Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 138,070,059 (GRCm38) |
Y1670H |
probably damaging |
Het |
Abca12 |
T |
C |
1: 71,307,053 (GRCm38) |
K886R |
possibly damaging |
Het |
Adcy3 |
G |
A |
12: 4,200,992 (GRCm38) |
E584K |
probably benign |
Het |
Ano3 |
A |
T |
2: 110,862,860 (GRCm38) |
V131D |
probably benign |
Het |
Arhgdig |
C |
T |
17: 26,199,363 (GRCm38) |
W215* |
probably null |
Het |
Cad |
G |
T |
5: 31,067,612 (GRCm38) |
W953L |
possibly damaging |
Het |
Calhm2 |
T |
C |
19: 47,135,641 (GRCm38) |
Y88C |
probably benign |
Het |
Cdk5rap2 |
A |
T |
4: 70,238,231 (GRCm38) |
D1681E |
probably benign |
Het |
Cenpl |
T |
A |
1: 161,082,912 (GRCm38) |
L143H |
possibly damaging |
Het |
Cherp |
T |
C |
8: 72,468,386 (GRCm38) |
K270E |
|
Het |
Cmss1 |
A |
G |
16: 57,311,355 (GRCm38) |
I136T |
probably benign |
Het |
Col23a1 |
T |
C |
11: 51,565,223 (GRCm38) |
|
probably null |
Het |
Crnn |
C |
A |
3: 93,148,382 (GRCm38) |
D158E |
probably damaging |
Het |
Dnmt3a |
A |
T |
12: 3,872,844 (GRCm38) |
Q149L |
probably benign |
Het |
Dst |
T |
A |
1: 34,189,882 (GRCm38) |
N2185K |
probably benign |
Het |
Elp2 |
T |
A |
18: 24,604,069 (GRCm38) |
N25K |
probably benign |
Het |
Ephb4 |
A |
T |
5: 137,372,046 (GRCm38) |
D845V |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,319,574 (GRCm38) |
T561A |
probably damaging |
Het |
F3 |
G |
T |
3: 121,731,586 (GRCm38) |
V159L |
probably damaging |
Het |
Fam81a |
A |
T |
9: 70,110,278 (GRCm38) |
D128E |
probably damaging |
Het |
Flot1 |
T |
G |
17: 35,824,943 (GRCm38) |
H155Q |
probably benign |
Het |
Fut9 |
T |
A |
4: 25,620,507 (GRCm38) |
K102N |
probably damaging |
Het |
Gm16368 |
G |
T |
12: 88,083,827 (GRCm38) |
C44F |
probably benign |
Het |
Gm6309 |
T |
C |
5: 146,170,290 (GRCm38) |
Q82R |
possibly damaging |
Het |
H13 |
A |
G |
2: 152,681,072 (GRCm38) |
N102D |
probably damaging |
Het |
Lamc2 |
C |
G |
1: 153,130,772 (GRCm38) |
A878P |
possibly damaging |
Het |
Lepr |
C |
T |
4: 101,752,197 (GRCm38) |
T327I |
probably benign |
Het |
Lrp2 |
A |
G |
2: 69,454,808 (GRCm38) |
|
probably null |
Het |
Ly86 |
A |
G |
13: 37,377,010 (GRCm38) |
K116E |
probably damaging |
Het |
Mapk8ip2 |
T |
A |
15: 89,458,998 (GRCm38) |
F648I |
possibly damaging |
Het |
Muc16 |
G |
A |
9: 18,655,580 (GRCm38) |
T1881I |
unknown |
Het |
Myh13 |
T |
G |
11: 67,354,740 (GRCm38) |
S1069A |
probably benign |
Het |
Myh4 |
T |
A |
11: 67,260,228 (GRCm38) |
I1903N |
possibly damaging |
Het |
Myo18b |
A |
T |
5: 112,817,679 (GRCm38) |
L1341* |
probably null |
Het |
Naa25 |
G |
T |
5: 121,417,489 (GRCm38) |
|
probably null |
Het |
Nbeal1 |
G |
C |
1: 60,237,151 (GRCm38) |
V684L |
probably benign |
Het |
Ncapg |
C |
T |
5: 45,670,030 (GRCm38) |
A3V |
possibly damaging |
Het |
Ncln |
T |
C |
10: 81,488,252 (GRCm38) |
H481R |
probably benign |
Het |
Nek4 |
C |
A |
14: 30,982,348 (GRCm38) |
Q607K |
probably damaging |
Het |
Neo1 |
T |
C |
9: 58,889,179 (GRCm38) |
Y1182C |
probably damaging |
Het |
Npnt |
T |
C |
3: 132,909,931 (GRCm38) |
N165S |
probably benign |
Het |
Olfr1076 |
T |
C |
2: 86,508,528 (GRCm38) |
L23P |
probably damaging |
Het |
Olfr1184 |
C |
T |
2: 88,487,377 (GRCm38) |
S215L |
probably damaging |
Het |
Olfr145 |
A |
G |
9: 37,897,563 (GRCm38) |
H53R |
probably benign |
Het |
Otulin |
T |
C |
15: 27,608,770 (GRCm38) |
Y229C |
probably damaging |
Het |
Palld |
A |
T |
8: 61,532,017 (GRCm38) |
D1071E |
unknown |
Het |
Pcdhb20 |
T |
C |
18: 37,505,089 (GRCm38) |
S223P |
probably damaging |
Het |
Pcdhga6 |
T |
A |
18: 37,707,728 (GRCm38) |
I167N |
probably damaging |
Het |
Pcdhgb4 |
A |
G |
18: 37,721,790 (GRCm38) |
N413D |
probably benign |
Het |
Pcdhgb8 |
T |
A |
18: 37,762,997 (GRCm38) |
Y373* |
probably null |
Het |
Plxna2 |
G |
T |
1: 194,649,522 (GRCm38) |
V419L |
probably benign |
Het |
Rpgrip1l |
A |
T |
8: 91,232,806 (GRCm38) |
|
probably null |
Het |
Rsrc2 |
A |
G |
5: 123,739,567 (GRCm38) |
|
probably benign |
Het |
Scaper |
C |
T |
9: 55,912,111 (GRCm38) |
D107N |
unknown |
Het |
Scgb2b3 |
T |
A |
7: 31,360,148 (GRCm38) |
Y67F |
probably benign |
Het |
Scn5a |
G |
A |
9: 119,486,371 (GRCm38) |
T1757I |
probably damaging |
Het |
Sgo2b |
G |
A |
8: 63,928,184 (GRCm38) |
P538L |
probably damaging |
Het |
Slc9a3 |
A |
G |
13: 74,150,678 (GRCm38) |
K72R |
probably damaging |
Het |
Smchd1 |
T |
A |
17: 71,378,207 (GRCm38) |
T1409S |
probably benign |
Het |
Stab1 |
A |
T |
14: 31,145,073 (GRCm38) |
|
probably null |
Het |
Sult2b1 |
T |
C |
7: 45,733,632 (GRCm38) |
E242G |
probably damaging |
Het |
Tcaf1 |
A |
T |
6: 42,686,753 (GRCm38) |
H64Q |
probably damaging |
Het |
Tle6 |
T |
C |
10: 81,600,076 (GRCm38) |
T2A |
possibly damaging |
Het |
Tmem115 |
T |
C |
9: 107,535,086 (GRCm38) |
V203A |
probably benign |
Het |
Tmem45b |
G |
A |
9: 31,429,041 (GRCm38) |
T108I |
probably damaging |
Het |
Tmf1 |
A |
T |
6: 97,176,118 (GRCm38) |
D331E |
probably damaging |
Het |
Txndc9 |
T |
C |
1: 37,990,296 (GRCm38) |
Y157C |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,559,051 (GRCm38) |
N549S |
possibly damaging |
Het |
Vmn2r27 |
C |
A |
6: 124,191,752 (GRCm38) |
R806S |
probably benign |
Het |
Vmn2r59 |
G |
A |
7: 42,045,764 (GRCm38) |
A408V |
probably damaging |
Het |
Ythdc1 |
T |
C |
5: 86,816,608 (GRCm38) |
V92A |
probably benign |
Het |
|
Other mutations in Olfr167 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01535:Olfr167
|
APN |
16 |
19,515,478 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02115:Olfr167
|
APN |
16 |
19,515,103 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02562:Olfr167
|
APN |
16 |
19,514,964 (GRCm38) |
missense |
possibly damaging |
0.74 |
BB008:Olfr167
|
UTSW |
16 |
19,515,508 (GRCm38) |
missense |
possibly damaging |
0.94 |
BB018:Olfr167
|
UTSW |
16 |
19,515,508 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0366:Olfr167
|
UTSW |
16 |
19,514,848 (GRCm38) |
missense |
probably benign |
0.13 |
R0673:Olfr167
|
UTSW |
16 |
19,515,396 (GRCm38) |
missense |
probably damaging |
1.00 |
R1187:Olfr167
|
UTSW |
16 |
19,515,046 (GRCm38) |
missense |
probably benign |
0.01 |
R1237:Olfr167
|
UTSW |
16 |
19,515,625 (GRCm38) |
missense |
probably benign |
0.01 |
R1975:Olfr167
|
UTSW |
16 |
19,514,836 (GRCm38) |
missense |
probably damaging |
0.99 |
R1977:Olfr167
|
UTSW |
16 |
19,514,836 (GRCm38) |
missense |
probably damaging |
0.99 |
R1997:Olfr167
|
UTSW |
16 |
19,515,042 (GRCm38) |
missense |
probably damaging |
1.00 |
R2225:Olfr167
|
UTSW |
16 |
19,515,246 (GRCm38) |
missense |
probably benign |
0.05 |
R2226:Olfr167
|
UTSW |
16 |
19,515,246 (GRCm38) |
missense |
probably benign |
0.05 |
R4078:Olfr167
|
UTSW |
16 |
19,515,232 (GRCm38) |
missense |
possibly damaging |
0.76 |
R5019:Olfr167
|
UTSW |
16 |
19,515,535 (GRCm38) |
missense |
probably damaging |
0.99 |
R5071:Olfr167
|
UTSW |
16 |
19,515,027 (GRCm38) |
missense |
probably benign |
0.00 |
R5278:Olfr167
|
UTSW |
16 |
19,515,378 (GRCm38) |
nonsense |
probably null |
|
R5415:Olfr167
|
UTSW |
16 |
19,515,246 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5744:Olfr167
|
UTSW |
16 |
19,515,336 (GRCm38) |
missense |
probably benign |
0.00 |
R5991:Olfr167
|
UTSW |
16 |
19,514,757 (GRCm38) |
missense |
probably damaging |
0.99 |
R6151:Olfr167
|
UTSW |
16 |
19,515,531 (GRCm38) |
missense |
probably damaging |
1.00 |
R6540:Olfr167
|
UTSW |
16 |
19,514,821 (GRCm38) |
missense |
probably benign |
|
R7014:Olfr167
|
UTSW |
16 |
19,515,456 (GRCm38) |
missense |
probably benign |
0.20 |
R7535:Olfr167
|
UTSW |
16 |
19,514,794 (GRCm38) |
missense |
probably damaging |
1.00 |
R7677:Olfr167
|
UTSW |
16 |
19,514,928 (GRCm38) |
missense |
probably benign |
0.42 |
R7715:Olfr167
|
UTSW |
16 |
19,514,730 (GRCm38) |
missense |
probably benign |
0.00 |
R7931:Olfr167
|
UTSW |
16 |
19,515,508 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8137:Olfr167
|
UTSW |
16 |
19,515,096 (GRCm38) |
missense |
possibly damaging |
0.89 |
R8671:Olfr167
|
UTSW |
16 |
19,515,054 (GRCm38) |
missense |
possibly damaging |
0.63 |
|