Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars2 |
T |
A |
17: 45,819,549 (GRCm39) |
L188* |
probably null |
Het |
Acod1 |
C |
T |
14: 103,292,471 (GRCm39) |
R332C |
probably damaging |
Het |
Adamts3 |
T |
A |
5: 89,839,194 (GRCm39) |
K852M |
probably damaging |
Het |
Adm |
A |
T |
7: 110,226,903 (GRCm39) |
|
probably benign |
Het |
Aff4 |
A |
G |
11: 53,263,837 (GRCm39) |
S286G |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,753,300 (GRCm39) |
|
probably null |
Het |
Aqr |
A |
T |
2: 113,973,530 (GRCm39) |
Y427* |
probably null |
Het |
Arid1b |
C |
A |
17: 5,045,231 (GRCm39) |
|
probably benign |
Het |
Arpp21 |
T |
A |
9: 111,972,553 (GRCm39) |
R259* |
probably null |
Het |
Cep290 |
C |
T |
10: 100,379,183 (GRCm39) |
A55V |
possibly damaging |
Het |
Chsy3 |
GT |
G |
18: 59,309,238 (GRCm39) |
163 |
probably null |
Het |
Clcn2 |
T |
C |
16: 20,532,404 (GRCm39) |
E68G |
possibly damaging |
Het |
Corin |
T |
A |
5: 72,473,732 (GRCm39) |
H699L |
probably benign |
Het |
Cyld |
T |
C |
8: 89,459,681 (GRCm39) |
Y446H |
probably damaging |
Het |
Dcst1 |
T |
A |
3: 89,259,883 (GRCm39) |
E613V |
probably damaging |
Het |
Dlk1 |
T |
C |
12: 109,421,507 (GRCm39) |
C74R |
probably damaging |
Het |
Dnah12 |
A |
C |
14: 26,418,496 (GRCm39) |
K128T |
probably benign |
Het |
Dspp |
T |
A |
5: 104,326,317 (GRCm39) |
S893R |
unknown |
Het |
Dtl |
A |
T |
1: 191,300,684 (GRCm39) |
|
probably null |
Het |
F2rl1 |
T |
A |
13: 95,650,778 (GRCm39) |
S35C |
probably benign |
Het |
Fcgbp |
A |
T |
7: 27,819,959 (GRCm39) |
Y2562F |
probably benign |
Het |
Fgf10 |
A |
T |
13: 118,852,044 (GRCm39) |
D42V |
probably benign |
Het |
Gm10271 |
A |
T |
10: 116,808,497 (GRCm39) |
F6L |
probably damaging |
Het |
Gm21190 |
T |
A |
5: 15,729,849 (GRCm39) |
E256D |
probably damaging |
Het |
Gm5157 |
A |
G |
7: 20,919,346 (GRCm39) |
S66P |
probably damaging |
Het |
Hal |
T |
G |
10: 93,326,778 (GRCm39) |
L138R |
probably damaging |
Het |
Hsd17b3 |
T |
C |
13: 64,207,284 (GRCm39) |
|
probably null |
Het |
Lrrc37 |
A |
T |
11: 103,504,618 (GRCm39) |
M2450K |
possibly damaging |
Het |
Lrsam1 |
T |
C |
2: 32,845,234 (GRCm39) |
T94A |
probably benign |
Het |
Macc1 |
T |
C |
12: 119,411,320 (GRCm39) |
V696A |
probably damaging |
Het |
Magi2 |
G |
A |
5: 19,432,289 (GRCm39) |
M1I |
probably null |
Het |
Marchf7 |
C |
A |
2: 60,075,564 (GRCm39) |
N674K |
probably benign |
Het |
Mfap1b |
A |
G |
2: 121,300,776 (GRCm39) |
V34A |
probably benign |
Het |
Mob3b |
G |
A |
4: 35,084,069 (GRCm39) |
S40L |
probably benign |
Het |
Ndufs2 |
A |
T |
1: 171,063,987 (GRCm39) |
V386E |
probably damaging |
Het |
Nfic |
C |
T |
10: 81,256,581 (GRCm39) |
A19T |
probably damaging |
Het |
Nfs1 |
G |
A |
2: 155,976,373 (GRCm39) |
R174W |
probably damaging |
Het |
Nin |
G |
T |
12: 70,092,298 (GRCm39) |
S670R |
possibly damaging |
Het |
Nrxn1 |
T |
C |
17: 90,930,935 (GRCm39) |
I754V |
probably benign |
Het |
Nwd1 |
T |
C |
8: 73,380,201 (GRCm39) |
|
probably null |
Het |
Or4c1 |
T |
A |
2: 89,133,703 (GRCm39) |
T78S |
possibly damaging |
Het |
Or51a6 |
G |
T |
7: 102,604,216 (GRCm39) |
N197K |
probably benign |
Het |
Pcdhgb8 |
A |
G |
18: 37,896,502 (GRCm39) |
E524G |
probably damaging |
Het |
Phlpp1 |
A |
T |
1: 106,246,723 (GRCm39) |
R638* |
probably null |
Het |
Pkmyt1 |
G |
C |
17: 23,954,300 (GRCm39) |
W360S |
probably benign |
Het |
Plxnd1 |
C |
A |
6: 115,944,748 (GRCm39) |
|
probably null |
Het |
Poldip3 |
A |
T |
15: 83,013,430 (GRCm39) |
N322K |
probably damaging |
Het |
Prmt3 |
A |
T |
7: 49,478,695 (GRCm39) |
I419L |
probably benign |
Het |
Prss36 |
A |
T |
7: 127,544,002 (GRCm39) |
V123E |
probably damaging |
Het |
Prss58 |
A |
G |
6: 40,874,703 (GRCm39) |
I46T |
probably damaging |
Het |
Rac1 |
T |
C |
5: 143,492,753 (GRCm39) |
|
probably benign |
Het |
Rb1cc1 |
A |
G |
1: 6,304,220 (GRCm39) |
Y36C |
probably damaging |
Het |
Rif1 |
C |
G |
2: 51,985,856 (GRCm39) |
L614V |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,218,926 (GRCm39) |
F951L |
unknown |
Het |
Rps6ka5 |
G |
T |
12: 100,541,509 (GRCm39) |
P417T |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,767,062 (GRCm39) |
W2967R |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,442,992 (GRCm39) |
S1679R |
probably damaging |
Het |
Scn1a |
A |
C |
2: 66,165,800 (GRCm39) |
W153G |
probably damaging |
Het |
Serpinb7 |
A |
G |
1: 107,373,726 (GRCm39) |
Y114C |
probably damaging |
Het |
Son |
T |
C |
16: 91,455,792 (GRCm39) |
M1513T |
probably benign |
Het |
Spag8 |
C |
T |
4: 43,651,534 (GRCm39) |
V447M |
probably benign |
Het |
St3gal2 |
T |
A |
8: 111,696,185 (GRCm39) |
Y257N |
probably damaging |
Het |
Tars1 |
A |
T |
15: 11,397,282 (GRCm39) |
D40E |
probably damaging |
Het |
Tlr3 |
T |
C |
8: 45,850,851 (GRCm39) |
H158R |
probably benign |
Het |
Tppp2 |
G |
T |
14: 52,156,392 (GRCm39) |
V50L |
probably benign |
Het |
Trrap |
T |
C |
5: 144,746,994 (GRCm39) |
S1503P |
probably benign |
Het |
Ttll4 |
T |
G |
1: 74,724,550 (GRCm39) |
S573R |
probably damaging |
Het |
Vmn2r104 |
A |
T |
17: 20,249,747 (GRCm39) |
N841K |
probably damaging |
Het |
Vmn2r3 |
A |
T |
3: 64,167,068 (GRCm39) |
C688S |
probably damaging |
Het |
Vps16 |
T |
C |
2: 130,266,369 (GRCm39) |
|
probably null |
Het |
Zfp608 |
G |
A |
18: 55,032,320 (GRCm39) |
T540I |
probably benign |
Het |
Zfp775 |
G |
A |
6: 48,596,750 (GRCm39) |
R208Q |
probably damaging |
Het |
|
Other mutations in Or4a39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01326:Or4a39
|
APN |
2 |
89,236,675 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01648:Or4a39
|
APN |
2 |
89,236,535 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03005:Or4a39
|
APN |
2 |
89,237,315 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0450:Or4a39
|
UTSW |
2 |
89,237,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R0469:Or4a39
|
UTSW |
2 |
89,237,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R0510:Or4a39
|
UTSW |
2 |
89,237,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R1983:Or4a39
|
UTSW |
2 |
89,236,770 (GRCm39) |
missense |
probably benign |
0.00 |
R4183:Or4a39
|
UTSW |
2 |
89,236,935 (GRCm39) |
missense |
probably benign |
|
R4737:Or4a39
|
UTSW |
2 |
89,236,830 (GRCm39) |
missense |
probably benign |
0.05 |
R4748:Or4a39
|
UTSW |
2 |
89,236,599 (GRCm39) |
missense |
probably benign |
0.02 |
R4749:Or4a39
|
UTSW |
2 |
89,236,599 (GRCm39) |
missense |
probably benign |
0.02 |
R4969:Or4a39
|
UTSW |
2 |
89,236,770 (GRCm39) |
missense |
probably benign |
0.00 |
R5047:Or4a39
|
UTSW |
2 |
89,237,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Or4a39
|
UTSW |
2 |
89,237,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Or4a39
|
UTSW |
2 |
89,237,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Or4a39
|
UTSW |
2 |
89,237,074 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6416:Or4a39
|
UTSW |
2 |
89,236,866 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7352:Or4a39
|
UTSW |
2 |
89,236,806 (GRCm39) |
missense |
probably benign |
0.00 |
R7515:Or4a39
|
UTSW |
2 |
89,237,250 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7796:Or4a39
|
UTSW |
2 |
89,237,157 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7893:Or4a39
|
UTSW |
2 |
89,237,414 (GRCm39) |
missense |
probably benign |
0.00 |
R8034:Or4a39
|
UTSW |
2 |
89,237,081 (GRCm39) |
missense |
probably benign |
0.44 |
R8399:Or4a39
|
UTSW |
2 |
89,237,028 (GRCm39) |
missense |
probably benign |
0.10 |
R8694:Or4a39
|
UTSW |
2 |
89,237,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R9085:Or4a39
|
UTSW |
2 |
89,236,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R9486:Or4a39
|
UTSW |
2 |
89,236,959 (GRCm39) |
missense |
possibly damaging |
0.53 |
|