Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
C |
11: 110,029,107 (GRCm39) |
E817G |
probably benign |
Het |
Abhd12b |
A |
G |
12: 70,215,988 (GRCm39) |
T182A |
probably benign |
Het |
Allc |
A |
T |
12: 28,607,414 (GRCm39) |
C279* |
probably null |
Het |
Ang |
A |
G |
14: 51,338,976 (GRCm39) |
D39G |
probably damaging |
Het |
Atp8b3 |
G |
A |
10: 80,360,197 (GRCm39) |
T958M |
probably damaging |
Het |
Ccn4 |
G |
A |
15: 66,784,900 (GRCm39) |
R191K |
probably benign |
Het |
Ccnyl1 |
A |
G |
1: 64,753,750 (GRCm39) |
Y187C |
probably damaging |
Het |
Cfhr4 |
A |
T |
1: 139,668,169 (GRCm39) |
S321R |
probably benign |
Het |
Chd3 |
A |
T |
11: 69,251,015 (GRCm39) |
W616R |
probably damaging |
Het |
Cyp17a1 |
C |
T |
19: 46,657,165 (GRCm39) |
R361H |
probably damaging |
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Dcp1a |
A |
G |
14: 30,201,691 (GRCm39) |
Q38R |
probably benign |
Het |
Ddias |
T |
C |
7: 92,507,560 (GRCm39) |
N785S |
probably benign |
Het |
Depdc5 |
A |
G |
5: 33,122,076 (GRCm39) |
N1133S |
probably benign |
Het |
Dhx8 |
T |
A |
11: 101,645,614 (GRCm39) |
Y877* |
probably null |
Het |
Dlk1 |
G |
A |
12: 109,420,889 (GRCm39) |
V15I |
unknown |
Het |
Fam120b |
G |
A |
17: 15,626,020 (GRCm39) |
A458T |
possibly damaging |
Het |
Fgd4 |
G |
A |
16: 16,308,353 (GRCm39) |
T9I |
probably benign |
Het |
Fhip1b |
C |
A |
7: 105,038,915 (GRCm39) |
R108L |
probably damaging |
Het |
Gfpt1 |
C |
T |
6: 87,062,323 (GRCm39) |
R561W |
probably damaging |
Het |
Gm5773 |
A |
G |
3: 93,680,340 (GRCm39) |
D4G |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,882,470 (GRCm39) |
T108S |
probably damaging |
Het |
Hivep1 |
G |
A |
13: 42,308,251 (GRCm39) |
D164N |
possibly damaging |
Het |
Kif15 |
G |
T |
9: 122,828,585 (GRCm39) |
L902F |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,261,497 (GRCm39) |
R4481S |
probably damaging |
Het |
Mcm3ap |
T |
C |
10: 76,332,310 (GRCm39) |
V1209A |
probably damaging |
Het |
Mkrn1 |
C |
T |
6: 39,376,838 (GRCm39) |
R377H |
probably benign |
Het |
Ms4a4a |
G |
A |
19: 11,367,708 (GRCm39) |
M191I |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,018,580 (GRCm39) |
N1922I |
|
Het |
Nbeal1 |
C |
T |
1: 60,290,287 (GRCm39) |
Q998* |
probably null |
Het |
Neil3 |
C |
A |
8: 54,061,770 (GRCm39) |
G204C |
probably damaging |
Het |
Nsmce1 |
T |
C |
7: 125,066,994 (GRCm39) |
E262G |
possibly damaging |
Het |
Oc90 |
G |
A |
15: 65,761,437 (GRCm39) |
P194S |
probably benign |
Het |
Oplah |
A |
G |
15: 76,193,787 (GRCm39) |
S57P |
probably benign |
Het |
Or10u4 |
A |
T |
10: 129,802,181 (GRCm39) |
F123L |
probably benign |
Het |
Or1x6 |
T |
A |
11: 50,939,223 (GRCm39) |
Y96* |
probably null |
Het |
Or2aj4 |
T |
A |
16: 19,384,722 (GRCm39) |
I304F |
possibly damaging |
Het |
Or4a73 |
C |
A |
2: 89,420,710 (GRCm39) |
V250F |
probably damaging |
Het |
Or51g1 |
A |
T |
7: 102,633,774 (GRCm39) |
I199N |
probably damaging |
Het |
Or5p70 |
A |
G |
7: 107,994,365 (GRCm39) |
T13A |
probably benign |
Het |
Or8g28 |
A |
C |
9: 39,169,756 (GRCm39) |
F71V |
possibly damaging |
Het |
Pdzd8 |
A |
T |
19: 59,333,574 (GRCm39) |
L149Q |
probably damaging |
Het |
Pid1 |
A |
G |
1: 84,137,032 (GRCm39) |
V33A |
probably benign |
Het |
Polr3gl |
A |
G |
3: 96,489,037 (GRCm39) |
V60A |
possibly damaging |
Het |
Prdm1 |
A |
G |
10: 44,317,242 (GRCm39) |
V527A |
probably benign |
Het |
Sbf2 |
T |
C |
7: 110,040,671 (GRCm39) |
I385M |
probably damaging |
Het |
Setbp1 |
C |
T |
18: 78,826,599 (GRCm39) |
S1338N |
probably benign |
Het |
Sh2b2 |
T |
C |
5: 136,253,006 (GRCm39) |
T389A |
probably benign |
Het |
Skint9 |
A |
T |
4: 112,248,915 (GRCm39) |
M171K |
probably benign |
Het |
Slx4 |
C |
A |
16: 3,805,820 (GRCm39) |
M577I |
probably benign |
Het |
Srcap |
T |
C |
7: 127,151,577 (GRCm39) |
S2092P |
probably damaging |
Het |
Traf6 |
T |
A |
2: 101,518,953 (GRCm39) |
H147Q |
probably benign |
Het |
Ttn |
T |
A |
2: 76,547,693 (GRCm39) |
E32159V |
possibly damaging |
Het |
Ubn1 |
T |
C |
16: 4,888,492 (GRCm39) |
S154P |
unknown |
Het |
Uchl1 |
T |
A |
5: 66,833,649 (GRCm39) |
M6K |
probably damaging |
Het |
Vmn1r193 |
A |
T |
13: 22,403,989 (GRCm39) |
M1K |
probably null |
Het |
Zfp429 |
T |
A |
13: 67,538,531 (GRCm39) |
K304N |
probably benign |
Het |
Zfp607b |
T |
A |
7: 27,402,464 (GRCm39) |
S307T |
probably damaging |
Het |
|
Other mutations in Or4d5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00946:Or4d5
|
APN |
9 |
40,012,450 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01402:Or4d5
|
APN |
9 |
40,012,558 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01404:Or4d5
|
APN |
9 |
40,012,558 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01445:Or4d5
|
APN |
9 |
40,012,608 (GRCm39) |
missense |
probably benign |
0.45 |
IGL01448:Or4d5
|
APN |
9 |
40,012,378 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02598:Or4d5
|
APN |
9 |
40,011,861 (GRCm39) |
missense |
probably benign |
|
IGL03106:Or4d5
|
APN |
9 |
40,012,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Or4d5
|
UTSW |
9 |
40,012,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0712:Or4d5
|
UTSW |
9 |
40,012,726 (GRCm39) |
missense |
probably benign |
|
R2049:Or4d5
|
UTSW |
9 |
40,012,415 (GRCm39) |
missense |
probably benign |
|
R2938:Or4d5
|
UTSW |
9 |
40,012,039 (GRCm39) |
missense |
probably benign |
0.20 |
R4609:Or4d5
|
UTSW |
9 |
40,012,102 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4907:Or4d5
|
UTSW |
9 |
40,011,955 (GRCm39) |
missense |
probably benign |
0.02 |
R5001:Or4d5
|
UTSW |
9 |
40,012,523 (GRCm39) |
missense |
probably benign |
0.02 |
R5174:Or4d5
|
UTSW |
9 |
40,012,043 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5587:Or4d5
|
UTSW |
9 |
40,012,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5880:Or4d5
|
UTSW |
9 |
40,012,543 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5896:Or4d5
|
UTSW |
9 |
40,012,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R6611:Or4d5
|
UTSW |
9 |
40,012,316 (GRCm39) |
missense |
probably benign |
0.03 |
R6904:Or4d5
|
UTSW |
9 |
40,012,652 (GRCm39) |
missense |
probably benign |
0.04 |
R7015:Or4d5
|
UTSW |
9 |
40,012,751 (GRCm39) |
missense |
probably benign |
0.30 |
R7870:Or4d5
|
UTSW |
9 |
40,011,973 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8191:Or4d5
|
UTSW |
9 |
40,012,767 (GRCm39) |
missense |
probably benign |
0.13 |
R8739:Or4d5
|
UTSW |
9 |
40,012,636 (GRCm39) |
missense |
probably benign |
0.13 |
R8799:Or4d5
|
UTSW |
9 |
40,011,985 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9307:Or4d5
|
UTSW |
9 |
40,012,451 (GRCm39) |
missense |
probably benign |
0.00 |
R9315:Or4d5
|
UTSW |
9 |
40,012,270 (GRCm39) |
missense |
probably benign |
0.02 |
R9497:Or4d5
|
UTSW |
9 |
40,011,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Or4d5
|
UTSW |
9 |
40,011,864 (GRCm39) |
missense |
probably benign |
0.01 |
|