Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
A |
T |
1: 179,580,199 (GRCm39) |
V2001E |
probably benign |
Het |
Ahsg |
A |
G |
16: 22,713,585 (GRCm39) |
D122G |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,840,553 (GRCm39) |
Y1616C |
probably damaging |
Het |
Arhgef1 |
A |
G |
7: 24,619,205 (GRCm39) |
|
probably null |
Het |
Atp7b |
T |
C |
8: 22,494,391 (GRCm39) |
I1023V |
probably benign |
Het |
Bod1l |
A |
T |
5: 41,979,216 (GRCm39) |
Y699* |
probably null |
Het |
Car12 |
C |
T |
9: 66,659,244 (GRCm39) |
S183L |
probably damaging |
Het |
Cep290 |
T |
C |
10: 100,324,490 (GRCm39) |
S57P |
probably damaging |
Het |
Cep57l1 |
T |
C |
10: 41,619,145 (GRCm39) |
D74G |
probably damaging |
Het |
Cers6 |
T |
C |
2: 68,938,903 (GRCm39) |
Y374H |
possibly damaging |
Het |
Chmp4c |
T |
A |
3: 10,432,195 (GRCm39) |
M35K |
possibly damaging |
Het |
Crkl |
G |
A |
16: 17,301,645 (GRCm39) |
D300N |
probably damaging |
Het |
Cyp3a41a |
A |
G |
5: 145,642,639 (GRCm39) |
M240T |
probably benign |
Het |
Dipk2a |
C |
T |
9: 94,406,502 (GRCm39) |
V302I |
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,523,470 (GRCm39) |
L1986F |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,867,439 (GRCm39) |
I297T |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,508,962 (GRCm39) |
I1610F |
probably damaging |
Het |
Dpys |
T |
A |
15: 39,720,559 (GRCm39) |
H67L |
probably damaging |
Het |
Epc2 |
T |
G |
2: 49,422,099 (GRCm39) |
V331G |
probably benign |
Het |
Fnbp1l |
G |
A |
3: 122,339,956 (GRCm39) |
R344* |
probably null |
Het |
Gmip |
G |
T |
8: 70,263,824 (GRCm39) |
L89F |
possibly damaging |
Het |
Gmip |
G |
C |
8: 70,263,826 (GRCm39) |
R90P |
probably damaging |
Het |
Gpi1 |
A |
G |
7: 33,928,415 (GRCm39) |
S74P |
probably damaging |
Het |
Gys1 |
G |
A |
7: 45,094,102 (GRCm39) |
E406K |
probably damaging |
Het |
Hspg2 |
G |
A |
4: 137,242,618 (GRCm39) |
G611E |
probably damaging |
Het |
Klhl29 |
C |
T |
12: 5,134,393 (GRCm39) |
V673M |
probably damaging |
Het |
Lnpk |
T |
C |
2: 74,360,020 (GRCm39) |
T332A |
probably benign |
Het |
Loxl4 |
T |
C |
19: 42,596,792 (GRCm39) |
D60G |
probably damaging |
Het |
Lrr1 |
T |
C |
12: 69,221,449 (GRCm39) |
I197T |
probably damaging |
Het |
Map1lc3b |
A |
G |
8: 122,320,316 (GRCm39) |
N43S |
probably benign |
Het |
Map3k21 |
A |
T |
8: 126,666,605 (GRCm39) |
D599V |
probably benign |
Het |
Mastl |
T |
C |
2: 23,023,710 (GRCm39) |
N338D |
probably benign |
Het |
Mepe |
A |
T |
5: 104,486,074 (GRCm39) |
R405* |
probably null |
Het |
Mrps30 |
T |
C |
13: 118,516,908 (GRCm39) |
E437G |
probably benign |
Het |
Mup15 |
A |
G |
4: 61,356,465 (GRCm39) |
V100A |
possibly damaging |
Het |
Olfml2a |
T |
A |
2: 38,850,238 (GRCm39) |
Y651* |
probably null |
Het |
Or2h1b |
T |
A |
17: 37,462,713 (GRCm39) |
D50V |
probably damaging |
Het |
Otog |
T |
C |
7: 45,947,741 (GRCm39) |
V113A |
probably damaging |
Het |
Parvg |
C |
T |
15: 84,210,464 (GRCm39) |
L44F |
possibly damaging |
Het |
Pcnx2 |
G |
T |
8: 126,498,839 (GRCm39) |
D1553E |
probably damaging |
Het |
Pcyt2 |
C |
T |
11: 120,505,200 (GRCm39) |
G122S |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,194,846 (GRCm39) |
L184P |
possibly damaging |
Het |
Polq |
C |
T |
16: 36,897,510 (GRCm39) |
T2134I |
probably damaging |
Het |
Prkce |
T |
G |
17: 86,937,489 (GRCm39) |
F641V |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,440,654 (GRCm39) |
I243T |
possibly damaging |
Het |
Pxmp2 |
A |
G |
5: 110,429,185 (GRCm39) |
F91L |
probably benign |
Het |
Ralgapb |
G |
A |
2: 158,278,486 (GRCm39) |
G5R |
probably damaging |
Het |
Rasgef1a |
T |
G |
6: 118,064,174 (GRCm39) |
M337R |
possibly damaging |
Het |
Rassf2 |
A |
G |
2: 131,844,845 (GRCm39) |
M199T |
probably damaging |
Het |
Rtbdn |
A |
T |
8: 85,679,303 (GRCm39) |
Y67F |
probably null |
Het |
Scamp3 |
T |
C |
3: 89,089,256 (GRCm39) |
V271A |
probably benign |
Het |
Sema3a |
A |
T |
5: 13,647,584 (GRCm39) |
R613W |
possibly damaging |
Het |
Slc4a3 |
A |
T |
1: 75,527,959 (GRCm39) |
I206F |
probably damaging |
Het |
Slc9b1 |
A |
G |
3: 135,063,518 (GRCm39) |
|
probably null |
Het |
Smchd1 |
C |
A |
17: 71,782,096 (GRCm39) |
V22F |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,783,794 (GRCm39) |
|
probably benign |
Het |
Spaca7b |
T |
C |
8: 11,728,584 (GRCm39) |
E29G |
possibly damaging |
Het |
Spata31e4 |
A |
C |
13: 50,857,131 (GRCm39) |
H923P |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,861,117 (GRCm39) |
L89P |
probably damaging |
Het |
Stim1 |
A |
G |
7: 102,076,498 (GRCm39) |
E152G |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 49,127,528 (GRCm39) |
F50S |
probably damaging |
Het |
Tpgs2 |
T |
G |
18: 25,262,927 (GRCm39) |
N231H |
probably benign |
Het |
Trank1 |
T |
A |
9: 111,219,747 (GRCm39) |
N2161K |
probably damaging |
Het |
Trim28 |
A |
G |
7: 12,759,273 (GRCm39) |
D129G |
probably benign |
Het |
Trim66 |
A |
T |
7: 109,076,961 (GRCm39) |
I326N |
probably damaging |
Het |
Trim80 |
A |
T |
11: 115,338,843 (GRCm39) |
T558S |
probably benign |
Het |
Uggt1 |
T |
A |
1: 36,269,769 (GRCm39) |
T83S |
probably benign |
Het |
Wdr91 |
A |
G |
6: 34,863,754 (GRCm39) |
I587T |
probably damaging |
Het |
Zpld1 |
A |
T |
16: 55,052,603 (GRCm39) |
V337D |
possibly damaging |
Het |
|
Other mutations in Olfml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01285:Olfml1
|
APN |
7 |
107,189,364 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02355:Olfml1
|
APN |
7 |
107,167,010 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02362:Olfml1
|
APN |
7 |
107,167,010 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03218:Olfml1
|
APN |
7 |
107,170,476 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03291:Olfml1
|
APN |
7 |
107,189,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Olfml1
|
UTSW |
7 |
107,189,393 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0041:Olfml1
|
UTSW |
7 |
107,189,393 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0081:Olfml1
|
UTSW |
7 |
107,170,506 (GRCm39) |
missense |
probably benign |
0.08 |
R0524:Olfml1
|
UTSW |
7 |
107,189,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R1311:Olfml1
|
UTSW |
7 |
107,167,103 (GRCm39) |
critical splice donor site |
probably null |
|
R1548:Olfml1
|
UTSW |
7 |
107,189,582 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1564:Olfml1
|
UTSW |
7 |
107,170,346 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4347:Olfml1
|
UTSW |
7 |
107,167,040 (GRCm39) |
missense |
probably benign |
0.00 |
R4997:Olfml1
|
UTSW |
7 |
107,170,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Olfml1
|
UTSW |
7 |
107,189,530 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7703:Olfml1
|
UTSW |
7 |
107,170,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Olfml1
|
UTSW |
7 |
107,170,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Olfml1
|
UTSW |
7 |
107,189,570 (GRCm39) |
missense |
probably benign |
0.04 |
R8441:Olfml1
|
UTSW |
7 |
107,166,977 (GRCm39) |
missense |
probably benign |
0.00 |
R9002:Olfml1
|
UTSW |
7 |
107,189,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Olfml1
|
UTSW |
7 |
107,167,007 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9797:Olfml1
|
UTSW |
7 |
107,167,069 (GRCm39) |
missense |
probably benign |
0.25 |
|