Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
T |
G |
6: 92,811,437 (GRCm39) |
I130S |
unknown |
Het |
Ano5 |
A |
G |
7: 51,220,141 (GRCm39) |
H427R |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,989,532 (GRCm39) |
V182E |
probably damaging |
Het |
B4galnt1 |
T |
C |
10: 127,002,923 (GRCm39) |
Y147H |
probably damaging |
Het |
C1s2 |
T |
C |
6: 124,605,289 (GRCm39) |
S349G |
possibly damaging |
Het |
Ccdc51 |
G |
T |
9: 108,920,655 (GRCm39) |
A181S |
probably damaging |
Het |
Dcc |
G |
A |
18: 72,087,939 (GRCm39) |
Q100* |
probably null |
Het |
Dchs2 |
A |
T |
3: 83,212,392 (GRCm39) |
I2064F |
probably damaging |
Het |
Depdc1a |
G |
A |
3: 159,221,706 (GRCm39) |
V217I |
probably benign |
Het |
Dnajc7 |
A |
T |
11: 100,492,629 (GRCm39) |
F31I |
probably benign |
Het |
Eftud2 |
C |
T |
11: 102,730,934 (GRCm39) |
R825H |
probably damaging |
Het |
Fam184a |
T |
C |
10: 53,551,256 (GRCm39) |
E237G |
probably damaging |
Het |
Fdx2 |
A |
T |
9: 20,984,623 (GRCm39) |
|
probably null |
Het |
Frem1 |
T |
C |
4: 82,934,643 (GRCm39) |
D106G |
possibly damaging |
Het |
Gabrg3 |
G |
A |
7: 56,374,229 (GRCm39) |
R446W |
probably damaging |
Het |
Get1 |
T |
A |
16: 95,946,768 (GRCm39) |
L31Q |
possibly damaging |
Het |
Gm42669 |
A |
G |
5: 107,656,572 (GRCm39) |
E362G |
|
Het |
Hmcn1 |
A |
T |
1: 150,533,221 (GRCm39) |
I3022N |
possibly damaging |
Het |
Ifna2 |
C |
A |
4: 88,601,506 (GRCm39) |
V171F |
probably damaging |
Het |
Igsf10 |
T |
C |
3: 59,235,748 (GRCm39) |
N1478D |
probably benign |
Het |
Kcnc1 |
C |
A |
7: 46,077,045 (GRCm39) |
D282E |
probably damaging |
Het |
Klhdc2 |
G |
A |
12: 69,351,406 (GRCm39) |
|
probably null |
Het |
Macrod2 |
G |
A |
2: 141,566,565 (GRCm39) |
G188S |
probably damaging |
Het |
Mapkbp1 |
T |
C |
2: 119,843,128 (GRCm39) |
F186L |
possibly damaging |
Het |
Mettl21a |
T |
C |
1: 64,654,343 (GRCm39) |
E58G |
probably damaging |
Het |
Muc16 |
A |
T |
9: 18,497,278 (GRCm39) |
C6625S |
probably benign |
Het |
Naip5 |
A |
T |
13: 100,382,689 (GRCm39) |
S7T |
probably benign |
Het |
Nfs1 |
T |
A |
2: 155,983,981 (GRCm39) |
D132V |
unknown |
Het |
Nlgn1 |
T |
C |
3: 25,490,071 (GRCm39) |
D552G |
probably damaging |
Het |
Numa1 |
C |
T |
7: 101,663,072 (GRCm39) |
T2066I |
probably benign |
Het |
Or10k2 |
T |
C |
8: 84,268,576 (GRCm39) |
S268P |
possibly damaging |
Het |
Or2t48 |
C |
A |
11: 58,419,880 (GRCm39) |
V311L |
probably benign |
Het |
Or4k2 |
A |
T |
14: 50,424,021 (GRCm39) |
Y219N |
probably damaging |
Het |
Or7a39 |
A |
G |
10: 78,715,657 (GRCm39) |
Y217C |
possibly damaging |
Het |
Pde11a |
C |
T |
2: 76,121,547 (GRCm39) |
V345I |
probably benign |
Het |
Pglyrp2 |
A |
G |
17: 32,637,735 (GRCm39) |
S98P |
possibly damaging |
Het |
Pik3c3 |
C |
T |
18: 30,452,641 (GRCm39) |
Q643* |
probably null |
Het |
Pold2 |
T |
C |
11: 5,822,714 (GRCm39) |
Y402C |
probably damaging |
Het |
Pom121 |
T |
C |
5: 135,410,848 (GRCm39) |
T770A |
unknown |
Het |
Pou4f1 |
A |
T |
14: 104,704,228 (GRCm39) |
V68E |
probably damaging |
Het |
Ppfia1 |
G |
T |
7: 144,073,020 (GRCm39) |
Q265K |
probably benign |
Het |
Pygl |
A |
G |
12: 70,253,130 (GRCm39) |
|
probably null |
Het |
Rdh19 |
A |
G |
10: 127,686,169 (GRCm39) |
T94A |
probably benign |
Het |
Scgb1b12 |
A |
G |
7: 32,033,922 (GRCm39) |
T61A |
probably damaging |
Het |
Sirpb1c |
C |
T |
3: 15,886,366 (GRCm39) |
A337T |
probably benign |
Het |
Sltm |
C |
G |
9: 70,493,955 (GRCm39) |
P802R |
possibly damaging |
Het |
Tbc1d23 |
T |
C |
16: 57,009,746 (GRCm39) |
E381G |
possibly damaging |
Het |
Tnik |
A |
G |
3: 28,720,288 (GRCm39) |
I1304V |
probably damaging |
Het |
Tpmt |
C |
A |
13: 47,193,638 (GRCm39) |
G54C |
probably damaging |
Het |
Usp25 |
A |
T |
16: 76,910,659 (GRCm39) |
Q905L |
probably damaging |
Het |
Vmn1r91 |
T |
A |
7: 19,835,490 (GRCm39) |
N136K |
probably benign |
Het |
Wdr70 |
C |
T |
15: 8,108,733 (GRCm39) |
E138K |
probably benign |
Het |
Zbed3 |
A |
G |
13: 95,472,633 (GRCm39) |
D19G |
possibly damaging |
Het |
Zfp369 |
A |
G |
13: 65,439,868 (GRCm39) |
K184R |
possibly damaging |
Het |
|
Other mutations in Or7g29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01150:Or7g29
|
APN |
9 |
19,286,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Or7g29
|
APN |
9 |
19,286,632 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01879:Or7g29
|
APN |
9 |
19,286,703 (GRCm39) |
nonsense |
probably null |
|
IGL03298:Or7g29
|
APN |
9 |
19,286,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R1350:Or7g29
|
UTSW |
9 |
19,286,710 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1400:Or7g29
|
UTSW |
9 |
19,286,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R2894:Or7g29
|
UTSW |
9 |
19,286,588 (GRCm39) |
nonsense |
probably null |
|
R4468:Or7g29
|
UTSW |
9 |
19,286,944 (GRCm39) |
missense |
probably benign |
0.00 |
R4694:Or7g29
|
UTSW |
9 |
19,286,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R4791:Or7g29
|
UTSW |
9 |
19,287,105 (GRCm39) |
missense |
probably benign |
0.28 |
R4794:Or7g29
|
UTSW |
9 |
19,286,841 (GRCm39) |
missense |
probably benign |
0.00 |
R5517:Or7g29
|
UTSW |
9 |
19,287,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Or7g29
|
UTSW |
9 |
19,286,925 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5777:Or7g29
|
UTSW |
9 |
19,287,014 (GRCm39) |
missense |
probably benign |
0.29 |
R6505:Or7g29
|
UTSW |
9 |
19,286,237 (GRCm39) |
makesense |
probably null |
|
R6509:Or7g29
|
UTSW |
9 |
19,286,439 (GRCm39) |
missense |
probably benign |
|
R7246:Or7g29
|
UTSW |
9 |
19,286,761 (GRCm39) |
nonsense |
probably null |
|
R7659:Or7g29
|
UTSW |
9 |
19,286,854 (GRCm39) |
missense |
probably benign |
0.03 |
R7789:Or7g29
|
UTSW |
9 |
19,286,361 (GRCm39) |
missense |
probably benign |
0.33 |
R8948:Or7g29
|
UTSW |
9 |
19,286,262 (GRCm39) |
missense |
probably benign |
0.03 |
R9326:Or7g29
|
UTSW |
9 |
19,286,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Or7g29
|
UTSW |
9 |
19,286,677 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9784:Or7g29
|
UTSW |
9 |
19,287,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R9798:Or7g29
|
UTSW |
9 |
19,286,577 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Or7g29
|
UTSW |
9 |
19,286,980 (GRCm39) |
missense |
probably damaging |
1.00 |
|