Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
A |
T |
12: 55,106,295 (GRCm39) |
S143T |
probably benign |
Het |
9030624G23Rik |
A |
T |
12: 24,094,724 (GRCm39) |
M149K |
unknown |
Het |
Aadacl4fm4 |
A |
T |
4: 144,396,913 (GRCm39) |
I273K |
possibly damaging |
Het |
Agpat3 |
T |
A |
10: 78,119,034 (GRCm39) |
I187F |
probably benign |
Het |
Ahcyl1 |
C |
T |
3: 107,576,467 (GRCm39) |
A332T |
probably damaging |
Het |
Aldh3b3 |
A |
G |
19: 4,014,871 (GRCm39) |
I123V |
possibly damaging |
Het |
Ap5z1 |
T |
A |
5: 142,456,313 (GRCm39) |
|
probably null |
Het |
Apob |
A |
T |
12: 8,061,933 (GRCm39) |
I3472F |
probably benign |
Het |
Arhgef33 |
C |
T |
17: 80,680,914 (GRCm39) |
P685S |
probably benign |
Het |
Arhgef4 |
T |
C |
1: 34,845,478 (GRCm39) |
I130T |
probably damaging |
Het |
Arnt2 |
A |
T |
7: 83,954,406 (GRCm39) |
F263I |
probably benign |
Het |
Bbof1 |
A |
G |
12: 84,466,763 (GRCm39) |
R177G |
probably damaging |
Het |
Bbs2 |
C |
A |
8: 94,807,764 (GRCm39) |
G372W |
probably damaging |
Het |
Blmh |
T |
A |
11: 76,836,721 (GRCm39) |
|
probably null |
Het |
Ccdc30 |
A |
T |
4: 119,209,910 (GRCm39) |
|
probably null |
Het |
Cdca7l |
G |
T |
12: 117,837,467 (GRCm39) |
L219F |
probably damaging |
Het |
Cenpu |
C |
A |
8: 47,015,499 (GRCm39) |
A138E |
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,972,321 (GRCm39) |
T13S |
probably benign |
Het |
Clasp2 |
A |
G |
9: 113,733,016 (GRCm39) |
M951V |
probably benign |
Het |
Clca4a |
A |
G |
3: 144,674,166 (GRCm39) |
S190P |
probably benign |
Het |
Clcn4 |
A |
G |
7: 7,298,167 (GRCm39) |
V74A |
probably benign |
Het |
Cntln |
C |
T |
4: 84,981,561 (GRCm39) |
T913M |
possibly damaging |
Het |
Cntnap4 |
T |
A |
8: 113,478,829 (GRCm39) |
V185E |
probably damaging |
Het |
Col26a1 |
C |
T |
5: 136,777,031 (GRCm39) |
|
probably null |
Het |
Ctcf |
A |
T |
8: 106,390,690 (GRCm39) |
Q99L |
possibly damaging |
Het |
Dgke |
T |
C |
11: 88,931,682 (GRCm39) |
Q524R |
probably damaging |
Het |
Dhrs7 |
A |
T |
12: 72,699,234 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
C |
1: 46,289,110 (GRCm39) |
Y2969H |
probably damaging |
Het |
Dync1h1 |
T |
G |
12: 110,582,891 (GRCm39) |
I358S |
probably damaging |
Het |
Efcab3 |
A |
C |
11: 105,008,150 (GRCm39) |
D410A |
probably benign |
Het |
Emilin2 |
T |
C |
17: 71,580,908 (GRCm39) |
D606G |
probably benign |
Het |
Ermard |
C |
T |
17: 15,283,875 (GRCm39) |
T622I |
possibly damaging |
Het |
Exo1 |
A |
G |
1: 175,728,562 (GRCm39) |
D542G |
probably benign |
Het |
Fgd5 |
A |
T |
6: 91,964,262 (GRCm39) |
D165V |
probably benign |
Het |
Gdap1 |
T |
C |
1: 17,231,368 (GRCm39) |
W238R |
probably damaging |
Het |
Gm11096 |
T |
G |
17: 81,749,328 (GRCm39) |
I7M |
unknown |
Het |
Gmppb |
A |
T |
9: 107,927,770 (GRCm39) |
M175L |
probably benign |
Het |
Gorasp2 |
G |
A |
2: 70,514,442 (GRCm39) |
S273N |
probably benign |
Het |
Gtf3c1 |
T |
C |
7: 125,271,994 (GRCm39) |
M642V |
possibly damaging |
Het |
Hmx2 |
T |
A |
7: 131,157,600 (GRCm39) |
L238Q |
probably damaging |
Het |
Kif13b |
A |
G |
14: 64,973,598 (GRCm39) |
D316G |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,578,174 (GRCm39) |
S701P |
possibly damaging |
Het |
Lama4 |
T |
A |
10: 38,964,325 (GRCm39) |
N1332K |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,288,823 (GRCm39) |
D3681G |
probably damaging |
Het |
Maml3 |
G |
T |
3: 51,605,143 (GRCm39) |
P722Q |
probably damaging |
Het |
Mier2 |
C |
A |
10: 79,377,719 (GRCm39) |
|
probably benign |
Het |
Ms4a15 |
A |
T |
19: 10,956,694 (GRCm39) |
|
probably null |
Het |
Msh5 |
T |
C |
17: 35,263,355 (GRCm39) |
M158V |
probably benign |
Het |
Nova2 |
A |
T |
7: 18,676,270 (GRCm39) |
K136I |
|
Het |
Npm1 |
A |
T |
11: 33,106,001 (GRCm39) |
|
probably null |
Het |
Nr4a3 |
T |
A |
4: 48,051,390 (GRCm39) |
M48K |
probably benign |
Het |
Nrap |
T |
G |
19: 56,342,584 (GRCm39) |
T806P |
probably benign |
Het |
Ntf3 |
G |
A |
6: 126,079,203 (GRCm39) |
T101M |
probably benign |
Het |
Or2aj4 |
G |
A |
16: 19,385,472 (GRCm39) |
R54* |
probably null |
Het |
Paxbp1 |
T |
A |
16: 90,822,166 (GRCm39) |
D648V |
probably damaging |
Het |
Pcdhb18 |
T |
A |
18: 37,623,520 (GRCm39) |
D283E |
probably benign |
Het |
Phrf1 |
C |
A |
7: 140,839,288 (GRCm39) |
Q828K |
unknown |
Het |
Pigq |
A |
T |
17: 26,156,299 (GRCm39) |
I43N |
probably benign |
Het |
Pou6f2 |
G |
T |
13: 18,300,033 (GRCm39) |
T542K |
|
Het |
Ppfibp2 |
T |
A |
7: 107,320,524 (GRCm39) |
|
probably null |
Het |
Rab1b |
A |
T |
19: 5,150,524 (GRCm39) |
M163K |
probably benign |
Het |
Ralgapa1 |
A |
G |
12: 55,793,934 (GRCm39) |
M567T |
probably benign |
Het |
Reck |
T |
C |
4: 43,890,970 (GRCm39) |
V36A |
probably benign |
Het |
Resp18 |
C |
T |
1: 75,254,846 (GRCm39) |
D36N |
probably null |
Het |
Rint1 |
A |
C |
5: 24,005,720 (GRCm39) |
H134P |
probably damaging |
Het |
Rps19 |
A |
T |
7: 24,587,764 (GRCm39) |
K77M |
possibly damaging |
Het |
Sec24b |
A |
T |
3: 129,789,598 (GRCm39) |
S808T |
probably benign |
Het |
Sema4c |
A |
C |
1: 36,592,199 (GRCm39) |
V216G |
probably damaging |
Het |
Septin10 |
T |
A |
10: 59,016,871 (GRCm39) |
T218S |
probably benign |
Het |
Septin3 |
A |
T |
15: 82,170,020 (GRCm39) |
H182L |
probably benign |
Het |
Sipa1 |
A |
G |
19: 5,702,690 (GRCm39) |
S836P |
probably benign |
Het |
Slc9a5 |
A |
G |
8: 106,089,998 (GRCm39) |
K652R |
probably damaging |
Het |
Slco5a1 |
T |
A |
1: 13,059,927 (GRCm39) |
I265F |
possibly damaging |
Het |
Snapc5 |
T |
A |
9: 64,086,614 (GRCm39) |
M1K |
probably null |
Het |
Snx5 |
T |
A |
2: 144,095,740 (GRCm39) |
D307V |
possibly damaging |
Het |
Srebf2 |
A |
T |
15: 82,061,441 (GRCm39) |
M381L |
probably benign |
Het |
Ssh2 |
G |
C |
11: 77,345,452 (GRCm39) |
E1146Q |
probably benign |
Het |
Suco |
A |
T |
1: 161,672,937 (GRCm39) |
|
probably null |
Het |
Tanc2 |
T |
A |
11: 105,812,651 (GRCm39) |
L1365Q |
probably damaging |
Het |
Tas1r3 |
A |
G |
4: 155,947,005 (GRCm39) |
L200P |
probably damaging |
Het |
Thbs2 |
T |
G |
17: 14,896,483 (GRCm39) |
D802A |
probably damaging |
Het |
Trav3-1 |
G |
A |
14: 52,818,550 (GRCm39) |
V75M |
probably benign |
Het |
Trim9 |
G |
A |
12: 70,301,961 (GRCm39) |
P559L |
probably benign |
Het |
Trpc6 |
G |
A |
9: 8,655,219 (GRCm39) |
G683D |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,615,509 (GRCm39) |
V164L |
possibly damaging |
Het |
Usf3 |
A |
T |
16: 44,036,565 (GRCm39) |
R348S |
possibly damaging |
Het |
Vmn1r236 |
T |
C |
17: 21,507,728 (GRCm39) |
V282A |
possibly damaging |
Het |
Vmn2r1 |
A |
G |
3: 63,997,130 (GRCm39) |
E262G |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,339,841 (GRCm39) |
E694G |
probably damaging |
Het |
Xpo4 |
T |
A |
14: 57,840,048 (GRCm39) |
H572L |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,307,259 (GRCm39) |
T162A |
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,571,020 (GRCm39) |
H59Q |
possibly damaging |
Het |
|
Other mutations in Gm40460 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6822:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7016:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R7053:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R7083:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7087:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R7110:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R7184:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7224:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R7367:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R7411:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R7481:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R7491:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7553:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7637:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7643:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7663:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R7785:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R7871:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R8054:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R8355:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R8389:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R8501:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R8509:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R8705:Gm40460
|
UTSW |
7 |
141,794,734 (GRCm39) |
missense |
unknown |
|
R8736:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R8815:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R8815:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R8862:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R8884:Gm40460
|
UTSW |
7 |
141,794,555 (GRCm39) |
nonsense |
probably null |
|
R8892:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R8915:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R8939:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R9034:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R9040:Gm40460
|
UTSW |
7 |
141,794,171 (GRCm39) |
small deletion |
probably benign |
|
R9122:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R9142:Gm40460
|
UTSW |
7 |
141,794,499 (GRCm39) |
missense |
unknown |
|
R9172:Gm40460
|
UTSW |
7 |
141,794,447 (GRCm39) |
small deletion |
probably benign |
|
R9217:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R9292:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R9314:Gm40460
|
UTSW |
7 |
141,794,447 (GRCm39) |
small deletion |
probably benign |
|
R9401:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R9556:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R9562:Gm40460
|
UTSW |
7 |
141,794,701 (GRCm39) |
missense |
unknown |
|
R9642:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R9731:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
R9741:Gm40460
|
UTSW |
7 |
141,794,450 (GRCm39) |
small deletion |
probably benign |
|
R9793:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
RF040:Gm40460
|
UTSW |
7 |
141,794,554 (GRCm39) |
small deletion |
probably benign |
|
Z1177:Gm40460
|
UTSW |
7 |
141,794,643 (GRCm39) |
missense |
unknown |
|
Z1177:Gm40460
|
UTSW |
7 |
141,794,509 (GRCm39) |
missense |
unknown |
|
|