Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
T |
A |
14: 118,790,764 (GRCm39) |
N748Y |
probably damaging |
Het |
Actbl2 |
A |
G |
13: 111,391,701 (GRCm39) |
D12G |
possibly damaging |
Het |
Adamts10 |
T |
C |
17: 33,747,785 (GRCm39) |
S74P |
probably benign |
Het |
Adprs |
C |
T |
4: 126,211,701 (GRCm39) |
|
probably benign |
Het |
Amn1 |
A |
G |
6: 149,070,944 (GRCm39) |
|
probably null |
Het |
Antxr1 |
A |
T |
6: 87,264,038 (GRCm39) |
I144N |
probably damaging |
Het |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
Cabp5 |
A |
T |
7: 13,132,269 (GRCm39) |
R13* |
probably null |
Het |
Cacna1e |
A |
G |
1: 154,296,859 (GRCm39) |
Y1669H |
probably damaging |
Het |
Ccdc174 |
A |
G |
6: 91,875,263 (GRCm39) |
E364G |
possibly damaging |
Het |
Ccdc18 |
C |
T |
5: 108,283,918 (GRCm39) |
P74S |
probably damaging |
Het |
Clec3a |
C |
T |
8: 115,152,240 (GRCm39) |
S82L |
probably benign |
Het |
Cnih3 |
A |
G |
1: 181,234,078 (GRCm39) |
D43G |
probably damaging |
Het |
Dpp10 |
G |
A |
1: 123,578,087 (GRCm39) |
T128M |
probably damaging |
Het |
Edar |
A |
T |
10: 58,464,403 (GRCm39) |
F79I |
probably damaging |
Het |
Eif2ak4 |
T |
A |
2: 118,251,272 (GRCm39) |
H199Q |
probably benign |
Het |
Fermt1 |
A |
G |
2: 132,783,871 (GRCm39) |
L46P |
probably damaging |
Het |
Glipr1 |
A |
G |
10: 111,824,799 (GRCm39) |
|
probably benign |
Het |
Gsdmc |
T |
C |
15: 63,675,428 (GRCm39) |
N129S |
probably damaging |
Het |
Ift88 |
T |
C |
14: 57,718,871 (GRCm39) |
S619P |
possibly damaging |
Het |
Itga9 |
T |
A |
9: 118,679,873 (GRCm39) |
V262E |
probably benign |
Het |
Med17 |
G |
A |
9: 15,188,963 (GRCm39) |
R101* |
probably null |
Het |
Mta1 |
T |
A |
12: 113,100,203 (GRCm39) |
I688N |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,570,894 (GRCm39) |
R651S |
probably benign |
Het |
Opcml |
A |
G |
9: 28,586,560 (GRCm39) |
I93V |
probably damaging |
Het |
Or12d17 |
C |
T |
17: 37,777,477 (GRCm39) |
P127S |
probably damaging |
Het |
Or9r7 |
A |
G |
10: 129,962,773 (GRCm39) |
V51A |
possibly damaging |
Het |
Parg |
T |
G |
14: 31,984,638 (GRCm39) |
|
probably null |
Het |
Rps3a3 |
A |
G |
13: 108,807,417 (GRCm39) |
|
probably benign |
Het |
Safb |
T |
A |
17: 56,907,813 (GRCm39) |
|
probably benign |
Het |
Sat2 |
G |
T |
11: 69,513,575 (GRCm39) |
C54F |
probably damaging |
Het |
Scin |
T |
A |
12: 40,127,530 (GRCm39) |
Y420F |
probably benign |
Het |
Slc22a29 |
A |
T |
19: 8,146,717 (GRCm39) |
S362T |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,738,254 (GRCm39) |
D537G |
probably null |
Het |
Spred3 |
A |
G |
7: 28,865,830 (GRCm39) |
S126P |
probably benign |
Het |
Ssh1 |
C |
T |
5: 114,080,578 (GRCm39) |
E951K |
probably damaging |
Het |
Ssmem1 |
A |
G |
6: 30,512,441 (GRCm39) |
E28G |
possibly damaging |
Het |
Stox1 |
A |
T |
10: 62,495,455 (GRCm39) |
|
probably benign |
Het |
Syn3 |
T |
C |
10: 85,900,770 (GRCm39) |
I373V |
probably benign |
Het |
Tecrl |
A |
T |
5: 83,502,674 (GRCm39) |
F58L |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,033,191 (GRCm39) |
N1655S |
possibly damaging |
Het |
Usp2 |
G |
T |
9: 44,002,524 (GRCm39) |
Q147H |
probably damaging |
Het |
Usp24 |
T |
A |
4: 106,264,326 (GRCm39) |
N1751K |
possibly damaging |
Het |
Wipf1 |
T |
A |
2: 73,264,487 (GRCm39) |
D438V |
probably damaging |
Het |
|
Other mutations in Or13p4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01823:Or13p4
|
APN |
4 |
118,546,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Or13p4
|
UTSW |
4 |
118,547,269 (GRCm39) |
missense |
probably benign |
|
R1565:Or13p4
|
UTSW |
4 |
118,547,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Or13p4
|
UTSW |
4 |
118,547,145 (GRCm39) |
missense |
probably benign |
0.00 |
R1823:Or13p4
|
UTSW |
4 |
118,547,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R2343:Or13p4
|
UTSW |
4 |
118,547,384 (GRCm39) |
missense |
probably benign |
0.30 |
R4618:Or13p4
|
UTSW |
4 |
118,546,667 (GRCm39) |
utr 3 prime |
probably benign |
|
R4941:Or13p4
|
UTSW |
4 |
118,547,089 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5408:Or13p4
|
UTSW |
4 |
118,547,641 (GRCm39) |
missense |
probably benign |
0.00 |
R5587:Or13p4
|
UTSW |
4 |
118,547,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R5895:Or13p4
|
UTSW |
4 |
118,547,314 (GRCm39) |
missense |
probably damaging |
0.97 |
R6023:Or13p4
|
UTSW |
4 |
118,547,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R6307:Or13p4
|
UTSW |
4 |
118,547,145 (GRCm39) |
missense |
probably benign |
0.00 |
R6324:Or13p4
|
UTSW |
4 |
118,547,728 (GRCm39) |
start gained |
probably benign |
|
R6890:Or13p4
|
UTSW |
4 |
118,546,728 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7218:Or13p4
|
UTSW |
4 |
118,547,215 (GRCm39) |
missense |
probably benign |
|
R7408:Or13p4
|
UTSW |
4 |
118,546,859 (GRCm39) |
missense |
probably damaging |
0.98 |
R7555:Or13p4
|
UTSW |
4 |
118,546,839 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7749:Or13p4
|
UTSW |
4 |
118,547,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Or13p4
|
UTSW |
4 |
118,547,406 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8493:Or13p4
|
UTSW |
4 |
118,547,229 (GRCm39) |
missense |
probably benign |
0.01 |
R9445:Or13p4
|
UTSW |
4 |
118,547,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R9500:Or13p4
|
UTSW |
4 |
118,546,930 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:Or13p4
|
UTSW |
4 |
118,547,469 (GRCm39) |
missense |
probably benign |
0.31 |
|