Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb8 |
T |
C |
5: 24,607,317 (GRCm39) |
L363P |
probably damaging |
Het |
Adam12 |
T |
A |
7: 133,599,959 (GRCm39) |
H85L |
probably damaging |
Het |
Adam34 |
A |
T |
8: 44,104,621 (GRCm39) |
H341Q |
probably damaging |
Het |
Adam34l |
A |
T |
8: 44,078,160 (GRCm39) |
M688K |
probably benign |
Het |
Adam7 |
A |
G |
14: 68,754,133 (GRCm39) |
L322P |
probably damaging |
Het |
Adcy5 |
T |
A |
16: 34,976,613 (GRCm39) |
S49T |
probably benign |
Het |
Arfgap2 |
T |
C |
2: 91,104,150 (GRCm39) |
S374P |
probably benign |
Het |
Arpp19 |
G |
A |
9: 74,944,967 (GRCm39) |
|
probably benign |
Het |
Baz1a |
T |
C |
12: 54,941,773 (GRCm39) |
K1478E |
probably damaging |
Het |
Cdc27 |
G |
T |
11: 104,396,467 (GRCm39) |
A812E |
possibly damaging |
Het |
Chtf8 |
G |
A |
8: 107,612,150 (GRCm39) |
T263I |
probably damaging |
Het |
Clcn6 |
T |
C |
4: 148,113,849 (GRCm39) |
N70D |
probably benign |
Het |
Cntnap5c |
A |
T |
17: 58,349,553 (GRCm39) |
T289S |
possibly damaging |
Het |
Dzip3 |
T |
C |
16: 48,795,840 (GRCm39) |
N177S |
probably damaging |
Het |
Edar |
G |
T |
10: 58,465,313 (GRCm39) |
|
probably null |
Het |
Enam |
T |
A |
5: 88,641,919 (GRCm39) |
N244K |
possibly damaging |
Het |
Fbxw10 |
A |
G |
11: 62,767,770 (GRCm39) |
K874E |
probably damaging |
Het |
Glra3 |
A |
G |
8: 56,578,239 (GRCm39) |
E432G |
possibly damaging |
Het |
Grin3b |
G |
A |
10: 79,807,062 (GRCm39) |
R110Q |
probably benign |
Het |
Herc3 |
T |
A |
6: 58,845,748 (GRCm39) |
V423D |
possibly damaging |
Het |
Ifit2 |
A |
T |
19: 34,550,984 (GRCm39) |
T175S |
probably benign |
Het |
Kcnj8 |
T |
G |
6: 142,511,627 (GRCm39) |
I327L |
possibly damaging |
Het |
Kcns2 |
A |
T |
15: 34,839,242 (GRCm39) |
I202F |
probably benign |
Het |
Kif12 |
T |
C |
4: 63,087,010 (GRCm39) |
R305G |
possibly damaging |
Het |
Limch1 |
A |
G |
5: 67,154,576 (GRCm39) |
D362G |
probably damaging |
Het |
Lrba |
T |
C |
3: 86,687,540 (GRCm39) |
I2815T |
probably damaging |
Het |
Lrrtm1 |
G |
T |
6: 77,221,843 (GRCm39) |
M433I |
probably damaging |
Het |
Myh7b |
A |
G |
2: 155,462,040 (GRCm39) |
D312G |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 90,344,758 (GRCm39) |
I382N |
probably damaging |
Het |
Nudt6 |
C |
T |
3: 37,459,502 (GRCm39) |
R161H |
probably benign |
Het |
Or10w1 |
T |
A |
19: 13,631,816 (GRCm39) |
W8R |
probably damaging |
Het |
Or11g2 |
A |
C |
14: 50,856,044 (GRCm39) |
M122L |
possibly damaging |
Het |
Or4m1 |
A |
T |
14: 50,558,186 (GRCm39) |
Y35* |
probably null |
Het |
Pmf1 |
A |
T |
3: 88,303,369 (GRCm39) |
V64D |
probably damaging |
Het |
Pomgnt1 |
T |
A |
4: 116,009,048 (GRCm39) |
V29D |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,380,790 (GRCm39) |
H411L |
possibly damaging |
Het |
Pramel26 |
A |
T |
4: 143,539,378 (GRCm39) |
D38E |
probably benign |
Het |
Prex1 |
C |
T |
2: 166,428,457 (GRCm39) |
A925T |
probably benign |
Het |
Pus3 |
A |
G |
9: 35,476,327 (GRCm39) |
Y72C |
probably damaging |
Het |
Rnf20 |
T |
C |
4: 49,642,176 (GRCm39) |
S247P |
probably damaging |
Het |
Rnf213 |
T |
A |
11: 119,305,396 (GRCm39) |
D542E |
probably benign |
Het |
Sidt1 |
T |
C |
16: 44,063,895 (GRCm39) |
D786G |
probably benign |
Het |
Sirt6 |
A |
T |
10: 81,458,475 (GRCm39) |
D219E |
probably damaging |
Het |
Slc36a2 |
A |
T |
11: 55,072,411 (GRCm39) |
I67N |
probably damaging |
Het |
Slc47a1 |
A |
G |
11: 61,264,248 (GRCm39) |
F57S |
probably damaging |
Het |
Spg11 |
T |
A |
2: 121,924,968 (GRCm39) |
T756S |
probably damaging |
Het |
Sptbn1 |
C |
A |
11: 30,071,591 (GRCm39) |
R1447L |
probably damaging |
Het |
Tcf7l2 |
A |
G |
19: 55,907,387 (GRCm39) |
M340V |
probably damaging |
Het |
Thap1 |
T |
C |
8: 26,652,733 (GRCm39) |
V157A |
probably benign |
Het |
Ubash3b |
G |
A |
9: 40,934,853 (GRCm39) |
Q354* |
probably null |
Het |
Ubtd1 |
G |
A |
19: 42,020,460 (GRCm39) |
W68* |
probably null |
Het |
Wdr64 |
G |
T |
1: 175,620,647 (GRCm39) |
R793L |
probably damaging |
Het |
Zbtb24 |
C |
T |
10: 41,327,432 (GRCm39) |
T106I |
probably benign |
Het |
Zbtb26 |
T |
C |
2: 37,326,337 (GRCm39) |
N233S |
possibly damaging |
Het |
Zcchc24 |
A |
T |
14: 25,757,585 (GRCm39) |
N99K |
possibly damaging |
Het |
|
Other mutations in Or7e166 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01510:Or7e166
|
APN |
9 |
19,624,575 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01919:Or7e166
|
APN |
9 |
19,624,638 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02157:Or7e166
|
APN |
9 |
19,624,585 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02550:Or7e166
|
APN |
9 |
19,624,343 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03329:Or7e166
|
APN |
9 |
19,624,597 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02799:Or7e166
|
UTSW |
9 |
19,624,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R0356:Or7e166
|
UTSW |
9 |
19,624,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R1161:Or7e166
|
UTSW |
9 |
19,624,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Or7e166
|
UTSW |
9 |
19,624,386 (GRCm39) |
missense |
probably benign |
0.01 |
R5191:Or7e166
|
UTSW |
9 |
19,624,630 (GRCm39) |
missense |
probably damaging |
0.98 |
R5216:Or7e166
|
UTSW |
9 |
19,624,585 (GRCm39) |
missense |
probably benign |
0.07 |
R5259:Or7e166
|
UTSW |
9 |
19,624,109 (GRCm39) |
splice site |
probably null |
|
R5342:Or7e166
|
UTSW |
9 |
19,624,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5506:Or7e166
|
UTSW |
9 |
19,624,570 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5526:Or7e166
|
UTSW |
9 |
19,624,994 (GRCm39) |
nonsense |
probably null |
|
R5594:Or7e166
|
UTSW |
9 |
19,624,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R5928:Or7e166
|
UTSW |
9 |
19,625,049 (GRCm39) |
missense |
probably benign |
0.02 |
R6569:Or7e166
|
UTSW |
9 |
19,624,638 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Or7e166
|
UTSW |
9 |
19,624,765 (GRCm39) |
missense |
probably damaging |
0.98 |
R7077:Or7e166
|
UTSW |
9 |
19,624,428 (GRCm39) |
missense |
probably benign |
|
R7378:Or7e166
|
UTSW |
9 |
19,624,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Or7e166
|
UTSW |
9 |
19,624,767 (GRCm39) |
missense |
probably benign |
|
R8038:Or7e166
|
UTSW |
9 |
19,624,976 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8160:Or7e166
|
UTSW |
9 |
19,624,085 (GRCm39) |
intron |
probably benign |
|
R8223:Or7e166
|
UTSW |
9 |
19,624,705 (GRCm39) |
missense |
probably benign |
|
R8400:Or7e166
|
UTSW |
9 |
19,624,389 (GRCm39) |
missense |
probably benign |
0.45 |
R8780:Or7e166
|
UTSW |
9 |
19,624,653 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8946:Or7e166
|
UTSW |
9 |
19,624,885 (GRCm39) |
missense |
probably damaging |
0.99 |
R9164:Or7e166
|
UTSW |
9 |
19,624,954 (GRCm39) |
missense |
probably benign |
0.25 |
R9475:Or7e166
|
UTSW |
9 |
19,624,939 (GRCm39) |
missense |
probably benign |
0.01 |
|