Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
C |
T |
1: 183,765,702 (GRCm39) |
S119N |
probably benign |
Het |
9030619P08Rik |
A |
C |
15: 75,301,846 (GRCm39) |
|
noncoding transcript |
Het |
Aldh1l2 |
T |
C |
10: 83,331,889 (GRCm39) |
I639V |
probably benign |
Het |
Ambra1 |
T |
C |
2: 91,601,241 (GRCm39) |
|
probably benign |
Het |
Ap5z1 |
T |
C |
5: 142,455,869 (GRCm39) |
Y299H |
probably damaging |
Het |
Atp6v1b1 |
A |
T |
6: 83,733,526 (GRCm39) |
|
probably benign |
Het |
Atr |
G |
A |
9: 95,832,689 (GRCm39) |
V2574I |
probably benign |
Het |
Atxn1l |
T |
A |
8: 110,459,612 (GRCm39) |
T217S |
probably benign |
Het |
Ccdc85a |
A |
G |
11: 28,346,150 (GRCm39) |
S89P |
probably benign |
Het |
Ccn5 |
T |
A |
2: 163,670,997 (GRCm39) |
M168K |
unknown |
Het |
Cd209e |
A |
T |
8: 3,899,124 (GRCm39) |
I196N |
probably damaging |
Het |
Cdhr4 |
A |
G |
9: 107,872,495 (GRCm39) |
S247G |
probably benign |
Het |
Cntn6 |
A |
T |
6: 104,809,470 (GRCm39) |
I502F |
probably damaging |
Het |
Crisp4 |
T |
C |
1: 18,193,018 (GRCm39) |
Y233C |
probably damaging |
Het |
Ctsb |
C |
A |
14: 63,376,553 (GRCm39) |
T261N |
probably benign |
Het |
Ctsk |
T |
C |
3: 95,408,185 (GRCm39) |
F14L |
probably benign |
Het |
Dchs1 |
T |
C |
7: 105,407,385 (GRCm39) |
I2110V |
probably damaging |
Het |
Dennd5b |
A |
G |
6: 148,969,988 (GRCm39) |
M155T |
probably benign |
Het |
Echdc3 |
T |
C |
2: 6,217,611 (GRCm39) |
D54G |
probably benign |
Het |
Egln3 |
G |
A |
12: 54,228,479 (GRCm39) |
T209I |
probably damaging |
Het |
Fbn1 |
A |
C |
2: 125,214,447 (GRCm39) |
|
probably benign |
Het |
Fkbp15 |
A |
T |
4: 62,222,846 (GRCm39) |
S1018T |
possibly damaging |
Het |
Flnb |
T |
C |
14: 7,896,503 (GRCm38) |
I898T |
probably benign |
Het |
Flt1 |
T |
A |
5: 147,536,456 (GRCm39) |
Y795F |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Fryl |
T |
C |
5: 73,267,614 (GRCm39) |
E417G |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,222,268 (GRCm39) |
|
probably benign |
Het |
Gcnt3 |
T |
C |
9: 69,941,615 (GRCm39) |
I318V |
probably benign |
Het |
Gm11437 |
T |
A |
11: 84,055,454 (GRCm39) |
H54L |
possibly damaging |
Het |
Huwe1 |
AGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGA |
X: 150,690,044 (GRCm39) |
|
probably benign |
Het |
Jarid2 |
G |
A |
13: 45,038,368 (GRCm39) |
|
probably benign |
Het |
Kif5b |
A |
T |
18: 6,214,044 (GRCm39) |
V653E |
probably benign |
Het |
Kmt2b |
A |
G |
7: 30,274,365 (GRCm39) |
V2113A |
probably damaging |
Het |
Knl1 |
C |
T |
2: 118,903,054 (GRCm39) |
T1585I |
probably benign |
Het |
Mlxipl |
T |
A |
5: 135,161,572 (GRCm39) |
M497K |
probably benign |
Het |
Mre11a |
T |
A |
9: 14,710,935 (GRCm39) |
W210R |
probably damaging |
Het |
Mrps22 |
A |
G |
9: 98,476,748 (GRCm39) |
V207A |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,390,256 (GRCm39) |
I2111V |
possibly damaging |
Het |
Myo1a |
C |
T |
10: 127,555,148 (GRCm39) |
P838L |
probably benign |
Het |
Nbea |
T |
A |
3: 55,965,461 (GRCm39) |
H484L |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Nlrp2 |
T |
A |
7: 5,331,430 (GRCm39) |
D322V |
probably damaging |
Het |
Nrcam |
T |
C |
12: 44,636,947 (GRCm39) |
C1057R |
probably damaging |
Het |
Ntsr1 |
T |
C |
2: 180,142,394 (GRCm39) |
S62P |
probably damaging |
Het |
Nudt18 |
A |
G |
14: 70,816,867 (GRCm39) |
H157R |
probably benign |
Het |
Or10s1 |
C |
A |
9: 39,986,192 (GRCm39) |
N200K |
probably damaging |
Het |
Sidt2 |
T |
C |
9: 45,857,002 (GRCm39) |
T435A |
probably damaging |
Het |
Snx27 |
T |
C |
3: 94,427,540 (GRCm39) |
T312A |
probably benign |
Het |
Srebf2 |
T |
C |
15: 82,061,720 (GRCm39) |
S429P |
probably damaging |
Het |
Suclg2 |
A |
G |
6: 95,474,563 (GRCm39) |
|
probably benign |
Het |
Tchh |
A |
T |
3: 93,352,279 (GRCm39) |
E573V |
unknown |
Het |
Tdrd1 |
A |
G |
19: 56,850,192 (GRCm39) |
T985A |
probably benign |
Het |
Ttc7b |
A |
G |
12: 100,369,698 (GRCm39) |
I357T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,626,008 (GRCm39) |
E13271G |
probably damaging |
Het |
Usp13 |
A |
G |
3: 32,969,857 (GRCm39) |
E661G |
probably damaging |
Het |
Vasp |
T |
G |
7: 18,992,958 (GRCm39) |
|
probably benign |
Het |
Vmn2r109 |
A |
T |
17: 20,775,503 (GRCm39) |
Y75N |
possibly damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,440,770 (GRCm39) |
N363Y |
probably damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,786,476 (GRCm39) |
N426K |
probably benign |
Het |
Znhit2 |
C |
A |
19: 6,112,288 (GRCm39) |
N344K |
probably damaging |
Het |
|
Other mutations in Or5g25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02591:Or5g25
|
APN |
2 |
85,478,487 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02873:Or5g25
|
APN |
2 |
85,478,096 (GRCm39) |
missense |
possibly damaging |
0.50 |
PIT4362001:Or5g25
|
UTSW |
2 |
85,478,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1261:Or5g25
|
UTSW |
2 |
85,478,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Or5g25
|
UTSW |
2 |
85,478,157 (GRCm39) |
nonsense |
probably null |
|
R1902:Or5g25
|
UTSW |
2 |
85,478,201 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1965:Or5g25
|
UTSW |
2 |
85,478,090 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2096:Or5g25
|
UTSW |
2 |
85,478,434 (GRCm39) |
missense |
probably benign |
0.20 |
R4239:Or5g25
|
UTSW |
2 |
85,478,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R4730:Or5g25
|
UTSW |
2 |
85,478,336 (GRCm39) |
missense |
probably benign |
0.39 |
R4948:Or5g25
|
UTSW |
2 |
85,477,916 (GRCm39) |
missense |
probably benign |
0.30 |
R5627:Or5g25
|
UTSW |
2 |
85,477,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R5844:Or5g25
|
UTSW |
2 |
85,478,239 (GRCm39) |
missense |
probably benign |
0.36 |
R6809:Or5g25
|
UTSW |
2 |
85,478,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Or5g25
|
UTSW |
2 |
85,477,768 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7476:Or5g25
|
UTSW |
2 |
85,478,512 (GRCm39) |
missense |
not run |
|
R7805:Or5g25
|
UTSW |
2 |
85,477,794 (GRCm39) |
nonsense |
probably null |
|
R7960:Or5g25
|
UTSW |
2 |
85,478,417 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8015:Or5g25
|
UTSW |
2 |
85,478,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R8355:Or5g25
|
UTSW |
2 |
85,478,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8455:Or5g25
|
UTSW |
2 |
85,478,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8479:Or5g25
|
UTSW |
2 |
85,478,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Or5g25
|
UTSW |
2 |
85,478,410 (GRCm39) |
missense |
probably benign |
0.35 |
R8699:Or5g25
|
UTSW |
2 |
85,478,330 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8762:Or5g25
|
UTSW |
2 |
85,478,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Or5g25
|
UTSW |
2 |
85,478,187 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9280:Or5g25
|
UTSW |
2 |
85,478,504 (GRCm39) |
nonsense |
probably null |
|
R9674:Or5g25
|
UTSW |
2 |
85,478,593 (GRCm39) |
missense |
possibly damaging |
0.94 |
|