Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
C |
G |
11: 58,770,823 (GRCm39) |
L102V |
not run |
Het |
Abca12 |
A |
T |
1: 71,331,580 (GRCm39) |
S1323R |
probably benign |
Het |
Abcb1a |
T |
A |
5: 8,748,623 (GRCm39) |
I318N |
probably benign |
Het |
Adam10 |
A |
T |
9: 70,674,209 (GRCm39) |
K524* |
probably null |
Het |
Adamts3 |
C |
T |
5: 90,009,349 (GRCm39) |
G105R |
probably damaging |
Het |
Adcy7 |
T |
C |
8: 89,042,387 (GRCm39) |
I418T |
probably damaging |
Het |
Alg9 |
T |
A |
9: 50,699,471 (GRCm39) |
F165L |
probably damaging |
Het |
Anapc2 |
G |
T |
2: 25,167,753 (GRCm39) |
R440L |
probably damaging |
Het |
Arhgef17 |
A |
T |
7: 100,526,052 (GRCm39) |
H1876Q |
probably benign |
Het |
Armc2 |
G |
A |
10: 41,802,856 (GRCm39) |
R606C |
probably benign |
Het |
Cd163 |
T |
C |
6: 124,281,738 (GRCm39) |
S14P |
probably benign |
Het |
Cfap74 |
T |
C |
4: 155,513,694 (GRCm39) |
V502A |
|
Het |
Copb2 |
T |
C |
9: 98,470,147 (GRCm39) |
I891T |
probably damaging |
Het |
Creb3 |
T |
C |
4: 43,566,322 (GRCm39) |
L276P |
probably damaging |
Het |
Crnkl1 |
T |
A |
2: 145,773,269 (GRCm39) |
M126L |
probably benign |
Het |
Csrp2 |
C |
T |
10: 110,771,045 (GRCm39) |
A50V |
probably damaging |
Het |
Ctsd |
A |
G |
7: 141,930,879 (GRCm39) |
C284R |
probably damaging |
Het |
Dll3 |
G |
A |
7: 27,994,075 (GRCm39) |
A454V |
probably damaging |
Het |
Dmbx1 |
C |
T |
4: 115,781,104 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
C |
A |
6: 73,104,902 (GRCm39) |
E1896* |
probably null |
Het |
Dtwd1 |
A |
G |
2: 126,006,679 (GRCm39) |
T234A |
probably damaging |
Het |
Fhod3 |
G |
A |
18: 25,248,947 (GRCm39) |
|
probably null |
Het |
Gm10549 |
C |
A |
18: 33,597,463 (GRCm39) |
|
probably benign |
Het |
Gm7298 |
T |
C |
6: 121,742,297 (GRCm39) |
I495T |
probably damaging |
Het |
Grhl3 |
T |
C |
4: 135,288,532 (GRCm39) |
N51S |
probably damaging |
Het |
Gtpbp4 |
A |
T |
13: 9,035,366 (GRCm39) |
|
probably null |
Het |
Hsd17b14 |
A |
C |
7: 45,216,209 (GRCm39) |
S260R |
probably benign |
Het |
Insig2 |
A |
T |
1: 121,235,058 (GRCm39) |
|
probably null |
Het |
Itgae |
T |
A |
11: 73,029,618 (GRCm39) |
V1046D |
probably benign |
Het |
Kif1b |
A |
T |
4: 149,305,447 (GRCm39) |
|
probably null |
Het |
Kmo |
A |
G |
1: 175,478,225 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
A |
G |
18: 77,496,483 (GRCm39) |
N29S |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,793,460 (GRCm39) |
C2484* |
probably null |
Het |
Lrrc23 |
T |
A |
6: 124,747,711 (GRCm39) |
M293L |
probably benign |
Het |
Mphosph6 |
T |
C |
8: 118,525,807 (GRCm39) |
D47G |
probably benign |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Naglu |
G |
A |
11: 100,967,436 (GRCm39) |
R462H |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nlrc5 |
T |
C |
8: 95,248,397 (GRCm39) |
S1711P |
probably damaging |
Het |
Or10al7 |
T |
C |
17: 38,366,220 (GRCm39) |
Y79C |
possibly damaging |
Het |
Or1o2 |
T |
C |
17: 37,543,201 (GRCm39) |
E20G |
probably benign |
Het |
Osbpl6 |
G |
A |
2: 76,423,731 (GRCm39) |
A857T |
probably damaging |
Het |
Oscp1 |
C |
A |
4: 125,982,201 (GRCm39) |
D380E |
probably benign |
Het |
Pdzd7 |
C |
A |
19: 45,027,678 (GRCm39) |
R265S |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,246,947 (GRCm39) |
|
probably null |
Het |
Pigc |
G |
A |
1: 161,798,033 (GRCm39) |
R5H |
probably benign |
Het |
Pla2g5 |
C |
A |
4: 138,531,845 (GRCm39) |
R53L |
probably benign |
Het |
Rbm6 |
T |
C |
9: 107,729,905 (GRCm39) |
R248G |
probably damaging |
Het |
Rev1 |
A |
T |
1: 38,095,526 (GRCm39) |
L877Q |
probably damaging |
Het |
Rpap3 |
A |
T |
15: 97,579,589 (GRCm39) |
N474K |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,842,493 (GRCm39) |
E468V |
possibly damaging |
Het |
Samd9l |
A |
C |
6: 3,374,749 (GRCm39) |
D837E |
probably benign |
Het |
Sipa1l2 |
T |
C |
8: 126,178,727 (GRCm39) |
N1124S |
probably damaging |
Het |
Slc11a2 |
G |
A |
15: 100,307,142 (GRCm39) |
A83V |
possibly damaging |
Het |
Slfn14 |
A |
G |
11: 83,172,643 (GRCm39) |
|
probably null |
Het |
Sry |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
GCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTGGTGGTGGTCATGGAACTGCTGCTTCTGCTG |
Y: 2,662,638 (GRCm39) |
|
probably benign |
Het |
Suclg1 |
A |
G |
6: 73,252,226 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
C |
10: 5,292,293 (GRCm39) |
V1325G |
probably damaging |
Het |
Tmprss15 |
T |
C |
16: 78,784,538 (GRCm39) |
S706G |
probably benign |
Het |
Tox2 |
T |
C |
2: 163,162,296 (GRCm39) |
Y389H |
probably damaging |
Het |
Trappc10 |
T |
C |
10: 78,034,909 (GRCm39) |
T946A |
probably benign |
Het |
Ubqln1 |
C |
T |
13: 58,325,719 (GRCm39) |
E546K |
probably damaging |
Het |
Zfp106 |
A |
G |
2: 120,354,538 (GRCm39) |
V1411A |
possibly damaging |
Het |
Zkscan5 |
A |
T |
5: 145,155,513 (GRCm39) |
K395* |
probably null |
Het |
|
Other mutations in Or6k2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Or6k2
|
APN |
1 |
173,986,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02479:Or6k2
|
APN |
1 |
173,986,520 (GRCm39) |
nonsense |
probably null |
|
IGL03190:Or6k2
|
APN |
1 |
173,987,110 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03270:Or6k2
|
APN |
1 |
173,987,119 (GRCm39) |
missense |
probably benign |
0.04 |
R0645:Or6k2
|
UTSW |
1 |
173,986,920 (GRCm39) |
missense |
probably benign |
0.00 |
R0834:Or6k2
|
UTSW |
1 |
173,986,930 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1432:Or6k2
|
UTSW |
1 |
173,986,483 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1508:Or6k2
|
UTSW |
1 |
173,986,930 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2351:Or6k2
|
UTSW |
1 |
173,986,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R3440:Or6k2
|
UTSW |
1 |
173,986,746 (GRCm39) |
missense |
probably benign |
0.14 |
R3441:Or6k2
|
UTSW |
1 |
173,986,746 (GRCm39) |
missense |
probably benign |
0.14 |
R4571:Or6k2
|
UTSW |
1 |
173,986,494 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5072:Or6k2
|
UTSW |
1 |
173,986,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R6060:Or6k2
|
UTSW |
1 |
173,986,907 (GRCm39) |
nonsense |
probably null |
|
R6166:Or6k2
|
UTSW |
1 |
173,986,659 (GRCm39) |
missense |
probably benign |
0.43 |
R6228:Or6k2
|
UTSW |
1 |
173,979,712 (GRCm39) |
missense |
probably benign |
0.00 |
R6272:Or6k2
|
UTSW |
1 |
173,986,741 (GRCm39) |
missense |
probably benign |
0.02 |
R6298:Or6k2
|
UTSW |
1 |
173,979,748 (GRCm39) |
missense |
probably benign |
0.02 |
R6400:Or6k2
|
UTSW |
1 |
173,986,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7581:Or6k2
|
UTSW |
1 |
173,986,337 (GRCm39) |
splice site |
probably null |
|
R7677:Or6k2
|
UTSW |
1 |
173,986,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Or6k2
|
UTSW |
1 |
173,987,254 (GRCm39) |
missense |
probably benign |
0.12 |
R8077:Or6k2
|
UTSW |
1 |
173,979,411 (GRCm39) |
unclassified |
probably benign |
|
R8519:Or6k2
|
UTSW |
1 |
173,986,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R9106:Or6k2
|
UTSW |
1 |
173,986,369 (GRCm39) |
missense |
probably benign |
0.00 |
R9205:Or6k2
|
UTSW |
1 |
173,986,456 (GRCm39) |
missense |
probably benign |
0.33 |
R9507:Or6k2
|
UTSW |
1 |
173,986,552 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9797:Or6k2
|
UTSW |
1 |
173,986,417 (GRCm39) |
missense |
probably benign |
|
Z1187:Or6k2
|
UTSW |
1 |
173,986,907 (GRCm39) |
nonsense |
probably null |
|
Z1192:Or6k2
|
UTSW |
1 |
173,986,907 (GRCm39) |
nonsense |
probably null |
|
|