Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300003K06Rik |
G |
T |
11: 99,837,904 (GRCm38) |
Q38K |
probably benign |
Het |
9930111J21Rik2 |
A |
T |
11: 49,019,307 (GRCm38) |
N766K |
probably benign |
Het |
Adam15 |
A |
C |
3: 89,343,883 (GRCm38) |
I505S |
probably benign |
Het |
Apc2 |
T |
C |
10: 80,306,420 (GRCm38) |
M391T |
probably damaging |
Het |
Bclaf1 |
A |
G |
10: 20,334,628 (GRCm38) |
S840G |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,239,060 (GRCm38) |
Y96C |
probably damaging |
Het |
Cald1 |
CAAAA |
CAAA |
6: 34,747,928 (GRCm38) |
|
probably null |
Het |
Ddhd1 |
A |
G |
14: 45,614,176 (GRCm38) |
L141P |
probably damaging |
Het |
Dnaaf3 |
A |
T |
7: 4,523,672 (GRCm38) |
S469T |
probably benign |
Het |
Dzip3 |
A |
T |
16: 48,958,465 (GRCm38) |
M323K |
possibly damaging |
Het |
E430018J23Rik |
C |
T |
7: 127,393,409 (GRCm38) |
A10T |
possibly damaging |
Het |
Eci2 |
T |
A |
13: 34,993,065 (GRCm38) |
|
probably null |
Het |
Fam109b |
T |
A |
15: 82,343,716 (GRCm38) |
H145Q |
probably benign |
Het |
Fam227b |
A |
T |
2: 126,126,962 (GRCm38) |
V64E |
probably damaging |
Het |
Galnt2 |
A |
G |
8: 124,343,315 (GRCm38) |
I524V |
probably benign |
Het |
Gm10549 |
C |
A |
18: 33,464,305 (GRCm38) |
|
probably benign |
Het |
Gm14548 |
A |
T |
7: 3,894,032 (GRCm38) |
S602T |
possibly damaging |
Het |
Gm3443 |
T |
A |
19: 21,555,746 (GRCm38) |
S25T |
probably damaging |
Het |
Gpr22 |
T |
A |
12: 31,711,617 (GRCm38) |
K14* |
probably null |
Het |
Grip1 |
T |
C |
10: 119,986,346 (GRCm38) |
S405P |
possibly damaging |
Het |
Helz2 |
C |
A |
2: 181,232,294 (GRCm38) |
V2136L |
probably benign |
Het |
Helz2 |
T |
C |
2: 181,235,945 (GRCm38) |
H1020R |
probably damaging |
Het |
Il1f5 |
G |
A |
2: 24,277,490 (GRCm38) |
|
probably benign |
Het |
Iqsec1 |
T |
A |
6: 90,689,635 (GRCm38) |
S607C |
probably damaging |
Het |
Klhl2 |
A |
T |
8: 64,752,767 (GRCm38) |
Y373* |
probably null |
Het |
L3mbtl3 |
T |
C |
10: 26,292,747 (GRCm38) |
I595V |
unknown |
Het |
Large2 |
T |
C |
2: 92,370,636 (GRCm38) |
D65G |
probably damaging |
Het |
Lrrfip1 |
T |
C |
1: 91,082,159 (GRCm38) |
Y122H |
probably damaging |
Het |
Map1b |
A |
T |
13: 99,433,206 (GRCm38) |
D1002E |
unknown |
Het |
Mink1 |
C |
T |
11: 70,598,894 (GRCm38) |
T59I |
possibly damaging |
Het |
Mrvi1 |
G |
A |
7: 110,876,905 (GRCm38) |
T819M |
probably benign |
Het |
Myo7b |
T |
C |
18: 31,959,454 (GRCm38) |
N2097D |
probably benign |
Het |
Nbea |
C |
A |
3: 55,628,484 (GRCm38) |
C2893F |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,436,093 (GRCm38) |
V490E |
probably damaging |
Het |
Olfr1230 |
G |
T |
2: 89,296,962 (GRCm38) |
H103N |
probably damaging |
Het |
Olfr131 |
A |
G |
17: 38,082,729 (GRCm38) |
M83T |
probably damaging |
Het |
Olfr1318 |
T |
C |
2: 112,156,356 (GRCm38) |
I135T |
probably damaging |
Het |
Olfr1369-ps1 |
G |
A |
13: 21,116,231 (GRCm38) |
E180K |
probably damaging |
Het |
Olfr730 |
C |
A |
14: 50,186,678 (GRCm38) |
D180Y |
probably damaging |
Het |
Pctp |
A |
G |
11: 89,987,318 (GRCm38) |
I130T |
probably benign |
Het |
Pdcl3 |
T |
C |
1: 38,988,071 (GRCm38) |
|
probably null |
Het |
Pkp1 |
T |
C |
1: 135,879,908 (GRCm38) |
K541E |
probably damaging |
Het |
Plekhh2 |
G |
A |
17: 84,591,564 (GRCm38) |
V990I |
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,718,431 (GRCm38) |
V828D |
probably damaging |
Het |
Prrc2b |
T |
C |
2: 32,208,811 (GRCm38) |
Y712H |
probably damaging |
Het |
Prune2 |
T |
C |
19: 17,121,562 (GRCm38) |
S1477P |
probably benign |
Het |
Psma5 |
A |
G |
3: 108,279,802 (GRCm38) |
K239R |
probably benign |
Het |
Rhobtb1 |
G |
C |
10: 69,270,456 (GRCm38) |
A284P |
probably benign |
Het |
Samsn1 |
G |
A |
16: 75,945,274 (GRCm38) |
|
noncoding transcript |
Het |
Scel |
A |
G |
14: 103,572,042 (GRCm38) |
T273A |
probably benign |
Het |
Slc22a5 |
T |
A |
11: 53,891,618 (GRCm38) |
|
probably benign |
Het |
Slc25a37 |
A |
T |
14: 69,249,504 (GRCm38) |
M110K |
possibly damaging |
Het |
Slc6a2 |
A |
T |
8: 92,981,981 (GRCm38) |
M242L |
probably benign |
Het |
Slc8a3 |
C |
A |
12: 81,199,567 (GRCm38) |
W904L |
probably benign |
Het |
Ss18l1 |
G |
A |
2: 180,055,112 (GRCm38) |
V109I |
probably benign |
Het |
Tbx5 |
C |
T |
5: 119,853,598 (GRCm38) |
H245Y |
probably damaging |
Het |
Thumpd2 |
C |
A |
17: 81,052,913 (GRCm38) |
L244F |
probably damaging |
Het |
Tmem107 |
T |
A |
11: 69,071,415 (GRCm38) |
V66E |
probably damaging |
Het |
Tnr |
T |
C |
1: 159,888,314 (GRCm38) |
V882A |
possibly damaging |
Het |
Top2b |
T |
G |
14: 16,409,189 (GRCm38) |
I777M |
probably damaging |
Het |
Ttbk1 |
A |
G |
17: 46,470,807 (GRCm38) |
V340A |
possibly damaging |
Het |
Veph1 |
T |
C |
3: 66,255,060 (GRCm38) |
E59G |
probably damaging |
Het |
Vmn1r234 |
T |
A |
17: 21,229,721 (GRCm38) |
M299K |
possibly damaging |
Het |
Vps13b |
T |
C |
15: 35,770,464 (GRCm38) |
Y2018H |
probably benign |
Het |
Zbtb11 |
A |
G |
16: 55,998,073 (GRCm38) |
E620G |
probably benign |
Het |
Zfp418 |
A |
G |
7: 7,182,628 (GRCm38) |
H530R |
possibly damaging |
Het |
|
Other mutations in Arsi |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Arsi
|
APN |
18 |
60,912,430 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02519:Arsi
|
APN |
18 |
60,917,067 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03186:Arsi
|
APN |
18 |
60,917,473 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03134:Arsi
|
UTSW |
18 |
60,917,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R0003:Arsi
|
UTSW |
18 |
60,916,986 (GRCm38) |
missense |
probably benign |
0.29 |
R0003:Arsi
|
UTSW |
18 |
60,916,986 (GRCm38) |
missense |
probably benign |
0.29 |
R0448:Arsi
|
UTSW |
18 |
60,917,302 (GRCm38) |
missense |
probably damaging |
0.98 |
R1147:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1147:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1148:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1148:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1190:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1261:Arsi
|
UTSW |
18 |
60,916,671 (GRCm38) |
missense |
probably damaging |
1.00 |
R1511:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1538:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1635:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1641:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1759:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1794:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1822:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1824:Arsi
|
UTSW |
18 |
60,912,297 (GRCm38) |
missense |
probably damaging |
1.00 |
R1824:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1930:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1932:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R1983:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2035:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2036:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2108:Arsi
|
UTSW |
18 |
60,916,371 (GRCm38) |
missense |
possibly damaging |
0.75 |
R2166:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2168:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2261:Arsi
|
UTSW |
18 |
60,916,665 (GRCm38) |
missense |
probably damaging |
1.00 |
R2263:Arsi
|
UTSW |
18 |
60,916,665 (GRCm38) |
missense |
probably damaging |
1.00 |
R2299:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2300:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2393:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2402:Arsi
|
UTSW |
18 |
60,916,467 (GRCm38) |
missense |
possibly damaging |
0.88 |
R2484:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2511:Arsi
|
UTSW |
18 |
60,916,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R2994:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2995:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2996:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R2997:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3625:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3694:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3695:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3883:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3884:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3907:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3932:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R3954:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4212:Arsi
|
UTSW |
18 |
60,916,701 (GRCm38) |
missense |
probably damaging |
1.00 |
R4256:Arsi
|
UTSW |
18 |
60,917,316 (GRCm38) |
missense |
probably damaging |
1.00 |
R4257:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4258:Arsi
|
UTSW |
18 |
60,917,316 (GRCm38) |
missense |
probably damaging |
1.00 |
R4459:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4469:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4601:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4603:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4610:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4649:Arsi
|
UTSW |
18 |
60,917,098 (GRCm38) |
missense |
probably damaging |
1.00 |
R4649:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4650:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4651:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4652:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4749:Arsi
|
UTSW |
18 |
60,917,461 (GRCm38) |
missense |
probably benign |
0.23 |
R4766:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4807:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4808:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4856:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4860:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4860:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R4886:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R5015:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R5121:Arsi
|
UTSW |
18 |
60,917,439 (GRCm38) |
missense |
probably damaging |
1.00 |
R5185:Arsi
|
UTSW |
18 |
60,916,912 (GRCm38) |
missense |
probably damaging |
1.00 |
R6191:Arsi
|
UTSW |
18 |
60,912,472 (GRCm38) |
missense |
probably damaging |
1.00 |
R6197:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R6219:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R6220:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R6378:Arsi
|
UTSW |
18 |
60,916,501 (GRCm38) |
missense |
probably damaging |
1.00 |
R6612:Arsi
|
UTSW |
18 |
60,912,456 (GRCm38) |
missense |
probably benign |
0.12 |
R6871:Arsi
|
UTSW |
18 |
60,916,651 (GRCm38) |
missense |
probably benign |
0.07 |
R7813:Arsi
|
UTSW |
18 |
60,916,654 (GRCm38) |
missense |
possibly damaging |
0.58 |
R7974:Arsi
|
UTSW |
18 |
60,912,406 (GRCm38) |
missense |
probably damaging |
1.00 |
R8035:Arsi
|
UTSW |
18 |
60,916,370 (GRCm38) |
missense |
probably damaging |
1.00 |
R9162:Arsi
|
UTSW |
18 |
60,917,497 (GRCm38) |
missense |
probably damaging |
0.96 |
R9200:Arsi
|
UTSW |
18 |
60,916,764 (GRCm38) |
missense |
possibly damaging |
0.87 |
R9581:Arsi
|
UTSW |
18 |
60,917,088 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Arsi
|
UTSW |
18 |
60,916,780 (GRCm38) |
missense |
probably damaging |
1.00 |
|