Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
C |
T |
8: 120,145,545 (GRCm38) |
R71C |
probably damaging |
Het |
Aanat |
A |
T |
11: 116,595,629 (GRCm38) |
|
probably benign |
Het |
Ahrr |
G |
T |
13: 74,257,545 (GRCm38) |
S91* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,088,442 (GRCm38) |
N223Y |
probably benign |
Het |
Ankar |
T |
G |
1: 72,680,058 (GRCm38) |
N544T |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,418,750 (GRCm38) |
S302P |
possibly damaging |
Het |
Bcr |
T |
C |
10: 75,157,100 (GRCm38) |
V809A |
probably benign |
Het |
Bpifb2 |
A |
G |
2: 153,890,540 (GRCm38) |
N353S |
possibly damaging |
Het |
Cyth1 |
A |
T |
11: 118,184,009 (GRCm38) |
|
probably null |
Het |
Ddx5 |
A |
T |
11: 106,782,180 (GRCm38) |
N506K |
probably benign |
Het |
Dnaja1 |
A |
T |
4: 40,730,244 (GRCm38) |
I239F |
probably benign |
Het |
Ethe1 |
C |
T |
7: 24,606,251 (GRCm38) |
T141I |
probably damaging |
Het |
Fam160b2 |
T |
C |
14: 70,594,007 (GRCm38) |
H29R |
probably damaging |
Het |
Gdap2 |
A |
T |
3: 100,202,066 (GRCm38) |
I36F |
unknown |
Het |
Gm13030 |
A |
T |
4: 138,871,266 (GRCm38) |
D115E |
unknown |
Het |
Gm13103 |
C |
T |
4: 143,853,209 (GRCm38) |
P455S |
probably benign |
Het |
Gm17019 |
A |
T |
5: 15,029,372 (GRCm38) |
L227Q |
probably damaging |
Het |
Gm9195 |
T |
A |
14: 72,435,777 (GRCm38) |
E2517D |
possibly damaging |
Het |
Gramd2 |
T |
A |
9: 59,708,071 (GRCm38) |
V39D |
possibly damaging |
Het |
Hmcn1 |
C |
T |
1: 150,630,266 (GRCm38) |
W3836* |
probably null |
Het |
Hspa14 |
C |
T |
2: 3,489,041 (GRCm38) |
D494N |
possibly damaging |
Het |
Ifit2 |
A |
G |
19: 34,573,198 (GRCm38) |
N46S |
probably benign |
Het |
Ifna6 |
A |
T |
4: 88,827,807 (GRCm38) |
E131V |
possibly damaging |
Het |
Ift140 |
T |
C |
17: 25,037,036 (GRCm38) |
V504A |
possibly damaging |
Het |
Irgc1 |
T |
C |
7: 24,432,228 (GRCm38) |
N388S |
probably damaging |
Het |
Itgal |
T |
A |
7: 127,317,365 (GRCm38) |
V743E |
probably benign |
Het |
Itih5 |
T |
C |
2: 10,245,637 (GRCm38) |
S716P |
probably damaging |
Het |
Kcnab1 |
A |
T |
3: 65,266,503 (GRCm38) |
K78N |
possibly damaging |
Het |
Kif1a |
A |
T |
1: 93,054,317 (GRCm38) |
V787E |
possibly damaging |
Het |
Krt15 |
A |
T |
11: 100,135,560 (GRCm38) |
V100E |
possibly damaging |
Het |
Krt39 |
A |
T |
11: 99,518,091 (GRCm38) |
V293E |
probably damaging |
Het |
Lrrn4 |
A |
G |
2: 132,869,743 (GRCm38) |
F720S |
possibly damaging |
Het |
Map2 |
G |
A |
1: 66,414,824 (GRCm38) |
A958T |
possibly damaging |
Het |
Map3k9 |
A |
G |
12: 81,724,097 (GRCm38) |
S906P |
probably benign |
Het |
Mdc1 |
T |
C |
17: 35,853,309 (GRCm38) |
S1250P |
probably benign |
Het |
Meltf |
G |
A |
16: 31,884,946 (GRCm38) |
V164I |
probably damaging |
Het |
Mtap |
T |
G |
4: 89,179,462 (GRCm38) |
|
probably null |
Het |
Mtus1 |
C |
A |
8: 41,022,406 (GRCm38) |
V184F |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,213,663 (GRCm38) |
D1015V |
probably damaging |
Het |
Ndrg1 |
T |
C |
15: 66,944,938 (GRCm38) |
|
probably null |
Het |
Nkd1 |
G |
T |
8: 88,585,175 (GRCm38) |
V130L |
probably benign |
Het |
Nsfl1c |
A |
G |
2: 151,500,753 (GRCm38) |
D81G |
probably benign |
Het |
Nt5c1b |
T |
A |
12: 10,381,391 (GRCm38) |
|
probably null |
Het |
Nucb1 |
T |
C |
7: 45,498,778 (GRCm38) |
K204E |
possibly damaging |
Het |
Nwd1 |
T |
G |
8: 72,675,173 (GRCm38) |
M774R |
possibly damaging |
Het |
Olfr165 |
A |
T |
16: 19,407,194 (GRCm38) |
V274E |
probably damaging |
Het |
Olfr654 |
G |
C |
7: 104,588,700 (GRCm38) |
E299Q |
probably damaging |
Het |
Pan3 |
T |
A |
5: 147,536,272 (GRCm38) |
|
probably null |
Het |
Pcdh15 |
A |
T |
10: 74,506,485 (GRCm38) |
T1135S |
probably benign |
Het |
Pfas |
A |
G |
11: 69,000,092 (GRCm38) |
I331T |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,806,339 (GRCm38) |
I1641N |
probably damaging |
Het |
Ptar1 |
A |
T |
19: 23,718,101 (GRCm38) |
R311W |
probably damaging |
Het |
Ranbp2 |
T |
G |
10: 58,479,194 (GRCm38) |
M1912R |
probably damaging |
Het |
Rbm12 |
A |
G |
2: 156,097,303 (GRCm38) |
F350L |
possibly damaging |
Het |
Sdhaf1 |
T |
C |
7: 30,322,043 (GRCm38) |
D96G |
probably benign |
Het |
Serpinb6b |
T |
A |
13: 32,968,667 (GRCm38) |
M53K |
probably damaging |
Het |
Sh2d6 |
A |
T |
6: 72,517,164 (GRCm38) |
L147Q |
probably benign |
Het |
Slc19a2 |
T |
A |
1: 164,260,876 (GRCm38) |
C298S |
probably benign |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,660,334 (GRCm38) |
|
probably benign |
Het |
St8sia2 |
T |
A |
7: 73,960,902 (GRCm38) |
Q211L |
possibly damaging |
Het |
Sult2a2 |
T |
C |
7: 13,734,897 (GRCm38) |
I96T |
possibly damaging |
Het |
Tab2 |
G |
T |
10: 7,907,483 (GRCm38) |
H678Q |
probably damaging |
Het |
Tnfaip6 |
A |
G |
2: 52,038,216 (GRCm38) |
E14G |
probably benign |
Het |
Trip11 |
A |
T |
12: 101,885,198 (GRCm38) |
L869H |
probably damaging |
Het |
Tslp |
T |
C |
18: 32,819,080 (GRCm38) |
Y133H |
not run |
Het |
Ttn |
T |
C |
2: 76,740,990 (GRCm38) |
I26520V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,932,143 (GRCm38) |
V3374A |
unknown |
Het |
Tubgcp2 |
T |
A |
7: 140,007,924 (GRCm38) |
I263F |
possibly damaging |
Het |
Uaca |
A |
G |
9: 60,870,110 (GRCm38) |
E593G |
probably damaging |
Het |
Unc13b |
C |
T |
4: 43,172,235 (GRCm38) |
T1021I |
unknown |
Het |
Ush1c |
T |
A |
7: 46,225,555 (GRCm38) |
I131F |
probably benign |
Het |
Usp24 |
C |
A |
4: 106,379,107 (GRCm38) |
D997E |
probably benign |
Het |
Usp54 |
T |
C |
14: 20,577,040 (GRCm38) |
T517A |
probably benign |
Het |
Vmn1r151 |
A |
T |
7: 22,499,080 (GRCm38) |
M200K |
possibly damaging |
Het |
Vmn2r43 |
T |
C |
7: 8,255,329 (GRCm38) |
D295G |
probably damaging |
Het |
Vmn2r70 |
G |
A |
7: 85,563,868 (GRCm38) |
P444S |
probably damaging |
Het |
Vmn2r85 |
G |
T |
10: 130,418,980 (GRCm38) |
P612T |
probably damaging |
Het |
Vps13d |
A |
T |
4: 145,148,747 (GRCm38) |
V1736D |
|
Het |
Zbtb11 |
A |
T |
16: 55,990,487 (GRCm38) |
H336L |
probably benign |
Het |
|
Other mutations in Olfr262 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01432:Olfr262
|
APN |
19 |
12,241,527 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02170:Olfr262
|
APN |
19 |
12,240,756 (GRCm38) |
missense |
probably benign |
|
IGL02748:Olfr262
|
APN |
19 |
12,240,840 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02896:Olfr262
|
APN |
19 |
12,240,989 (GRCm38) |
nonsense |
probably null |
|
R0365:Olfr262
|
UTSW |
19 |
12,241,076 (GRCm38) |
missense |
probably benign |
0.13 |
R0374:Olfr262
|
UTSW |
19 |
12,241,141 (GRCm38) |
missense |
probably damaging |
1.00 |
R1226:Olfr262
|
UTSW |
19 |
12,241,586 (GRCm38) |
missense |
probably benign |
|
R1319:Olfr262
|
UTSW |
19 |
12,241,502 (GRCm38) |
missense |
probably damaging |
1.00 |
R1426:Olfr262
|
UTSW |
19 |
12,241,182 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1453:Olfr262
|
UTSW |
19 |
12,241,592 (GRCm38) |
missense |
probably benign |
|
R1675:Olfr262
|
UTSW |
19 |
12,240,831 (GRCm38) |
missense |
probably benign |
0.37 |
R1773:Olfr262
|
UTSW |
19 |
12,241,659 (GRCm38) |
start codon destroyed |
probably null |
0.03 |
R1778:Olfr262
|
UTSW |
19 |
12,241,455 (GRCm38) |
missense |
probably benign |
|
R1820:Olfr262
|
UTSW |
19 |
12,241,248 (GRCm38) |
missense |
probably damaging |
1.00 |
R3161:Olfr262
|
UTSW |
19 |
12,241,496 (GRCm38) |
missense |
probably benign |
0.06 |
R3412:Olfr262
|
UTSW |
19 |
12,241,590 (GRCm38) |
missense |
probably benign |
0.00 |
R4387:Olfr262
|
UTSW |
19 |
12,241,139 (GRCm38) |
missense |
probably damaging |
0.98 |
R4389:Olfr262
|
UTSW |
19 |
12,241,139 (GRCm38) |
missense |
probably damaging |
0.98 |
R4782:Olfr262
|
UTSW |
19 |
12,241,572 (GRCm38) |
missense |
probably benign |
0.01 |
R4885:Olfr262
|
UTSW |
19 |
12,240,718 (GRCm38) |
splice site |
probably null |
|
R4915:Olfr262
|
UTSW |
19 |
12,241,373 (GRCm38) |
missense |
probably benign |
0.31 |
R5254:Olfr262
|
UTSW |
19 |
12,241,248 (GRCm38) |
missense |
probably damaging |
1.00 |
R5726:Olfr262
|
UTSW |
19 |
12,241,280 (GRCm38) |
missense |
probably damaging |
0.99 |
R6579:Olfr262
|
UTSW |
19 |
12,241,362 (GRCm38) |
missense |
probably benign |
|
R7062:Olfr262
|
UTSW |
19 |
12,240,725 (GRCm38) |
missense |
probably benign |
|
R9491:Olfr262
|
UTSW |
19 |
12,241,242 (GRCm38) |
missense |
probably benign |
0.01 |
R9736:Olfr262
|
UTSW |
19 |
12,241,556 (GRCm38) |
missense |
probably damaging |
0.97 |
|