Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700109H08Rik |
T |
A |
5: 3,630,442 (GRCm39) |
Y119* |
probably null |
Het |
Abcb9 |
C |
A |
5: 124,209,812 (GRCm39) |
E664* |
probably null |
Het |
Adgrl2 |
T |
C |
3: 148,564,578 (GRCm39) |
D334G |
probably damaging |
Het |
Ak9 |
T |
G |
10: 41,193,826 (GRCm39) |
C57G |
probably damaging |
Het |
Als2cl |
A |
G |
9: 110,724,952 (GRCm39) |
K809E |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp11a |
A |
G |
8: 12,896,099 (GRCm39) |
I223V |
probably benign |
Het |
Cacna2d3 |
A |
T |
14: 28,630,278 (GRCm39) |
V1022E |
probably benign |
Het |
Cc2d1b |
C |
T |
4: 108,490,422 (GRCm39) |
R825W |
probably damaging |
Het |
Cd37 |
A |
G |
7: 44,886,598 (GRCm39) |
C85R |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,063,764 (GRCm39) |
S7G |
probably benign |
Het |
Cltc |
T |
C |
11: 86,611,188 (GRCm39) |
N561S |
probably benign |
Het |
Cnbd2 |
A |
G |
2: 156,217,494 (GRCm39) |
E661G |
possibly damaging |
Het |
Col6a3 |
A |
T |
1: 90,750,063 (GRCm39) |
F257Y |
probably damaging |
Het |
Cpt1b |
T |
C |
15: 89,309,037 (GRCm39) |
Y55C |
possibly damaging |
Het |
Csmd1 |
A |
G |
8: 15,976,611 (GRCm39) |
V2869A |
probably benign |
Het |
Dnah11 |
T |
C |
12: 118,143,482 (GRCm39) |
E387G |
probably benign |
Het |
Eny2 |
T |
A |
15: 44,292,949 (GRCm39) |
|
probably null |
Het |
Fbxo10 |
G |
T |
4: 45,043,857 (GRCm39) |
H655Q |
probably benign |
Het |
Gm14403 |
AAACCCTA |
AA |
2: 177,201,448 (GRCm39) |
|
probably benign |
Het |
Gpx2 |
C |
T |
12: 76,842,068 (GRCm39) |
G28S |
probably damaging |
Het |
H2-Q5 |
G |
T |
17: 35,613,918 (GRCm39) |
A156S |
probably benign |
Het |
Hoxd4 |
A |
G |
2: 74,558,807 (GRCm39) |
D210G |
possibly damaging |
Het |
Hoxd9 |
A |
G |
2: 74,529,166 (GRCm39) |
Q256R |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,346,085 (GRCm39) |
V2571A |
probably damaging |
Het |
Mtus1 |
A |
G |
8: 41,537,074 (GRCm39) |
V214A |
possibly damaging |
Het |
Myh1 |
C |
T |
11: 67,111,793 (GRCm39) |
A1716V |
probably benign |
Het |
Nbeal1 |
A |
G |
1: 60,261,287 (GRCm39) |
D249G |
probably damaging |
Het |
Nup54 |
TCTGCTGCTGCTGCTGCTGCTGCTG |
TCTGCTGCTGCTGCTGCTGCTG |
5: 92,578,663 (GRCm39) |
|
probably benign |
Het |
Or10v9 |
G |
T |
19: 11,833,148 (GRCm39) |
H56Q |
probably damaging |
Het |
Or4c124 |
A |
T |
2: 89,155,677 (GRCm39) |
N282K |
probably damaging |
Het |
Or7a37 |
T |
G |
10: 78,805,974 (GRCm39) |
L164V |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pramel23 |
T |
C |
4: 143,423,886 (GRCm39) |
Y301C |
possibly damaging |
Het |
Prss59 |
A |
G |
6: 40,897,939 (GRCm39) |
I248T |
probably benign |
Het |
Pwwp2a |
A |
G |
11: 43,595,423 (GRCm39) |
D196G |
probably benign |
Het |
Rarg |
A |
T |
15: 102,150,327 (GRCm39) |
C93S |
possibly damaging |
Het |
Rcc1 |
T |
C |
4: 132,065,073 (GRCm39) |
D150G |
possibly damaging |
Het |
Ripk2 |
A |
G |
4: 16,163,330 (GRCm39) |
Y23H |
probably damaging |
Het |
Rragc |
A |
G |
4: 123,811,340 (GRCm39) |
Y5C |
possibly damaging |
Het |
Rubcnl |
G |
A |
14: 75,269,369 (GRCm39) |
G9D |
probably damaging |
Het |
Sephs2 |
A |
T |
7: 126,872,073 (GRCm39) |
V340E |
probably damaging |
Het |
Slc22a3 |
C |
T |
17: 12,677,438 (GRCm39) |
M243I |
probably benign |
Het |
Slco6c1 |
A |
G |
1: 97,000,518 (GRCm39) |
|
probably null |
Het |
Sncaip |
T |
G |
18: 53,039,966 (GRCm39) |
I308R |
probably damaging |
Het |
Supt16 |
G |
A |
14: 52,408,338 (GRCm39) |
T869M |
probably damaging |
Het |
Tanc1 |
G |
A |
2: 59,674,366 (GRCm39) |
E1817K |
possibly damaging |
Het |
Usp4 |
C |
A |
9: 108,248,154 (GRCm39) |
Q395K |
probably damaging |
Het |
Usp49 |
T |
A |
17: 47,984,272 (GRCm39) |
S210T |
possibly damaging |
Het |
Virma |
A |
G |
4: 11,505,498 (GRCm39) |
I124M |
probably damaging |
Het |
Vmn1r234 |
G |
A |
17: 21,449,589 (GRCm39) |
V168I |
probably benign |
Het |
Vnn3 |
T |
A |
10: 23,732,187 (GRCm39) |
C146S |
probably damaging |
Het |
Ylpm1 |
A |
G |
12: 85,088,953 (GRCm39) |
D1234G |
probably damaging |
Het |
Zfp617 |
T |
A |
8: 72,687,098 (GRCm39) |
V476E |
probably benign |
Het |
|
Other mutations in Or5w17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01143:Or5w17
|
APN |
2 |
87,584,278 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01412:Or5w17
|
APN |
2 |
87,583,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01533:Or5w17
|
APN |
2 |
87,583,412 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02455:Or5w17
|
APN |
2 |
87,583,927 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02698:Or5w17
|
APN |
2 |
87,584,188 (GRCm39) |
nonsense |
probably null |
|
PIT4480001:Or5w17
|
UTSW |
2 |
87,584,127 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0543:Or5w17
|
UTSW |
2 |
87,583,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Or5w17
|
UTSW |
2 |
87,583,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R1750:Or5w17
|
UTSW |
2 |
87,583,530 (GRCm39) |
missense |
probably damaging |
0.97 |
R1844:Or5w17
|
UTSW |
2 |
87,584,334 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R2248:Or5w17
|
UTSW |
2 |
87,584,287 (GRCm39) |
missense |
probably null |
0.05 |
R4064:Or5w17
|
UTSW |
2 |
87,584,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R5193:Or5w17
|
UTSW |
2 |
87,583,448 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5861:Or5w17
|
UTSW |
2 |
87,583,922 (GRCm39) |
missense |
probably benign |
0.01 |
R6146:Or5w17
|
UTSW |
2 |
87,583,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Or5w17
|
UTSW |
2 |
87,583,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Or5w17
|
UTSW |
2 |
87,583,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6904:Or5w17
|
UTSW |
2 |
87,584,223 (GRCm39) |
missense |
probably benign |
0.00 |
R6962:Or5w17
|
UTSW |
2 |
87,584,071 (GRCm39) |
missense |
probably benign |
|
R7014:Or5w17
|
UTSW |
2 |
87,584,215 (GRCm39) |
missense |
probably benign |
0.00 |
R8229:Or5w17
|
UTSW |
2 |
87,583,408 (GRCm39) |
missense |
probably benign |
0.00 |
R8723:Or5w17
|
UTSW |
2 |
87,583,501 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8883:Or5w17
|
UTSW |
2 |
87,583,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R9129:Or5w17
|
UTSW |
2 |
87,584,048 (GRCm39) |
missense |
probably benign |
0.00 |
R9587:Or5w17
|
UTSW |
2 |
87,584,184 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9665:Or5w17
|
UTSW |
2 |
87,583,671 (GRCm39) |
missense |
probably damaging |
0.97 |
T0722:Or5w17
|
UTSW |
2 |
87,583,467 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Or5w17
|
UTSW |
2 |
87,583,534 (GRCm39) |
missense |
possibly damaging |
0.95 |
|