Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402N03Rik |
T |
C |
7: 130,740,872 (GRCm39) |
M115V |
probably benign |
Het |
4933415A04Rik |
TTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT |
TTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT |
11: 43,478,227 (GRCm39) |
|
probably null |
Het |
Abca7 |
C |
T |
10: 79,843,185 (GRCm39) |
A1220V |
probably benign |
Het |
Adamts19 |
G |
A |
18: 59,060,372 (GRCm39) |
|
probably null |
Het |
Agbl1 |
G |
A |
7: 76,058,993 (GRCm39) |
V194M |
probably benign |
Het |
Arhgap20 |
G |
T |
9: 51,760,963 (GRCm39) |
S902I |
probably damaging |
Het |
Atp11b |
T |
G |
3: 35,861,093 (GRCm39) |
D193E |
probably damaging |
Het |
B3gntl1 |
A |
T |
11: 121,535,430 (GRCm39) |
|
probably benign |
Het |
C2cd2 |
T |
C |
16: 97,723,496 (GRCm39) |
E7G |
possibly damaging |
Het |
Camta2 |
A |
G |
11: 70,572,447 (GRCm39) |
L259P |
probably benign |
Het |
Ccni |
T |
C |
5: 93,335,563 (GRCm39) |
N192D |
probably benign |
Het |
Cgnl1 |
A |
G |
9: 71,558,535 (GRCm39) |
I946T |
possibly damaging |
Het |
Chil3 |
T |
C |
3: 106,068,548 (GRCm39) |
|
probably null |
Het |
Cntn5 |
A |
G |
9: 9,673,407 (GRCm39) |
|
probably benign |
Het |
Cpn2 |
C |
T |
16: 30,078,169 (GRCm39) |
G511S |
possibly damaging |
Het |
Dagla |
C |
A |
19: 10,232,170 (GRCm39) |
|
probably null |
Het |
Dcc |
T |
C |
18: 71,392,086 (GRCm39) |
N1440S |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,907,474 (GRCm39) |
N1069K |
probably benign |
Het |
Edc4 |
A |
G |
8: 106,616,060 (GRCm39) |
T812A |
probably benign |
Het |
Eml4 |
A |
G |
17: 83,747,471 (GRCm39) |
I238V |
probably benign |
Het |
Ep400 |
T |
C |
5: 110,852,882 (GRCm39) |
T1288A |
unknown |
Het |
Fastkd1 |
A |
C |
2: 69,532,750 (GRCm39) |
L539R |
probably damaging |
Het |
Fbln7 |
G |
A |
2: 128,719,454 (GRCm39) |
|
probably benign |
Het |
Fbxo39 |
A |
G |
11: 72,209,297 (GRCm39) |
I386V |
probably benign |
Het |
Gm17430 |
T |
C |
18: 9,726,267 (GRCm39) |
K135R |
probably damaging |
Het |
Gm3646 |
T |
A |
1: 39,843,483 (GRCm39) |
T8S |
unknown |
Het |
Gtsf1 |
A |
T |
15: 103,329,619 (GRCm39) |
V100E |
possibly damaging |
Het |
Helz2 |
A |
G |
2: 180,876,618 (GRCm39) |
F1292S |
possibly damaging |
Het |
Igf2bp3 |
G |
A |
6: 49,084,401 (GRCm39) |
|
probably benign |
Het |
Ip6k2 |
T |
G |
9: 108,681,826 (GRCm39) |
D252E |
probably damaging |
Het |
Iqck |
T |
A |
7: 118,514,817 (GRCm39) |
L232Q |
probably damaging |
Het |
Kif18b |
A |
G |
11: 102,806,001 (GRCm39) |
V186A |
probably damaging |
Het |
Klhl6 |
T |
A |
16: 19,768,197 (GRCm39) |
|
probably null |
Het |
Lao1 |
C |
T |
4: 118,820,999 (GRCm39) |
T75I |
probably benign |
Het |
Lyst |
T |
C |
13: 13,855,878 (GRCm39) |
F2400L |
probably benign |
Het |
Map3k9 |
A |
T |
12: 81,780,997 (GRCm39) |
S388T |
possibly damaging |
Het |
Mmp11 |
G |
T |
10: 75,762,767 (GRCm39) |
H229N |
probably damaging |
Het |
Myh7 |
T |
G |
14: 55,212,158 (GRCm39) |
I1529L |
probably benign |
Het |
Nckap5 |
G |
T |
1: 126,623,459 (GRCm39) |
D11E |
possibly damaging |
Het |
Ncoa1 |
A |
T |
12: 4,373,033 (GRCm39) |
F123I |
probably damaging |
Het |
Nelfb |
A |
T |
2: 25,093,992 (GRCm39) |
D385E |
probably benign |
Het |
Obscn |
C |
T |
11: 58,972,810 (GRCm39) |
V2288M |
probably damaging |
Het |
Or2f1b |
A |
G |
6: 42,739,154 (GRCm39) |
H56R |
probably damaging |
Het |
Or52x1 |
A |
T |
7: 104,853,367 (GRCm39) |
M61K |
probably damaging |
Het |
Or5b12b |
A |
G |
19: 12,861,458 (GRCm39) |
Y71C |
probably damaging |
Het |
Otog |
T |
A |
7: 45,918,673 (GRCm39) |
|
probably benign |
Het |
Oxa1l |
A |
G |
14: 54,605,646 (GRCm39) |
E375G |
possibly damaging |
Het |
Pan2 |
T |
A |
10: 128,144,091 (GRCm39) |
I129K |
possibly damaging |
Het |
Parp1 |
A |
G |
1: 180,426,616 (GRCm39) |
I919M |
probably benign |
Het |
Pnpla7 |
T |
C |
2: 24,885,305 (GRCm39) |
Y174H |
probably damaging |
Het |
Polr3b |
T |
C |
10: 84,473,928 (GRCm39) |
F169S |
probably damaging |
Het |
Rab10 |
T |
C |
12: 3,314,743 (GRCm39) |
D45G |
probably damaging |
Het |
Reln |
A |
G |
5: 22,185,107 (GRCm39) |
S1537P |
possibly damaging |
Het |
Sema6d |
T |
A |
2: 124,507,197 (GRCm39) |
S1045T |
probably benign |
Het |
Setd2 |
T |
C |
9: 110,402,741 (GRCm39) |
V1794A |
probably damaging |
Het |
Spidr |
T |
A |
16: 15,733,229 (GRCm39) |
I589F |
probably damaging |
Het |
Stmn4 |
A |
C |
14: 66,595,388 (GRCm39) |
I165L |
probably benign |
Het |
Stx5a |
T |
C |
19: 8,727,301 (GRCm39) |
M177T |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,491,486 (GRCm39) |
|
probably null |
Het |
Tmem192 |
T |
C |
8: 65,416,912 (GRCm39) |
Y168H |
probably damaging |
Het |
Ttc21a |
C |
T |
9: 119,785,892 (GRCm39) |
|
probably benign |
Het |
Ush2a |
A |
G |
1: 188,446,663 (GRCm39) |
|
probably benign |
Het |
Vezf1 |
A |
G |
11: 87,972,403 (GRCm39) |
M255V |
possibly damaging |
Het |
Vmn2r25 |
A |
G |
6: 123,816,786 (GRCm39) |
F265S |
probably damaging |
Het |
Vps13a |
A |
G |
19: 16,681,941 (GRCm39) |
S1021P |
probably benign |
Het |
Wfdc16 |
T |
C |
2: 164,477,773 (GRCm39) |
E92G |
possibly damaging |
Het |
Zkscan2 |
T |
C |
7: 123,079,423 (GRCm39) |
T845A |
possibly damaging |
Het |
|
Other mutations in Or4d6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03062:Or4d6
|
APN |
19 |
12,086,512 (GRCm39) |
missense |
probably benign |
0.00 |
BB006:Or4d6
|
UTSW |
19 |
12,086,118 (GRCm39) |
missense |
unknown |
|
BB016:Or4d6
|
UTSW |
19 |
12,086,118 (GRCm39) |
missense |
unknown |
|
IGL02796:Or4d6
|
UTSW |
19 |
12,086,248 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4495001:Or4d6
|
UTSW |
19 |
12,086,076 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1169:Or4d6
|
UTSW |
19 |
12,086,853 (GRCm39) |
missense |
probably benign |
|
R1918:Or4d6
|
UTSW |
19 |
12,086,871 (GRCm39) |
missense |
probably benign |
0.06 |
R2915:Or4d6
|
UTSW |
19 |
12,085,989 (GRCm39) |
missense |
probably benign |
0.09 |
R3835:Or4d6
|
UTSW |
19 |
12,086,764 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4470:Or4d6
|
UTSW |
19 |
12,086,547 (GRCm39) |
splice site |
probably null |
|
R4682:Or4d6
|
UTSW |
19 |
12,086,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Or4d6
|
UTSW |
19 |
12,086,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5467:Or4d6
|
UTSW |
19 |
12,086,023 (GRCm39) |
missense |
probably benign |
0.20 |
R5513:Or4d6
|
UTSW |
19 |
12,086,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Or4d6
|
UTSW |
19 |
12,086,490 (GRCm39) |
missense |
probably benign |
0.25 |
R7385:Or4d6
|
UTSW |
19 |
12,086,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R7569:Or4d6
|
UTSW |
19 |
12,086,385 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7929:Or4d6
|
UTSW |
19 |
12,086,118 (GRCm39) |
missense |
unknown |
|
R8442:Or4d6
|
UTSW |
19 |
12,086,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R9215:Or4d6
|
UTSW |
19 |
12,086,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9467:Or4d6
|
UTSW |
19 |
12,086,313 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9753:Or4d6
|
UTSW |
19 |
12,086,056 (GRCm39) |
missense |
probably benign |
0.02 |
|