Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
G |
C |
1: 120,096,840 (GRCm39) |
|
probably benign |
Het |
3110009E18Rik |
C |
T |
1: 120,096,850 (GRCm39) |
|
probably benign |
Het |
3110009E18Rik |
G |
T |
1: 120,096,849 (GRCm39) |
|
probably benign |
Het |
4930562C15Rik |
A |
G |
16: 4,672,816 (GRCm39) |
K866E |
probably damaging |
Het |
Afap1l2 |
T |
C |
19: 56,931,879 (GRCm39) |
M49V |
probably benign |
Het |
Atf7ip |
C |
T |
6: 136,583,808 (GRCm39) |
R1280C |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,599,643 (GRCm39) |
F583L |
probably benign |
Het |
Atxn7l3b |
A |
G |
10: 112,764,501 (GRCm39) |
C43R |
probably damaging |
Het |
Axin2 |
T |
C |
11: 108,833,904 (GRCm39) |
V617A |
probably damaging |
Het |
Bltp3a |
T |
A |
17: 28,108,958 (GRCm39) |
|
probably null |
Het |
Brd1 |
A |
T |
15: 88,614,316 (GRCm39) |
F193Y |
probably damaging |
Het |
Cdc27 |
T |
C |
11: 104,420,221 (GRCm39) |
S141G |
probably damaging |
Het |
Chst9 |
A |
T |
18: 15,851,045 (GRCm39) |
F7Y |
probably damaging |
Het |
Cpn2 |
T |
A |
16: 30,079,233 (GRCm39) |
Q156L |
possibly damaging |
Het |
Dcaf6 |
A |
T |
1: 165,216,354 (GRCm39) |
D416E |
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
Eif2s3y |
A |
G |
Y: 1,023,407 (GRCm39) |
T430A |
possibly damaging |
Het |
Enah |
G |
A |
1: 181,745,854 (GRCm39) |
T401I |
probably damaging |
Het |
Esp38 |
T |
G |
17: 40,266,053 (GRCm39) |
I54R |
probably damaging |
Het |
Ffar4 |
C |
T |
19: 38,086,028 (GRCm39) |
R152W |
probably benign |
Het |
Flvcr1 |
A |
G |
1: 190,758,383 (GRCm39) |
|
probably benign |
Het |
Fzd9 |
G |
A |
5: 135,278,796 (GRCm39) |
A363V |
probably damaging |
Het |
Gadl1 |
T |
A |
9: 115,869,987 (GRCm39) |
I451N |
probably benign |
Het |
Hmg20a |
A |
G |
9: 56,388,948 (GRCm39) |
T172A |
probably damaging |
Het |
Ints1 |
G |
A |
5: 139,742,885 (GRCm39) |
T1695M |
probably damaging |
Het |
Ipo13 |
G |
A |
4: 117,758,768 (GRCm39) |
A699V |
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,331,960 (GRCm39) |
|
probably null |
Het |
Klra17 |
A |
G |
6: 129,850,279 (GRCm39) |
L57P |
probably damaging |
Het |
Map3k8 |
A |
C |
18: 4,339,530 (GRCm39) |
D280E |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,524,675 (GRCm39) |
F662L |
probably damaging |
Het |
Ncor1 |
T |
A |
11: 62,231,431 (GRCm39) |
H792L |
probably damaging |
Het |
Nlrx1 |
T |
A |
9: 44,173,909 (GRCm39) |
K431* |
probably null |
Het |
Nos1 |
A |
G |
5: 118,085,575 (GRCm39) |
N1301S |
probably benign |
Het |
Obp2b |
A |
G |
2: 25,627,087 (GRCm39) |
T7A |
probably damaging |
Het |
Odc1 |
T |
C |
12: 17,597,958 (GRCm39) |
I95T |
probably damaging |
Het |
Or2t43 |
A |
G |
11: 58,457,344 (GRCm39) |
Y276H |
probably damaging |
Het |
Or4c127 |
G |
A |
2: 89,833,187 (GRCm39) |
V146M |
probably benign |
Het |
Or5b97 |
C |
T |
19: 12,878,963 (GRCm39) |
M60I |
probably damaging |
Het |
Or6c1 |
A |
T |
10: 129,517,968 (GRCm39) |
F213L |
probably benign |
Het |
Pcif1 |
A |
T |
2: 164,731,610 (GRCm39) |
Q521L |
probably damaging |
Het |
Plekhg2 |
A |
C |
7: 28,067,780 (GRCm39) |
L223R |
probably damaging |
Het |
Plod3 |
A |
G |
5: 137,018,772 (GRCm39) |
N270D |
probably damaging |
Het |
Ppp1r37 |
A |
T |
7: 19,266,636 (GRCm39) |
L417* |
probably null |
Het |
Psmd6 |
C |
T |
14: 14,116,166 (GRCm38) |
V141I |
probably benign |
Het |
Rcn1 |
A |
T |
2: 105,225,121 (GRCm39) |
Y111* |
probably null |
Het |
Rell2 |
G |
A |
18: 38,090,758 (GRCm39) |
R145H |
probably damaging |
Het |
Scaper |
T |
C |
9: 55,745,426 (GRCm39) |
K614R |
probably damaging |
Het |
Scart2 |
A |
G |
7: 139,878,275 (GRCm39) |
I1001V |
probably benign |
Het |
Shbg |
C |
T |
11: 69,508,045 (GRCm39) |
E107K |
probably damaging |
Het |
Slc30a3 |
G |
A |
5: 31,244,247 (GRCm39) |
P345L |
possibly damaging |
Het |
Tchp |
A |
C |
5: 114,857,681 (GRCm39) |
E391D |
probably damaging |
Het |
Timeless |
A |
G |
10: 128,077,520 (GRCm39) |
D200G |
probably damaging |
Het |
Tspear |
A |
G |
10: 77,700,601 (GRCm39) |
T144A |
possibly damaging |
Het |
Usp5 |
C |
G |
6: 124,799,593 (GRCm39) |
K318N |
possibly damaging |
Het |
Vgll3 |
T |
C |
16: 65,624,820 (GRCm39) |
V56A |
possibly damaging |
Het |
Vmn2r71 |
C |
T |
7: 85,268,436 (GRCm39) |
T213I |
probably benign |
Het |
Wtap |
T |
C |
17: 13,186,423 (GRCm39) |
T375A |
probably benign |
Het |
Yipf2 |
T |
G |
9: 21,503,204 (GRCm39) |
T88P |
probably damaging |
Het |
Zfp382 |
T |
A |
7: 29,830,979 (GRCm39) |
D89E |
probably benign |
Het |
Zfp955b |
C |
T |
17: 33,524,209 (GRCm39) |
|
probably benign |
Het |
Zpr1 |
C |
T |
9: 46,185,961 (GRCm39) |
T144I |
probably damaging |
Het |
|
Other mutations in Or6ae1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01806:Or6ae1
|
APN |
7 |
139,742,841 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02121:Or6ae1
|
APN |
7 |
139,742,607 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02399:Or6ae1
|
APN |
7 |
139,742,513 (GRCm39) |
missense |
probably benign |
|
IGL02803:Or6ae1
|
APN |
7 |
139,742,287 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0446:Or6ae1
|
UTSW |
7 |
139,742,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Or6ae1
|
UTSW |
7 |
139,742,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Or6ae1
|
UTSW |
7 |
139,742,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Or6ae1
|
UTSW |
7 |
139,742,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Or6ae1
|
UTSW |
7 |
139,742,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Or6ae1
|
UTSW |
7 |
139,742,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Or6ae1
|
UTSW |
7 |
139,742,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R1895:Or6ae1
|
UTSW |
7 |
139,742,726 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2004:Or6ae1
|
UTSW |
7 |
139,742,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R2060:Or6ae1
|
UTSW |
7 |
139,742,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Or6ae1
|
UTSW |
7 |
139,742,822 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4841:Or6ae1
|
UTSW |
7 |
139,742,602 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4842:Or6ae1
|
UTSW |
7 |
139,742,602 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5189:Or6ae1
|
UTSW |
7 |
139,742,632 (GRCm39) |
missense |
probably damaging |
0.98 |
R5325:Or6ae1
|
UTSW |
7 |
139,742,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Or6ae1
|
UTSW |
7 |
139,742,564 (GRCm39) |
missense |
probably benign |
0.36 |
R5618:Or6ae1
|
UTSW |
7 |
139,742,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Or6ae1
|
UTSW |
7 |
139,742,722 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6031:Or6ae1
|
UTSW |
7 |
139,742,722 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6609:Or6ae1
|
UTSW |
7 |
139,742,476 (GRCm39) |
missense |
probably benign |
|
R7154:Or6ae1
|
UTSW |
7 |
139,741,997 (GRCm39) |
missense |
probably benign |
0.00 |
R8370:Or6ae1
|
UTSW |
7 |
139,742,681 (GRCm39) |
missense |
probably damaging |
0.98 |
R8765:Or6ae1
|
UTSW |
7 |
139,742,467 (GRCm39) |
missense |
probably benign |
|
R9002:Or6ae1
|
UTSW |
7 |
139,742,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R9112:Or6ae1
|
UTSW |
7 |
139,742,660 (GRCm39) |
missense |
|
|
R9431:Or6ae1
|
UTSW |
7 |
139,741,942 (GRCm39) |
missense |
probably benign |
0.04 |
R9513:Or6ae1
|
UTSW |
7 |
139,742,822 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9563:Or6ae1
|
UTSW |
7 |
139,742,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Or6ae1
|
UTSW |
7 |
139,742,771 (GRCm39) |
missense |
probably benign |
|
|