Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
T |
C |
16: 88,424,081 (GRCm39) |
M137V |
probably benign |
Het |
Aak1 |
T |
A |
6: 86,932,172 (GRCm39) |
I381N |
probably benign |
Het |
Abcd4 |
C |
T |
12: 84,658,533 (GRCm39) |
M223I |
probably benign |
Het |
Adgrf2 |
A |
G |
17: 43,023,979 (GRCm39) |
V164A |
probably damaging |
Het |
Ahdc1 |
G |
A |
4: 132,793,297 (GRCm39) |
A1513T |
possibly damaging |
Het |
Akap13 |
T |
C |
7: 75,235,929 (GRCm39) |
M168T |
probably damaging |
Het |
Aox1 |
C |
T |
1: 58,095,374 (GRCm39) |
T196I |
probably benign |
Het |
Aqr |
A |
G |
2: 113,949,150 (GRCm39) |
|
probably benign |
Het |
Astn1 |
A |
G |
1: 158,495,102 (GRCm39) |
E1042G |
possibly damaging |
Het |
Azi2 |
A |
G |
9: 117,876,508 (GRCm39) |
D8G |
possibly damaging |
Het |
Bcam |
T |
C |
7: 19,498,118 (GRCm39) |
T302A |
probably benign |
Het |
Cct6b |
A |
T |
11: 82,651,183 (GRCm39) |
I110N |
probably damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Ceacam5 |
G |
A |
7: 17,493,263 (GRCm39) |
S762N |
possibly damaging |
Het |
Cecr2 |
T |
C |
6: 120,735,221 (GRCm39) |
L819P |
probably damaging |
Het |
Cers3 |
G |
T |
7: 66,435,823 (GRCm39) |
A261S |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,121,538 (GRCm39) |
|
probably benign |
Het |
Col7a1 |
G |
T |
9: 108,793,508 (GRCm39) |
G1357* |
probably null |
Het |
Cux1 |
A |
G |
5: 136,594,397 (GRCm39) |
|
probably benign |
Het |
Cwh43 |
A |
T |
5: 73,595,835 (GRCm39) |
I535F |
probably damaging |
Het |
Dexi |
A |
T |
16: 10,360,553 (GRCm39) |
M1K |
probably null |
Het |
Dnah12 |
T |
C |
14: 26,534,747 (GRCm39) |
V2081A |
probably benign |
Het |
Efcab5 |
A |
T |
11: 77,007,008 (GRCm39) |
L872Q |
probably damaging |
Het |
Enpp7 |
A |
G |
11: 118,881,344 (GRCm39) |
Y163C |
probably damaging |
Het |
Fam221a |
T |
C |
6: 49,349,548 (GRCm39) |
Y38H |
probably damaging |
Het |
Foxred1 |
A |
G |
9: 35,122,186 (GRCm39) |
M1T |
probably null |
Het |
Fscn3 |
C |
T |
6: 28,428,091 (GRCm39) |
T26I |
possibly damaging |
Het |
Galp |
A |
T |
7: 6,216,836 (GRCm39) |
D72V |
probably damaging |
Het |
Gm9843 |
A |
G |
16: 76,200,419 (GRCm39) |
|
noncoding transcript |
Het |
Grm7 |
G |
T |
6: 110,623,309 (GRCm39) |
V161F |
probably damaging |
Het |
Lmbrd1 |
T |
C |
1: 24,732,076 (GRCm39) |
Y98H |
probably damaging |
Het |
Lrrc63 |
T |
G |
14: 75,344,776 (GRCm39) |
Y437S |
probably benign |
Het |
Macc1 |
A |
G |
12: 119,410,576 (GRCm39) |
E448G |
probably benign |
Het |
Madcam1 |
A |
G |
10: 79,504,194 (GRCm39) |
H404R |
probably benign |
Het |
Mink1 |
G |
T |
11: 70,499,776 (GRCm39) |
R773L |
possibly damaging |
Het |
Mroh2b |
A |
G |
15: 4,973,131 (GRCm39) |
I1045V |
probably benign |
Het |
Mroh3 |
T |
C |
1: 136,113,714 (GRCm39) |
T692A |
probably benign |
Het |
Myo15a |
A |
T |
11: 60,370,057 (GRCm39) |
E939V |
possibly damaging |
Het |
Naip2 |
A |
G |
13: 100,298,410 (GRCm39) |
F542S |
probably damaging |
Het |
Napsa |
A |
G |
7: 44,230,852 (GRCm39) |
Y73C |
probably damaging |
Het |
Ndst4 |
A |
T |
3: 125,355,154 (GRCm39) |
H354L |
possibly damaging |
Het |
Neil1 |
A |
T |
9: 57,054,254 (GRCm39) |
V22E |
probably damaging |
Het |
Nol4 |
T |
C |
18: 23,172,994 (GRCm39) |
I36V |
probably damaging |
Het |
Nprl3 |
G |
A |
11: 32,205,464 (GRCm39) |
T111I |
probably damaging |
Het |
Or12k8 |
A |
G |
2: 36,975,517 (GRCm39) |
M81T |
possibly damaging |
Het |
Or4p22 |
C |
A |
2: 88,317,787 (GRCm39) |
T237N |
probably damaging |
Het |
Pald1 |
G |
A |
10: 61,178,144 (GRCm39) |
T624I |
possibly damaging |
Het |
Pcdhb13 |
C |
T |
18: 37,576,786 (GRCm39) |
P388L |
probably damaging |
Het |
Pcdhga6 |
T |
C |
18: 37,840,976 (GRCm39) |
V232A |
probably damaging |
Het |
Pde6b |
A |
G |
5: 108,570,928 (GRCm39) |
I388V |
probably damaging |
Het |
Phactr2 |
C |
A |
10: 13,264,476 (GRCm39) |
|
probably benign |
Het |
Prdx5 |
T |
C |
19: 6,885,477 (GRCm39) |
D56G |
probably damaging |
Het |
Ptprh |
A |
T |
7: 4,574,969 (GRCm39) |
I350N |
probably damaging |
Het |
Rangap1 |
C |
A |
15: 81,594,661 (GRCm39) |
E389D |
probably benign |
Het |
Reln |
A |
G |
5: 22,109,732 (GRCm39) |
V3126A |
probably damaging |
Het |
Rpl21 |
G |
A |
5: 146,771,847 (GRCm39) |
G59S |
possibly damaging |
Het |
Rsph6a |
G |
A |
7: 18,791,475 (GRCm39) |
V215M |
probably damaging |
Het |
Smcp |
T |
C |
3: 92,491,431 (GRCm39) |
K139E |
unknown |
Het |
Stag1 |
A |
G |
9: 100,771,671 (GRCm39) |
T699A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,338,700 (GRCm39) |
|
probably null |
Het |
Tle1 |
G |
T |
4: 72,044,659 (GRCm39) |
H459Q |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,561,363 (GRCm39) |
P27302S |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,571,610 (GRCm39) |
V26428I |
probably damaging |
Het |
Usp53 |
T |
C |
3: 122,742,968 (GRCm39) |
E656G |
probably benign |
Het |
Vmn1r218 |
A |
T |
13: 23,321,081 (GRCm39) |
N63Y |
probably damaging |
Het |
Vmn1r79 |
A |
G |
7: 11,910,139 (GRCm39) |
N40S |
possibly damaging |
Het |
Wdr35 |
A |
G |
12: 9,077,648 (GRCm39) |
D1107G |
possibly damaging |
Het |
Zfp101 |
A |
G |
17: 33,600,880 (GRCm39) |
M292T |
probably benign |
Het |
Zfp108 |
T |
A |
7: 23,961,270 (GRCm39) |
C620* |
probably null |
Het |
Zscan4b |
T |
C |
7: 10,635,818 (GRCm39) |
T170A |
probably benign |
Het |
|
Other mutations in Or1e26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01570:Or1e26
|
APN |
11 |
73,480,209 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02045:Or1e26
|
APN |
11 |
73,480,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02324:Or1e26
|
APN |
11 |
73,480,081 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02328:Or1e26
|
APN |
11 |
73,480,081 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02562:Or1e26
|
APN |
11 |
73,480,237 (GRCm39) |
missense |
probably benign |
|
IGL02715:Or1e26
|
APN |
11 |
73,479,947 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03182:Or1e26
|
APN |
11 |
73,480,268 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03048:Or1e26
|
UTSW |
11 |
73,479,831 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0346:Or1e26
|
UTSW |
11 |
73,480,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Or1e26
|
UTSW |
11 |
73,480,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R0751:Or1e26
|
UTSW |
11 |
73,479,970 (GRCm39) |
missense |
probably benign |
0.02 |
R1220:Or1e26
|
UTSW |
11 |
73,480,203 (GRCm39) |
nonsense |
probably null |
|
R1389:Or1e26
|
UTSW |
11 |
73,480,369 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1484:Or1e26
|
UTSW |
11 |
73,480,187 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1619:Or1e26
|
UTSW |
11 |
73,480,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Or1e26
|
UTSW |
11 |
73,479,745 (GRCm39) |
missense |
probably benign |
0.37 |
R3781:Or1e26
|
UTSW |
11 |
73,480,194 (GRCm39) |
nonsense |
probably null |
|
R3781:Or1e26
|
UTSW |
11 |
73,479,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R3782:Or1e26
|
UTSW |
11 |
73,480,194 (GRCm39) |
nonsense |
probably null |
|
R3782:Or1e26
|
UTSW |
11 |
73,479,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Or1e26
|
UTSW |
11 |
73,480,081 (GRCm39) |
missense |
probably benign |
0.02 |
R4721:Or1e26
|
UTSW |
11 |
73,480,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R5157:Or1e26
|
UTSW |
11 |
73,480,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Or1e26
|
UTSW |
11 |
73,480,076 (GRCm39) |
missense |
probably benign |
|
R6373:Or1e26
|
UTSW |
11 |
73,479,724 (GRCm39) |
missense |
probably benign |
0.42 |
R6658:Or1e26
|
UTSW |
11 |
73,479,874 (GRCm39) |
missense |
probably damaging |
0.99 |
R7046:Or1e26
|
UTSW |
11 |
73,480,558 (GRCm39) |
missense |
probably benign |
|
R7096:Or1e26
|
UTSW |
11 |
73,480,463 (GRCm39) |
missense |
probably benign |
0.03 |
R7238:Or1e26
|
UTSW |
11 |
73,480,561 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R7537:Or1e26
|
UTSW |
11 |
73,480,094 (GRCm39) |
missense |
probably benign |
0.04 |
R7548:Or1e26
|
UTSW |
11 |
73,479,802 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7888:Or1e26
|
UTSW |
11 |
73,480,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R7968:Or1e26
|
UTSW |
11 |
73,480,154 (GRCm39) |
missense |
probably benign |
0.05 |
R8923:Or1e26
|
UTSW |
11 |
73,480,076 (GRCm39) |
missense |
probably benign |
|
R9006:Or1e26
|
UTSW |
11 |
73,480,036 (GRCm39) |
missense |
probably benign |
0.40 |
R9281:Or1e26
|
UTSW |
11 |
73,480,133 (GRCm39) |
missense |
probably benign |
|
R9689:Or1e26
|
UTSW |
11 |
73,479,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|