Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
A |
G |
9: 104,003,855 (GRCm39) |
E649G |
probably damaging |
Het |
Adgre1 |
C |
A |
17: 57,726,335 (GRCm39) |
T402K |
probably benign |
Het |
Agap3 |
A |
G |
5: 24,706,000 (GRCm39) |
|
probably benign |
Het |
Amy1 |
T |
C |
3: 113,349,689 (GRCm39) |
I494V |
probably benign |
Het |
Arhgef40 |
G |
A |
14: 52,229,155 (GRCm39) |
|
probably null |
Het |
Atp2c2 |
T |
C |
8: 120,472,329 (GRCm39) |
V461A |
probably benign |
Het |
Bub1 |
A |
G |
2: 127,652,583 (GRCm39) |
S595P |
probably damaging |
Het |
Cdcp3 |
T |
A |
7: 130,844,836 (GRCm39) |
Y692* |
probably null |
Het |
Cmya5 |
C |
T |
13: 93,234,414 (GRCm39) |
V225I |
probably benign |
Het |
Cnbd1 |
T |
C |
4: 18,906,988 (GRCm39) |
|
probably benign |
Het |
Cux1 |
A |
T |
5: 136,340,345 (GRCm39) |
|
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,656,664 (GRCm39) |
I178N |
probably benign |
Het |
Dus2 |
T |
A |
8: 106,752,533 (GRCm39) |
|
probably null |
Het |
Enpp1 |
G |
A |
10: 24,529,929 (GRCm39) |
H570Y |
probably damaging |
Het |
Ephb3 |
A |
C |
16: 21,036,044 (GRCm39) |
T57P |
probably benign |
Het |
Fat3 |
C |
A |
9: 15,910,390 (GRCm39) |
V1871F |
possibly damaging |
Het |
Fbll1 |
T |
C |
11: 35,688,874 (GRCm39) |
T130A |
probably benign |
Het |
Fbxl20 |
C |
T |
11: 98,001,800 (GRCm39) |
S99N |
probably damaging |
Het |
Folr2 |
T |
C |
7: 101,489,593 (GRCm39) |
E182G |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,703,080 (GRCm39) |
D281G |
probably benign |
Het |
Gm17175 |
G |
T |
14: 51,810,526 (GRCm39) |
Q34K |
possibly damaging |
Het |
Gm5592 |
T |
A |
7: 40,938,519 (GRCm39) |
D600E |
probably damaging |
Het |
Gtf2e1 |
T |
C |
16: 37,336,092 (GRCm39) |
E294G |
probably benign |
Het |
Gtf3c2 |
A |
G |
5: 31,327,517 (GRCm39) |
|
probably benign |
Het |
Heg1 |
T |
C |
16: 33,530,977 (GRCm39) |
L151P |
probably damaging |
Het |
Hmcn2 |
T |
G |
2: 31,319,006 (GRCm39) |
V3902G |
probably damaging |
Het |
Ift140 |
A |
G |
17: 25,237,776 (GRCm39) |
Y4C |
probably damaging |
Het |
Ighv1-19 |
A |
C |
12: 114,672,569 (GRCm39) |
V17G |
possibly damaging |
Het |
Iqca1 |
T |
A |
1: 89,973,379 (GRCm39) |
I770F |
probably benign |
Het |
Jak3 |
T |
A |
8: 72,131,656 (GRCm39) |
C115S |
probably benign |
Het |
Kif18b |
A |
T |
11: 102,805,501 (GRCm39) |
M252K |
probably damaging |
Het |
Klhdc7a |
A |
T |
4: 139,694,236 (GRCm39) |
V237D |
probably benign |
Het |
Klhl11 |
C |
T |
11: 100,354,031 (GRCm39) |
V597I |
possibly damaging |
Het |
Krt72 |
T |
A |
15: 101,689,396 (GRCm39) |
Y312F |
probably damaging |
Het |
Lonp2 |
T |
A |
8: 87,360,600 (GRCm39) |
I191N |
probably damaging |
Het |
Npc2 |
A |
T |
12: 84,819,619 (GRCm39) |
I8N |
possibly damaging |
Het |
Nr4a1 |
T |
C |
15: 101,170,669 (GRCm39) |
L413P |
probably damaging |
Het |
Nup133 |
T |
C |
8: 124,638,645 (GRCm39) |
N895S |
probably damaging |
Het |
Ppef1 |
A |
G |
X: 159,468,290 (GRCm39) |
I94T |
probably benign |
Het |
Prrt4 |
G |
A |
6: 29,176,455 (GRCm39) |
T290I |
probably benign |
Het |
Ptpru |
A |
T |
4: 131,499,927 (GRCm39) |
V1239E |
probably damaging |
Het |
Rab8b |
T |
G |
9: 66,760,274 (GRCm39) |
M117L |
probably benign |
Het |
S1pr5 |
T |
A |
9: 21,155,512 (GRCm39) |
I305F |
possibly damaging |
Het |
Sdr39u1 |
A |
G |
14: 56,135,463 (GRCm39) |
V160A |
probably damaging |
Het |
Slc6a21 |
C |
T |
7: 44,937,668 (GRCm39) |
T653M |
probably benign |
Het |
Stk39 |
T |
A |
2: 68,042,302 (GRCm39) |
E544D |
probably benign |
Het |
Tgfbr3 |
T |
C |
5: 107,290,367 (GRCm39) |
T313A |
probably benign |
Het |
Tle6 |
A |
T |
10: 81,430,292 (GRCm39) |
L287M |
probably damaging |
Het |
Tmc2 |
A |
G |
2: 130,105,932 (GRCm39) |
H821R |
probably benign |
Het |
Tmem230 |
G |
T |
2: 132,087,897 (GRCm39) |
D26E |
probably benign |
Het |
Tnfaip3 |
A |
G |
10: 18,880,885 (GRCm39) |
F394S |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,641,721 (GRCm39) |
L13458F |
probably damaging |
Het |
Vwa5a |
A |
T |
9: 38,634,675 (GRCm39) |
N161I |
probably benign |
Het |
Wdr87-ps |
C |
A |
7: 29,236,888 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Or7e175 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01550:Or7e175
|
APN |
9 |
20,048,750 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02247:Or7e175
|
APN |
9 |
20,048,516 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02448:Or7e175
|
APN |
9 |
20,048,937 (GRCm39) |
nonsense |
probably null |
|
IGL03076:Or7e175
|
APN |
9 |
20,049,023 (GRCm39) |
missense |
probably benign |
0.25 |
R0045:Or7e175
|
UTSW |
9 |
20,048,487 (GRCm39) |
missense |
probably benign |
0.25 |
R0962:Or7e175
|
UTSW |
9 |
20,048,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R4588:Or7e175
|
UTSW |
9 |
20,049,383 (GRCm39) |
makesense |
probably null |
|
R4931:Or7e175
|
UTSW |
9 |
20,048,858 (GRCm39) |
missense |
probably benign |
0.19 |
R5030:Or7e175
|
UTSW |
9 |
20,049,363 (GRCm39) |
missense |
probably benign |
0.01 |
R5759:Or7e175
|
UTSW |
9 |
20,049,228 (GRCm39) |
missense |
probably benign |
0.12 |
R5780:Or7e175
|
UTSW |
9 |
20,048,793 (GRCm39) |
missense |
probably damaging |
0.98 |
R6440:Or7e175
|
UTSW |
9 |
20,048,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R6599:Or7e175
|
UTSW |
9 |
20,049,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R6710:Or7e175
|
UTSW |
9 |
20,049,378 (GRCm39) |
missense |
probably benign |
0.01 |
R6953:Or7e175
|
UTSW |
9 |
20,049,299 (GRCm39) |
missense |
probably benign |
0.00 |
R7288:Or7e175
|
UTSW |
9 |
20,048,737 (GRCm39) |
nonsense |
probably null |
|
R7585:Or7e175
|
UTSW |
9 |
20,040,307 (GRCm39) |
|
|
|
R7860:Or7e175
|
UTSW |
9 |
20,048,871 (GRCm39) |
missense |
probably benign |
0.16 |
R8025:Or7e175
|
UTSW |
9 |
20,048,928 (GRCm39) |
missense |
probably benign |
0.01 |
R8178:Or7e175
|
UTSW |
9 |
20,048,571 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8794:Or7e175
|
UTSW |
9 |
20,048,630 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8954:Or7e175
|
UTSW |
9 |
20,048,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R9116:Or7e175
|
UTSW |
9 |
20,048,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R9162:Or7e175
|
UTSW |
9 |
20,040,457 (GRCm39) |
missense |
probably benign |
0.00 |
R9269:Or7e175
|
UTSW |
9 |
20,048,757 (GRCm39) |
missense |
probably damaging |
1.00 |
|