Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
T |
C |
11: 23,468,839 (GRCm39) |
I31V |
probably benign |
Het |
Adamts17 |
A |
G |
7: 66,701,665 (GRCm39) |
K40E |
|
Het |
Akr1c14 |
G |
A |
13: 4,138,952 (GRCm39) |
D312N |
probably benign |
Het |
Alg6 |
T |
C |
4: 99,641,295 (GRCm39) |
V398A |
probably benign |
Het |
Ankmy1 |
A |
T |
1: 92,823,801 (GRCm39) |
M155K |
probably benign |
Het |
Arid5b |
C |
A |
10: 67,954,096 (GRCm39) |
R396L |
probably damaging |
Het |
Armt1 |
C |
A |
10: 4,382,706 (GRCm39) |
D12E |
probably benign |
Het |
Arrb2 |
T |
A |
11: 70,328,796 (GRCm39) |
N217K |
probably benign |
Het |
Atg2b |
A |
T |
12: 105,627,463 (GRCm39) |
L508Q |
probably damaging |
Het |
Atg2b |
A |
T |
12: 105,630,957 (GRCm39) |
S323T |
probably benign |
Het |
Atp1a3 |
G |
A |
7: 24,705,300 (GRCm39) |
|
probably benign |
Het |
Atp6v0e |
T |
C |
17: 26,901,672 (GRCm39) |
V42A |
probably benign |
Het |
Atp9b |
A |
G |
18: 80,809,056 (GRCm39) |
V621A |
|
Het |
Atrnl1 |
A |
C |
19: 57,743,956 (GRCm39) |
D1186A |
probably damaging |
Het |
Atxn2l |
A |
T |
7: 126,093,046 (GRCm39) |
M821K |
possibly damaging |
Het |
Blnk |
G |
A |
19: 40,948,301 (GRCm39) |
R123* |
probably null |
Het |
Bud13 |
T |
A |
9: 46,198,372 (GRCm39) |
S98T |
probably benign |
Het |
Ccdc183 |
T |
C |
2: 25,499,469 (GRCm39) |
M455V |
probably benign |
Het |
Cd109 |
A |
G |
9: 78,622,225 (GRCm39) |
Y1405C |
possibly damaging |
Het |
Cdan1 |
A |
T |
2: 120,553,236 (GRCm39) |
L989Q |
probably damaging |
Het |
Clec16a |
T |
C |
16: 10,506,419 (GRCm39) |
I713T |
possibly damaging |
Het |
Clta |
T |
A |
4: 44,032,419 (GRCm39) |
F168L |
possibly damaging |
Het |
Cnnm1 |
A |
T |
19: 43,456,710 (GRCm39) |
H583L |
probably benign |
Het |
Cyp4f18 |
A |
G |
8: 72,749,906 (GRCm39) |
Y248H |
probably benign |
Het |
Dsg4 |
G |
T |
18: 20,579,323 (GRCm39) |
G20* |
probably null |
Het |
Dusp12 |
T |
A |
1: 170,707,345 (GRCm39) |
K248* |
probably null |
Het |
Eeig2 |
C |
T |
3: 108,910,723 (GRCm39) |
A51T |
probably damaging |
Het |
Elp1 |
C |
T |
4: 56,776,925 (GRCm39) |
G624D |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,134,966 (GRCm39) |
D359G |
possibly damaging |
Het |
Frmpd2 |
C |
A |
14: 33,229,510 (GRCm39) |
F365L |
probably damaging |
Het |
Gab1 |
A |
G |
8: 81,515,298 (GRCm39) |
I340T |
probably benign |
Het |
Gabpa |
C |
T |
16: 84,654,408 (GRCm39) |
Q362* |
probably null |
Het |
Gcnt2 |
A |
T |
13: 41,040,688 (GRCm39) |
|
probably benign |
Het |
Gm12728 |
T |
A |
4: 105,651,486 (GRCm39) |
L32Q |
probably damaging |
Het |
Gpatch4 |
A |
G |
3: 87,959,003 (GRCm39) |
N35D |
probably damaging |
Het |
Grid2 |
G |
T |
6: 64,252,854 (GRCm39) |
V441L |
possibly damaging |
Het |
H2-M2 |
A |
G |
17: 37,792,361 (GRCm39) |
|
probably null |
Het |
Hip1r |
T |
C |
5: 124,129,829 (GRCm39) |
F180L |
probably benign |
Het |
Il17re |
T |
C |
6: 113,439,332 (GRCm39) |
F81L |
probably benign |
Het |
Il3ra |
T |
C |
14: 14,350,691 (GRCm38) |
V235A |
possibly damaging |
Het |
Krtap6-2 |
C |
T |
16: 89,216,761 (GRCm39) |
G69S |
unknown |
Het |
Lmln |
T |
C |
16: 32,909,738 (GRCm39) |
L373P |
probably damaging |
Het |
Lmo7 |
C |
A |
14: 102,139,551 (GRCm39) |
Q945K |
probably benign |
Het |
Loxhd1 |
G |
T |
18: 77,383,547 (GRCm39) |
V149L |
possibly damaging |
Het |
Lrrc73 |
T |
C |
17: 46,566,709 (GRCm39) |
|
probably null |
Het |
Mapkapk5 |
G |
A |
5: 121,675,234 (GRCm39) |
H112Y |
possibly damaging |
Het |
Maz |
A |
G |
7: 126,622,220 (GRCm39) |
V467A |
probably benign |
Het |
Med13l |
T |
G |
5: 118,890,003 (GRCm39) |
V1884G |
probably damaging |
Het |
Nlrp12 |
A |
C |
7: 3,271,213 (GRCm39) |
N1033K |
probably benign |
Het |
Nos3 |
T |
A |
5: 24,572,613 (GRCm39) |
V184E |
probably damaging |
Het |
Npr2 |
T |
C |
4: 43,647,155 (GRCm39) |
V737A |
probably damaging |
Het |
Nsd1 |
A |
G |
13: 55,361,187 (GRCm39) |
T52A |
probably benign |
Het |
Obscn |
C |
T |
11: 58,919,733 (GRCm39) |
R108Q |
|
Het |
Or4k50-ps1 |
A |
G |
2: 111,522,401 (GRCm39) |
*179W |
probably null |
Het |
Or4x11 |
A |
T |
2: 89,867,528 (GRCm39) |
K88N |
probably damaging |
Het |
Or5t5 |
G |
T |
2: 86,616,565 (GRCm39) |
G164* |
probably null |
Het |
Or5w22 |
T |
C |
2: 87,362,784 (GRCm39) |
S136P |
probably damaging |
Het |
Or6c70 |
T |
C |
10: 129,709,719 (GRCm39) |
I302M |
probably benign |
Het |
Or9a4 |
C |
A |
6: 40,549,240 (GRCm39) |
R307S |
probably benign |
Het |
Ovol2 |
A |
G |
2: 144,159,792 (GRCm39) |
V116A |
probably benign |
Het |
Pcdha5 |
C |
A |
18: 37,095,379 (GRCm39) |
S629R |
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,602,408 (GRCm39) |
M2274L |
probably benign |
Het |
Pdpk1 |
T |
C |
17: 24,320,643 (GRCm39) |
T185A |
probably benign |
Het |
Pip5k1a |
T |
G |
3: 94,981,431 (GRCm39) |
T67P |
probably benign |
Het |
Plat |
G |
T |
8: 23,263,667 (GRCm39) |
V189F |
probably damaging |
Het |
Ppm1a |
C |
T |
12: 72,830,916 (GRCm39) |
S147L |
probably damaging |
Het |
Prim1 |
T |
A |
10: 127,851,885 (GRCm39) |
D52E |
probably damaging |
Het |
Prkab1 |
C |
G |
5: 116,162,221 (GRCm39) |
D30H |
possibly damaging |
Het |
Psma6 |
A |
T |
12: 55,445,613 (GRCm39) |
|
probably benign |
Het |
Psmd2 |
T |
A |
16: 20,473,675 (GRCm39) |
M196K |
probably damaging |
Het |
Ralgapa2 |
G |
T |
2: 146,276,776 (GRCm39) |
T488K |
probably benign |
Het |
Rapgefl1 |
A |
G |
11: 98,741,940 (GRCm39) |
K635E |
probably damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,118,424 (GRCm39) |
I522V |
probably damaging |
Het |
Rcor3 |
C |
A |
1: 191,822,173 (GRCm39) |
G8V |
probably damaging |
Het |
Rgs11 |
G |
A |
17: 26,426,734 (GRCm39) |
V289M |
probably damaging |
Het |
Scmh1 |
T |
C |
4: 120,386,353 (GRCm39) |
L631P |
probably damaging |
Het |
Sema3e |
T |
G |
5: 14,274,404 (GRCm39) |
D218E |
probably damaging |
Het |
Sh3rf2 |
T |
C |
18: 42,187,091 (GRCm39) |
V70A |
probably damaging |
Het |
Slc12a1 |
G |
T |
2: 125,047,960 (GRCm39) |
V801L |
probably benign |
Het |
Slc25a51 |
C |
G |
4: 45,399,765 (GRCm39) |
A142P |
possibly damaging |
Het |
Slc41a1 |
C |
T |
1: 131,758,694 (GRCm39) |
T112I |
probably damaging |
Het |
Slc44a2 |
T |
C |
9: 21,254,511 (GRCm39) |
M264T |
probably benign |
Het |
Snapc1 |
T |
A |
12: 74,015,068 (GRCm39) |
M134K |
probably benign |
Het |
Snrk |
T |
C |
9: 121,986,276 (GRCm39) |
F215S |
probably damaging |
Het |
Stab2 |
T |
C |
10: 86,721,547 (GRCm39) |
E1526G |
probably damaging |
Het |
Tbc1d10a |
C |
A |
11: 4,163,016 (GRCm39) |
Y260* |
probably null |
Het |
Tdrd5 |
A |
T |
1: 156,130,002 (GRCm39) |
L56Q |
probably damaging |
Het |
Tenm2 |
T |
C |
11: 36,755,768 (GRCm39) |
T77A |
probably benign |
Het |
Tmprss11g |
T |
G |
5: 86,644,366 (GRCm39) |
R159S |
possibly damaging |
Het |
Traj38 |
T |
A |
14: 54,418,034 (GRCm39) |
N1K |
|
Het |
Ttn |
A |
G |
2: 76,596,631 (GRCm39) |
I20094T |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,115,693 (GRCm39) |
L64P |
probably damaging |
Het |
Utp20 |
C |
T |
10: 88,634,260 (GRCm39) |
R812Q |
probably benign |
Het |
Vmn2r57 |
C |
A |
7: 41,076,148 (GRCm39) |
V455L |
probably benign |
Het |
Wdcp |
T |
C |
12: 4,900,246 (GRCm39) |
V34A |
probably damaging |
Het |
Zfp27 |
C |
T |
7: 29,594,784 (GRCm39) |
V394I |
probably benign |
Het |
Zfp512b |
T |
C |
2: 181,231,649 (GRCm39) |
H177R |
probably benign |
Het |
Zfp648 |
T |
A |
1: 154,080,783 (GRCm39) |
M314K |
possibly damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,733 (GRCm39) |
I102M |
possibly damaging |
Het |
Zkscan6 |
A |
G |
11: 65,705,189 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ro60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01563:Ro60
|
APN |
1 |
143,637,120 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01578:Ro60
|
APN |
1 |
143,637,038 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02006:Ro60
|
APN |
1 |
143,636,084 (GRCm39) |
splice site |
probably benign |
|
IGL02155:Ro60
|
APN |
1 |
143,637,007 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02219:Ro60
|
APN |
1 |
143,637,013 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02637:Ro60
|
APN |
1 |
143,646,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03013:Ro60
|
APN |
1 |
143,646,446 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Ro60
|
APN |
1 |
143,646,509 (GRCm39) |
missense |
probably benign |
|
R0415:Ro60
|
UTSW |
1 |
143,635,813 (GRCm39) |
missense |
probably benign |
0.00 |
R0443:Ro60
|
UTSW |
1 |
143,641,661 (GRCm39) |
splice site |
probably benign |
|
R0479:Ro60
|
UTSW |
1 |
143,633,489 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1696:Ro60
|
UTSW |
1 |
143,633,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R1728:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1728:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1729:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1729:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1730:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1730:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1739:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1739:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1762:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1762:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1783:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1783:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1784:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1784:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1785:Ro60
|
UTSW |
1 |
143,635,752 (GRCm39) |
missense |
probably benign |
|
R1785:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R1857:Ro60
|
UTSW |
1 |
143,646,488 (GRCm39) |
missense |
probably benign |
0.00 |
R2049:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R2130:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R2131:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R2133:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R2141:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R2142:Ro60
|
UTSW |
1 |
143,635,772 (GRCm39) |
missense |
probably benign |
|
R2372:Ro60
|
UTSW |
1 |
143,646,620 (GRCm39) |
nonsense |
probably null |
|
R2929:Ro60
|
UTSW |
1 |
143,633,616 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4191:Ro60
|
UTSW |
1 |
143,646,524 (GRCm39) |
missense |
probably benign |
0.00 |
R5520:Ro60
|
UTSW |
1 |
143,646,509 (GRCm39) |
missense |
probably benign |
|
R5821:Ro60
|
UTSW |
1 |
143,642,503 (GRCm39) |
missense |
probably benign |
0.09 |
R7658:Ro60
|
UTSW |
1 |
143,646,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Ro60
|
UTSW |
1 |
143,641,517 (GRCm39) |
nonsense |
probably null |
|
R8924:Ro60
|
UTSW |
1 |
143,641,170 (GRCm39) |
critical splice donor site |
probably null |
|
R9079:Ro60
|
UTSW |
1 |
143,641,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|