Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
G |
A |
5: 138,561,188 (GRCm39) |
T158M |
probably benign |
Het |
Actl7b |
T |
A |
4: 56,740,251 (GRCm39) |
D369V |
probably damaging |
Het |
Apc |
A |
G |
18: 34,445,804 (GRCm39) |
D900G |
possibly damaging |
Het |
Bola1 |
G |
A |
3: 96,104,573 (GRCm39) |
A7V |
probably benign |
Het |
Bud13 |
A |
G |
9: 46,199,377 (GRCm39) |
N246S |
possibly damaging |
Het |
Cdkal1 |
G |
A |
13: 29,538,663 (GRCm39) |
P499S |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Cntnap5c |
C |
T |
17: 58,362,687 (GRCm39) |
R347W |
probably damaging |
Het |
Cox8b |
T |
A |
7: 140,478,929 (GRCm39) |
E62V |
probably null |
Het |
Cyp2t4 |
G |
A |
7: 26,857,162 (GRCm39) |
A342T |
probably benign |
Het |
Cyp8b1 |
A |
G |
9: 121,744,997 (GRCm39) |
Y112H |
probably damaging |
Het |
Dlg5 |
G |
T |
14: 24,241,261 (GRCm39) |
A212D |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,466,986 (GRCm39) |
E3626G |
probably null |
Het |
Dpys |
T |
C |
15: 39,656,720 (GRCm39) |
E449G |
possibly damaging |
Het |
Fam187a |
C |
A |
11: 102,777,400 (GRCm39) |
C401* |
probably null |
Het |
Fsip2 |
A |
T |
2: 82,814,937 (GRCm39) |
I3557L |
probably benign |
Het |
Gpr165 |
C |
A |
X: 95,757,623 (GRCm39) |
D7E |
probably benign |
Het |
H2bc7 |
A |
G |
13: 23,758,219 (GRCm39) |
V49A |
probably damaging |
Het |
Ifi213 |
T |
C |
1: 173,422,835 (GRCm39) |
K10R |
possibly damaging |
Het |
Lrrfip1 |
T |
C |
1: 90,926,541 (GRCm39) |
S8P |
probably benign |
Het |
Morc2b |
T |
C |
17: 33,356,476 (GRCm39) |
D432G |
probably damaging |
Het |
Mrgpra4 |
T |
A |
7: 47,631,425 (GRCm39) |
I59F |
probably damaging |
Het |
Mttp |
A |
T |
3: 137,818,374 (GRCm39) |
D361E |
probably damaging |
Het |
Mysm1 |
A |
G |
4: 94,863,510 (GRCm39) |
S28P |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,876,260 (GRCm39) |
V284D |
probably damaging |
Het |
Nrip2 |
A |
T |
6: 128,384,957 (GRCm39) |
D203V |
probably damaging |
Het |
Oog4 |
A |
T |
4: 143,164,047 (GRCm39) |
Y495N |
probably benign |
Het |
Or52n4 |
A |
T |
7: 104,293,736 (GRCm39) |
V281E |
possibly damaging |
Het |
Or7g19 |
T |
A |
9: 18,856,459 (GRCm39) |
L172M |
possibly damaging |
Het |
Or8c11 |
A |
T |
9: 38,289,647 (GRCm39) |
M151L |
probably benign |
Het |
Pacrg |
T |
A |
17: 10,795,523 (GRCm39) |
R146* |
probably null |
Het |
Pcdh18 |
A |
T |
3: 49,699,624 (GRCm39) |
M946K |
possibly damaging |
Het |
Perm1 |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
TGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCTGAGCCTGACACGGCTTTGTCTACACCCGCCTCT |
4: 156,302,525 (GRCm39) |
|
probably benign |
Het |
Pign |
A |
G |
1: 105,575,917 (GRCm39) |
I241T |
probably benign |
Het |
Pik3cg |
A |
G |
12: 32,243,639 (GRCm39) |
I944T |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Ppp2r5c |
T |
A |
12: 110,510,511 (GRCm39) |
F99L |
probably benign |
Het |
Prex1 |
A |
T |
2: 166,431,493 (GRCm39) |
N756K |
probably benign |
Het |
Prex2 |
A |
T |
1: 11,355,363 (GRCm39) |
M1555L |
probably benign |
Het |
Prex2 |
T |
G |
1: 11,355,364 (GRCm39) |
M1555R |
probably benign |
Het |
Prl3c1 |
T |
A |
13: 27,386,385 (GRCm39) |
D123E |
probably benign |
Het |
Prr22 |
G |
A |
17: 57,078,311 (GRCm39) |
G155R |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,698,899 (GRCm39) |
D1132G |
probably damaging |
Het |
Rnf180 |
A |
T |
13: 105,318,056 (GRCm39) |
F452Y |
probably damaging |
Het |
Scn4b |
A |
T |
9: 45,058,039 (GRCm39) |
I44F |
possibly damaging |
Het |
Sirpb1b |
T |
A |
3: 15,607,410 (GRCm39) |
I291L |
probably benign |
Het |
Slc12a9 |
C |
A |
5: 137,313,737 (GRCm39) |
V741L |
probably benign |
Het |
Tbc1d8 |
G |
T |
1: 39,444,438 (GRCm39) |
R174S |
probably damaging |
Het |
Tenm2 |
A |
G |
11: 35,914,428 (GRCm39) |
F2370L |
probably damaging |
Het |
Tfec |
T |
A |
6: 16,844,202 (GRCm39) |
H115L |
probably damaging |
Het |
Tnxb |
A |
T |
17: 34,908,381 (GRCm39) |
T1345S |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,568,831 (GRCm39) |
N27354I |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,838,290 (GRCm39) |
Y854H |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,689,253 (GRCm39) |
W11R |
probably benign |
Het |
Vmn2r26 |
A |
G |
6: 124,016,577 (GRCm39) |
Q347R |
probably benign |
Het |
|
Other mutations in Or52h1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02121:Or52h1
|
APN |
7 |
103,829,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Or52h1
|
APN |
7 |
103,829,478 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02956:Or52h1
|
APN |
7 |
103,829,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0001:Or52h1
|
UTSW |
7 |
103,828,680 (GRCm39) |
nonsense |
probably null |
|
R0057:Or52h1
|
UTSW |
7 |
103,829,536 (GRCm39) |
missense |
probably benign |
0.13 |
R1054:Or52h1
|
UTSW |
7 |
103,829,498 (GRCm39) |
missense |
probably benign |
0.02 |
R1262:Or52h1
|
UTSW |
7 |
103,828,623 (GRCm39) |
splice site |
probably null |
|
R4589:Or52h1
|
UTSW |
7 |
103,828,636 (GRCm39) |
splice site |
probably null |
|
R4975:Or52h1
|
UTSW |
7 |
103,828,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Or52h1
|
UTSW |
7 |
103,829,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R5643:Or52h1
|
UTSW |
7 |
103,829,091 (GRCm39) |
missense |
probably benign |
0.00 |
R6195:Or52h1
|
UTSW |
7 |
103,828,961 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6211:Or52h1
|
UTSW |
7 |
103,828,954 (GRCm39) |
nonsense |
probably null |
|
R6233:Or52h1
|
UTSW |
7 |
103,828,961 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6259:Or52h1
|
UTSW |
7 |
103,829,261 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7138:Or52h1
|
UTSW |
7 |
103,829,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R7357:Or52h1
|
UTSW |
7 |
103,828,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Or52h1
|
UTSW |
7 |
103,828,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Or52h1
|
UTSW |
7 |
103,829,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R8712:Or52h1
|
UTSW |
7 |
103,829,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R8937:Or52h1
|
UTSW |
7 |
103,828,949 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0018:Or52h1
|
UTSW |
7 |
103,828,797 (GRCm39) |
missense |
probably benign |
0.00 |
|