 27,371,728 (GRCm39) |
G575D |
probably benign |
Het |
Rnf157 |
C |
A |
11: 116,251,192 (GRCm39) |
A111S |
probably benign |
Het |
Robo3 |
A |
G |
9: 37,344,212 (GRCm39) |
L29P |
probably damaging |
Het |
Smarca5 |
T |
C |
8: 81,452,680 (GRCm39) |
N342S |
probably damaging |
Het |
Specc1 |
T |
A |
11: 62,009,078 (GRCm39) |
I198K |
probably benign |
Het |
Tmem177 |
A |
T |
1: 119,837,744 (GRCm39) |
*312R |
probably null |
Het |
Tom1l2 |
A |
T |
11: 60,152,026 (GRCm39) |
M172K |
probably benign |
Het |
Tsc22d4 |
T |
C |
5: 137,756,414 (GRCm39) |
V3A |
unknown |
Het |
Vmn1r128 |
G |
T |
7: 21,083,668 (GRCm39) |
G124V |
probably damaging |
Het |
Vmn1r15 |
T |
C |
6: 57,235,342 (GRCm39) |
I70T |
probably benign |
Het |
Vmn2r60 |
A |
G |
7: 41,844,631 (GRCm39) |
T665A |
probably damaging |
Het |
Vmn2r83 |
T |
C |
10: 79,314,790 (GRCm39) |
F346S |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,910,691 (GRCm39) |
D694E |
probably damaging |
Het |
|
Other mutations in Pbx3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02468:Pbx3
|
APN |
2 |
34,114,589 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02524:Pbx3
|
APN |
2 |
34,260,830 (GRCm39) |
splice site |
probably benign |
|
PIT4812001:Pbx3
|
UTSW |
2 |
34,114,631 (GRCm39) |
missense |
probably damaging |
0.96 |
R0302:Pbx3
|
UTSW |
2 |
34,114,572 (GRCm39) |
missense |
probably benign |
0.42 |
R1526:Pbx3
|
UTSW |
2 |
34,261,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R1529:Pbx3
|
UTSW |
2 |
34,094,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1627:Pbx3
|
UTSW |
2 |
34,065,965 (GRCm39) |
missense |
probably benign |
0.00 |
R1652:Pbx3
|
UTSW |
2 |
34,114,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Pbx3
|
UTSW |
2 |
34,114,464 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1850:Pbx3
|
UTSW |
2 |
34,066,832 (GRCm39) |
missense |
probably benign |
0.34 |
R2908:Pbx3
|
UTSW |
2 |
34,062,933 (GRCm39) |
missense |
probably damaging |
0.96 |
R4073:Pbx3
|
UTSW |
2 |
34,114,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R5212:Pbx3
|
UTSW |
2 |
34,178,793 (GRCm39) |
intron |
probably benign |
|
R5897:Pbx3
|
UTSW |
2 |
34,261,920 (GRCm39) |
missense |
probably benign |
0.01 |
R7504:Pbx3
|
UTSW |
2 |
34,065,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R7812:Pbx3
|
UTSW |
2 |
34,114,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R8079:Pbx3
|
UTSW |
2 |
34,068,240 (GRCm39) |
missense |
probably benign |
0.36 |
R9104:Pbx3
|
UTSW |
2 |
34,114,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R9114:Pbx3
|
UTSW |
2 |
34,103,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Pbx3
|
UTSW |
2 |
34,260,938 (GRCm39) |
unclassified |
probably benign |
|
R9336:Pbx3
|
UTSW |
2 |
34,261,832 (GRCm39) |
missense |
probably benign |
0.30 |
R9420:Pbx3
|
UTSW |
2 |
34,103,348 (GRCm39) |
missense |
probably damaging |
0.96 |
R9445:Pbx3
|
UTSW |
2 |
34,114,555 (GRCm39) |
critical splice donor site |
probably benign |
|
|