Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025B11Rik |
C |
T |
15: 77,443,189 (GRCm39) |
V17I |
unknown |
Het |
Acad8 |
T |
A |
9: 26,889,726 (GRCm39) |
K323* |
probably null |
Het |
Adam18 |
A |
T |
8: 25,137,824 (GRCm39) |
C339S |
probably damaging |
Het |
Anxa7 |
A |
G |
14: 20,510,263 (GRCm39) |
F396L |
probably damaging |
Het |
Ap2m1 |
T |
A |
16: 20,358,201 (GRCm39) |
V73D |
probably damaging |
Het |
Asic2 |
A |
T |
11: 80,862,340 (GRCm39) |
I270N |
probably damaging |
Het |
Atrn |
T |
G |
2: 130,828,664 (GRCm39) |
C1070G |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,361,921 (GRCm39) |
N517S |
unknown |
Het |
Bhmt1b |
A |
G |
18: 87,775,590 (GRCm39) |
D371G |
possibly damaging |
Het |
Bltp3b |
A |
T |
10: 89,644,503 (GRCm39) |
Q1181L |
probably benign |
Het |
Cavin1 |
A |
C |
11: 100,861,284 (GRCm39) |
D3E |
probably benign |
Het |
Cc2d2b |
T |
C |
19: 40,779,751 (GRCm39) |
L571P |
unknown |
Het |
Ccbe1 |
A |
T |
18: 66,216,199 (GRCm39) |
C175S |
probably damaging |
Het |
Cd19 |
A |
G |
7: 126,013,995 (GRCm39) |
L5P |
unknown |
Het |
Cd46 |
A |
G |
1: 194,724,314 (GRCm39) |
S362P |
possibly damaging |
Het |
Celf5 |
A |
G |
10: 81,303,863 (GRCm39) |
S198P |
probably damaging |
Het |
Cep170b |
A |
G |
12: 112,704,359 (GRCm39) |
R706G |
possibly damaging |
Het |
Chd3 |
G |
T |
11: 69,260,037 (GRCm39) |
R61S |
unknown |
Het |
Cpsf6 |
A |
C |
10: 117,197,727 (GRCm39) |
W253G |
unknown |
Het |
Cyp27a1 |
G |
A |
1: 74,776,507 (GRCm39) |
G481D |
probably damaging |
Het |
Ddr1 |
C |
T |
17: 36,002,039 (GRCm39) |
D218N |
possibly damaging |
Het |
Dhx34 |
A |
T |
7: 15,932,801 (GRCm39) |
V1046D |
probably damaging |
Het |
Dhx9 |
A |
T |
1: 153,341,423 (GRCm39) |
D608E |
probably benign |
Het |
Dnajc6 |
C |
A |
4: 101,496,569 (GRCm39) |
A912E |
probably damaging |
Het |
Ehmt1 |
T |
C |
2: 24,694,794 (GRCm39) |
D1051G |
probably damaging |
Het |
Fam217b |
C |
A |
2: 178,062,996 (GRCm39) |
A320E |
probably benign |
Het |
Farsa |
T |
A |
8: 85,590,689 (GRCm39) |
I169N |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,170,142 (GRCm39) |
C2210R |
probably damaging |
Het |
Fbxo3 |
T |
A |
2: 103,880,642 (GRCm39) |
S251T |
probably benign |
Het |
Fer1l6 |
C |
T |
15: 58,462,384 (GRCm39) |
T813I |
probably benign |
Het |
Ftl1-ps1 |
A |
T |
13: 74,555,114 (GRCm39) |
E131V |
probably damaging |
Het |
Gins3 |
T |
A |
8: 96,364,499 (GRCm39) |
I83N |
probably damaging |
Het |
Gja3 |
T |
C |
14: 57,273,350 (GRCm39) |
T341A |
probably benign |
Het |
Gja5 |
A |
G |
3: 96,958,174 (GRCm39) |
Y77C |
probably damaging |
Het |
Gm7247 |
A |
G |
14: 51,602,808 (GRCm39) |
K48R |
probably damaging |
Het |
Gsx2 |
C |
A |
5: 75,236,621 (GRCm39) |
S67* |
probably null |
Het |
H2-Q5 |
T |
A |
17: 35,616,089 (GRCm39) |
L217Q |
|
Het |
Impg2 |
T |
A |
16: 56,087,467 (GRCm39) |
C1095* |
probably null |
Het |
Itga7 |
G |
T |
10: 128,776,801 (GRCm39) |
W222L |
probably damaging |
Het |
Kdm2b |
T |
A |
5: 123,059,512 (GRCm39) |
D530V |
possibly damaging |
Het |
Klhdc8a |
A |
T |
1: 132,230,344 (GRCm39) |
D153V |
probably damaging |
Het |
Lin28a |
C |
T |
4: 133,733,619 (GRCm39) |
G143S |
probably damaging |
Het |
Memo1 |
A |
G |
17: 74,509,338 (GRCm39) |
L227S |
probably damaging |
Het |
Mettl27 |
T |
A |
5: 134,964,657 (GRCm39) |
V138E |
probably damaging |
Het |
Mov10 |
G |
T |
3: 104,708,328 (GRCm39) |
L474I |
probably damaging |
Het |
Nat10 |
T |
C |
2: 103,557,098 (GRCm39) |
N852S |
probably benign |
Het |
Nfkbie |
T |
C |
17: 45,870,153 (GRCm39) |
V166A |
possibly damaging |
Het |
Nktr |
T |
C |
9: 121,575,599 (GRCm39) |
M369T |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,258,149 (GRCm39) |
N589I |
probably benign |
Het |
Nrn1 |
G |
A |
13: 36,914,577 (GRCm39) |
R8C |
probably benign |
Het |
Nrsn1 |
A |
G |
13: 25,437,451 (GRCm39) |
I159T |
probably damaging |
Het |
Or2h15 |
C |
T |
17: 38,441,324 (GRCm39) |
G253D |
probably benign |
Het |
Or5p61 |
A |
T |
7: 107,758,164 (GRCm39) |
D305E |
probably benign |
Het |
Or6c88 |
G |
A |
10: 129,406,584 (GRCm39) |
G20D |
probably benign |
Het |
Osbp |
T |
A |
19: 11,956,031 (GRCm39) |
D385E |
probably benign |
Het |
Pan3 |
T |
A |
5: 147,463,802 (GRCm39) |
N547K |
probably damaging |
Het |
Pip4p2 |
T |
A |
4: 14,892,464 (GRCm39) |
D109E |
probably damaging |
Het |
Pum1 |
C |
A |
4: 130,499,292 (GRCm39) |
T1036K |
probably damaging |
Het |
Rad54l2 |
C |
A |
9: 106,590,671 (GRCm39) |
R485L |
probably damaging |
Het |
Rps26 |
A |
T |
10: 128,461,087 (GRCm39) |
F101I |
unknown |
Het |
Sdsl |
T |
C |
5: 120,598,702 (GRCm39) |
N138S |
probably benign |
Het |
Slc28a2b |
C |
A |
2: 122,353,013 (GRCm39) |
R453S |
probably benign |
Het |
Slc39a6 |
A |
T |
18: 24,717,084 (GRCm39) |
H649Q |
probably damaging |
Het |
Snip1 |
T |
A |
4: 124,965,273 (GRCm39) |
F226Y |
probably benign |
Het |
Srrd |
T |
C |
5: 112,485,322 (GRCm39) |
T334A |
unknown |
Het |
St14 |
C |
T |
9: 31,011,448 (GRCm39) |
D448N |
possibly damaging |
Het |
Tmem270 |
T |
A |
5: 134,930,538 (GRCm39) |
Q241L |
probably benign |
Het |
Tubb4b |
T |
C |
2: 25,114,180 (GRCm39) |
D41G |
probably benign |
Het |
Usf3 |
T |
C |
16: 44,040,368 (GRCm39) |
M1616T |
possibly damaging |
Het |
Vmn2r95 |
A |
T |
17: 18,672,245 (GRCm39) |
I733F |
possibly damaging |
Het |
Zfp976 |
A |
T |
7: 42,262,684 (GRCm39) |
C385* |
probably null |
Het |
|
Other mutations in Or1e29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01458:Or1e29
|
APN |
11 |
73,667,532 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01766:Or1e29
|
APN |
11 |
73,667,901 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01771:Or1e29
|
APN |
11 |
73,667,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02535:Or1e29
|
APN |
11 |
73,667,442 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02639:Or1e29
|
APN |
11 |
73,667,371 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03060:Or1e29
|
APN |
11 |
73,667,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Or1e29
|
APN |
11 |
73,667,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Or1e29
|
UTSW |
11 |
73,667,935 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0426:Or1e29
|
UTSW |
11 |
73,667,263 (GRCm39) |
missense |
probably benign |
0.13 |
R1140:Or1e29
|
UTSW |
11 |
73,667,680 (GRCm39) |
missense |
probably benign |
|
R1638:Or1e29
|
UTSW |
11 |
73,667,974 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2001:Or1e29
|
UTSW |
11 |
73,667,539 (GRCm39) |
missense |
probably benign |
|
R2214:Or1e29
|
UTSW |
11 |
73,667,655 (GRCm39) |
nonsense |
probably null |
|
R3076:Or1e29
|
UTSW |
11 |
73,667,466 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3077:Or1e29
|
UTSW |
11 |
73,667,466 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3078:Or1e29
|
UTSW |
11 |
73,667,466 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3081:Or1e29
|
UTSW |
11 |
73,668,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Or1e29
|
UTSW |
11 |
73,667,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R3731:Or1e29
|
UTSW |
11 |
73,667,565 (GRCm39) |
missense |
probably benign |
0.08 |
R4090:Or1e29
|
UTSW |
11 |
73,667,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R4303:Or1e29
|
UTSW |
11 |
73,667,664 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4516:Or1e29
|
UTSW |
11 |
73,667,866 (GRCm39) |
missense |
probably benign |
0.06 |
R4556:Or1e29
|
UTSW |
11 |
73,667,307 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4557:Or1e29
|
UTSW |
11 |
73,667,307 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4775:Or1e29
|
UTSW |
11 |
73,667,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Or1e29
|
UTSW |
11 |
73,667,372 (GRCm39) |
missense |
probably benign |
0.44 |
R5015:Or1e29
|
UTSW |
11 |
73,668,007 (GRCm39) |
missense |
probably benign |
0.07 |
R5087:Or1e29
|
UTSW |
11 |
73,668,084 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6599:Or1e29
|
UTSW |
11 |
73,667,506 (GRCm39) |
missense |
probably benign |
|
R6701:Or1e29
|
UTSW |
11 |
73,667,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R6784:Or1e29
|
UTSW |
11 |
73,667,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6916:Or1e29
|
UTSW |
11 |
73,667,895 (GRCm39) |
missense |
probably benign |
0.00 |
R7066:Or1e29
|
UTSW |
11 |
73,668,018 (GRCm39) |
missense |
probably damaging |
0.99 |
R7457:Or1e29
|
UTSW |
11 |
73,667,652 (GRCm39) |
missense |
probably benign |
0.06 |
R7486:Or1e29
|
UTSW |
11 |
73,667,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7990:Or1e29
|
UTSW |
11 |
73,667,497 (GRCm39) |
missense |
probably benign |
0.00 |
R8289:Or1e29
|
UTSW |
11 |
73,667,839 (GRCm39) |
missense |
probably benign |
|
R9131:Or1e29
|
UTSW |
11 |
73,668,150 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9160:Or1e29
|
UTSW |
11 |
73,667,881 (GRCm39) |
missense |
probably benign |
0.01 |
R9239:Or1e29
|
UTSW |
11 |
73,667,346 (GRCm39) |
missense |
probably benign |
0.00 |
R9666:Or1e29
|
UTSW |
11 |
73,667,976 (GRCm39) |
missense |
probably damaging |
1.00 |
|