Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
A |
G |
4: 144,184,464 (GRCm39) |
I98T |
probably damaging |
Het |
Ahnak |
T |
C |
19: 8,988,529 (GRCm39) |
I3271T |
probably damaging |
Het |
Aox1 |
G |
A |
1: 58,086,304 (GRCm39) |
V70I |
probably benign |
Het |
Ap1g2 |
A |
G |
14: 55,337,206 (GRCm39) |
S710P |
probably damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
Cacna1e |
T |
C |
1: 154,347,162 (GRCm39) |
K1064E |
probably benign |
Het |
Capn11 |
T |
A |
17: 45,944,891 (GRCm39) |
I459F |
probably damaging |
Het |
Ccnc |
A |
G |
4: 21,732,220 (GRCm39) |
I48V |
probably damaging |
Het |
Ces1d |
T |
A |
8: 93,904,667 (GRCm39) |
I358F |
probably benign |
Het |
Clgn |
A |
T |
8: 84,147,185 (GRCm39) |
N379I |
probably damaging |
Het |
Cym |
T |
C |
3: 107,121,548 (GRCm39) |
Y248C |
probably damaging |
Het |
Epha8 |
T |
C |
4: 136,666,100 (GRCm39) |
D352G |
possibly damaging |
Het |
Eya2 |
T |
C |
2: 165,558,050 (GRCm39) |
|
probably null |
Het |
Fam219a |
A |
C |
4: 41,569,208 (GRCm39) |
V10G |
probably benign |
Het |
Fbxl5 |
C |
T |
5: 43,978,891 (GRCm39) |
V20I |
probably benign |
Het |
Fbxl9 |
A |
G |
8: 106,042,388 (GRCm39) |
C147R |
probably benign |
Het |
Fscb |
T |
C |
12: 64,520,059 (GRCm39) |
E469G |
possibly damaging |
Het |
Glt8d2 |
A |
T |
10: 82,496,659 (GRCm39) |
|
probably null |
Het |
Grep1 |
A |
T |
17: 23,936,302 (GRCm39) |
F8L |
probably benign |
Het |
Helt |
T |
C |
8: 46,746,630 (GRCm39) |
|
probably benign |
Het |
Igkv8-27 |
G |
T |
6: 70,148,887 (GRCm39) |
T89K |
probably benign |
Het |
Ipo5 |
T |
A |
14: 121,183,567 (GRCm39) |
H1048Q |
probably benign |
Het |
Kalrn |
T |
C |
16: 34,212,464 (GRCm39) |
D28G |
probably damaging |
Het |
Kcnh4 |
G |
A |
11: 100,632,680 (GRCm39) |
P936S |
probably benign |
Het |
Klrd1 |
A |
G |
6: 129,570,701 (GRCm39) |
I37M |
possibly damaging |
Het |
Kmt2e |
T |
C |
5: 23,705,271 (GRCm39) |
V1267A |
probably damaging |
Het |
Marchf1 |
A |
T |
8: 66,920,965 (GRCm39) |
Q214L |
probably damaging |
Het |
Mlip |
G |
T |
9: 77,020,279 (GRCm39) |
H52N |
probably damaging |
Het |
Oas1e |
T |
C |
5: 120,927,021 (GRCm39) |
R229G |
probably benign |
Het |
Ogfr |
T |
A |
2: 180,234,300 (GRCm39) |
|
probably null |
Het |
Or5m10 |
T |
A |
2: 85,717,482 (GRCm39) |
Y113N |
probably damaging |
Het |
Pde4d |
T |
C |
13: 110,087,541 (GRCm39) |
I636T |
probably benign |
Het |
Pex5l |
C |
T |
3: 33,008,625 (GRCm39) |
V426I |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,252,006 (GRCm39) |
K384E |
possibly damaging |
Het |
Pramel22 |
A |
T |
4: 143,380,675 (GRCm39) |
Y449* |
probably null |
Het |
Prl6a1 |
T |
G |
13: 27,498,221 (GRCm39) |
|
probably null |
Het |
Prss23 |
A |
T |
7: 89,159,038 (GRCm39) |
W344R |
probably damaging |
Het |
Ptar1 |
T |
A |
19: 23,697,680 (GRCm39) |
D397E |
probably benign |
Het |
Qrsl1 |
G |
A |
10: 43,752,513 (GRCm39) |
R437C |
probably damaging |
Het |
Rab6a |
G |
T |
7: 100,257,404 (GRCm39) |
|
probably benign |
Het |
Samd14 |
C |
A |
11: 94,912,239 (GRCm39) |
S205R |
probably benign |
Het |
Sel1l3 |
T |
C |
5: 53,343,326 (GRCm39) |
Y322C |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,940,480 (GRCm39) |
L669I |
probably benign |
Het |
Ssc4d |
A |
G |
5: 135,991,887 (GRCm39) |
L419P |
probably damaging |
Het |
Tbc1d2b |
A |
T |
9: 90,101,063 (GRCm39) |
Y642* |
probably null |
Het |
Tbc1d2b |
A |
C |
9: 90,108,301 (GRCm39) |
F417V |
probably benign |
Het |
Top2a |
T |
C |
11: 98,907,005 (GRCm39) |
D212G |
probably damaging |
Het |
Trim39 |
A |
T |
17: 36,571,807 (GRCm39) |
V317E |
probably damaging |
Het |
Uncx |
G |
A |
5: 139,530,261 (GRCm39) |
R113H |
probably damaging |
Het |
Usp4 |
A |
G |
9: 108,256,543 (GRCm39) |
S655G |
probably benign |
Het |
Vmn2r114 |
C |
T |
17: 23,510,000 (GRCm39) |
V827I |
probably benign |
Het |
Vmn2r28 |
T |
A |
7: 5,491,200 (GRCm39) |
N349I |
probably benign |
Het |
Vmn2r3 |
A |
G |
3: 64,182,770 (GRCm39) |
W310R |
possibly damaging |
Het |
Xirp2 |
T |
C |
2: 67,340,245 (GRCm39) |
W829R |
probably damaging |
Het |
Zfp574 |
C |
A |
7: 24,780,777 (GRCm39) |
H600N |
possibly damaging |
Het |
|
Other mutations in Or4g16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01095:Or4g16
|
APN |
2 |
111,136,966 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01355:Or4g16
|
APN |
2 |
111,137,438 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01864:Or4g16
|
APN |
2 |
111,137,400 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Or4g16
|
APN |
2 |
111,137,143 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02183:Or4g16
|
APN |
2 |
111,136,763 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4377001:Or4g16
|
UTSW |
2 |
111,137,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0280:Or4g16
|
UTSW |
2 |
111,137,417 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0636:Or4g16
|
UTSW |
2 |
111,136,757 (GRCm39) |
missense |
probably benign |
0.06 |
R0732:Or4g16
|
UTSW |
2 |
111,137,325 (GRCm39) |
nonsense |
probably null |
|
R1661:Or4g16
|
UTSW |
2 |
111,137,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1665:Or4g16
|
UTSW |
2 |
111,137,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R2251:Or4g16
|
UTSW |
2 |
111,136,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Or4g16
|
UTSW |
2 |
111,136,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R2253:Or4g16
|
UTSW |
2 |
111,136,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R2473:Or4g16
|
UTSW |
2 |
111,137,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R3408:Or4g16
|
UTSW |
2 |
111,136,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5020:Or4g16
|
UTSW |
2 |
111,136,637 (GRCm39) |
missense |
probably benign |
0.01 |
R5634:Or4g16
|
UTSW |
2 |
111,137,437 (GRCm39) |
missense |
probably benign |
|
R5647:Or4g16
|
UTSW |
2 |
111,137,392 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6782:Or4g16
|
UTSW |
2 |
111,137,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R6911:Or4g16
|
UTSW |
2 |
111,136,618 (GRCm39) |
missense |
probably benign |
0.00 |
R7135:Or4g16
|
UTSW |
2 |
111,137,365 (GRCm39) |
missense |
probably benign |
0.05 |
R7167:Or4g16
|
UTSW |
2 |
111,136,793 (GRCm39) |
missense |
probably benign |
0.10 |
R7452:Or4g16
|
UTSW |
2 |
111,137,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7582:Or4g16
|
UTSW |
2 |
111,136,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R8949:Or4g16
|
UTSW |
2 |
111,137,379 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Or4g16
|
UTSW |
2 |
111,136,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|