Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Amigo1 |
T |
A |
3: 108,099,009 (GRCm39) |
C189* |
probably null |
Het |
Auts2 |
G |
T |
5: 131,505,828 (GRCm39) |
|
probably benign |
Het |
Cadps2 |
C |
A |
6: 23,626,670 (GRCm39) |
W177L |
probably damaging |
Het |
Camk2b |
G |
T |
11: 5,939,635 (GRCm39) |
P223Q |
probably damaging |
Het |
Ccdc74a |
C |
A |
16: 17,464,591 (GRCm39) |
S9* |
probably null |
Het |
Ccnt1 |
A |
C |
15: 98,441,205 (GRCm39) |
Y688D |
probably damaging |
Het |
Cdhr1 |
T |
C |
14: 36,801,600 (GRCm39) |
N781S |
probably benign |
Het |
Ceacam3 |
C |
T |
7: 16,885,484 (GRCm39) |
T29I |
probably benign |
Het |
Cep170b |
T |
C |
12: 112,710,589 (GRCm39) |
S1473P |
probably damaging |
Het |
Col19a1 |
T |
A |
1: 24,565,564 (GRCm39) |
T256S |
unknown |
Het |
Eif2d |
T |
A |
1: 131,094,079 (GRCm39) |
D423E |
probably damaging |
Het |
Fam13a |
A |
G |
6: 58,966,723 (GRCm39) |
|
probably null |
Het |
Gaa |
G |
A |
11: 119,175,012 (GRCm39) |
R871H |
probably benign |
Het |
Galnt12 |
T |
A |
4: 47,112,405 (GRCm39) |
V37D |
probably damaging |
Het |
Glp2r |
A |
G |
11: 67,637,640 (GRCm39) |
S13P |
unknown |
Het |
Gnptab |
C |
T |
10: 88,268,940 (GRCm39) |
L548F |
probably damaging |
Het |
Heg1 |
C |
T |
16: 33,547,573 (GRCm39) |
P787S |
possibly damaging |
Het |
Hivep2 |
T |
A |
10: 14,007,485 (GRCm39) |
M1361K |
probably benign |
Het |
Hivep3 |
T |
C |
4: 119,954,891 (GRCm39) |
I1069T |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,268,046 (GRCm39) |
D2121G |
probably benign |
Het |
Htatip2 |
A |
G |
7: 49,422,322 (GRCm39) |
|
probably null |
Het |
Ighv1-75 |
T |
C |
12: 115,798,007 (GRCm39) |
S4G |
probably benign |
Het |
Ip6k1 |
A |
G |
9: 107,901,308 (GRCm39) |
|
probably benign |
Het |
Kcna6 |
A |
G |
6: 126,716,242 (GRCm39) |
S216P |
probably benign |
Het |
Kif21a |
T |
A |
15: 90,865,095 (GRCm39) |
T526S |
probably benign |
Het |
Kng2 |
C |
T |
16: 22,819,346 (GRCm39) |
G230D |
probably benign |
Het |
Lgi2 |
A |
T |
5: 52,703,984 (GRCm39) |
F216I |
probably benign |
Het |
Lratd1 |
G |
A |
12: 14,200,512 (GRCm39) |
H72Y |
probably benign |
Het |
Lss |
T |
A |
10: 76,379,693 (GRCm39) |
N383K |
probably damaging |
Het |
Mical1 |
T |
C |
10: 41,362,061 (GRCm39) |
M929T |
probably benign |
Het |
Mroh2a |
A |
G |
1: 88,186,386 (GRCm39) |
S64G |
probably benign |
Het |
Nat8f4 |
A |
G |
6: 85,878,169 (GRCm39) |
V118A |
probably damaging |
Het |
Or4p23 |
A |
C |
2: 88,576,566 (GRCm39) |
L222R |
probably damaging |
Het |
Or6b2 |
G |
A |
1: 92,407,497 (GRCm39) |
T282M |
probably benign |
Het |
Osbpl11 |
T |
A |
16: 33,030,335 (GRCm39) |
S188T |
probably benign |
Het |
Pea15a |
C |
T |
1: 172,026,752 (GRCm39) |
R85H |
possibly damaging |
Het |
Ppp1r13b |
A |
G |
12: 111,798,836 (GRCm39) |
I919T |
probably damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,835,968 (GRCm39) |
D232G |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,415,602 (GRCm39) |
S1837P |
probably benign |
Het |
Samd5 |
T |
A |
10: 9,550,334 (GRCm39) |
Y125F |
possibly damaging |
Het |
Skint5 |
T |
C |
4: 113,662,397 (GRCm39) |
T597A |
unknown |
Het |
Slc25a12 |
A |
G |
2: 71,106,798 (GRCm39) |
F605L |
probably benign |
Het |
Slc39a12 |
C |
T |
2: 14,412,290 (GRCm39) |
Q321* |
probably null |
Het |
Slc6a19 |
T |
C |
13: 73,837,882 (GRCm39) |
S206G |
probably benign |
Het |
Tacc2 |
T |
A |
7: 130,227,165 (GRCm39) |
H1283Q |
possibly damaging |
Het |
Thumpd3 |
A |
G |
6: 113,036,971 (GRCm39) |
E290G |
possibly damaging |
Het |
Timd2 |
C |
T |
11: 46,577,999 (GRCm39) |
G44D |
possibly damaging |
Het |
Tmem74 |
A |
G |
15: 43,730,134 (GRCm39) |
V303A |
possibly damaging |
Het |
Tpo |
A |
G |
12: 30,128,186 (GRCm39) |
V785A |
probably benign |
Het |
Tpra1 |
T |
A |
6: 88,888,919 (GRCm39) |
I367N |
possibly damaging |
Het |
Txnrd2 |
T |
C |
16: 18,256,297 (GRCm39) |
I95T |
probably damaging |
Het |
Usp32 |
A |
G |
11: 84,885,399 (GRCm39) |
V1216A |
probably benign |
Het |
Usp54 |
C |
A |
14: 20,602,167 (GRCm39) |
M1394I |
probably benign |
Het |
Vmn2r13 |
A |
G |
5: 109,322,167 (GRCm39) |
F177L |
probably benign |
Het |
Vmn2r82 |
T |
A |
10: 79,232,377 (GRCm39) |
V792E |
probably damaging |
Het |
Wdfy4 |
C |
T |
14: 32,805,596 (GRCm39) |
|
probably null |
Het |
Wnk2 |
A |
T |
13: 49,204,875 (GRCm39) |
C458S |
probably damaging |
Het |
Xkr6 |
T |
G |
14: 63,844,519 (GRCm39) |
F181V |
possibly damaging |
Het |
Zfp212 |
T |
A |
6: 47,903,986 (GRCm39) |
C149* |
probably null |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
Zfp661 |
A |
G |
2: 127,419,793 (GRCm39) |
S116P |
probably benign |
Het |
Zfp770 |
A |
G |
2: 114,026,870 (GRCm39) |
Y400H |
possibly damaging |
Het |
|
Other mutations in Or10j5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Or10j5
|
APN |
1 |
172,785,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00336:Or10j5
|
APN |
1 |
172,785,045 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01155:Or10j5
|
APN |
1 |
172,784,491 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01549:Or10j5
|
APN |
1 |
172,784,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Or10j5
|
APN |
1 |
172,784,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03071:Or10j5
|
APN |
1 |
172,784,502 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03352:Or10j5
|
APN |
1 |
172,784,850 (GRCm39) |
missense |
probably benign |
0.00 |
R0449:Or10j5
|
UTSW |
1 |
172,784,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Or10j5
|
UTSW |
1 |
172,784,908 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1726:Or10j5
|
UTSW |
1 |
172,784,658 (GRCm39) |
missense |
probably benign |
0.00 |
R1735:Or10j5
|
UTSW |
1 |
172,784,374 (GRCm39) |
missense |
probably benign |
|
R1928:Or10j5
|
UTSW |
1 |
172,784,881 (GRCm39) |
missense |
probably damaging |
0.98 |
R4258:Or10j5
|
UTSW |
1 |
172,785,205 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4359:Or10j5
|
UTSW |
1 |
172,784,647 (GRCm39) |
missense |
probably benign |
|
R4434:Or10j5
|
UTSW |
1 |
172,785,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Or10j5
|
UTSW |
1 |
172,785,157 (GRCm39) |
missense |
probably benign |
|
R4874:Or10j5
|
UTSW |
1 |
172,785,166 (GRCm39) |
missense |
probably benign |
0.00 |
R5063:Or10j5
|
UTSW |
1 |
172,785,009 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5988:Or10j5
|
UTSW |
1 |
172,784,723 (GRCm39) |
nonsense |
probably null |
|
R7021:Or10j5
|
UTSW |
1 |
172,784,494 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Or10j5
|
UTSW |
1 |
172,784,673 (GRCm39) |
missense |
probably damaging |
0.96 |
R7527:Or10j5
|
UTSW |
1 |
172,784,511 (GRCm39) |
missense |
probably benign |
0.00 |
R8271:Or10j5
|
UTSW |
1 |
172,784,744 (GRCm39) |
nonsense |
probably null |
|
R8890:Or10j5
|
UTSW |
1 |
172,785,045 (GRCm39) |
missense |
probably benign |
0.30 |
R8906:Or10j5
|
UTSW |
1 |
172,784,186 (GRCm39) |
start gained |
probably benign |
|
R9048:Or10j5
|
UTSW |
1 |
172,784,929 (GRCm39) |
missense |
probably benign |
|
R9583:Or10j5
|
UTSW |
1 |
172,784,893 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or10j5
|
UTSW |
1 |
172,784,891 (GRCm39) |
missense |
probably damaging |
1.00 |
|