Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003H04Rik |
T |
A |
3: 124,350,509 (GRCm39) |
D143V |
unknown |
Het |
Abca8a |
A |
T |
11: 109,962,277 (GRCm39) |
N525K |
probably damaging |
Het |
Abhd12 |
T |
A |
2: 150,690,338 (GRCm39) |
D119V |
probably damaging |
Het |
Adamts20 |
A |
T |
15: 94,184,225 (GRCm39) |
M1526K |
probably benign |
Het |
Ankdd1a |
A |
T |
9: 65,411,771 (GRCm39) |
|
probably null |
Het |
Ankrd1 |
C |
T |
19: 36,092,378 (GRCm39) |
C283Y |
possibly damaging |
Het |
Arfgef1 |
G |
C |
1: 10,275,115 (GRCm39) |
I312M |
probably benign |
Het |
Bhlhe22 |
G |
A |
3: 18,109,139 (GRCm39) |
C63Y |
probably damaging |
Het |
Bmp8a |
A |
T |
4: 123,218,885 (GRCm39) |
|
probably benign |
Het |
Ccdc148 |
A |
T |
2: 58,891,911 (GRCm39) |
S235T |
probably damaging |
Het |
Ccdc88b |
G |
A |
19: 6,830,900 (GRCm39) |
Q681* |
probably null |
Het |
Cep104 |
T |
A |
4: 154,087,003 (GRCm39) |
V842E |
probably benign |
Het |
Chac2 |
T |
C |
11: 30,927,568 (GRCm39) |
N117S |
probably benign |
Het |
Cimap3 |
C |
T |
3: 105,921,912 (GRCm39) |
E4K |
possibly damaging |
Het |
Cldn8 |
T |
A |
16: 88,359,746 (GRCm39) |
I60F |
probably benign |
Het |
Col16a1 |
G |
A |
4: 129,970,850 (GRCm39) |
|
probably null |
Het |
Col4a1 |
A |
G |
8: 11,264,644 (GRCm39) |
|
probably benign |
Het |
Cyp2a4 |
G |
T |
7: 26,011,635 (GRCm39) |
E285D |
probably damaging |
Het |
Cyp4a31 |
G |
A |
4: 115,426,928 (GRCm39) |
G176D |
probably benign |
Het |
Dmxl2 |
A |
C |
9: 54,368,233 (GRCm39) |
Y246D |
probably damaging |
Het |
Dync1h1 |
A |
G |
12: 110,580,493 (GRCm39) |
K118R |
probably damaging |
Het |
Dync2i1 |
T |
A |
12: 116,171,363 (GRCm39) |
S958C |
probably damaging |
Het |
Eif3h |
T |
C |
15: 51,728,832 (GRCm39) |
T8A |
possibly damaging |
Het |
Fbh1 |
G |
T |
2: 11,772,211 (GRCm39) |
L157I |
probably benign |
Het |
Fbxo40 |
C |
A |
16: 36,789,218 (GRCm39) |
G631* |
probably null |
Het |
Gabrb1 |
T |
A |
5: 72,279,281 (GRCm39) |
|
probably null |
Het |
Galc |
A |
G |
12: 98,200,499 (GRCm39) |
|
probably null |
Het |
Garin2 |
G |
A |
12: 78,762,280 (GRCm39) |
|
probably benign |
Het |
H2-Q7 |
C |
A |
17: 35,658,675 (GRCm39) |
S104R |
probably benign |
Het |
Igkv13-54-1 |
A |
T |
6: 69,594,277 (GRCm39) |
M31L |
probably benign |
Het |
Lamc2 |
C |
T |
1: 153,041,933 (GRCm39) |
R67Q |
possibly damaging |
Het |
Lcn10 |
A |
G |
2: 25,575,151 (GRCm39) |
D173G |
probably damaging |
Het |
Llgl2 |
G |
T |
11: 115,741,926 (GRCm39) |
R656L |
probably damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Lrrc66 |
G |
A |
5: 73,764,769 (GRCm39) |
S758L |
possibly damaging |
Het |
Ly6d |
T |
C |
15: 74,634,615 (GRCm39) |
K46E |
probably damaging |
Het |
Map3k5 |
A |
G |
10: 19,975,306 (GRCm39) |
N88D |
probably damaging |
Het |
Mertk |
A |
T |
2: 128,604,132 (GRCm39) |
E422V |
probably benign |
Het |
Mixl1 |
A |
G |
1: 180,522,296 (GRCm39) |
V195A |
probably benign |
Het |
Nmnat3 |
T |
C |
9: 98,281,521 (GRCm39) |
V41A |
probably damaging |
Het |
Or2a7 |
A |
G |
6: 43,151,834 (GRCm39) |
R305G |
probably benign |
Het |
Or7g34 |
A |
G |
9: 19,478,492 (GRCm39) |
Y63H |
possibly damaging |
Het |
Pappa2 |
T |
A |
1: 158,684,886 (GRCm39) |
E751V |
probably damaging |
Het |
Pcsk2 |
A |
G |
2: 143,635,189 (GRCm39) |
S355G |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,390,134 (GRCm39) |
V821A |
probably damaging |
Het |
Plxna4 |
A |
C |
6: 32,174,761 (GRCm39) |
D1109E |
probably benign |
Het |
Ppard |
A |
G |
17: 28,516,084 (GRCm39) |
M103V |
probably benign |
Het |
Pramel51 |
T |
C |
12: 88,145,218 (GRCm39) |
E44G |
possibly damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,804,752 (GRCm39) |
T515A |
probably benign |
Het |
Rin2 |
A |
G |
2: 145,703,091 (GRCm39) |
I596V |
possibly damaging |
Het |
Rnls |
A |
G |
19: 33,145,895 (GRCm39) |
S75P |
possibly damaging |
Het |
Rsph10b |
A |
T |
5: 143,903,997 (GRCm39) |
Y236F |
possibly damaging |
Het |
Runx1t1 |
C |
T |
4: 13,835,628 (GRCm39) |
|
probably benign |
Het |
Sardh |
A |
G |
2: 27,125,581 (GRCm39) |
V311A |
possibly damaging |
Het |
Sbno2 |
G |
T |
10: 79,896,439 (GRCm39) |
Y889* |
probably null |
Het |
Sclt1 |
A |
G |
3: 41,681,546 (GRCm39) |
V91A |
probably damaging |
Het |
Sema4g |
T |
A |
19: 44,987,456 (GRCm39) |
V534E |
probably benign |
Het |
Shoc1 |
T |
G |
4: 59,066,441 (GRCm39) |
I768L |
probably benign |
Het |
Slc10a1 |
G |
A |
12: 81,000,446 (GRCm39) |
S351F |
probably benign |
Het |
Slc19a3 |
A |
T |
1: 83,000,468 (GRCm39) |
V183E |
probably damaging |
Het |
Slc25a12 |
A |
G |
2: 71,164,054 (GRCm39) |
Y74H |
possibly damaging |
Het |
Slc6a19 |
T |
A |
13: 73,841,069 (GRCm39) |
I114L |
probably benign |
Het |
Smpd2 |
A |
T |
10: 41,364,232 (GRCm39) |
C189S |
probably benign |
Het |
Spon1 |
T |
A |
7: 113,616,018 (GRCm39) |
V295D |
probably benign |
Het |
Tet3 |
A |
G |
6: 83,380,627 (GRCm39) |
S514P |
probably benign |
Het |
Tnk1 |
T |
C |
11: 69,747,754 (GRCm39) |
I49M |
probably damaging |
Het |
Trim80 |
A |
G |
11: 115,337,619 (GRCm39) |
T431A |
probably benign |
Het |
Vgf |
A |
T |
5: 137,060,153 (GRCm39) |
Q105L |
possibly damaging |
Het |
Vmn1r37 |
G |
T |
6: 66,708,780 (GRCm39) |
L135F |
probably benign |
Het |
Vps37d |
C |
T |
5: 135,102,594 (GRCm39) |
A128T |
possibly damaging |
Het |
Wwp1 |
T |
C |
4: 19,650,197 (GRCm39) |
D323G |
probably benign |
Het |
Zfp456 |
T |
A |
13: 67,515,482 (GRCm39) |
I75L |
probably benign |
Het |
Zfp990 |
A |
G |
4: 145,264,780 (GRCm39) |
I593V |
possibly damaging |
Het |
|
Other mutations in Or1r1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01084:Or1r1
|
APN |
11 |
73,875,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01116:Or1r1
|
APN |
11 |
73,875,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Or1r1
|
UTSW |
11 |
73,874,538 (GRCm39) |
missense |
probably benign |
|
R0242:Or1r1
|
UTSW |
11 |
73,874,538 (GRCm39) |
missense |
probably benign |
|
R0647:Or1r1
|
UTSW |
11 |
73,874,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R0906:Or1r1
|
UTSW |
11 |
73,874,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R1581:Or1r1
|
UTSW |
11 |
73,875,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Or1r1
|
UTSW |
11 |
73,874,673 (GRCm39) |
missense |
probably benign |
0.34 |
R1879:Or1r1
|
UTSW |
11 |
73,875,368 (GRCm39) |
missense |
probably benign |
0.00 |
R2138:Or1r1
|
UTSW |
11 |
73,875,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R2988:Or1r1
|
UTSW |
11 |
73,874,627 (GRCm39) |
missense |
probably benign |
0.13 |
R4557:Or1r1
|
UTSW |
11 |
73,875,425 (GRCm39) |
missense |
probably benign |
0.25 |
R4606:Or1r1
|
UTSW |
11 |
73,874,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Or1r1
|
UTSW |
11 |
73,875,221 (GRCm39) |
missense |
probably benign |
0.01 |
R4783:Or1r1
|
UTSW |
11 |
73,874,834 (GRCm39) |
missense |
probably damaging |
0.97 |
R5047:Or1r1
|
UTSW |
11 |
73,875,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Or1r1
|
UTSW |
11 |
73,875,362 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6379:Or1r1
|
UTSW |
11 |
73,875,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Or1r1
|
UTSW |
11 |
73,875,121 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7254:Or1r1
|
UTSW |
11 |
73,874,603 (GRCm39) |
missense |
probably benign |
0.40 |
R7324:Or1r1
|
UTSW |
11 |
73,874,669 (GRCm39) |
missense |
probably benign |
0.06 |
R7444:Or1r1
|
UTSW |
11 |
73,874,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Or1r1
|
UTSW |
11 |
73,875,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R8540:Or1r1
|
UTSW |
11 |
73,875,153 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Or1r1
|
UTSW |
11 |
73,875,120 (GRCm39) |
missense |
probably benign |
0.01 |
|