Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
T |
A |
4: 53,092,887 (GRCm39) |
Q299L |
probably null |
Het |
Adamts9 |
T |
G |
6: 92,885,692 (GRCm39) |
K399N |
possibly damaging |
Het |
Alox12b |
T |
C |
11: 69,056,711 (GRCm39) |
F369S |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,483,301 (GRCm39) |
Y236H |
probably benign |
Het |
Ankrd36 |
T |
C |
11: 5,585,329 (GRCm39) |
L380P |
probably damaging |
Het |
Atp2a1 |
C |
T |
7: 126,051,844 (GRCm39) |
A468T |
possibly damaging |
Het |
Caprin1 |
A |
T |
2: 103,606,332 (GRCm39) |
F303I |
possibly damaging |
Het |
Casp7 |
A |
T |
19: 56,421,684 (GRCm39) |
R41* |
probably null |
Het |
Ccdc66 |
T |
A |
14: 27,208,463 (GRCm39) |
H753L |
probably benign |
Het |
Ccnc |
T |
C |
4: 21,742,671 (GRCm39) |
M166T |
probably benign |
Het |
Cdkl3 |
T |
A |
11: 51,923,337 (GRCm39) |
M538K |
possibly damaging |
Het |
Cemip2 |
T |
A |
19: 21,775,346 (GRCm39) |
Y196* |
probably null |
Het |
Cercam |
G |
A |
2: 29,766,251 (GRCm39) |
A345T |
probably benign |
Het |
Chmp3 |
T |
A |
6: 71,537,954 (GRCm39) |
C60* |
probably null |
Het |
Ddx1 |
C |
T |
12: 13,289,542 (GRCm39) |
G125S |
probably damaging |
Het |
Defb7 |
A |
G |
8: 19,547,567 (GRCm39) |
D24G |
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,077,452 (GRCm39) |
Y653N |
probably damaging |
Het |
Dsc2 |
T |
C |
18: 20,183,208 (GRCm39) |
D70G |
probably damaging |
Het |
Erich3 |
T |
G |
3: 154,419,705 (GRCm39) |
N266K |
probably damaging |
Het |
Fastk |
A |
T |
5: 24,649,045 (GRCm39) |
|
probably null |
Het |
Fat4 |
A |
G |
3: 38,943,135 (GRCm39) |
N676S |
probably damaging |
Het |
Fermt1 |
A |
T |
2: 132,776,739 (GRCm39) |
|
probably null |
Het |
Fmn1 |
A |
G |
2: 113,523,463 (GRCm39) |
T1149A |
possibly damaging |
Het |
Foxo3 |
A |
G |
10: 42,073,068 (GRCm39) |
V483A |
probably damaging |
Het |
Fpgs |
T |
C |
2: 32,575,852 (GRCm39) |
T364A |
possibly damaging |
Het |
Gm12185 |
A |
G |
11: 48,806,262 (GRCm39) |
S310P |
probably damaging |
Het |
Gm15056 |
A |
T |
8: 21,391,949 (GRCm39) |
|
probably benign |
Het |
Hcn1 |
T |
C |
13: 118,112,112 (GRCm39) |
V692A |
unknown |
Het |
Izumo3 |
A |
C |
4: 92,035,140 (GRCm39) |
C26G |
probably damaging |
Het |
Kcnf1 |
T |
C |
12: 17,225,474 (GRCm39) |
Y249C |
probably damaging |
Het |
Kcnj6 |
T |
C |
16: 94,563,358 (GRCm39) |
E380G |
possibly damaging |
Het |
Kdm3b |
A |
G |
18: 34,942,149 (GRCm39) |
T747A |
probably damaging |
Het |
Lrba |
G |
A |
3: 86,258,622 (GRCm39) |
G1370R |
probably damaging |
Het |
Mei1 |
G |
A |
15: 81,991,334 (GRCm39) |
R504Q |
probably damaging |
Het |
Mgat4f |
G |
A |
1: 134,318,512 (GRCm39) |
G428D |
probably damaging |
Het |
Mipol1 |
T |
C |
12: 57,379,127 (GRCm39) |
I195T |
probably damaging |
Het |
Ncor2 |
G |
A |
5: 125,110,610 (GRCm39) |
T1350I |
probably damaging |
Het |
Npy |
A |
G |
6: 49,800,705 (GRCm39) |
E43G |
probably damaging |
Het |
Or5w19 |
T |
A |
2: 87,698,459 (GRCm39) |
N41K |
probably damaging |
Het |
Or8d2 |
T |
A |
9: 38,760,200 (GRCm39) |
N263K |
probably benign |
Het |
Pcdhb3 |
T |
C |
18: 37,434,634 (GRCm39) |
L200P |
probably damaging |
Het |
Pcnt |
G |
A |
10: 76,258,756 (GRCm39) |
H570Y |
possibly damaging |
Het |
Phf8-ps |
T |
A |
17: 33,284,679 (GRCm39) |
I708F |
probably benign |
Het |
Pkd1l2 |
A |
C |
8: 117,808,991 (GRCm39) |
D66E |
possibly damaging |
Het |
Plekhg4 |
A |
G |
8: 106,108,467 (GRCm39) |
D1170G |
possibly damaging |
Het |
Poln |
T |
A |
5: 34,190,143 (GRCm39) |
H672L |
probably benign |
Het |
Ptprq |
T |
C |
10: 107,479,904 (GRCm39) |
Y1122C |
probably damaging |
Het |
Ptrhd1 |
A |
G |
12: 4,286,505 (GRCm39) |
Y132C |
probably damaging |
Het |
Pwwp3a |
G |
T |
10: 80,068,778 (GRCm39) |
R307S |
probably benign |
Het |
Riok1 |
G |
T |
13: 38,234,831 (GRCm39) |
R300L |
probably damaging |
Het |
Sbf2 |
G |
T |
7: 110,027,553 (GRCm39) |
T481K |
probably damaging |
Het |
Sidt2 |
A |
T |
9: 45,863,098 (GRCm39) |
M11K |
probably damaging |
Het |
Slc66a1 |
A |
T |
4: 139,027,391 (GRCm39) |
|
probably benign |
Het |
Syne1 |
G |
A |
10: 5,299,280 (GRCm39) |
R992* |
probably null |
Het |
Tmem8b |
C |
A |
4: 43,681,134 (GRCm39) |
R384S |
possibly damaging |
Het |
Trim28 |
T |
C |
7: 12,761,761 (GRCm39) |
Y243H |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,764,192 (GRCm39) |
M266T |
probably benign |
Het |
Tsg101 |
A |
T |
7: 46,539,437 (GRCm39) |
S368T |
probably damaging |
Het |
Ttc28 |
G |
A |
5: 111,373,543 (GRCm39) |
S962N |
probably damaging |
Het |
Ttc6 |
G |
A |
12: 57,733,132 (GRCm39) |
V1092I |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,534,465 (GRCm39) |
T927I |
probably damaging |
Het |
Zfr |
C |
T |
15: 12,140,730 (GRCm39) |
T259I |
unknown |
Het |
|
Other mutations in Or4e5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01336:Or4e5
|
APN |
14 |
52,728,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01367:Or4e5
|
APN |
14 |
52,727,624 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01664:Or4e5
|
APN |
14 |
52,728,002 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02890:Or4e5
|
APN |
14 |
52,728,368 (GRCm39) |
missense |
probably benign |
|
IGL03108:Or4e5
|
APN |
14 |
52,727,533 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03184:Or4e5
|
APN |
14 |
52,728,380 (GRCm39) |
missense |
probably benign |
0.20 |
R0563:Or4e5
|
UTSW |
14 |
52,727,714 (GRCm39) |
nonsense |
probably null |
|
R1080:Or4e5
|
UTSW |
14 |
52,728,042 (GRCm39) |
nonsense |
probably null |
|
R1653:Or4e5
|
UTSW |
14 |
52,728,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Or4e5
|
UTSW |
14 |
52,727,871 (GRCm39) |
splice site |
probably null |
|
R1720:Or4e5
|
UTSW |
14 |
52,728,051 (GRCm39) |
nonsense |
probably null |
|
R3430:Or4e5
|
UTSW |
14 |
52,727,882 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4995:Or4e5
|
UTSW |
14 |
52,727,988 (GRCm39) |
nonsense |
probably null |
|
R5954:Or4e5
|
UTSW |
14 |
52,727,624 (GRCm39) |
missense |
probably benign |
0.42 |
R6183:Or4e5
|
UTSW |
14 |
52,728,188 (GRCm39) |
missense |
probably benign |
0.05 |
R6518:Or4e5
|
UTSW |
14 |
52,728,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R6651:Or4e5
|
UTSW |
14 |
52,728,250 (GRCm39) |
missense |
probably benign |
0.07 |
R6652:Or4e5
|
UTSW |
14 |
52,728,250 (GRCm39) |
missense |
probably benign |
0.07 |
R6653:Or4e5
|
UTSW |
14 |
52,728,250 (GRCm39) |
missense |
probably benign |
0.07 |
R7385:Or4e5
|
UTSW |
14 |
52,727,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R7524:Or4e5
|
UTSW |
14 |
52,727,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Or4e5
|
UTSW |
14 |
52,728,010 (GRCm39) |
missense |
probably benign |
0.02 |
R9165:Or4e5
|
UTSW |
14 |
52,727,830 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9763:Or4e5
|
UTSW |
14 |
52,728,307 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Or4e5
|
UTSW |
14 |
52,727,923 (GRCm39) |
missense |
probably damaging |
0.99 |
|