Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
AGCTTCCCTGCTT |
AGCTT |
9: 57,165,505 (GRCm39) |
|
probably null |
Het |
Aars2 |
T |
C |
17: 45,819,885 (GRCm39) |
Y221H |
probably damaging |
Het |
Abca8b |
G |
A |
11: 109,836,648 (GRCm39) |
R1216* |
probably null |
Het |
Acad8 |
A |
T |
9: 26,888,967 (GRCm39) |
|
probably null |
Het |
Acer2 |
A |
G |
4: 86,805,287 (GRCm39) |
T84A |
probably null |
Het |
Adgrb2 |
A |
G |
4: 129,903,315 (GRCm39) |
N613S |
probably damaging |
Het |
Arap2 |
T |
C |
5: 62,798,729 (GRCm39) |
D1300G |
possibly damaging |
Het |
Castor1 |
T |
C |
11: 4,168,949 (GRCm39) |
C39R |
probably damaging |
Het |
Ccl11 |
A |
T |
11: 81,948,665 (GRCm39) |
|
probably benign |
Het |
Cfh |
A |
T |
1: 140,016,505 (GRCm39) |
Y1151* |
probably null |
Het |
Cobll1 |
A |
G |
2: 64,928,882 (GRCm39) |
S815P |
probably benign |
Het |
Cryz |
T |
C |
3: 154,327,205 (GRCm39) |
S240P |
probably damaging |
Het |
Csmd2 |
A |
G |
4: 128,404,826 (GRCm39) |
Y2404C |
|
Het |
F13a1 |
T |
C |
13: 37,100,860 (GRCm39) |
D428G |
probably damaging |
Het |
Fbxo42 |
A |
G |
4: 140,927,396 (GRCm39) |
S559G |
probably benign |
Het |
Fry |
A |
G |
5: 150,393,232 (GRCm39) |
S263G |
|
Het |
Fshr |
C |
T |
17: 89,292,897 (GRCm39) |
A594T |
probably damaging |
Het |
Gm1527 |
A |
G |
3: 28,980,690 (GRCm39) |
M597V |
probably null |
Het |
Gpr158 |
A |
T |
2: 21,815,412 (GRCm39) |
T602S |
probably damaging |
Het |
Hmgxb4 |
C |
A |
8: 75,756,624 (GRCm39) |
T583K |
probably damaging |
Het |
Igkv8-30 |
C |
T |
6: 70,094,069 (GRCm39) |
C114Y |
probably damaging |
Het |
Igsf5 |
T |
A |
16: 96,204,546 (GRCm39) |
N366K |
probably damaging |
Het |
Kif15 |
T |
C |
9: 122,838,991 (GRCm39) |
|
probably null |
Het |
Klk1b26 |
T |
A |
7: 43,665,821 (GRCm39) |
|
probably null |
Het |
Lama1 |
G |
T |
17: 68,044,700 (GRCm39) |
E200* |
probably null |
Het |
Lpar5 |
C |
T |
6: 125,059,347 (GRCm39) |
T356I |
probably benign |
Het |
Lrch3 |
A |
T |
16: 32,810,665 (GRCm39) |
T538S |
probably damaging |
Het |
Mansc4 |
A |
G |
6: 146,977,203 (GRCm39) |
S138P |
probably damaging |
Het |
Mief1 |
T |
C |
15: 80,134,061 (GRCm39) |
S373P |
possibly damaging |
Het |
Nbas |
G |
T |
12: 13,570,751 (GRCm39) |
V2053F |
possibly damaging |
Het |
Nek11 |
T |
C |
9: 105,121,614 (GRCm39) |
E435G |
probably damaging |
Het |
Nynrin |
A |
T |
14: 56,109,380 (GRCm39) |
I1496F |
probably benign |
Het |
Odf1 |
A |
T |
15: 38,219,794 (GRCm39) |
M41L |
probably benign |
Het |
Or4c115 |
A |
G |
2: 88,927,626 (GRCm39) |
V215A |
probably benign |
Het |
Or4c29 |
A |
T |
2: 88,740,708 (GRCm39) |
F10I |
probably benign |
Het |
Or7h8 |
T |
G |
9: 20,123,851 (GRCm39) |
S69A |
probably benign |
Het |
Oxnad1 |
T |
C |
14: 31,818,473 (GRCm39) |
V106A |
possibly damaging |
Het |
Padi4 |
C |
A |
4: 140,488,969 (GRCm39) |
E157* |
probably null |
Het |
Parp10 |
A |
T |
15: 76,126,616 (GRCm39) |
F217L |
probably damaging |
Het |
Pcdhb18 |
T |
A |
18: 37,623,436 (GRCm39) |
S255R |
probably benign |
Het |
Pde4c |
G |
T |
8: 71,197,978 (GRCm39) |
G102W |
probably damaging |
Het |
Pde6a |
T |
C |
18: 61,391,295 (GRCm39) |
Y547H |
probably damaging |
Het |
Phf11b |
A |
T |
14: 59,563,507 (GRCm39) |
L137I |
probably benign |
Het |
Pigh |
A |
C |
12: 79,130,463 (GRCm39) |
I134S |
probably damaging |
Het |
Pigt |
G |
A |
2: 164,344,436 (GRCm39) |
V362M |
probably damaging |
Het |
Pld1 |
A |
G |
3: 28,078,401 (GRCm39) |
D20G |
probably damaging |
Het |
Pou3f2 |
T |
C |
4: 22,487,288 (GRCm39) |
R282G |
probably damaging |
Het |
Ppp2r5d |
A |
G |
17: 46,996,527 (GRCm39) |
V382A |
probably damaging |
Het |
Prdm16 |
T |
C |
4: 154,425,967 (GRCm39) |
E606G |
probably damaging |
Het |
Psg28 |
A |
G |
7: 18,164,509 (GRCm39) |
Y68H |
probably damaging |
Het |
Qpctl |
C |
A |
7: 18,882,944 (GRCm39) |
W56L |
probably damaging |
Het |
Rab11fip5 |
G |
A |
6: 85,319,137 (GRCm39) |
P584L |
probably damaging |
Het |
Sde2 |
C |
T |
1: 180,678,843 (GRCm39) |
H36Y |
probably benign |
Het |
Sema4d |
T |
C |
13: 51,856,872 (GRCm39) |
S787G |
probably benign |
Het |
Sgca |
C |
T |
11: 94,864,014 (GRCm39) |
|
probably null |
Het |
Shroom3 |
A |
G |
5: 93,090,463 (GRCm39) |
E1071G |
probably damaging |
Het |
Skint5 |
A |
G |
4: 113,437,679 (GRCm39) |
|
probably null |
Het |
Slc44a3 |
T |
A |
3: 121,319,411 (GRCm39) |
D110V |
probably benign |
Het |
Slc4a4 |
A |
C |
5: 89,082,433 (GRCm39) |
|
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,688,857 (GRCm39) |
D389G |
probably damaging |
Het |
Sp3 |
C |
G |
2: 72,809,953 (GRCm39) |
E11Q |
probably benign |
Het |
Srrm2 |
A |
G |
17: 24,037,198 (GRCm39) |
S1281G |
unknown |
Het |
Tat |
A |
T |
8: 110,723,459 (GRCm39) |
I316F |
probably benign |
Het |
Thoc5 |
A |
G |
11: 4,865,563 (GRCm39) |
T381A |
probably benign |
Het |
Tiam1 |
T |
C |
16: 89,681,826 (GRCm39) |
Y384C |
probably damaging |
Het |
Tmem45a |
A |
T |
16: 56,632,026 (GRCm39) |
F197L |
probably damaging |
Het |
Trav8d-1 |
A |
G |
14: 53,016,435 (GRCm39) |
Y107C |
probably damaging |
Het |
Trim10 |
T |
A |
17: 37,187,846 (GRCm39) |
V354D |
probably damaging |
Het |
Unc45b |
A |
T |
11: 82,831,013 (GRCm39) |
|
probably null |
Het |
Unc79 |
A |
G |
12: 103,078,765 (GRCm39) |
I1643M |
probably benign |
Het |
Unc80 |
G |
T |
1: 66,560,725 (GRCm39) |
G818* |
probably null |
Het |
Usp15 |
A |
T |
10: 122,966,910 (GRCm39) |
M470K |
possibly damaging |
Het |
Vldlr |
T |
C |
19: 27,212,241 (GRCm39) |
V85A |
probably benign |
Het |
Vma21-ps |
A |
G |
4: 52,496,994 (GRCm39) |
V84A |
probably benign |
Het |
Vmn2r67 |
C |
T |
7: 84,785,774 (GRCm39) |
V744I |
possibly damaging |
Het |
Wdr73 |
A |
G |
7: 80,542,946 (GRCm39) |
C221R |
probably benign |
Het |
Zxdc |
C |
T |
6: 90,355,819 (GRCm39) |
H443Y |
probably damaging |
Het |
|
Other mutations in Or10a5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01324:Or10a5
|
APN |
7 |
106,636,054 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01630:Or10a5
|
APN |
7 |
106,636,318 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02539:Or10a5
|
APN |
7 |
106,635,641 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02727:Or10a5
|
APN |
7 |
106,635,902 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03336:Or10a5
|
APN |
7 |
106,635,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R0501:Or10a5
|
UTSW |
7 |
106,635,439 (GRCm39) |
missense |
probably benign |
|
R0684:Or10a5
|
UTSW |
7 |
106,635,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R0909:Or10a5
|
UTSW |
7 |
106,635,401 (GRCm39) |
missense |
probably benign |
0.19 |
R1481:Or10a5
|
UTSW |
7 |
106,635,356 (GRCm39) |
missense |
probably benign |
0.05 |
R1958:Or10a5
|
UTSW |
7 |
106,635,478 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1965:Or10a5
|
UTSW |
7 |
106,635,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Or10a5
|
UTSW |
7 |
106,635,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Or10a5
|
UTSW |
7 |
106,635,545 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3012:Or10a5
|
UTSW |
7 |
106,635,569 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3428:Or10a5
|
UTSW |
7 |
106,635,923 (GRCm39) |
missense |
probably benign |
|
R4425:Or10a5
|
UTSW |
7 |
106,635,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Or10a5
|
UTSW |
7 |
106,636,121 (GRCm39) |
missense |
probably benign |
0.00 |
R4796:Or10a5
|
UTSW |
7 |
106,636,121 (GRCm39) |
missense |
probably benign |
0.00 |
R4908:Or10a5
|
UTSW |
7 |
106,635,364 (GRCm39) |
start codon destroyed |
probably benign |
0.02 |
R4945:Or10a5
|
UTSW |
7 |
106,635,526 (GRCm39) |
missense |
probably benign |
0.00 |
R5122:Or10a5
|
UTSW |
7 |
106,636,055 (GRCm39) |
nonsense |
probably null |
|
R5721:Or10a5
|
UTSW |
7 |
106,635,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Or10a5
|
UTSW |
7 |
106,635,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Or10a5
|
UTSW |
7 |
106,636,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R6981:Or10a5
|
UTSW |
7 |
106,635,956 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7228:Or10a5
|
UTSW |
7 |
106,636,307 (GRCm39) |
missense |
probably benign |
|
R7444:Or10a5
|
UTSW |
7 |
106,635,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Or10a5
|
UTSW |
7 |
106,635,889 (GRCm39) |
missense |
probably benign |
0.28 |
R9109:Or10a5
|
UTSW |
7 |
106,635,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Or10a5
|
UTSW |
7 |
106,635,640 (GRCm39) |
missense |
probably damaging |
1.00 |
|