Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
G |
16: 4,667,138 (GRCm39) |
T204A |
unknown |
Het |
Abca12 |
T |
C |
1: 71,327,836 (GRCm39) |
T1415A |
probably benign |
Het |
Adamtsl3 |
A |
G |
7: 81,986,459 (GRCm39) |
T24A |
probably benign |
Het |
Ankrd13b |
A |
C |
11: 77,367,327 (GRCm39) |
V194G |
probably benign |
Het |
Aurkc |
C |
T |
7: 7,003,006 (GRCm39) |
T167I |
probably benign |
Het |
Capn1 |
T |
C |
19: 6,064,469 (GRCm39) |
Y10C |
probably benign |
Het |
Ccnk |
T |
C |
12: 108,152,724 (GRCm39) |
S14P |
possibly damaging |
Het |
Cebpe |
T |
A |
14: 54,949,298 (GRCm39) |
I40F |
probably damaging |
Het |
Cers3 |
G |
A |
7: 66,439,377 (GRCm39) |
C296Y |
probably damaging |
Het |
Cog8 |
A |
T |
8: 107,776,861 (GRCm39) |
C505S |
possibly damaging |
Het |
Col4a3 |
A |
G |
1: 82,626,338 (GRCm39) |
I92V |
unknown |
Het |
Col5a3 |
T |
A |
9: 20,708,689 (GRCm39) |
H645L |
unknown |
Het |
Crispld1 |
A |
T |
1: 17,798,990 (GRCm39) |
E37V |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,357,591 (GRCm39) |
Y1684C |
|
Het |
Cstdc5 |
A |
T |
16: 36,187,862 (GRCm39) |
M1K |
probably null |
Het |
Dcst1 |
C |
A |
3: 89,260,599 (GRCm39) |
S555I |
probably benign |
Het |
Drc1 |
A |
G |
5: 30,499,060 (GRCm39) |
S70G |
possibly damaging |
Het |
Elavl2 |
A |
T |
4: 91,199,808 (GRCm39) |
|
probably null |
Het |
Emc1 |
A |
G |
4: 139,087,877 (GRCm39) |
H300R |
probably benign |
Het |
Gcnt4 |
G |
A |
13: 97,083,669 (GRCm39) |
V322I |
probably benign |
Het |
Gsg1l2 |
A |
G |
11: 67,665,584 (GRCm39) |
N51D |
probably benign |
Het |
Gucy2e |
A |
T |
11: 69,114,150 (GRCm39) |
|
probably null |
Het |
Hip1r |
A |
G |
5: 124,136,036 (GRCm39) |
E579G |
probably benign |
Het |
Hoxa4 |
T |
C |
6: 52,168,520 (GRCm39) |
H50R |
unknown |
Het |
Htr7 |
T |
C |
19: 36,034,292 (GRCm39) |
Y121C |
probably damaging |
Het |
Ift43 |
G |
A |
12: 86,207,964 (GRCm39) |
D111N |
probably damaging |
Het |
Itih3 |
A |
G |
14: 30,630,722 (GRCm39) |
V863A |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,304,686 (GRCm39) |
|
probably benign |
Het |
Mgat3 |
A |
G |
15: 80,095,193 (GRCm39) |
K7E |
probably damaging |
Het |
Ndst4 |
T |
A |
3: 125,364,436 (GRCm39) |
V371E |
probably damaging |
Het |
Npr1 |
T |
G |
3: 90,372,323 (GRCm39) |
D163A |
possibly damaging |
Het |
Nudt12 |
T |
C |
17: 59,313,589 (GRCm39) |
I330V |
probably benign |
Het |
Or4k2 |
T |
A |
14: 50,424,020 (GRCm39) |
Y219F |
probably damaging |
Het |
Or51l4 |
C |
A |
7: 103,404,279 (GRCm39) |
C171F |
probably damaging |
Het |
Or7g32 |
C |
A |
9: 19,389,128 (GRCm39) |
M139I |
possibly damaging |
Het |
Poc1a |
A |
T |
9: 106,226,967 (GRCm39) |
R402S |
probably benign |
Het |
Prex2 |
G |
T |
1: 11,193,437 (GRCm39) |
V470L |
probably damaging |
Het |
Prom1 |
T |
C |
5: 44,220,469 (GRCm39) |
E93G |
probably damaging |
Het |
Psma1 |
A |
T |
7: 113,868,961 (GRCm39) |
M180K |
probably benign |
Het |
Pudp |
A |
T |
18: 50,701,053 (GRCm39) |
F227I |
probably damaging |
Het |
Rab15 |
T |
A |
12: 76,851,223 (GRCm39) |
Q60L |
probably damaging |
Het |
Scaf8 |
T |
C |
17: 3,221,497 (GRCm39) |
|
probably null |
Het |
Septin9 |
T |
A |
11: 117,181,488 (GRCm39) |
I96N |
probably damaging |
Het |
Sez6 |
T |
C |
11: 77,868,876 (GRCm39) |
S976P |
probably damaging |
Het |
Slc2a12 |
A |
G |
10: 22,540,802 (GRCm39) |
Y219C |
probably damaging |
Het |
Slc38a9 |
T |
A |
13: 112,831,889 (GRCm39) |
I213K |
probably damaging |
Het |
Stil |
T |
A |
4: 114,881,005 (GRCm39) |
D516E |
probably benign |
Het |
Supt20 |
A |
G |
3: 54,614,543 (GRCm39) |
D184G |
probably damaging |
Het |
Tars3 |
G |
A |
7: 65,308,619 (GRCm39) |
S263N |
probably benign |
Het |
Tmem181a |
C |
A |
17: 6,339,295 (GRCm39) |
T68K |
probably benign |
Het |
Trav21-dv12 |
G |
T |
14: 54,113,997 (GRCm39) |
C39F |
probably damaging |
Het |
Tshz1 |
T |
C |
18: 84,032,173 (GRCm39) |
E745G |
probably damaging |
Het |
Ugt1a8 |
T |
A |
1: 88,015,904 (GRCm39) |
F106I |
probably benign |
Het |
Vmn1r39 |
C |
A |
6: 66,781,428 (GRCm39) |
V297L |
probably benign |
Het |
Vmn2r101 |
G |
A |
17: 19,811,443 (GRCm39) |
|
probably null |
Het |
Vmn2r69 |
GAAAA |
GAAAAA |
7: 85,060,768 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Or2a20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Or2a20
|
APN |
6 |
43,194,782 (GRCm39) |
missense |
probably benign |
0.00 |
R0347:Or2a20
|
UTSW |
6 |
43,194,296 (GRCm39) |
missense |
probably benign |
|
R1099:Or2a20
|
UTSW |
6 |
43,194,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Or2a20
|
UTSW |
6 |
43,194,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R1147:Or2a20
|
UTSW |
6 |
43,194,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R1353:Or2a20
|
UTSW |
6 |
43,194,624 (GRCm39) |
missense |
probably benign |
0.41 |
R1570:Or2a20
|
UTSW |
6 |
43,194,285 (GRCm39) |
missense |
probably benign |
|
R1720:Or2a20
|
UTSW |
6 |
43,194,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R2098:Or2a20
|
UTSW |
6 |
43,194,437 (GRCm39) |
missense |
probably benign |
0.02 |
R4707:Or2a20
|
UTSW |
6 |
43,193,883 (GRCm39) |
missense |
probably benign |
0.27 |
R4942:Or2a20
|
UTSW |
6 |
43,193,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5008:Or2a20
|
UTSW |
6 |
43,193,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R5084:Or2a20
|
UTSW |
6 |
43,194,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R6472:Or2a20
|
UTSW |
6 |
43,194,293 (GRCm39) |
missense |
probably benign |
|
R7756:Or2a20
|
UTSW |
6 |
43,193,950 (GRCm39) |
nonsense |
probably null |
|
R7784:Or2a20
|
UTSW |
6 |
43,194,322 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8056:Or2a20
|
UTSW |
6 |
43,193,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R9093:Or2a20
|
UTSW |
6 |
43,194,500 (GRCm39) |
missense |
probably benign |
|
R9193:Or2a20
|
UTSW |
6 |
43,194,086 (GRCm39) |
missense |
probably benign |
0.45 |
R9745:Or2a20
|
UTSW |
6 |
43,194,258 (GRCm39) |
nonsense |
probably null |
|
R9749:Or2a20
|
UTSW |
6 |
43,194,258 (GRCm39) |
nonsense |
probably null |
|
|