Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
C |
G |
4: 40,180,284 (GRCm39) |
A395G |
probably benign |
Het |
Adgrf5 |
G |
A |
17: 43,741,503 (GRCm39) |
C380Y |
probably damaging |
Het |
Astn2 |
T |
C |
4: 65,977,418 (GRCm39) |
T422A |
unknown |
Het |
Baz1b |
G |
T |
5: 135,233,916 (GRCm39) |
V148F |
probably benign |
Het |
Bicd1 |
A |
C |
6: 149,451,854 (GRCm39) |
S823R |
probably damaging |
Het |
Bltp3b |
C |
T |
10: 89,647,928 (GRCm39) |
T1330M |
possibly damaging |
Het |
Blvra |
A |
C |
2: 126,937,047 (GRCm39) |
S167R |
probably damaging |
Het |
Camsap2 |
G |
T |
1: 136,225,132 (GRCm39) |
|
probably null |
Het |
Card14 |
T |
C |
11: 119,228,623 (GRCm39) |
S650P |
probably damaging |
Het |
Ccdc121rt2 |
A |
G |
5: 112,597,993 (GRCm39) |
D180G |
possibly damaging |
Het |
Cdh2 |
A |
G |
18: 16,781,593 (GRCm39) |
I166T |
probably damaging |
Het |
Cdnf |
T |
C |
2: 3,514,228 (GRCm39) |
V22A |
probably benign |
Het |
Cfhr4 |
T |
A |
1: 139,625,868 (GRCm39) |
I869F |
probably damaging |
Het |
Chd2 |
T |
A |
7: 73,079,504 (GRCm39) |
K1799* |
probably null |
Het |
Col20a1 |
G |
A |
2: 180,658,126 (GRCm39) |
|
probably null |
Het |
Cyp4a31 |
T |
C |
4: 115,426,943 (GRCm39) |
I182T |
probably benign |
Het |
Dap3 |
A |
T |
3: 88,843,543 (GRCm39) |
F25L |
probably benign |
Het |
Dcc |
T |
A |
18: 71,943,928 (GRCm39) |
Y241F |
probably benign |
Het |
Ddx46 |
A |
G |
13: 55,814,029 (GRCm39) |
I662V |
possibly damaging |
Het |
Dzip3 |
T |
C |
16: 48,772,499 (GRCm39) |
D390G |
probably damaging |
Het |
Eif1 |
A |
G |
11: 100,211,624 (GRCm39) |
D55G |
probably benign |
Het |
Exosc5 |
T |
A |
7: 25,358,790 (GRCm39) |
S44T |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,163,997 (GRCm39) |
V3086A |
probably damaging |
Het |
Fcamr |
T |
A |
1: 130,730,665 (GRCm39) |
|
probably null |
Het |
Gcg |
T |
C |
2: 62,309,004 (GRCm39) |
D50G |
probably damaging |
Het |
Gm7298 |
A |
G |
6: 121,763,537 (GRCm39) |
|
probably null |
Het |
Hfe |
A |
G |
13: 23,892,175 (GRCm39) |
V63A |
probably damaging |
Het |
Hoxd11 |
T |
A |
2: 74,514,298 (GRCm39) |
I276N |
probably damaging |
Het |
Htt |
T |
C |
5: 34,919,287 (GRCm39) |
S13P |
probably benign |
Het |
Il12a |
T |
A |
3: 68,598,872 (GRCm39) |
C18S |
unknown |
Het |
Itk |
G |
T |
11: 46,222,776 (GRCm39) |
Y564* |
probably null |
Het |
Lrrc46 |
A |
T |
11: 96,931,705 (GRCm39) |
L39Q |
probably damaging |
Het |
Myom3 |
T |
A |
4: 135,507,231 (GRCm39) |
L537Q |
probably damaging |
Het |
Nrap |
A |
C |
19: 56,325,010 (GRCm39) |
Y1234* |
probably null |
Het |
Or51q1 |
T |
C |
7: 103,628,743 (GRCm39) |
S121P |
probably damaging |
Het |
Parn |
T |
C |
16: 13,359,020 (GRCm39) |
D574G |
probably benign |
Het |
Pbrm1 |
A |
G |
14: 30,789,773 (GRCm39) |
I807V |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,725,193 (GRCm39) |
S1350R |
unknown |
Het |
Pira13 |
T |
C |
7: 3,826,126 (GRCm39) |
H289R |
unknown |
Het |
Plaa |
T |
C |
4: 94,474,586 (GRCm39) |
Q272R |
probably damaging |
Het |
Rfx6 |
T |
A |
10: 51,594,292 (GRCm39) |
I174N |
probably benign |
Het |
Ripk2 |
T |
A |
4: 16,139,218 (GRCm39) |
K226N |
probably damaging |
Het |
Scgb1b2 |
T |
C |
7: 30,990,946 (GRCm39) |
D54G |
possibly damaging |
Het |
Slc45a4 |
T |
C |
15: 73,456,383 (GRCm39) |
Y599C |
probably benign |
Het |
Slc7a13 |
T |
C |
4: 19,819,082 (GRCm39) |
V94A |
probably benign |
Het |
Slc7a8 |
A |
G |
14: 54,972,579 (GRCm39) |
F281L |
probably benign |
Het |
Slco4c1 |
T |
A |
1: 96,772,261 (GRCm39) |
T243S |
probably damaging |
Het |
Smim30 |
C |
T |
6: 13,870,541 (GRCm39) |
G57E |
probably damaging |
Het |
Stat5b |
A |
G |
11: 100,692,262 (GRCm39) |
I174T |
probably damaging |
Het |
Styk1 |
C |
A |
6: 131,281,848 (GRCm39) |
V257L |
probably benign |
Het |
Tmem268 |
T |
C |
4: 63,498,209 (GRCm39) |
F210L |
probably damaging |
Het |
Ugt2b35 |
T |
A |
5: 87,149,302 (GRCm39) |
S184R |
probably damaging |
Het |
Vps50 |
T |
A |
6: 3,562,297 (GRCm39) |
L464* |
probably null |
Het |
Zfhx2 |
A |
T |
14: 55,301,898 (GRCm39) |
S2029T |
probably benign |
Het |
Zfp235 |
T |
A |
7: 23,841,296 (GRCm39) |
F572I |
probably damaging |
Het |
Zfp280d |
T |
C |
9: 72,267,615 (GRCm39) |
I766T |
probably benign |
Het |
Zfr |
T |
G |
15: 12,171,904 (GRCm39) |
C933W |
probably damaging |
Het |
|
Other mutations in Or8b9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01862:Or8b9
|
APN |
9 |
37,766,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02108:Or8b9
|
APN |
9 |
37,766,234 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02474:Or8b9
|
APN |
9 |
37,766,656 (GRCm39) |
missense |
probably benign |
0.08 |
R0006:Or8b9
|
UTSW |
9 |
37,766,516 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0893:Or8b9
|
UTSW |
9 |
37,766,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1051:Or8b9
|
UTSW |
9 |
37,766,657 (GRCm39) |
missense |
probably damaging |
0.99 |
R1432:Or8b9
|
UTSW |
9 |
37,766,548 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1718:Or8b9
|
UTSW |
9 |
37,766,749 (GRCm39) |
missense |
probably benign |
0.03 |
R1864:Or8b9
|
UTSW |
9 |
37,766,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Or8b9
|
UTSW |
9 |
37,766,705 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4507:Or8b9
|
UTSW |
9 |
37,766,201 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4900:Or8b9
|
UTSW |
9 |
37,766,608 (GRCm39) |
missense |
probably benign |
|
R5406:Or8b9
|
UTSW |
9 |
37,766,515 (GRCm39) |
missense |
probably benign |
0.02 |
R6813:Or8b9
|
UTSW |
9 |
37,766,810 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7061:Or8b9
|
UTSW |
9 |
37,766,942 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7315:Or8b9
|
UTSW |
9 |
37,766,543 (GRCm39) |
missense |
probably benign |
|
R7500:Or8b9
|
UTSW |
9 |
37,766,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R8021:Or8b9
|
UTSW |
9 |
37,766,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R9093:Or8b9
|
UTSW |
9 |
37,766,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9331:Or8b9
|
UTSW |
9 |
37,766,710 (GRCm39) |
missense |
probably benign |
0.03 |
R9373:Or8b9
|
UTSW |
9 |
37,766,750 (GRCm39) |
missense |
probably damaging |
0.97 |
R9696:Or8b9
|
UTSW |
9 |
37,766,671 (GRCm39) |
missense |
probably benign |
0.35 |
Z1088:Or8b9
|
UTSW |
9 |
37,766,614 (GRCm39) |
missense |
probably benign |
0.31 |
Z1177:Or8b9
|
UTSW |
9 |
37,766,794 (GRCm39) |
missense |
possibly damaging |
0.72 |
|