Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap2 |
T |
C |
5: 62,828,297 (GRCm39) |
D958G |
possibly damaging |
Het |
Bag4 |
T |
C |
8: 26,261,259 (GRCm39) |
T161A |
probably benign |
Het |
Bora |
A |
T |
14: 99,299,730 (GRCm39) |
Q234L |
possibly damaging |
Het |
Cacna2d2 |
T |
C |
9: 107,374,720 (GRCm39) |
|
probably null |
Het |
Cass4 |
G |
T |
2: 172,268,832 (GRCm39) |
A307S |
probably benign |
Het |
Cbln4 |
A |
T |
2: 171,884,016 (GRCm39) |
V68E |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,826,015 (GRCm39) |
N2K |
probably benign |
Het |
Ccnf |
T |
A |
17: 24,450,811 (GRCm39) |
D389V |
probably damaging |
Het |
Cdipt |
T |
C |
7: 126,578,773 (GRCm39) |
S161P |
probably benign |
Het |
Ceacam19 |
T |
C |
7: 19,616,812 (GRCm39) |
I161V |
probably benign |
Het |
Cfap65 |
A |
G |
1: 74,959,564 (GRCm39) |
I862T |
probably damaging |
Het |
Cfi |
T |
A |
3: 129,652,019 (GRCm39) |
L230Q |
probably benign |
Het |
Chac2 |
G |
A |
11: 30,936,159 (GRCm39) |
R30W |
probably damaging |
Het |
Cmc2 |
G |
A |
8: 117,616,566 (GRCm39) |
|
probably benign |
Het |
Col1a2 |
A |
T |
6: 4,505,840 (GRCm39) |
M1L |
probably benign |
Het |
Cox8a |
C |
A |
19: 7,194,783 (GRCm39) |
R32L |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,435,708 (GRCm39) |
N1083Y |
probably damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,059,504 (GRCm39) |
D132G |
probably damaging |
Het |
Dedd2 |
G |
A |
7: 24,910,715 (GRCm39) |
P154S |
probably benign |
Het |
Dnaaf3 |
T |
C |
7: 4,527,212 (GRCm39) |
D358G |
probably benign |
Het |
Dysf |
T |
A |
6: 83,996,586 (GRCm39) |
F29L |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,089,101 (GRCm39) |
L888P |
probably damaging |
Het |
Ebf4 |
A |
G |
2: 130,151,643 (GRCm39) |
D277G |
probably damaging |
Het |
Ecm2 |
T |
A |
13: 49,668,570 (GRCm39) |
L91* |
probably null |
Het |
Foxs1 |
T |
C |
2: 152,774,762 (GRCm39) |
D97G |
possibly damaging |
Het |
Frs2 |
A |
C |
10: 116,912,714 (GRCm39) |
|
probably null |
Het |
Grp |
A |
T |
18: 66,013,008 (GRCm39) |
D58V |
probably damaging |
Het |
Hif1a |
T |
G |
12: 73,988,616 (GRCm39) |
F537C |
probably damaging |
Het |
Icam4 |
G |
A |
9: 20,940,835 (GRCm39) |
S29N |
probably benign |
Het |
Itfg1 |
T |
C |
8: 86,452,799 (GRCm39) |
E523G |
probably benign |
Het |
Jph2 |
T |
C |
2: 163,217,600 (GRCm39) |
K359E |
probably damaging |
Het |
Katnip |
G |
A |
7: 125,414,037 (GRCm39) |
G394R |
probably benign |
Het |
Kcnq2 |
A |
T |
2: 180,729,449 (GRCm39) |
V490E |
possibly damaging |
Het |
Klhl18 |
C |
T |
9: 110,257,795 (GRCm39) |
M548I |
possibly damaging |
Het |
Lpin3 |
A |
G |
2: 160,737,721 (GRCm39) |
Y197C |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,396,422 (GRCm39) |
N2381D |
probably benign |
Het |
Man1a |
A |
T |
10: 53,795,307 (GRCm39) |
W649R |
probably damaging |
Het |
Map4 |
T |
C |
9: 109,893,360 (GRCm39) |
L542P |
probably damaging |
Het |
Mboat2 |
A |
T |
12: 24,928,284 (GRCm39) |
H52L |
probably damaging |
Het |
Mok |
C |
G |
12: 110,781,380 (GRCm39) |
S91T |
probably benign |
Het |
Mtmr11 |
G |
T |
3: 96,075,400 (GRCm39) |
R360L |
probably damaging |
Het |
Myt1l |
G |
A |
12: 29,882,331 (GRCm39) |
G509R |
unknown |
Het |
Ncoa4-ps |
A |
G |
12: 119,225,386 (GRCm39) |
|
noncoding transcript |
Het |
Or1j13 |
A |
G |
2: 36,369,524 (GRCm39) |
V206A |
probably benign |
Het |
Or4g7 |
A |
T |
2: 111,309,734 (GRCm39) |
N202Y |
probably damaging |
Het |
Or52z1 |
C |
T |
7: 103,437,162 (GRCm39) |
M107I |
probably benign |
Het |
Or55b4 |
T |
C |
7: 102,133,596 (GRCm39) |
T244A |
probably damaging |
Het |
Or7d11 |
A |
T |
9: 19,966,179 (GRCm39) |
H75Q |
possibly damaging |
Het |
Padi3 |
G |
T |
4: 140,523,154 (GRCm39) |
T292N |
probably damaging |
Het |
Pard6g |
A |
C |
18: 80,160,420 (GRCm39) |
T178P |
possibly damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,740,726 (GRCm39) |
Y2124N |
probably damaging |
Het |
Plxdc1 |
G |
A |
11: 97,819,289 (GRCm39) |
T398I |
probably damaging |
Het |
Prickle2 |
A |
T |
6: 92,393,829 (GRCm39) |
C225* |
probably null |
Het |
Prmt2 |
G |
A |
10: 76,046,278 (GRCm39) |
T317I |
probably benign |
Het |
Psg22 |
T |
G |
7: 18,453,705 (GRCm39) |
N172K |
probably benign |
Het |
Ptpn9 |
C |
T |
9: 56,940,447 (GRCm39) |
R196* |
probably null |
Het |
Rap1b |
C |
T |
10: 117,660,516 (GRCm39) |
V14I |
probably damaging |
Het |
Rapgef4 |
T |
A |
2: 72,026,622 (GRCm39) |
|
probably null |
Het |
Rlf |
A |
T |
4: 121,006,412 (GRCm39) |
M856K |
possibly damaging |
Het |
Rnf149 |
A |
G |
1: 39,616,255 (GRCm39) |
L34P |
probably benign |
Het |
Rock1 |
T |
C |
18: 10,101,007 (GRCm39) |
E636G |
probably benign |
Het |
Rsad2 |
A |
T |
12: 26,504,122 (GRCm39) |
Y136N |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,738,838 (GRCm39) |
H563R |
probably damaging |
Het |
Slc18b1 |
A |
G |
10: 23,680,110 (GRCm39) |
M102V |
probably benign |
Het |
Slc34a2 |
T |
A |
5: 53,224,989 (GRCm39) |
C377S |
possibly damaging |
Het |
Slco1c1 |
T |
C |
6: 141,492,496 (GRCm39) |
V293A |
probably benign |
Het |
Spidr |
A |
T |
16: 15,957,888 (GRCm39) |
S80T |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 5,298,994 (GRCm39) |
E1031K |
probably damaging |
Het |
Synj2 |
G |
A |
17: 6,067,889 (GRCm39) |
V121I |
probably damaging |
Het |
Synj2 |
A |
T |
17: 6,088,373 (GRCm39) |
T1430S |
probably damaging |
Het |
Tecpr2 |
G |
T |
12: 110,895,543 (GRCm39) |
K343N |
probably damaging |
Het |
Tmem132d |
T |
A |
5: 127,861,164 (GRCm39) |
I986F |
probably benign |
Het |
Trib1 |
G |
A |
15: 59,526,324 (GRCm39) |
R298H |
probably damaging |
Het |
Ttll10 |
T |
A |
4: 156,129,814 (GRCm39) |
D283V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,645,123 (GRCm39) |
K673* |
probably null |
Het |
Ubqlnl |
T |
A |
7: 103,797,905 (GRCm39) |
M531L |
probably benign |
Het |
Vmn2r120 |
A |
T |
17: 57,832,721 (GRCm39) |
W153R |
probably benign |
Het |
Vmn2r2 |
A |
C |
3: 64,024,467 (GRCm39) |
S705A |
probably benign |
Het |
Vmn2r32 |
T |
A |
7: 7,467,209 (GRCm39) |
D773V |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,366,205 (GRCm39) |
Q243L |
probably damaging |
Het |
Wdr24 |
C |
A |
17: 26,043,504 (GRCm39) |
R109S |
probably damaging |
Het |
Zfp113 |
T |
C |
5: 138,143,930 (GRCm39) |
M107V |
probably benign |
Het |
Zfp426 |
G |
T |
9: 20,381,923 (GRCm39) |
Q341K |
possibly damaging |
Het |
Zfp616 |
A |
T |
11: 73,974,672 (GRCm39) |
K314* |
probably null |
Het |
|
Other mutations in Or7g21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00907:Or7g21
|
APN |
9 |
19,032,528 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01316:Or7g21
|
APN |
9 |
19,032,718 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01412:Or7g21
|
APN |
9 |
19,032,895 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01815:Or7g21
|
APN |
9 |
19,032,622 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Or7g21
|
APN |
9 |
19,032,361 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02313:Or7g21
|
APN |
9 |
19,032,671 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03185:Or7g21
|
APN |
9 |
19,033,034 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03186:Or7g21
|
APN |
9 |
19,033,200 (GRCm39) |
missense |
probably benign |
0.16 |
R1337:Or7g21
|
UTSW |
9 |
19,033,099 (GRCm39) |
missense |
probably benign |
|
R2267:Or7g21
|
UTSW |
9 |
19,032,737 (GRCm39) |
missense |
probably benign |
0.22 |
R3969:Or7g21
|
UTSW |
9 |
19,032,956 (GRCm39) |
missense |
probably benign |
0.00 |
R4695:Or7g21
|
UTSW |
9 |
19,032,306 (GRCm39) |
missense |
probably null |
0.04 |
R4976:Or7g21
|
UTSW |
9 |
19,032,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5176:Or7g21
|
UTSW |
9 |
19,032,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R5379:Or7g21
|
UTSW |
9 |
19,032,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Or7g21
|
UTSW |
9 |
19,032,676 (GRCm39) |
missense |
probably benign |
0.00 |
R6236:Or7g21
|
UTSW |
9 |
19,032,409 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6329:Or7g21
|
UTSW |
9 |
19,032,253 (GRCm39) |
start codon destroyed |
probably benign |
0.08 |
R7151:Or7g21
|
UTSW |
9 |
19,033,037 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7326:Or7g21
|
UTSW |
9 |
19,032,965 (GRCm39) |
missense |
probably benign |
0.42 |
R8460:Or7g21
|
UTSW |
9 |
19,032,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R8767:Or7g21
|
UTSW |
9 |
19,032,922 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8978:Or7g21
|
UTSW |
9 |
19,032,582 (GRCm39) |
nonsense |
probably null |
|
R9099:Or7g21
|
UTSW |
9 |
19,032,890 (GRCm39) |
missense |
probably benign |
0.35 |
R9220:Or7g21
|
UTSW |
9 |
19,033,193 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9236:Or7g21
|
UTSW |
9 |
19,033,206 (GRCm39) |
makesense |
probably null |
|
R9265:Or7g21
|
UTSW |
9 |
19,032,984 (GRCm39) |
nonsense |
probably null |
|
R9530:Or7g21
|
UTSW |
9 |
19,033,051 (GRCm39) |
missense |
probably benign |
0.24 |
R9612:Or7g21
|
UTSW |
9 |
19,032,760 (GRCm39) |
missense |
probably benign |
0.16 |
|