Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
C |
10: 79,843,221 (GRCm39) |
L1232P |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,188,351 (GRCm39) |
I1922F |
possibly damaging |
Het |
Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
Arpc5 |
T |
C |
1: 152,647,206 (GRCm39) |
V103A |
possibly damaging |
Het |
Atp9a |
C |
A |
2: 168,510,090 (GRCm39) |
V430F |
probably benign |
Het |
Bod1 |
A |
G |
11: 31,616,932 (GRCm39) |
S110P |
probably damaging |
Het |
Cacna1c |
C |
A |
6: 118,590,914 (GRCm39) |
V1453F |
probably damaging |
Het |
Capn8 |
T |
A |
1: 182,435,264 (GRCm39) |
M414K |
probably damaging |
Het |
Cbl |
A |
T |
9: 44,069,809 (GRCm39) |
|
probably null |
Het |
Ccdc42 |
A |
T |
11: 68,479,106 (GRCm39) |
Q98L |
probably damaging |
Het |
Ccn3 |
T |
C |
15: 54,611,421 (GRCm39) |
|
probably null |
Het |
Cd200 |
C |
A |
16: 45,217,545 (GRCm39) |
V49L |
probably benign |
Het |
Celsr1 |
A |
G |
15: 85,812,531 (GRCm39) |
S2060P |
probably benign |
Het |
Ces1g |
A |
T |
8: 94,057,820 (GRCm39) |
H160Q |
possibly damaging |
Het |
Chrnb2 |
G |
T |
3: 89,668,831 (GRCm39) |
H161Q |
probably damaging |
Het |
Ctns |
G |
A |
11: 73,082,559 (GRCm39) |
T57I |
probably benign |
Het |
Cyp3a25 |
A |
T |
5: 145,931,766 (GRCm39) |
M114K |
possibly damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,057,871 (GRCm39) |
F536L |
probably benign |
Het |
Dcc |
C |
T |
18: 71,943,826 (GRCm39) |
R275Q |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,289,990 (GRCm39) |
H2508Q |
possibly damaging |
Het |
Elf5 |
C |
A |
2: 103,269,757 (GRCm39) |
Q113K |
probably damaging |
Het |
Fam83a |
T |
G |
15: 57,849,507 (GRCm39) |
V17G |
possibly damaging |
Het |
Farsa |
T |
C |
8: 85,587,674 (GRCm39) |
|
probably null |
Het |
Fat2 |
G |
C |
11: 55,172,106 (GRCm39) |
T2869S |
possibly damaging |
Het |
Fgg |
A |
T |
3: 82,920,283 (GRCm39) |
Q354L |
probably damaging |
Het |
Folh1 |
T |
C |
7: 86,372,517 (GRCm39) |
D679G |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,270,975 (GRCm39) |
R83* |
probably null |
Het |
Gm17482 |
T |
A |
6: 115,204,311 (GRCm39) |
|
probably benign |
Het |
Hmgxb4 |
T |
A |
8: 75,749,927 (GRCm39) |
V481D |
possibly damaging |
Het |
Ifi207 |
A |
C |
1: 173,552,619 (GRCm39) |
Y926D |
probably damaging |
Het |
Ikzf5 |
T |
A |
7: 130,993,377 (GRCm39) |
N264Y |
probably damaging |
Het |
Kat6a |
T |
A |
8: 23,430,384 (GRCm39) |
M1913K |
unknown |
Het |
Krt33b |
A |
T |
11: 99,915,694 (GRCm39) |
C351S |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,427,944 (GRCm39) |
D543G |
probably damaging |
Het |
Lrrfip2 |
C |
T |
9: 111,053,021 (GRCm39) |
R339W |
probably damaging |
Het |
Mapk3 |
T |
G |
7: 126,363,454 (GRCm39) |
M276R |
probably benign |
Het |
Mgst1 |
T |
C |
6: 138,127,827 (GRCm39) |
V137A |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,558,884 (GRCm39) |
T2470A |
unknown |
Het |
Muc4 |
C |
T |
16: 32,575,237 (GRCm39) |
S1274F |
possibly damaging |
Het |
Myo5c |
A |
C |
9: 75,180,198 (GRCm39) |
K713T |
possibly damaging |
Het |
Myzap |
T |
C |
9: 71,466,146 (GRCm39) |
D170G |
possibly damaging |
Het |
Naa50 |
T |
C |
16: 43,979,831 (GRCm39) |
V113A |
probably damaging |
Het |
Neu3 |
T |
C |
7: 99,462,929 (GRCm39) |
T265A |
probably benign |
Het |
Nin |
T |
C |
12: 70,061,631 (GRCm39) |
T2078A |
possibly damaging |
Het |
Nomo1 |
G |
A |
7: 45,683,260 (GRCm39) |
|
probably benign |
Het |
Nprl3 |
A |
G |
11: 32,189,828 (GRCm39) |
L273P |
probably damaging |
Het |
Oaf |
T |
A |
9: 43,136,216 (GRCm39) |
H120L |
possibly damaging |
Het |
Or10s1 |
T |
C |
9: 39,985,824 (GRCm39) |
S78P |
probably damaging |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Or8k21 |
T |
C |
2: 86,145,468 (GRCm39) |
H54R |
probably benign |
Het |
Pcdhga3 |
T |
A |
18: 37,809,674 (GRCm39) |
|
probably benign |
Het |
Polq |
G |
A |
16: 36,837,718 (GRCm39) |
|
probably null |
Het |
Prdm8 |
C |
T |
5: 98,333,162 (GRCm39) |
P243L |
possibly damaging |
Het |
Prim2 |
T |
C |
1: 33,701,373 (GRCm39) |
D138G |
probably benign |
Het |
Prl2c5 |
A |
G |
13: 13,365,175 (GRCm39) |
E107G |
probably benign |
Het |
Prr14l |
T |
A |
5: 32,984,869 (GRCm39) |
H1542L |
probably damaging |
Het |
Rab26 |
T |
C |
17: 24,749,072 (GRCm39) |
E203G |
probably damaging |
Het |
Rtkn2 |
A |
T |
10: 67,871,662 (GRCm39) |
H350L |
possibly damaging |
Het |
Scara3 |
T |
C |
14: 66,175,710 (GRCm39) |
D19G |
probably benign |
Het |
Scn3a |
A |
G |
2: 65,302,685 (GRCm39) |
S1254P |
probably damaging |
Het |
Sdcbp |
A |
G |
4: 6,385,059 (GRCm39) |
M93V |
probably benign |
Het |
Sema6a |
C |
A |
18: 47,382,231 (GRCm39) |
R772L |
probably damaging |
Het |
Slc5a7 |
T |
C |
17: 54,584,006 (GRCm39) |
K428R |
probably benign |
Het |
Sptbn2 |
G |
A |
19: 4,774,674 (GRCm39) |
G109D |
probably damaging |
Het |
Tmppe |
T |
C |
9: 114,233,812 (GRCm39) |
L37P |
probably benign |
Het |
Tuba1a |
T |
C |
15: 98,849,410 (GRCm39) |
T56A |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,412,817 (GRCm39) |
I1506N |
probably damaging |
Het |
Vmn2r111 |
A |
G |
17: 22,792,070 (GRCm39) |
I62T |
probably benign |
Het |
Vmn2r73 |
A |
G |
7: 85,506,828 (GRCm39) |
I828T |
probably damaging |
Het |
Vmn2r79 |
T |
A |
7: 86,686,976 (GRCm39) |
W786R |
probably damaging |
Het |
Zp1 |
G |
A |
19: 10,894,084 (GRCm39) |
T405M |
probably null |
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 |
IGL02391:Or13p4
|
APN |
4 |
118,547,538 (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 |
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 |
|