Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930451I11Rik |
C |
T |
7: 126,430,662 (GRCm39) |
|
probably benign |
Het |
4930578I06Rik |
C |
T |
14: 64,210,658 (GRCm39) |
R190H |
probably benign |
Het |
Akap13 |
T |
A |
7: 75,261,033 (GRCm39) |
I1219K |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,229,771 (GRCm39) |
|
probably benign |
Het |
Arhgap24 |
A |
G |
5: 102,811,983 (GRCm39) |
E70G |
probably benign |
Het |
Babam2 |
T |
C |
5: 31,859,414 (GRCm39) |
S40P |
possibly damaging |
Het |
Brwd1 |
A |
G |
16: 95,824,696 (GRCm39) |
V1190A |
probably damaging |
Het |
Ccpg1 |
A |
G |
9: 72,919,909 (GRCm39) |
E508G |
probably damaging |
Het |
Ckm |
T |
C |
7: 19,155,279 (GRCm39) |
S372P |
probably benign |
Het |
Egflam |
T |
A |
15: 7,283,907 (GRCm39) |
|
probably null |
Het |
Farp1 |
G |
A |
14: 121,492,891 (GRCm39) |
V498M |
probably benign |
Het |
Galnt14 |
T |
A |
17: 73,811,899 (GRCm39) |
I441F |
probably benign |
Het |
Gm5414 |
A |
G |
15: 101,533,107 (GRCm39) |
L440P |
probably damaging |
Het |
Gm6563 |
A |
G |
19: 23,653,339 (GRCm39) |
E43G |
possibly damaging |
Het |
Gm9755 |
A |
T |
8: 67,967,129 (GRCm39) |
|
noncoding transcript |
Het |
Gmds |
A |
G |
13: 32,004,172 (GRCm39) |
S337P |
possibly damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,156,020 (GRCm39) |
Q754L |
unknown |
Het |
Ltk |
G |
A |
2: 119,583,485 (GRCm39) |
T300I |
possibly damaging |
Het |
Or5d46 |
A |
C |
2: 88,170,621 (GRCm39) |
K237N |
probably damaging |
Het |
Pbx2 |
C |
A |
17: 34,813,619 (GRCm39) |
H184Q |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,327,083 (GRCm39) |
F339S |
probably damaging |
Het |
Prkaa2 |
A |
T |
4: 104,897,153 (GRCm39) |
D353E |
probably benign |
Het |
Prss36 |
G |
A |
7: 127,532,010 (GRCm39) |
|
probably benign |
Het |
Rimbp2 |
A |
G |
5: 128,851,324 (GRCm39) |
V874A |
probably damaging |
Het |
Rspo2 |
C |
A |
15: 42,939,307 (GRCm39) |
R161L |
probably benign |
Het |
Ryr1 |
T |
C |
7: 28,781,875 (GRCm39) |
D2038G |
possibly damaging |
Het |
Stkld1 |
A |
G |
2: 26,833,146 (GRCm39) |
M111V |
probably benign |
Het |
Tprn |
A |
G |
2: 25,154,494 (GRCm39) |
I599V |
probably damaging |
Het |
Upp2 |
A |
T |
2: 58,670,106 (GRCm39) |
I219F |
probably damaging |
Het |
Vmn2r94 |
A |
T |
17: 18,464,433 (GRCm39) |
F619Y |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,346,383 (GRCm39) |
T2875A |
probably benign |
Het |
Zfp64 |
A |
G |
2: 168,768,298 (GRCm39) |
L438P |
probably 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 |
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 |
R4650: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 |
|