Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
C |
T |
4: 103,088,180 (GRCm39) |
G342D |
possibly damaging |
Het |
Acvr2b |
C |
T |
9: 119,261,675 (GRCm39) |
R399W |
probably damaging |
Het |
Arb2a |
T |
A |
13: 77,982,832 (GRCm39) |
|
probably benign |
Het |
Atf6 |
A |
G |
1: 170,662,492 (GRCm39) |
V256A |
probably benign |
Het |
Atp2b4 |
A |
T |
1: 133,656,454 (GRCm39) |
I732N |
probably damaging |
Het |
C1qtnf9 |
A |
C |
14: 61,009,820 (GRCm39) |
Q25H |
probably damaging |
Het |
Ccdc6 |
T |
A |
10: 69,978,401 (GRCm39) |
|
probably benign |
Het |
Cds2 |
T |
C |
2: 132,127,887 (GRCm39) |
|
probably null |
Het |
Chdh |
A |
G |
14: 29,756,603 (GRCm39) |
Y343C |
probably damaging |
Het |
Col5a2 |
T |
C |
1: 45,421,262 (GRCm39) |
|
probably benign |
Het |
Cts3 |
G |
A |
13: 61,716,024 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
T |
A |
7: 55,541,802 (GRCm39) |
D362E |
probably benign |
Het |
Dsg1b |
T |
A |
18: 20,529,082 (GRCm39) |
S273T |
probably benign |
Het |
Dysf |
A |
T |
6: 84,117,649 (GRCm39) |
H1274L |
probably benign |
Het |
Eva1c |
T |
C |
16: 90,672,986 (GRCm39) |
S187P |
probably benign |
Het |
Fam13b |
G |
A |
18: 34,578,581 (GRCm39) |
|
probably benign |
Het |
Fbn2 |
C |
T |
18: 58,168,408 (GRCm39) |
G2310S |
probably damaging |
Het |
Fcna |
T |
C |
2: 25,515,520 (GRCm39) |
Y183C |
probably damaging |
Het |
Fnta |
T |
C |
8: 26,491,056 (GRCm39) |
T263A |
probably benign |
Het |
Gm94 |
T |
C |
18: 43,914,309 (GRCm39) |
D83G |
possibly damaging |
Het |
Gnal |
C |
T |
18: 67,268,720 (GRCm39) |
|
probably benign |
Het |
Grb7 |
T |
G |
11: 98,343,014 (GRCm39) |
S244A |
probably benign |
Het |
Grm3 |
T |
C |
5: 9,562,477 (GRCm39) |
T458A |
probably benign |
Het |
Hdac2 |
C |
T |
10: 36,867,832 (GRCm39) |
R193C |
probably damaging |
Het |
Hycc2 |
T |
C |
1: 58,573,638 (GRCm39) |
|
probably benign |
Het |
Ighmbp2 |
T |
C |
19: 3,315,072 (GRCm39) |
R783G |
probably benign |
Het |
Inpp5j |
G |
T |
11: 3,453,122 (GRCm39) |
L43I |
possibly damaging |
Het |
Itga11 |
A |
T |
9: 62,604,243 (GRCm39) |
T44S |
probably damaging |
Het |
Itsn1 |
C |
T |
16: 91,665,036 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
G |
T |
11: 69,297,822 (GRCm39) |
C233* |
probably null |
Het |
Lamb3 |
T |
C |
1: 193,025,700 (GRCm39) |
L1130P |
probably damaging |
Het |
Lrch3 |
T |
C |
16: 32,807,250 (GRCm39) |
F508L |
probably damaging |
Het |
Lrrd1 |
T |
A |
5: 3,916,425 (GRCm39) |
V814E |
probably benign |
Het |
Megf10 |
C |
T |
18: 57,386,054 (GRCm39) |
P356S |
probably benign |
Het |
Myorg |
G |
A |
4: 41,499,538 (GRCm39) |
R31* |
probably null |
Het |
Naip1 |
A |
T |
13: 100,559,727 (GRCm39) |
D1092E |
probably benign |
Het |
Nus1 |
T |
A |
10: 52,306,190 (GRCm39) |
V42E |
probably damaging |
Het |
Or2a51 |
A |
C |
6: 43,179,006 (GRCm39) |
M143L |
probably benign |
Het |
Padi3 |
T |
C |
4: 140,523,024 (GRCm39) |
N306S |
probably damaging |
Het |
Pex13 |
T |
C |
11: 23,605,949 (GRCm39) |
S94G |
probably benign |
Het |
Ppm1h |
G |
T |
10: 122,638,229 (GRCm39) |
Q166H |
probably benign |
Het |
Ptafr |
A |
T |
4: 132,307,396 (GRCm39) |
Y262F |
probably benign |
Het |
Rabgap1 |
T |
A |
2: 37,377,132 (GRCm39) |
D321E |
probably damaging |
Het |
Samsn1 |
C |
T |
16: 75,742,113 (GRCm39) |
|
noncoding transcript |
Het |
Scarb1 |
T |
C |
5: 125,366,745 (GRCm39) |
N63D |
probably damaging |
Het |
Serpinb7 |
T |
C |
1: 107,379,340 (GRCm39) |
I249T |
possibly damaging |
Het |
Srpra |
A |
G |
9: 35,126,277 (GRCm39) |
K490R |
probably benign |
Het |
Sycn |
A |
G |
7: 28,240,398 (GRCm39) |
N22D |
probably benign |
Het |
Tarbp1 |
C |
T |
8: 127,167,612 (GRCm39) |
A1067T |
probably benign |
Het |
Tex14 |
A |
G |
11: 87,405,131 (GRCm39) |
D681G |
possibly damaging |
Het |
Usp34 |
C |
T |
11: 23,396,741 (GRCm39) |
|
probably benign |
Het |
Vmn2r107 |
T |
C |
17: 20,595,085 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
T |
6: 13,187,528 (GRCm39) |
M653K |
probably benign |
Het |
Wrap73 |
T |
A |
4: 154,233,200 (GRCm39) |
S125T |
possibly damaging |
Het |
|
Other mutations in Or11g24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01719:Or11g24
|
APN |
14 |
50,662,018 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02430:Or11g24
|
APN |
14 |
50,662,608 (GRCm39) |
missense |
probably benign |
|
IGL02603:Or11g24
|
APN |
14 |
50,662,657 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02959:Or11g24
|
APN |
14 |
50,662,389 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03154:Or11g24
|
APN |
14 |
50,662,080 (GRCm39) |
missense |
probably benign |
0.00 |
R1984:Or11g24
|
UTSW |
14 |
50,662,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3160:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3161:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Or11g24
|
UTSW |
14 |
50,662,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R4821:Or11g24
|
UTSW |
14 |
50,662,206 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4880:Or11g24
|
UTSW |
14 |
50,662,758 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5047:Or11g24
|
UTSW |
14 |
50,662,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5385:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5386:Or11g24
|
UTSW |
14 |
50,662,846 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5640:Or11g24
|
UTSW |
14 |
50,662,111 (GRCm39) |
missense |
probably benign |
0.18 |
R5809:Or11g24
|
UTSW |
14 |
50,662,905 (GRCm39) |
makesense |
probably null |
|
R6035:Or11g24
|
UTSW |
14 |
50,661,984 (GRCm39) |
missense |
probably benign |
|
R6035:Or11g24
|
UTSW |
14 |
50,661,984 (GRCm39) |
missense |
probably benign |
|
R6229:Or11g24
|
UTSW |
14 |
50,662,662 (GRCm39) |
missense |
probably benign |
0.38 |
R6614:Or11g24
|
UTSW |
14 |
50,662,546 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Or11g24
|
UTSW |
14 |
50,662,722 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7443:Or11g24
|
UTSW |
14 |
50,662,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Or11g24
|
UTSW |
14 |
50,662,792 (GRCm39) |
missense |
probably benign |
|
R7700:Or11g24
|
UTSW |
14 |
50,662,792 (GRCm39) |
missense |
probably benign |
|
R7851:Or11g24
|
UTSW |
14 |
50,662,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R8397:Or11g24
|
UTSW |
14 |
50,662,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Or11g24
|
UTSW |
14 |
50,662,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Or11g24
|
UTSW |
14 |
50,662,255 (GRCm39) |
missense |
probably benign |
0.00 |
|