Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110025L11Rik |
T |
A |
16: 88,860,603 (GRCm39) |
Y77F |
unknown |
Het |
4933409G03Rik |
G |
A |
2: 68,436,559 (GRCm39) |
E168K |
unknown |
Het |
Aldoa |
A |
G |
7: 126,396,879 (GRCm39) |
S71P |
possibly damaging |
Het |
Arhgef12 |
A |
G |
9: 42,893,266 (GRCm39) |
V979A |
probably damaging |
Het |
Brd8 |
T |
C |
18: 34,739,752 (GRCm39) |
T674A |
probably benign |
Het |
Cacna1d |
C |
T |
14: 29,817,365 (GRCm39) |
M1232I |
probably benign |
Het |
Capza1 |
A |
G |
3: 104,752,296 (GRCm39) |
V14A |
probably damaging |
Het |
Cdk2 |
A |
T |
10: 128,538,364 (GRCm39) |
I135N |
probably damaging |
Het |
Celf4 |
A |
T |
18: 25,629,302 (GRCm39) |
M407K |
possibly damaging |
Het |
Cenpf |
A |
T |
1: 189,392,235 (GRCm39) |
D532E |
probably benign |
Het |
Cideb |
A |
G |
14: 55,992,688 (GRCm39) |
V76A |
possibly damaging |
Het |
Dbpht2 |
C |
G |
12: 74,345,933 (GRCm39) |
|
noncoding transcript |
Het |
Dis3l2 |
A |
G |
1: 86,918,043 (GRCm39) |
D550G |
possibly damaging |
Het |
Dnah1 |
A |
T |
14: 31,006,844 (GRCm39) |
|
probably null |
Het |
Edc4 |
T |
A |
8: 106,619,307 (GRCm39) |
L1293* |
probably null |
Het |
Elp5 |
A |
G |
11: 69,860,398 (GRCm39) |
V203A |
possibly damaging |
Het |
Fndc7 |
T |
C |
3: 108,770,135 (GRCm39) |
N597S |
probably benign |
Het |
Gjb3 |
T |
C |
4: 127,220,484 (GRCm39) |
Y16C |
probably damaging |
Het |
Gm5773 |
A |
G |
3: 93,680,712 (GRCm39) |
D128G |
probably benign |
Het |
Gnb1l |
T |
C |
16: 18,363,025 (GRCm39) |
|
probably null |
Het |
Gon4l |
G |
A |
3: 88,770,859 (GRCm39) |
D514N |
possibly damaging |
Het |
Grhl3 |
T |
A |
4: 135,276,547 (GRCm39) |
|
probably null |
Het |
Hoxc10 |
T |
C |
15: 102,875,698 (GRCm39) |
S136P |
probably benign |
Het |
Ift22 |
G |
A |
5: 136,940,655 (GRCm39) |
V107I |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lamc1 |
T |
G |
1: 153,104,523 (GRCm39) |
S59R |
probably damaging |
Het |
Lgi4 |
G |
A |
7: 30,768,554 (GRCm39) |
A518T |
probably benign |
Het |
Lhx2 |
T |
A |
2: 38,250,052 (GRCm39) |
N290K |
probably damaging |
Het |
Ltbp4 |
A |
T |
7: 27,013,734 (GRCm39) |
C1092S |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,367,412 (GRCm39) |
I2450V |
probably benign |
Het |
Mefv |
A |
G |
16: 3,535,682 (GRCm39) |
L82P |
probably damaging |
Het |
Myb |
A |
G |
10: 21,028,840 (GRCm39) |
L86P |
probably damaging |
Het |
Myh3 |
C |
T |
11: 66,977,270 (GRCm39) |
T333M |
probably damaging |
Het |
Nek11 |
T |
C |
9: 105,225,279 (GRCm39) |
N78D |
possibly damaging |
Het |
Nmi |
C |
A |
2: 51,838,646 (GRCm39) |
C296F |
probably benign |
Het |
Nphs1 |
A |
T |
7: 30,181,895 (GRCm39) |
T1163S |
probably benign |
Het |
Npy4r |
C |
T |
14: 33,868,181 (GRCm39) |
G369D |
possibly damaging |
Het |
Ola1 |
T |
C |
2: 72,972,309 (GRCm39) |
T221A |
probably damaging |
Het |
Or51d1 |
A |
G |
7: 102,348,027 (GRCm39) |
D194G |
probably damaging |
Het |
Or8c11 |
T |
C |
9: 38,289,699 (GRCm39) |
F168S |
probably damaging |
Het |
Pfkfb2 |
A |
T |
1: 130,633,200 (GRCm39) |
N184K |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,513,088 (GRCm39) |
V129A |
probably benign |
Het |
Prps2 |
T |
C |
X: 166,135,288 (GRCm39) |
D183G |
probably damaging |
Het |
Pth |
A |
T |
7: 112,985,026 (GRCm39) |
*116K |
probably null |
Het |
R3hdm1 |
T |
C |
1: 128,112,181 (GRCm39) |
S422P |
probably damaging |
Het |
Rhox2a |
G |
C |
X: 36,508,962 (GRCm39) |
R43P |
probably benign |
Het |
Rwdd3 |
A |
G |
3: 120,952,826 (GRCm39) |
F55S |
probably damaging |
Het |
Serpinb9d |
A |
T |
13: 33,386,836 (GRCm39) |
L301F |
probably benign |
Het |
Slc35e4 |
A |
G |
11: 3,862,677 (GRCm39) |
C171R |
probably damaging |
Het |
Slco1a4 |
A |
T |
6: 141,758,424 (GRCm39) |
I529K |
possibly damaging |
Het |
Styk1 |
A |
T |
6: 131,277,532 (GRCm39) |
W370R |
probably damaging |
Het |
Tmprss11e |
C |
A |
5: 86,875,212 (GRCm39) |
W18L |
probably damaging |
Het |
Trpv1 |
A |
C |
11: 73,129,089 (GRCm39) |
E2A |
probably benign |
Het |
Unc13b |
T |
A |
4: 43,261,035 (GRCm39) |
I1799N |
probably damaging |
Het |
Vmn1r213 |
G |
A |
13: 23,196,422 (GRCm39) |
C335Y |
possibly damaging |
Het |
Vps37c |
C |
T |
19: 10,690,273 (GRCm39) |
S245L |
probably benign |
Het |
Wrn |
T |
C |
8: 33,745,537 (GRCm39) |
T1191A |
probably benign |
Het |
Zfp13 |
A |
G |
17: 23,799,112 (GRCm39) |
L153P |
probably damaging |
Het |
Zfp472 |
T |
G |
17: 33,196,631 (GRCm39) |
S235R |
possibly damaging |
Het |
|
Other mutations in Arsi |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Arsi
|
APN |
18 |
61,045,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02519:Arsi
|
APN |
18 |
61,050,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03186:Arsi
|
APN |
18 |
61,050,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Arsi
|
UTSW |
18 |
61,050,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Arsi
|
UTSW |
18 |
61,050,058 (GRCm39) |
missense |
probably benign |
0.29 |
R0003:Arsi
|
UTSW |
18 |
61,050,058 (GRCm39) |
missense |
probably benign |
0.29 |
R0448:Arsi
|
UTSW |
18 |
61,050,374 (GRCm39) |
missense |
probably damaging |
0.98 |
R1147:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1147:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1148:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1148:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1190:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1261:Arsi
|
UTSW |
18 |
61,049,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1538:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1635:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1641:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1759:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1794:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1822:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1824:Arsi
|
UTSW |
18 |
61,045,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1930:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1932:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R1983:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2035:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2036:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2108:Arsi
|
UTSW |
18 |
61,049,443 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2166:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2168:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2261:Arsi
|
UTSW |
18 |
61,049,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Arsi
|
UTSW |
18 |
61,049,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R2299:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2300:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2393:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2402:Arsi
|
UTSW |
18 |
61,049,539 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2484:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2511:Arsi
|
UTSW |
18 |
61,049,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R2994:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2995:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2996:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R2997:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3625:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3694:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3695:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3883:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3884:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3907:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3932:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R3954:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4212:Arsi
|
UTSW |
18 |
61,049,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4256:Arsi
|
UTSW |
18 |
61,050,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R4257:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4258:Arsi
|
UTSW |
18 |
61,050,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R4459:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4469:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4601:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4603:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4610:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4649:Arsi
|
UTSW |
18 |
61,050,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4651:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4652:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4749:Arsi
|
UTSW |
18 |
61,050,533 (GRCm39) |
missense |
probably benign |
0.23 |
R4766:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4807:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4808:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4856:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4860:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4860:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R4886:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R5015:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R5121:Arsi
|
UTSW |
18 |
61,050,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5185:Arsi
|
UTSW |
18 |
61,049,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Arsi
|
UTSW |
18 |
61,045,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R6197:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R6218:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R6219:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R6220:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R6378:Arsi
|
UTSW |
18 |
61,049,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R6612:Arsi
|
UTSW |
18 |
61,045,528 (GRCm39) |
missense |
probably benign |
0.12 |
R6871:Arsi
|
UTSW |
18 |
61,049,723 (GRCm39) |
missense |
probably benign |
0.07 |
R7813:Arsi
|
UTSW |
18 |
61,049,726 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7974:Arsi
|
UTSW |
18 |
61,045,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R8035:Arsi
|
UTSW |
18 |
61,049,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R9162:Arsi
|
UTSW |
18 |
61,050,569 (GRCm39) |
missense |
probably damaging |
0.96 |
R9200:Arsi
|
UTSW |
18 |
61,049,836 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9581:Arsi
|
UTSW |
18 |
61,050,160 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arsi
|
UTSW |
18 |
61,049,852 (GRCm39) |
missense |
probably damaging |
1.00 |
|