Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
C |
A |
10: 10,253,636 (GRCm39) |
E1209* |
probably null |
Het |
Adgrg5 |
G |
T |
8: 95,668,696 (GRCm39) |
R503L |
probably benign |
Het |
Anks1b |
C |
T |
10: 90,733,189 (GRCm39) |
|
probably benign |
Het |
Anxa5 |
A |
T |
3: 36,519,451 (GRCm39) |
F13I |
probably damaging |
Het |
Bicd1 |
A |
G |
6: 149,385,503 (GRCm39) |
I79V |
probably benign |
Het |
Bnip1 |
A |
G |
17: 27,008,719 (GRCm39) |
D107G |
probably damaging |
Het |
Ccdc42 |
A |
G |
11: 68,479,046 (GRCm39) |
E78G |
probably damaging |
Het |
Ccnk |
A |
G |
12: 108,153,446 (GRCm39) |
D69G |
probably damaging |
Het |
Clec2i |
G |
T |
6: 128,870,692 (GRCm39) |
V77F |
probably damaging |
Het |
Clec4g |
A |
C |
8: 3,768,803 (GRCm39) |
V62G |
probably benign |
Het |
Col4a4 |
G |
A |
1: 82,465,304 (GRCm39) |
A957V |
unknown |
Het |
Csnk1d |
A |
G |
11: 120,862,449 (GRCm39) |
F277L |
probably damaging |
Het |
Dip2c |
G |
A |
13: 9,625,264 (GRCm39) |
|
probably null |
Het |
Dpf2 |
T |
A |
19: 5,955,560 (GRCm39) |
K108* |
probably null |
Het |
Dync1h1 |
G |
A |
12: 110,583,171 (GRCm39) |
D423N |
probably damaging |
Het |
Fbxl13 |
T |
C |
5: 21,766,554 (GRCm39) |
|
probably null |
Homo |
Flad1 |
T |
C |
3: 89,310,490 (GRCm39) |
R488G |
probably damaging |
Het |
Galnt6 |
A |
C |
15: 100,591,236 (GRCm39) |
*623E |
probably null |
Het |
Gtf2e1 |
T |
C |
16: 37,331,816 (GRCm39) |
T420A |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,282,586 (GRCm39) |
V3442A |
probably damaging |
Het |
Itpr1 |
A |
G |
6: 108,365,237 (GRCm39) |
D55G |
probably damaging |
Het |
Kdm2a |
C |
A |
19: 4,374,854 (GRCm39) |
R759L |
possibly damaging |
Het |
Kif19a |
A |
G |
11: 114,676,605 (GRCm39) |
E478G |
probably damaging |
Het |
Lamb3 |
G |
A |
1: 193,017,761 (GRCm39) |
V881I |
probably benign |
Het |
Map3k6 |
T |
C |
4: 132,977,335 (GRCm39) |
L894P |
possibly damaging |
Het |
Mast4 |
A |
G |
13: 102,897,801 (GRCm39) |
|
probably null |
Het |
Mst1r |
G |
A |
9: 107,790,438 (GRCm39) |
V684M |
probably benign |
Het |
Naa15 |
T |
C |
3: 51,378,935 (GRCm39) |
S727P |
probably damaging |
Het |
Nap1l1 |
T |
C |
10: 111,330,084 (GRCm39) |
L330S |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,247,281 (GRCm39) |
T2205A |
probably damaging |
Het |
Ncf2 |
T |
C |
1: 152,703,214 (GRCm39) |
|
probably null |
Het |
Opa1 |
T |
A |
16: 29,444,332 (GRCm39) |
N839K |
probably benign |
Het |
Or4c104 |
T |
C |
2: 88,586,452 (GRCm39) |
D189G |
probably damaging |
Het |
Or52a33 |
T |
C |
7: 103,288,504 (GRCm39) |
Y281C |
probably damaging |
Het |
Pcdha7 |
T |
C |
18: 37,106,995 (GRCm39) |
Y7H |
possibly damaging |
Het |
Pcdhb15 |
T |
C |
18: 37,607,314 (GRCm39) |
V182A |
probably benign |
Het |
Phf10 |
A |
T |
17: 15,176,269 (GRCm39) |
I128N |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,736,965 (GRCm39) |
|
probably null |
Het |
Plxnb2 |
T |
C |
15: 89,048,629 (GRCm39) |
N626S |
probably benign |
Het |
Prh1 |
G |
A |
6: 132,548,996 (GRCm39) |
G168R |
unknown |
Het |
Prss51 |
A |
G |
14: 64,334,855 (GRCm39) |
T137A |
possibly damaging |
Het |
Ptprcap |
C |
T |
19: 4,206,183 (GRCm39) |
R89C |
possibly damaging |
Het |
Scfd1 |
A |
G |
12: 51,478,324 (GRCm39) |
K512R |
probably benign |
Het |
Serpina1b |
A |
C |
12: 103,701,296 (GRCm39) |
|
probably null |
Het |
Setbp1 |
T |
C |
18: 78,900,605 (GRCm39) |
T1021A |
probably damaging |
Het |
Slco1b2 |
G |
A |
6: 141,601,145 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
C |
T |
2: 127,063,747 (GRCm39) |
T642I |
probably benign |
Het |
Tenm4 |
A |
C |
7: 96,492,251 (GRCm39) |
I1063L |
possibly damaging |
Het |
Tfb2m |
G |
A |
1: 179,373,611 (GRCm39) |
A29V |
probably benign |
Het |
Tfeb |
T |
C |
17: 48,100,627 (GRCm39) |
V140A |
probably damaging |
Het |
Tmem104 |
A |
T |
11: 115,134,579 (GRCm39) |
I372F |
probably damaging |
Het |
Tmem132d |
G |
T |
5: 127,860,832 (GRCm39) |
H1096Q |
probably benign |
Het |
Trim12c |
A |
T |
7: 103,997,531 (GRCm39) |
N8K |
probably benign |
Het |
Tti2 |
A |
G |
8: 31,643,631 (GRCm39) |
I249V |
probably null |
Het |
Vps8 |
T |
A |
16: 21,261,129 (GRCm39) |
L90I |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,639,926 (GRCm39) |
|
probably null |
Het |
Wdfy4 |
A |
G |
14: 32,868,901 (GRCm39) |
S376P |
probably damaging |
Het |
|
Other mutations in Or52n4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01308:Or52n4b
|
APN |
7 |
108,143,933 (GRCm39) |
nonsense |
probably null |
|
IGL02031:Or52n4b
|
APN |
7 |
108,144,137 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02426:Or52n4b
|
APN |
7 |
108,144,187 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02502:Or52n4b
|
APN |
7 |
108,143,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03208:Or52n4b
|
APN |
7 |
108,144,326 (GRCm39) |
missense |
probably benign |
0.02 |
R0507:Or52n4b
|
UTSW |
7 |
108,144,292 (GRCm39) |
missense |
probably damaging |
0.98 |
R0967:Or52n4b
|
UTSW |
7 |
108,143,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1181:Or52n4b
|
UTSW |
7 |
108,144,509 (GRCm39) |
missense |
probably benign |
0.00 |
R1501:Or52n4b
|
UTSW |
7 |
108,143,782 (GRCm39) |
missense |
probably benign |
|
R1596:Or52n4b
|
UTSW |
7 |
108,144,290 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1657:Or52n4b
|
UTSW |
7 |
108,144,584 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1708:Or52n4b
|
UTSW |
7 |
108,143,781 (GRCm39) |
missense |
probably benign |
0.04 |
R2215:Or52n4b
|
UTSW |
7 |
108,144,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Or52n4b
|
UTSW |
7 |
108,143,744 (GRCm39) |
nonsense |
probably null |
|
R4772:Or52n4b
|
UTSW |
7 |
108,144,092 (GRCm39) |
missense |
probably damaging |
0.98 |
R5009:Or52n4b
|
UTSW |
7 |
108,144,055 (GRCm39) |
missense |
probably benign |
0.01 |
R5297:Or52n4b
|
UTSW |
7 |
108,144,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R5788:Or52n4b
|
UTSW |
7 |
108,144,551 (GRCm39) |
missense |
probably damaging |
0.97 |
R5944:Or52n4b
|
UTSW |
7 |
108,144,484 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7045:Or52n4b
|
UTSW |
7 |
108,144,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R7339:Or52n4b
|
UTSW |
7 |
108,144,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Or52n4b
|
UTSW |
7 |
108,143,928 (GRCm39) |
nonsense |
probably null |
|
R7585:Or52n4b
|
UTSW |
7 |
108,144,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Or52n4b
|
UTSW |
7 |
108,144,664 (GRCm39) |
missense |
probably benign |
0.00 |
|