Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
A |
8: 73,198,923 (GRCm39) |
A110D |
probably benign |
Het |
4930407I10Rik |
A |
G |
15: 81,947,615 (GRCm39) |
E504G |
probably benign |
Het |
Apbb2 |
T |
C |
5: 66,609,018 (GRCm39) |
K210E |
probably benign |
Het |
Arhgef37 |
G |
T |
18: 61,651,072 (GRCm39) |
A151D |
probably damaging |
Het |
Btaf1 |
A |
G |
19: 36,964,114 (GRCm39) |
Y895C |
probably benign |
Het |
Catsperb |
A |
G |
12: 101,560,600 (GRCm39) |
I864V |
possibly damaging |
Het |
Cdhr17 |
T |
A |
5: 16,996,855 (GRCm39) |
C10* |
probably null |
Het |
Cmklr1 |
G |
C |
5: 113,752,043 (GRCm39) |
H319Q |
probably benign |
Het |
Col18a1 |
G |
A |
10: 76,893,204 (GRCm39) |
T1057M |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,515,260 (GRCm39) |
|
probably null |
Het |
Col6a4 |
A |
G |
9: 105,945,534 (GRCm39) |
I860T |
probably damaging |
Het |
Csmd3 |
A |
C |
15: 47,617,187 (GRCm39) |
H1000Q |
|
Het |
Cyp4a29 |
T |
A |
4: 115,108,395 (GRCm39) |
M373K |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,333,173 (GRCm39) |
E215G |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,597,087 (GRCm39) |
E1972G |
probably damaging |
Het |
Dusp19 |
T |
C |
2: 80,447,729 (GRCm39) |
M1T |
probably null |
Het |
Eif4b |
A |
G |
15: 101,990,449 (GRCm39) |
T18A |
possibly damaging |
Het |
Exosc6 |
G |
A |
8: 111,783,513 (GRCm39) |
A171T |
probably damaging |
Het |
Fau |
G |
A |
19: 6,108,297 (GRCm39) |
R6H |
probably benign |
Het |
Flrt3 |
T |
C |
2: 140,501,879 (GRCm39) |
D583G |
probably damaging |
Het |
Fpgt |
A |
T |
3: 154,792,695 (GRCm39) |
L444* |
probably null |
Het |
Gm10226 |
A |
G |
17: 21,910,768 (GRCm39) |
E1G |
probably null |
Het |
Gm14443 |
A |
T |
2: 175,011,869 (GRCm39) |
C192* |
probably null |
Het |
Gm4353 |
T |
A |
7: 115,682,843 (GRCm39) |
N246I |
probably benign |
Het |
Igfn1 |
A |
G |
1: 135,926,327 (GRCm39) |
L41P |
probably benign |
Het |
Iigp1 |
T |
G |
18: 60,523,063 (GRCm39) |
D60E |
probably benign |
Het |
Kcnt2 |
T |
A |
1: 140,353,035 (GRCm39) |
V248D |
probably damaging |
Het |
Kctd14 |
A |
G |
7: 97,107,243 (GRCm39) |
K166R |
probably benign |
Het |
Kdm4d |
G |
A |
9: 14,375,336 (GRCm39) |
T174M |
probably damaging |
Het |
Kdm5b |
T |
C |
1: 134,528,493 (GRCm39) |
|
probably null |
Het |
Maz |
CGCGGCCTCGGCGGCTGGTGCGG |
CGCGG |
7: 126,625,075 (GRCm39) |
|
probably benign |
Het |
Mrtfb |
A |
G |
16: 13,202,082 (GRCm39) |
Q115R |
probably benign |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Or10a5 |
A |
T |
7: 106,635,640 (GRCm39) |
I93F |
probably damaging |
Het |
Or5b95 |
T |
A |
19: 12,658,190 (GRCm39) |
C239* |
probably null |
Het |
Pigc |
C |
T |
1: 161,798,032 (GRCm39) |
R5C |
probably benign |
Het |
Plekhm2 |
C |
A |
4: 141,356,829 (GRCm39) |
M771I |
probably benign |
Het |
Runx1 |
T |
A |
16: 92,441,147 (GRCm39) |
T221S |
possibly damaging |
Het |
S100pbp |
A |
G |
4: 129,044,847 (GRCm39) |
Y363H |
probably damaging |
Het |
Sema5a |
A |
G |
15: 32,619,040 (GRCm39) |
T523A |
probably benign |
Het |
Slc38a8 |
A |
G |
8: 120,212,851 (GRCm39) |
F270S |
possibly damaging |
Het |
Slc4a1ap |
T |
C |
5: 31,693,538 (GRCm39) |
S491P |
probably damaging |
Het |
Slc66a2 |
T |
C |
18: 80,300,300 (GRCm39) |
L57P |
probably damaging |
Het |
Slc7a6 |
T |
C |
8: 106,922,534 (GRCm39) |
V440A |
probably damaging |
Het |
Sobp |
A |
T |
10: 42,898,902 (GRCm39) |
C228S |
probably damaging |
Het |
Svop |
G |
A |
5: 114,168,231 (GRCm39) |
T456M |
probably benign |
Het |
Synrg |
A |
G |
11: 83,900,278 (GRCm39) |
D750G |
probably damaging |
Het |
Syt14 |
C |
A |
1: 192,612,944 (GRCm39) |
E336* |
probably null |
Het |
Tcp11l1 |
C |
T |
2: 104,528,897 (GRCm39) |
V134I |
possibly damaging |
Het |
Tex51 |
T |
C |
18: 32,594,029 (GRCm39) |
R110G |
possibly damaging |
Het |
Tle3 |
T |
A |
9: 61,319,562 (GRCm39) |
H443Q |
possibly damaging |
Het |
Unc13a |
C |
T |
8: 72,108,335 (GRCm39) |
R506Q |
possibly damaging |
Het |
Vmn1r121 |
A |
C |
7: 20,832,344 (GRCm39) |
V32G |
probably damaging |
Het |
Wiz |
A |
G |
17: 32,580,714 (GRCm39) |
F246L |
probably benign |
Het |
Zfp672 |
A |
T |
11: 58,220,590 (GRCm39) |
M3K |
unknown |
Het |
Zfp709 |
A |
T |
8: 72,644,648 (GRCm39) |
E692D |
possibly damaging |
Het |
Zglp1 |
A |
T |
9: 20,977,482 (GRCm39) |
L111Q |
probably benign |
Het |
|
Other mutations in Or2h1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01087:Or2h1b
|
APN |
17 |
37,462,332 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02369:Or2h1b
|
APN |
17 |
37,462,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02392:Or2h1b
|
APN |
17 |
37,461,979 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02516:Or2h1b
|
APN |
17 |
37,462,163 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03089:Or2h1b
|
APN |
17 |
37,462,534 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4515001:Or2h1b
|
UTSW |
17 |
37,462,270 (GRCm39) |
missense |
probably benign |
|
R0396:Or2h1b
|
UTSW |
17 |
37,462,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R2276:Or2h1b
|
UTSW |
17 |
37,462,145 (GRCm39) |
nonsense |
probably null |
|
R2278:Or2h1b
|
UTSW |
17 |
37,462,145 (GRCm39) |
nonsense |
probably null |
|
R3419:Or2h1b
|
UTSW |
17 |
37,462,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R4254:Or2h1b
|
UTSW |
17 |
37,462,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4353:Or2h1b
|
UTSW |
17 |
37,462,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Or2h1b
|
UTSW |
17 |
37,462,498 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4666:Or2h1b
|
UTSW |
17 |
37,462,270 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5583:Or2h1b
|
UTSW |
17 |
37,462,485 (GRCm39) |
missense |
probably benign |
0.00 |
R5834:Or2h1b
|
UTSW |
17 |
37,462,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Or2h1b
|
UTSW |
17 |
37,462,497 (GRCm39) |
missense |
probably damaging |
0.96 |
R6461:Or2h1b
|
UTSW |
17 |
37,462,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Or2h1b
|
UTSW |
17 |
37,462,713 (GRCm39) |
missense |
probably damaging |
0.98 |
R7969:Or2h1b
|
UTSW |
17 |
37,462,077 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8374:Or2h1b
|
UTSW |
17 |
37,462,636 (GRCm39) |
missense |
probably damaging |
0.97 |
R9126:Or2h1b
|
UTSW |
17 |
37,462,123 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Or2h1b
|
UTSW |
17 |
37,462,716 (GRCm39) |
missense |
probably damaging |
0.99 |
|