Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
T |
11: 109,921,743 (GRCm39) |
V1437E |
probably null |
Het |
Adam12 |
G |
A |
7: 133,614,017 (GRCm39) |
R80* |
probably null |
Het |
Adgrb3 |
G |
T |
1: 25,133,038 (GRCm39) |
F479L |
probably damaging |
Het |
Atf7ip |
T |
A |
6: 136,582,485 (GRCm39) |
V1165E |
possibly damaging |
Het |
Atm |
C |
T |
9: 53,379,264 (GRCm39) |
|
probably null |
Het |
Atp11c |
A |
G |
X: 59,322,143 (GRCm39) |
Y593H |
probably damaging |
Het |
Btnl1 |
A |
G |
17: 34,604,608 (GRCm39) |
D463G |
possibly damaging |
Het |
Cdc34b |
T |
G |
11: 94,633,252 (GRCm39) |
W151G |
probably damaging |
Het |
Cdkal1 |
A |
G |
13: 29,538,660 (GRCm39) |
S500P |
possibly damaging |
Het |
Cenpf |
T |
C |
1: 189,390,839 (GRCm39) |
N998D |
probably benign |
Het |
Ces2e |
T |
A |
8: 105,659,171 (GRCm39) |
|
probably null |
Het |
Chd7 |
A |
G |
4: 8,753,147 (GRCm39) |
Q548R |
probably damaging |
Het |
Chfr |
T |
A |
5: 110,292,627 (GRCm39) |
|
probably null |
Het |
Clu |
A |
G |
14: 66,212,290 (GRCm39) |
|
probably null |
Het |
Cntnap5c |
A |
G |
17: 58,714,717 (GRCm39) |
D1235G |
probably damaging |
Het |
Col6a4 |
T |
C |
9: 105,943,860 (GRCm39) |
S1205G |
probably benign |
Het |
Ddx47 |
G |
T |
6: 134,992,313 (GRCm39) |
E113* |
probably null |
Het |
Dock4 |
A |
G |
12: 40,795,667 (GRCm39) |
Y828C |
probably benign |
Het |
Dync1h1 |
T |
A |
12: 110,623,065 (GRCm39) |
N3553K |
possibly damaging |
Het |
Egflam |
C |
T |
15: 7,263,760 (GRCm39) |
C730Y |
probably damaging |
Het |
Fam83b |
T |
C |
9: 76,398,298 (GRCm39) |
Y935C |
probably damaging |
Het |
Fam83g |
A |
G |
11: 61,594,510 (GRCm39) |
I681M |
probably benign |
Het |
Fastk |
T |
C |
5: 24,650,139 (GRCm39) |
R3G |
probably damaging |
Het |
Fxr1 |
A |
T |
3: 34,112,196 (GRCm39) |
E367D |
probably damaging |
Het |
Gatb |
A |
G |
3: 85,518,677 (GRCm39) |
D261G |
probably damaging |
Het |
Gm5617 |
T |
C |
9: 48,407,117 (GRCm39) |
S84P |
possibly damaging |
Het |
Hecw1 |
C |
T |
13: 14,552,285 (GRCm39) |
E104K |
probably damaging |
Het |
Il31ra |
T |
C |
13: 112,680,422 (GRCm39) |
K265R |
possibly damaging |
Het |
Khsrp |
GTCATT |
GT |
17: 57,331,410 (GRCm39) |
|
probably null |
Het |
Lrp2 |
T |
A |
2: 69,341,411 (GRCm39) |
D923V |
probably damaging |
Het |
Ltn1 |
A |
G |
16: 87,179,601 (GRCm39) |
L1520P |
probably damaging |
Het |
Magel2 |
G |
A |
7: 62,028,844 (GRCm39) |
V583I |
unknown |
Het |
Map1s |
T |
G |
8: 71,366,526 (GRCm39) |
V477G |
probably benign |
Het |
Mical1 |
T |
C |
10: 41,358,708 (GRCm39) |
L542P |
probably damaging |
Het |
Mtcl3 |
T |
A |
10: 29,072,395 (GRCm39) |
Y562* |
probably null |
Het |
Mycbp2 |
T |
C |
14: 103,446,329 (GRCm39) |
Y1800C |
probably damaging |
Het |
Mylk |
A |
T |
16: 34,806,846 (GRCm39) |
D1697V |
probably benign |
Het |
Nlrp1a |
A |
T |
11: 71,015,014 (GRCm39) |
F79I |
probably benign |
Het |
Pde9a |
A |
G |
17: 31,605,284 (GRCm39) |
Y6C |
probably damaging |
Het |
Plxnd1 |
A |
T |
6: 115,934,509 (GRCm39) |
I1808N |
probably damaging |
Het |
Ppp1r13b |
T |
A |
12: 111,800,167 (GRCm39) |
T537S |
probably benign |
Het |
Ppp2r2a |
A |
G |
14: 67,253,924 (GRCm39) |
F415L |
possibly damaging |
Het |
Rabgap1 |
C |
T |
2: 37,453,499 (GRCm39) |
R976* |
probably null |
Het |
Rbfox3 |
T |
C |
11: 118,387,842 (GRCm39) |
H195R |
probably damaging |
Het |
Ripk4 |
A |
T |
16: 97,544,933 (GRCm39) |
D571E |
probably damaging |
Het |
Sdhaf4 |
T |
A |
1: 24,044,634 (GRCm39) |
R16S |
probably benign |
Het |
Slc17a1 |
G |
T |
13: 24,059,658 (GRCm39) |
G130* |
probably null |
Het |
Slc6a1 |
G |
T |
6: 114,278,977 (GRCm39) |
A23S |
probably benign |
Het |
Slco1a8 |
T |
C |
6: 141,926,704 (GRCm39) |
I541V |
probably damaging |
Het |
Spock1 |
T |
A |
13: 57,583,952 (GRCm39) |
Q321L |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,999,560 (GRCm39) |
I2318V |
probably damaging |
Het |
Terf2ip |
T |
C |
8: 112,738,271 (GRCm39) |
V53A |
possibly damaging |
Het |
Thrb |
T |
C |
14: 18,033,487 (GRCm38) |
F403L |
probably benign |
Het |
Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
Uqcrfs1 |
T |
C |
13: 30,724,787 (GRCm39) |
K251R |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,792,085 (GRCm39) |
E57G |
possibly damaging |
Het |
Vmn2r114 |
T |
A |
17: 23,510,737 (GRCm39) |
Y581F |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,874,909 (GRCm39) |
V1866A |
probably benign |
Het |
Washc5 |
A |
T |
15: 59,241,083 (GRCm39) |
F84Y |
probably damaging |
Het |
Yars1 |
T |
A |
4: 129,090,992 (GRCm39) |
Y28* |
probably null |
Het |
Zfp638 |
A |
G |
6: 83,905,964 (GRCm39) |
Y43C |
probably damaging |
Het |
Zfp750 |
T |
A |
11: 121,404,758 (GRCm39) |
H39L |
probably damaging |
Het |
Zfr2 |
C |
A |
10: 81,078,735 (GRCm39) |
S322R |
probably damaging |
Het |
Zzef1 |
A |
G |
11: 72,771,450 (GRCm39) |
D1644G |
probably benign |
Het |
|
Other mutations in Or52d3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01588:Or52d3
|
APN |
7 |
104,229,150 (GRCm39) |
missense |
probably damaging |
1.00 |
I2288:Or52d3
|
UTSW |
7 |
104,229,593 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Or52d3
|
UTSW |
7 |
104,229,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R0325:Or52d3
|
UTSW |
7 |
104,229,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Or52d3
|
UTSW |
7 |
104,229,268 (GRCm39) |
nonsense |
probably null |
|
R1599:Or52d3
|
UTSW |
7 |
104,228,855 (GRCm39) |
start codon destroyed |
probably null |
|
R1956:Or52d3
|
UTSW |
7 |
104,229,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R2418:Or52d3
|
UTSW |
7 |
104,229,141 (GRCm39) |
missense |
probably benign |
0.00 |
R2483:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R4049:Or52d3
|
UTSW |
7 |
104,229,575 (GRCm39) |
missense |
probably benign |
|
R4755:Or52d3
|
UTSW |
7 |
104,229,268 (GRCm39) |
nonsense |
probably null |
|
R4757:Or52d3
|
UTSW |
7 |
104,229,404 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4828:Or52d3
|
UTSW |
7 |
104,229,180 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4842:Or52d3
|
UTSW |
7 |
104,229,422 (GRCm39) |
missense |
probably benign |
0.45 |
R5496:Or52d3
|
UTSW |
7 |
104,229,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Or52d3
|
UTSW |
7 |
104,229,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Or52d3
|
UTSW |
7 |
104,229,645 (GRCm39) |
nonsense |
probably null |
|
R7590:Or52d3
|
UTSW |
7 |
104,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7968:Or52d3
|
UTSW |
7 |
104,229,595 (GRCm39) |
nonsense |
probably null |
|
R8491:Or52d3
|
UTSW |
7 |
104,229,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R9306:Or52d3
|
UTSW |
7 |
104,229,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R9521:Or52d3
|
UTSW |
7 |
104,228,855 (GRCm39) |
start codon destroyed |
probably null |
|
R9557:Or52d3
|
UTSW |
7 |
104,229,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9682:Or52d3
|
UTSW |
7 |
104,229,434 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Or52d3
|
UTSW |
7 |
104,229,497 (GRCm39) |
missense |
probably benign |
0.00 |
|