Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210010C04Rik |
A |
G |
6: 41,035,462 (GRCm38) |
F6S |
probably benign |
Het |
2810474O19Rik |
T |
A |
6: 149,328,822 (GRCm38) |
I1122K |
probably benign |
Het |
A930003A15Rik |
T |
G |
16: 19,883,780 (GRCm38) |
|
noncoding transcript |
Het |
Abca5 |
T |
C |
11: 110,319,832 (GRCm38) |
T174A |
probably benign |
Het |
Abcg3 |
G |
A |
5: 104,966,814 (GRCm38) |
S279L |
probably benign |
Het |
Acap3 |
T |
C |
4: 155,896,912 (GRCm38) |
L85P |
probably damaging |
Het |
Adgrl3 |
A |
G |
5: 81,512,254 (GRCm38) |
K290R |
probably damaging |
Het |
Ankhd1 |
A |
G |
18: 36,647,621 (GRCm38) |
T1909A |
probably benign |
Het |
Asap1 |
T |
C |
15: 64,110,959 (GRCm38) |
D832G |
probably damaging |
Het |
Atp6v0a2 |
T |
A |
5: 124,718,488 (GRCm38) |
L702Q |
possibly damaging |
Het |
Bsn |
A |
G |
9: 108,113,231 (GRCm38) |
V1774A |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,853,248 (GRCm38) |
E48G |
probably benign |
Het |
Cdadc1 |
T |
C |
14: 59,568,044 (GRCm38) |
|
probably null |
Het |
Cfap65 |
C |
CA |
1: 74,917,273 (GRCm38) |
|
probably null |
Het |
Cln3 |
A |
C |
7: 126,582,799 (GRCm38) |
S30R |
probably benign |
Het |
Cluap1 |
C |
T |
16: 3,933,772 (GRCm38) |
R332W |
probably damaging |
Het |
Crb1 |
A |
T |
1: 139,337,425 (GRCm38) |
V85E |
probably benign |
Het |
Crocc |
G |
A |
4: 141,032,954 (GRCm38) |
R789W |
probably damaging |
Het |
Cwh43 |
A |
G |
5: 73,415,054 (GRCm38) |
I212V |
probably benign |
Het |
Cyp2t4 |
C |
A |
7: 27,158,160 (GRCm38) |
F391L |
probably benign |
Het |
Dhx35 |
G |
T |
2: 158,831,861 (GRCm38) |
R404L |
probably damaging |
Het |
Disp1 |
A |
G |
1: 183,088,378 (GRCm38) |
L826S |
probably damaging |
Het |
Dync2h1 |
T |
A |
9: 7,122,772 (GRCm38) |
E2061D |
probably damaging |
Het |
Ep300 |
T |
A |
15: 81,640,447 (GRCm38) |
Y1393N |
unknown |
Het |
Fap |
C |
T |
2: 62,524,207 (GRCm38) |
G446D |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 16,377,051 (GRCm38) |
I392T |
probably benign |
Het |
Fpr-rs4 |
CAGGAA |
CA |
17: 18,022,334 (GRCm38) |
|
probably null |
Het |
Glipr1l1 |
T |
C |
10: 112,060,476 (GRCm38) |
V56A |
probably damaging |
Het |
Grsf1 |
A |
G |
5: 88,672,658 (GRCm38) |
V7A |
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,633,659 (GRCm38) |
A3646V |
probably damaging |
Het |
Ipo9 |
A |
T |
1: 135,394,285 (GRCm38) |
I569N |
probably damaging |
Het |
Irs1 |
G |
T |
1: 82,290,042 (GRCm38) |
P151Q |
probably damaging |
Het |
Kalrn |
T |
C |
16: 34,307,724 (GRCm38) |
D491G |
possibly damaging |
Het |
Kctd7 |
T |
C |
5: 130,152,366 (GRCm38) |
L210P |
probably damaging |
Het |
Lifr |
C |
A |
15: 7,181,857 (GRCm38) |
D625E |
possibly damaging |
Het |
Lrguk |
T |
C |
6: 34,043,519 (GRCm38) |
V201A |
probably benign |
Het |
Mark1 |
A |
G |
1: 184,919,573 (GRCm38) |
V135A |
probably damaging |
Het |
Mical2 |
T |
A |
7: 112,271,515 (GRCm38) |
D70E |
possibly damaging |
Het |
Mrc1 |
T |
C |
2: 14,270,189 (GRCm38) |
Y434H |
probably damaging |
Het |
Myh10 |
C |
A |
11: 68,804,714 (GRCm38) |
Q1556K |
probably damaging |
Het |
Nav1 |
G |
A |
1: 135,454,436 (GRCm38) |
T1400I |
probably null |
Het |
Olfr1173 |
T |
C |
2: 88,274,240 (GRCm38) |
K270E |
probably damaging |
Het |
Olfr1178 |
T |
A |
2: 88,391,319 (GRCm38) |
I24N |
probably benign |
Het |
Olfr1289 |
T |
C |
2: 111,483,616 (GRCm38) |
V62A |
probably damaging |
Het |
Olfr13 |
A |
G |
6: 43,174,501 (GRCm38) |
K172E |
probably benign |
Het |
Olfr339 |
A |
G |
2: 36,421,938 (GRCm38) |
D180G |
probably damaging |
Het |
Olfr513 |
G |
A |
7: 108,755,223 (GRCm38) |
M122I |
possibly damaging |
Het |
Osmr |
T |
A |
15: 6,852,462 (GRCm38) |
Q67L |
probably damaging |
Het |
Pan2 |
T |
G |
10: 128,313,637 (GRCm38) |
V522G |
possibly damaging |
Het |
Pard3 |
T |
G |
8: 127,376,885 (GRCm38) |
|
probably null |
Het |
Pcdhgc5 |
G |
T |
18: 37,820,113 (GRCm38) |
A147S |
possibly damaging |
Het |
Pcsk9 |
T |
C |
4: 106,446,770 (GRCm38) |
I506V |
probably benign |
Het |
Polr3d |
GCCCCC |
GCCCC |
14: 70,443,047 (GRCm38) |
|
probably null |
Het |
Prdm4 |
G |
A |
10: 85,893,351 (GRCm38) |
R731* |
probably null |
Het |
Prdx6b |
T |
A |
2: 80,293,163 (GRCm38) |
D105E |
probably damaging |
Het |
Rab42 |
A |
G |
4: 132,302,479 (GRCm38) |
L144P |
probably damaging |
Het |
Ralbp1 |
T |
A |
17: 65,864,666 (GRCm38) |
K104M |
probably damaging |
Het |
Rrp12 |
A |
G |
19: 41,892,599 (GRCm38) |
V131A |
probably damaging |
Het |
Sbno1 |
C |
T |
5: 124,387,534 (GRCm38) |
|
probably null |
Het |
Sbno2 |
A |
T |
10: 80,062,693 (GRCm38) |
I645N |
probably damaging |
Het |
Scfd2 |
T |
C |
5: 74,206,367 (GRCm38) |
K624R |
probably benign |
Het |
Sgk2 |
C |
A |
2: 162,999,179 (GRCm38) |
|
probably null |
Het |
Sirt4 |
A |
G |
5: 115,479,701 (GRCm38) |
S299P |
probably benign |
Het |
Slit2 |
C |
T |
5: 48,304,225 (GRCm38) |
A1521V |
probably benign |
Het |
Socs7 |
T |
G |
11: 97,373,107 (GRCm38) |
V275G |
possibly damaging |
Het |
Spink11 |
G |
A |
18: 44,190,487 (GRCm38) |
P102S |
probably benign |
Het |
Tacc3 |
A |
G |
5: 33,671,404 (GRCm38) |
N534D |
probably damaging |
Het |
Tas2r115 |
T |
C |
6: 132,737,346 (GRCm38) |
Y214C |
probably damaging |
Het |
Tcaf1 |
A |
T |
6: 42,673,520 (GRCm38) |
M875K |
probably benign |
Het |
Ttc22 |
T |
A |
4: 106,622,672 (GRCm38) |
L41Q |
possibly damaging |
Het |
Ttc37 |
T |
C |
13: 76,173,354 (GRCm38) |
S1322P |
possibly damaging |
Het |
Vasn |
T |
A |
16: 4,649,795 (GRCm38) |
C535* |
probably null |
Het |
Vcan |
T |
A |
13: 89,689,737 (GRCm38) |
I2563F |
probably damaging |
Het |
Vmn2r63 |
T |
G |
7: 42,926,873 (GRCm38) |
Q505H |
probably damaging |
Het |
Vmn2r65 |
T |
G |
7: 84,943,573 (GRCm38) |
Q475H |
probably damaging |
Het |
Zbtb43 |
T |
C |
2: 33,454,520 (GRCm38) |
Y231C |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,810,266 (GRCm38) |
V931A |
probably benign |
Het |
|
Other mutations in Olfr142 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01622:Olfr142
|
APN |
2 |
90,252,609 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01623:Olfr142
|
APN |
2 |
90,252,609 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01810:Olfr142
|
APN |
2 |
90,252,132 (GRCm38) |
nonsense |
probably null |
|
IGL01918:Olfr142
|
APN |
2 |
90,252,331 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02619:Olfr142
|
APN |
2 |
90,252,505 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02732:Olfr142
|
APN |
2 |
90,252,308 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02738:Olfr142
|
APN |
2 |
90,252,355 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL02795:Olfr142
|
APN |
2 |
90,252,562 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02830:Olfr142
|
APN |
2 |
90,252,781 (GRCm38) |
missense |
probably damaging |
1.00 |
R0601:Olfr142
|
UTSW |
2 |
90,252,934 (GRCm38) |
missense |
probably benign |
0.05 |
R2004:Olfr142
|
UTSW |
2 |
90,252,692 (GRCm38) |
missense |
probably benign |
0.04 |
R2377:Olfr142
|
UTSW |
2 |
90,252,911 (GRCm38) |
missense |
probably damaging |
1.00 |
R3615:Olfr142
|
UTSW |
2 |
90,252,409 (GRCm38) |
missense |
possibly damaging |
0.94 |
R3616:Olfr142
|
UTSW |
2 |
90,252,409 (GRCm38) |
missense |
possibly damaging |
0.94 |
R3777:Olfr142
|
UTSW |
2 |
90,252,625 (GRCm38) |
missense |
probably damaging |
1.00 |
R4763:Olfr142
|
UTSW |
2 |
90,252,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R4765:Olfr142
|
UTSW |
2 |
90,252,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R5421:Olfr142
|
UTSW |
2 |
90,252,745 (GRCm38) |
missense |
probably benign |
0.01 |
R5426:Olfr142
|
UTSW |
2 |
90,252,611 (GRCm38) |
nonsense |
probably null |
|
R6063:Olfr142
|
UTSW |
2 |
90,252,427 (GRCm38) |
missense |
probably benign |
0.40 |
R6717:Olfr142
|
UTSW |
2 |
90,252,524 (GRCm38) |
missense |
probably benign |
0.00 |
R6931:Olfr142
|
UTSW |
2 |
90,252,777 (GRCm38) |
nonsense |
probably null |
|
R6936:Olfr142
|
UTSW |
2 |
90,252,334 (GRCm38) |
missense |
probably benign |
0.17 |
R7013:Olfr142
|
UTSW |
2 |
90,252,097 (GRCm38) |
missense |
possibly damaging |
0.87 |
R7091:Olfr142
|
UTSW |
2 |
90,252,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R7247:Olfr142
|
UTSW |
2 |
90,252,821 (GRCm38) |
missense |
probably damaging |
1.00 |
R8169:Olfr142
|
UTSW |
2 |
90,252,098 (GRCm38) |
nonsense |
probably null |
|
R8345:Olfr142
|
UTSW |
2 |
90,252,217 (GRCm38) |
missense |
possibly damaging |
0.50 |
R9222:Olfr142
|
UTSW |
2 |
90,252,476 (GRCm38) |
missense |
possibly damaging |
0.95 |
|