Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 138,069,871 (GRCm38) |
L1607P |
probably damaging |
Het |
1700016H13Rik |
T |
C |
5: 103,648,821 (GRCm38) |
*118W |
probably null |
Het |
1700061G19Rik |
A |
T |
17: 56,883,835 (GRCm38) |
N468Y |
probably benign |
Het |
2610507B11Rik |
A |
C |
11: 78,269,704 (GRCm38) |
|
probably benign |
Het |
4930452B06Rik |
C |
T |
14: 8,518,695 (GRCm38) |
G254R |
probably damaging |
Het |
Abcc2 |
A |
T |
19: 43,826,614 (GRCm38) |
R1147* |
probably null |
Het |
Agap2 |
A |
G |
10: 127,091,702 (GRCm38) |
T1131A |
possibly damaging |
Het |
Aldh9a1 |
A |
G |
1: 167,361,847 (GRCm38) |
D388G |
probably damaging |
Het |
Ap3d1 |
G |
T |
10: 80,730,042 (GRCm38) |
A97E |
probably damaging |
Het |
Arhgef10 |
T |
A |
8: 14,962,636 (GRCm38) |
V320E |
probably damaging |
Het |
Baiap2l1 |
C |
A |
5: 144,266,010 (GRCm38) |
V498L |
probably damaging |
Het |
Ccdc189 |
T |
C |
7: 127,584,862 (GRCm38) |
E261G |
probably damaging |
Het |
Cdh2 |
T |
C |
18: 16,629,576 (GRCm38) |
N437S |
probably benign |
Het |
Chd1 |
C |
A |
17: 15,725,431 (GRCm38) |
N72K |
probably benign |
Het |
Col4a3bp |
T |
A |
13: 96,549,287 (GRCm38) |
Y63N |
probably benign |
Het |
Cstf2t |
A |
T |
19: 31,084,626 (GRCm38) |
M521L |
probably benign |
Het |
Dlx5 |
T |
C |
6: 6,881,619 (GRCm38) |
K90E |
possibly damaging |
Het |
Dmp1 |
A |
G |
5: 104,207,630 (GRCm38) |
E32G |
possibly damaging |
Het |
Espnl |
T |
G |
1: 91,344,489 (GRCm38) |
Y524D |
probably damaging |
Het |
Fam20c |
T |
C |
5: 138,755,724 (GRCm38) |
L30P |
probably damaging |
Het |
Fat1 |
G |
T |
8: 45,026,553 (GRCm38) |
A2879S |
probably benign |
Het |
Gabrg1 |
A |
T |
5: 70,774,389 (GRCm38) |
V337D |
probably damaging |
Het |
Gart |
C |
A |
16: 91,623,403 (GRCm38) |
D851Y |
possibly damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,616 (GRCm38) |
H234R |
probably damaging |
Het |
Gemin6 |
T |
A |
17: 80,228,095 (GRCm38) |
H161Q |
probably damaging |
Het |
Glt6d1 |
A |
G |
2: 25,794,070 (GRCm38) |
I308T |
probably benign |
Het |
Gm10320 |
T |
C |
13: 98,491,983 (GRCm38) |
T7A |
probably benign |
Het |
Gm10912 |
T |
C |
2: 104,066,530 (GRCm38) |
S5P |
probably benign |
Het |
Gm13088 |
C |
T |
4: 143,656,440 (GRCm38) |
E70K |
possibly damaging |
Het |
Gmpr2 |
T |
A |
14: 55,672,735 (GRCm38) |
D7E |
possibly damaging |
Het |
Hc |
A |
G |
2: 34,984,750 (GRCm38) |
Y1620H |
probably damaging |
Het |
Hoxa3 |
T |
C |
6: 52,170,143 (GRCm38) |
|
probably benign |
Het |
Ift140 |
A |
G |
17: 25,090,933 (GRCm38) |
T1105A |
probably benign |
Het |
Kdr |
G |
T |
5: 75,968,422 (GRCm38) |
T188N |
possibly damaging |
Het |
Lepr |
A |
T |
4: 101,752,152 (GRCm38) |
D312V |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,810,105 (GRCm38) |
V501A |
probably damaging |
Het |
Mcur1 |
T |
C |
13: 43,545,740 (GRCm38) |
Y267C |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,307,038 (GRCm38) |
T736S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,671,002 (GRCm38) |
|
probably benign |
Het |
Mroh2a |
G |
C |
1: 88,246,042 (GRCm38) |
A871P |
probably damaging |
Het |
Ndrg2 |
T |
A |
14: 51,907,003 (GRCm38) |
|
probably benign |
Het |
Oas3 |
G |
A |
5: 120,756,145 (GRCm38) |
R39C |
probably damaging |
Het |
Olfr1258 |
A |
G |
2: 89,930,201 (GRCm38) |
T131A |
probably benign |
Het |
Olfr1298 |
C |
T |
2: 111,645,791 (GRCm38) |
V69I |
probably benign |
Het |
Olfr558 |
T |
A |
7: 102,709,995 (GRCm38) |
H245Q |
probably damaging |
Het |
Onecut2 |
T |
A |
18: 64,341,472 (GRCm38) |
S365T |
possibly damaging |
Het |
Pds5b |
C |
A |
5: 150,754,431 (GRCm38) |
Q505K |
probably benign |
Het |
Rfx2 |
T |
C |
17: 56,803,722 (GRCm38) |
Y88C |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,208,478 (GRCm38) |
V214A |
probably benign |
Het |
Samd3 |
T |
A |
10: 26,271,854 (GRCm38) |
C476S |
possibly damaging |
Het |
Sfi1 |
TCGC |
TC |
11: 3,146,254 (GRCm38) |
|
probably null |
Het |
Shank1 |
C |
T |
7: 44,352,294 (GRCm38) |
R1146W |
unknown |
Het |
Smcr8 |
T |
C |
11: 60,778,115 (GRCm38) |
Y30H |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,641,597 (GRCm38) |
|
probably null |
Het |
Strip1 |
C |
A |
3: 107,614,613 (GRCm38) |
D750Y |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,070,851 (GRCm38) |
K2312E |
possibly damaging |
Het |
Taf1c |
A |
T |
8: 119,599,983 (GRCm38) |
I438N |
probably damaging |
Het |
Tnfaip1 |
A |
T |
11: 78,530,014 (GRCm38) |
|
probably benign |
Het |
Unc45b |
T |
A |
11: 82,940,205 (GRCm38) |
L797Q |
possibly damaging |
Het |
Usp24 |
T |
A |
4: 106,407,133 (GRCm38) |
W1754R |
probably damaging |
Het |
Utp20 |
G |
A |
10: 88,777,516 (GRCm38) |
P1301L |
probably benign |
Het |
Vmn2r115 |
T |
A |
17: 23,359,781 (GRCm38) |
S743T |
probably damaging |
Het |
Vps41 |
T |
G |
13: 18,854,663 (GRCm38) |
|
probably null |
Het |
Vps72 |
G |
T |
3: 95,122,583 (GRCm38) |
L304F |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,356,441 (GRCm38) |
I907N |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,845,062 (GRCm38) |
T765A |
probably benign |
Het |
Zfp616 |
A |
T |
11: 74,085,674 (GRCm38) |
H923L |
probably damaging |
Het |
Zp2 |
A |
T |
7: 120,143,576 (GRCm38) |
|
probably benign |
Het |
|
Other mutations in Olfr272 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Olfr272
|
APN |
4 |
52,911,618 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL02224:Olfr272
|
APN |
4 |
52,911,392 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL03293:Olfr272
|
APN |
4 |
52,910,835 (GRCm38) |
makesense |
probably null |
|
K3955:Olfr272
|
UTSW |
4 |
52,911,081 (GRCm38) |
missense |
probably damaging |
1.00 |
R0195:Olfr272
|
UTSW |
4 |
52,910,849 (GRCm38) |
missense |
probably benign |
0.00 |
R0445:Olfr272
|
UTSW |
4 |
52,910,849 (GRCm38) |
missense |
probably benign |
0.00 |
R1517:Olfr272
|
UTSW |
4 |
52,911,502 (GRCm38) |
nonsense |
probably null |
|
R1536:Olfr272
|
UTSW |
4 |
52,911,260 (GRCm38) |
missense |
probably benign |
0.43 |
R1540:Olfr272
|
UTSW |
4 |
52,910,996 (GRCm38) |
missense |
probably benign |
0.00 |
R1551:Olfr272
|
UTSW |
4 |
52,911,397 (GRCm38) |
nonsense |
probably null |
|
R1612:Olfr272
|
UTSW |
4 |
52,911,501 (GRCm38) |
missense |
probably benign |
|
R1920:Olfr272
|
UTSW |
4 |
52,910,849 (GRCm38) |
missense |
probably benign |
|
R2181:Olfr272
|
UTSW |
4 |
52,911,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R5410:Olfr272
|
UTSW |
4 |
52,910,991 (GRCm38) |
missense |
probably benign |
0.01 |
R6331:Olfr272
|
UTSW |
4 |
52,911,399 (GRCm38) |
missense |
probably damaging |
1.00 |
R6336:Olfr272
|
UTSW |
4 |
52,911,459 (GRCm38) |
missense |
probably damaging |
1.00 |
R7085:Olfr272
|
UTSW |
4 |
52,910,961 (GRCm38) |
missense |
probably benign |
0.02 |
R7541:Olfr272
|
UTSW |
4 |
52,911,376 (GRCm38) |
missense |
probably benign |
0.04 |
R7727:Olfr272
|
UTSW |
4 |
52,911,368 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7891:Olfr272
|
UTSW |
4 |
52,911,663 (GRCm38) |
missense |
probably benign |
0.01 |
R8782:Olfr272
|
UTSW |
4 |
52,911,693 (GRCm38) |
missense |
probably benign |
0.16 |
R9321:Olfr272
|
UTSW |
4 |
52,911,314 (GRCm38) |
missense |
probably damaging |
1.00 |
|