Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
G |
3: 59,651,112 (GRCm39) |
N78S |
probably damaging |
Het |
Abca12 |
G |
A |
1: 71,453,837 (GRCm39) |
|
probably benign |
Het |
Abcb1b |
T |
C |
5: 8,887,747 (GRCm39) |
S878P |
probably damaging |
Het |
Adamts20 |
T |
C |
15: 94,223,814 (GRCm39) |
R1305G |
probably damaging |
Het |
Adcy2 |
A |
T |
13: 68,837,400 (GRCm39) |
C650S |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,982,708 (GRCm39) |
K1331* |
probably null |
Het |
Alpk1 |
A |
T |
3: 127,473,700 (GRCm39) |
S768T |
probably benign |
Het |
Ap4b1 |
T |
G |
3: 103,722,398 (GRCm39) |
L124R |
probably damaging |
Het |
Arrdc2 |
A |
T |
8: 71,292,038 (GRCm39) |
F3Y |
probably damaging |
Het |
Atp9a |
A |
G |
2: 168,547,114 (GRCm39) |
V155A |
probably benign |
Het |
Bptf |
A |
G |
11: 106,938,013 (GRCm39) |
S87P |
probably benign |
Het |
Carmil1 |
A |
T |
13: 24,220,421 (GRCm39) |
M697K |
probably benign |
Het |
Ccdc42 |
G |
A |
11: 68,485,022 (GRCm39) |
V32M |
probably benign |
Het |
Cert1 |
A |
G |
13: 96,753,563 (GRCm39) |
H391R |
probably damaging |
Het |
Ces1d |
A |
G |
8: 93,924,294 (GRCm39) |
|
probably null |
Het |
Dcpp2 |
T |
G |
17: 24,119,566 (GRCm39) |
Y127D |
probably damaging |
Het |
Def8 |
C |
A |
8: 124,174,060 (GRCm39) |
T7K |
probably benign |
Het |
Dnah8 |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
CGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTTTGACTTTCCTGTGTCTTCAATATTTTGTTCCCTTTCCCGTAGGTGCCGTCCTT |
17: 30,979,841 (GRCm39) |
|
probably null |
Het |
En2 |
G |
A |
5: 28,371,594 (GRCm39) |
G24S |
probably benign |
Het |
Evi2a |
T |
C |
11: 79,418,688 (GRCm39) |
|
probably benign |
Het |
Fam117b |
A |
T |
1: 59,952,837 (GRCm39) |
H172L |
possibly damaging |
Het |
Fam169b |
A |
G |
7: 67,954,338 (GRCm39) |
I67M |
probably benign |
Het |
Fbxo40 |
T |
A |
16: 36,789,861 (GRCm39) |
E416D |
probably damaging |
Het |
Gja8 |
T |
A |
3: 96,827,635 (GRCm39) |
N9I |
possibly damaging |
Het |
Gsg1l2 |
T |
A |
11: 67,676,097 (GRCm39) |
C154S |
probably benign |
Het |
Hdhd3 |
C |
A |
4: 62,418,232 (GRCm39) |
|
probably benign |
Het |
Hunk |
C |
T |
16: 90,278,214 (GRCm39) |
P341L |
possibly damaging |
Het |
Ighv8-5 |
T |
C |
12: 115,031,258 (GRCm39) |
T94A |
possibly damaging |
Het |
Ints3 |
T |
C |
3: 90,331,319 (GRCm39) |
N75D |
probably benign |
Het |
Krt39 |
T |
C |
11: 99,409,901 (GRCm39) |
E212G |
probably damaging |
Het |
Ldlrad4 |
A |
G |
18: 68,387,495 (GRCm39) |
H269R |
probably damaging |
Het |
Lrrc2 |
T |
A |
9: 110,790,049 (GRCm39) |
V102E |
possibly damaging |
Het |
Ltbp2 |
T |
A |
12: 84,836,655 (GRCm39) |
I1292L |
probably benign |
Het |
Mad2l1bp |
A |
T |
17: 46,458,993 (GRCm39) |
V179E |
possibly damaging |
Het |
Map3k1 |
A |
G |
13: 111,892,663 (GRCm39) |
V864A |
probably benign |
Het |
Mapk8ip2 |
T |
G |
15: 89,342,322 (GRCm39) |
V511G |
probably damaging |
Het |
Mknk2 |
A |
C |
10: 80,503,021 (GRCm39) |
S434A |
probably benign |
Het |
Mllt11 |
A |
G |
3: 95,127,548 (GRCm39) |
F74S |
probably damaging |
Het |
Muc16 |
G |
T |
9: 18,506,519 (GRCm39) |
T6412K |
possibly damaging |
Het |
Nek5 |
C |
A |
8: 22,573,403 (GRCm39) |
A518S |
possibly damaging |
Het |
Npy1r |
T |
C |
8: 67,156,864 (GRCm39) |
F95L |
possibly damaging |
Het |
Nup98 |
G |
A |
7: 101,773,569 (GRCm39) |
T1586I |
probably benign |
Het |
Olig3 |
A |
T |
10: 19,232,518 (GRCm39) |
M48L |
probably benign |
Het |
Or13n4 |
A |
G |
7: 106,422,932 (GRCm39) |
M267T |
probably benign |
Het |
Or14j7 |
T |
A |
17: 38,234,568 (GRCm39) |
L37* |
probably null |
Het |
Or5b120 |
T |
G |
19: 13,480,587 (GRCm39) |
N293K |
probably damaging |
Het |
Pcdhb16 |
A |
G |
18: 37,611,904 (GRCm39) |
D288G |
possibly damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Phip |
T |
C |
9: 82,790,886 (GRCm39) |
I687V |
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,209,659 (GRCm39) |
T2348M |
probably damaging |
Het |
Plod3 |
A |
G |
5: 137,018,835 (GRCm39) |
T291A |
probably benign |
Het |
Pmpca |
G |
A |
2: 26,280,144 (GRCm39) |
V89I |
possibly damaging |
Het |
Polr1b |
C |
A |
2: 128,967,464 (GRCm39) |
F952L |
probably damaging |
Het |
Pou6f2 |
C |
A |
13: 18,553,092 (GRCm39) |
A81S |
|
Het |
Ppl |
T |
A |
16: 4,905,828 (GRCm39) |
E1489V |
probably damaging |
Het |
Ptpdc1 |
A |
G |
13: 48,733,264 (GRCm39) |
F792S |
probably damaging |
Het |
Pus1 |
A |
G |
5: 110,927,582 (GRCm39) |
Y58H |
probably damaging |
Het |
Rex2 |
C |
A |
4: 147,142,547 (GRCm39) |
T345N |
possibly damaging |
Het |
Rnf144a |
T |
C |
12: 26,389,439 (GRCm39) |
M1V |
probably null |
Het |
Siglec15 |
A |
T |
18: 78,100,445 (GRCm39) |
C13* |
probably null |
Het |
Skint10 |
G |
A |
4: 112,632,003 (GRCm39) |
Q6* |
probably null |
Het |
Slc5a1 |
T |
C |
5: 33,304,057 (GRCm39) |
W291R |
probably damaging |
Het |
Snx27 |
A |
G |
3: 94,426,366 (GRCm39) |
F378L |
probably benign |
Het |
Strip2 |
A |
T |
6: 29,923,928 (GRCm39) |
T81S |
probably benign |
Het |
Tas2r143 |
A |
G |
6: 42,377,656 (GRCm39) |
N162S |
probably damaging |
Het |
Tatdn1 |
T |
C |
15: 58,776,607 (GRCm39) |
D256G |
probably benign |
Het |
Tbc1d5 |
A |
G |
17: 51,089,291 (GRCm39) |
S630P |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,598,611 (GRCm39) |
D199G |
probably benign |
Het |
Tmed8 |
C |
A |
12: 87,246,991 (GRCm39) |
|
probably benign |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Ttll3 |
TAA |
TAAAGCAA |
6: 113,376,123 (GRCm39) |
|
probably null |
Het |
U2af2 |
T |
C |
7: 5,077,661 (GRCm39) |
|
probably null |
Het |
Ywhag |
C |
T |
5: 135,940,394 (GRCm39) |
E67K |
probably damaging |
Het |
Zfp105 |
A |
G |
9: 122,759,808 (GRCm39) |
H493R |
probably damaging |
Het |
Zfp426 |
A |
T |
9: 20,381,446 (GRCm39) |
C514S |
probably damaging |
Het |
Zfp536 |
T |
A |
7: 37,269,113 (GRCm39) |
D101V |
probably damaging |
Het |
|
Other mutations in Or6aa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02228:Or6aa1
|
APN |
7 |
86,044,286 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02902:Or6aa1
|
APN |
7 |
86,043,743 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02937:Or6aa1
|
APN |
7 |
86,043,798 (GRCm39) |
missense |
possibly damaging |
0.89 |
BB001:Or6aa1
|
UTSW |
7 |
86,043,938 (GRCm39) |
missense |
probably damaging |
1.00 |
BB011:Or6aa1
|
UTSW |
7 |
86,043,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Or6aa1
|
UTSW |
7 |
86,043,803 (GRCm39) |
missense |
probably damaging |
0.97 |
R1524:Or6aa1
|
UTSW |
7 |
86,044,020 (GRCm39) |
missense |
probably benign |
0.01 |
R1762:Or6aa1
|
UTSW |
7 |
86,044,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R3014:Or6aa1
|
UTSW |
7 |
86,043,884 (GRCm39) |
missense |
probably benign |
0.19 |
R3027:Or6aa1
|
UTSW |
7 |
86,043,761 (GRCm39) |
missense |
probably benign |
0.00 |
R4073:Or6aa1
|
UTSW |
7 |
86,044,155 (GRCm39) |
missense |
probably damaging |
0.98 |
R4502:Or6aa1
|
UTSW |
7 |
86,044,485 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4503:Or6aa1
|
UTSW |
7 |
86,044,485 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4607:Or6aa1
|
UTSW |
7 |
86,043,718 (GRCm39) |
splice site |
probably null |
|
R4608:Or6aa1
|
UTSW |
7 |
86,043,718 (GRCm39) |
splice site |
probably null |
|
R7134:Or6aa1
|
UTSW |
7 |
86,044,752 (GRCm39) |
start gained |
probably benign |
|
R7298:Or6aa1
|
UTSW |
7 |
86,044,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Or6aa1
|
UTSW |
7 |
86,043,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R8160:Or6aa1
|
UTSW |
7 |
86,044,473 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8294:Or6aa1
|
UTSW |
7 |
86,044,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R9465:Or6aa1
|
UTSW |
7 |
86,043,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9725:Or6aa1
|
UTSW |
7 |
86,043,973 (GRCm39) |
missense |
probably damaging |
0.99 |
|