Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,126,989 (GRCm39) |
I1227V |
probably benign |
Het |
Abhd8 |
A |
G |
8: 71,911,148 (GRCm39) |
V261A |
possibly damaging |
Het |
Adam34 |
A |
T |
8: 44,104,416 (GRCm39) |
C410S |
probably damaging |
Het |
Adamts17 |
T |
C |
7: 66,489,645 (GRCm39) |
L21P |
probably damaging |
Het |
Adgre1 |
A |
G |
17: 57,748,275 (GRCm39) |
N492D |
probably benign |
Het |
Aldh1b1 |
G |
A |
4: 45,803,811 (GRCm39) |
V450M |
probably damaging |
Het |
Apob |
A |
G |
12: 8,058,053 (GRCm39) |
I2178M |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,517,163 (GRCm39) |
I390N |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,098,969 (GRCm39) |
I1277V |
|
Het |
Cacng2 |
T |
G |
15: 77,897,542 (GRCm39) |
Y89S |
possibly damaging |
Het |
Capn10 |
T |
C |
1: 92,871,665 (GRCm39) |
|
probably null |
Het |
Casq2 |
A |
G |
3: 102,052,700 (GRCm39) |
D404G |
unknown |
Het |
Cdh9 |
T |
A |
15: 16,832,138 (GRCm39) |
Y342N |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,392,271 (GRCm39) |
|
probably null |
Het |
Cep295nl |
G |
A |
11: 118,224,766 (GRCm39) |
P26L |
possibly damaging |
Het |
Chmp4c |
T |
G |
3: 10,454,974 (GRCm39) |
S214A |
probably benign |
Het |
Clstn2 |
T |
A |
9: 97,343,537 (GRCm39) |
I637F |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 16,011,532 (GRCm39) |
T2507K |
probably benign |
Het |
Ddx55 |
C |
T |
5: 124,705,012 (GRCm39) |
S427F |
probably damaging |
Het |
Dpysl5 |
T |
C |
5: 30,948,959 (GRCm39) |
W405R |
probably damaging |
Het |
Esyt1 |
A |
G |
10: 128,355,388 (GRCm39) |
V451A |
possibly damaging |
Het |
Fads2b |
A |
T |
2: 85,330,649 (GRCm39) |
C219* |
probably null |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Foxa3 |
A |
G |
7: 18,748,961 (GRCm39) |
L55P |
possibly damaging |
Het |
Gng2 |
G |
T |
14: 19,925,961 (GRCm39) |
H44N |
probably damaging |
Het |
Hps5 |
G |
A |
7: 46,438,619 (GRCm39) |
T38I |
possibly damaging |
Het |
Igf2 |
G |
A |
7: 142,208,153 (GRCm39) |
R64C |
probably damaging |
Het |
Klb |
T |
A |
5: 65,505,988 (GRCm39) |
Y78* |
probably null |
Het |
Krt32 |
T |
C |
11: 99,972,029 (GRCm39) |
T440A |
probably benign |
Het |
Kynu |
T |
A |
2: 43,569,768 (GRCm39) |
F350Y |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,618,574 (GRCm39) |
S281T |
|
Het |
Lrrc43 |
C |
T |
5: 123,646,219 (GRCm39) |
A657V |
unknown |
Het |
Mief2 |
C |
A |
11: 60,622,042 (GRCm39) |
P204Q |
possibly damaging |
Het |
Morc3 |
G |
T |
16: 93,667,302 (GRCm39) |
R560L |
probably benign |
Het |
Or2y3 |
A |
T |
17: 38,393,629 (GRCm39) |
V80D |
probably damaging |
Het |
Orc3 |
G |
A |
4: 34,607,181 (GRCm39) |
R50* |
probably null |
Het |
Osbpl6 |
T |
A |
2: 76,378,716 (GRCm39) |
D124E |
probably damaging |
Het |
Parp4 |
TG |
T |
14: 56,832,790 (GRCm39) |
|
probably null |
Het |
Parp4 |
T |
C |
14: 56,852,224 (GRCm39) |
|
probably null |
Het |
Pcdhb18 |
A |
C |
18: 37,625,004 (GRCm39) |
H778P |
probably benign |
Het |
Polg |
A |
T |
7: 79,105,860 (GRCm39) |
Y710N |
probably benign |
Het |
Ppp2r2b |
C |
A |
18: 42,779,025 (GRCm39) |
R370L |
possibly damaging |
Het |
Prune2 |
A |
G |
19: 17,097,625 (GRCm39) |
D1043G |
probably benign |
Het |
Rpl6 |
T |
C |
5: 121,346,516 (GRCm39) |
S206P |
possibly damaging |
Het |
Serpina3i |
T |
C |
12: 104,234,881 (GRCm39) |
V404A |
probably damaging |
Het |
Serpinb8 |
T |
C |
1: 107,526,769 (GRCm39) |
|
probably null |
Het |
Stx11 |
A |
T |
10: 12,817,564 (GRCm39) |
D53E |
probably benign |
Het |
Thoc3 |
C |
T |
13: 54,607,998 (GRCm39) |
W315* |
probably null |
Het |
Tmem26 |
G |
A |
10: 68,559,816 (GRCm39) |
W29* |
probably null |
Het |
Togaram2 |
A |
G |
17: 71,996,408 (GRCm39) |
E137G |
probably damaging |
Het |
Ttc39b |
A |
G |
4: 83,151,023 (GRCm39) |
L524S |
probably damaging |
Het |
Usp43 |
T |
C |
11: 67,767,345 (GRCm39) |
N675S |
probably damaging |
Het |
Vmn2r104 |
A |
G |
17: 20,268,439 (GRCm39) |
L10P |
possibly damaging |
Het |
Zbtb1 |
G |
A |
12: 76,432,773 (GRCm39) |
R253Q |
probably damaging |
Het |
Zfc3h1 |
A |
G |
10: 115,255,771 (GRCm39) |
D1474G |
probably benign |
Het |
Zfp873 |
T |
C |
10: 81,896,514 (GRCm39) |
F415S |
probably benign |
Het |
|
Other mutations in Or8c20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Or8c20
|
APN |
9 |
38,261,101 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02477:Or8c20
|
APN |
9 |
38,260,421 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02858:Or8c20
|
APN |
9 |
38,260,469 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4362001:Or8c20
|
UTSW |
9 |
38,260,494 (GRCm39) |
missense |
probably benign |
0.34 |
R0060:Or8c20
|
UTSW |
9 |
38,260,808 (GRCm39) |
missense |
probably benign |
0.23 |
R0518:Or8c20
|
UTSW |
9 |
38,260,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R0521:Or8c20
|
UTSW |
9 |
38,260,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R0622:Or8c20
|
UTSW |
9 |
38,260,667 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0898:Or8c20
|
UTSW |
9 |
38,260,738 (GRCm39) |
missense |
probably damaging |
0.97 |
R1562:Or8c20
|
UTSW |
9 |
38,260,658 (GRCm39) |
nonsense |
probably null |
|
R3903:Or8c20
|
UTSW |
9 |
38,260,954 (GRCm39) |
nonsense |
probably null |
|
R4375:Or8c20
|
UTSW |
9 |
38,260,465 (GRCm39) |
missense |
probably benign |
|
R4459:Or8c20
|
UTSW |
9 |
38,261,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R4762:Or8c20
|
UTSW |
9 |
38,260,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Or8c20
|
UTSW |
9 |
38,260,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Or8c20
|
UTSW |
9 |
38,260,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R5442:Or8c20
|
UTSW |
9 |
38,261,158 (GRCm39) |
missense |
probably benign |
0.06 |
R5863:Or8c20
|
UTSW |
9 |
38,261,083 (GRCm39) |
missense |
probably benign |
0.09 |
R5988:Or8c20
|
UTSW |
9 |
38,261,045 (GRCm39) |
missense |
probably benign |
0.30 |
R7077:Or8c20
|
UTSW |
9 |
38,261,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7509:Or8c20
|
UTSW |
9 |
38,260,868 (GRCm39) |
missense |
probably benign |
0.26 |
R7709:Or8c20
|
UTSW |
9 |
38,260,573 (GRCm39) |
missense |
probably benign |
0.02 |
|