Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,793,587 (GRCm39) |
M1T |
probably null |
Het |
Akap3 |
T |
C |
6: 126,842,226 (GRCm39) |
S282P |
probably damaging |
Het |
Anxa10 |
A |
G |
8: 62,516,054 (GRCm39) |
I206T |
probably damaging |
Het |
Apobec3 |
A |
G |
15: 79,779,713 (GRCm39) |
D52G |
probably damaging |
Het |
Arl6 |
A |
T |
16: 59,439,228 (GRCm39) |
|
probably null |
Het |
Calcoco1 |
T |
C |
15: 102,626,329 (GRCm39) |
E87G |
probably damaging |
Het |
Ccdc88b |
C |
A |
19: 6,825,636 (GRCm39) |
A1206S |
probably damaging |
Het |
Ccpg1 |
A |
G |
9: 72,923,197 (GRCm39) |
|
probably benign |
Het |
Cdon |
A |
G |
9: 35,389,901 (GRCm39) |
N852D |
probably damaging |
Het |
Cobl |
T |
A |
11: 12,336,665 (GRCm39) |
Q41L |
possibly damaging |
Het |
Cspg4b |
A |
G |
13: 113,516,020 (GRCm39) |
T145A |
unknown |
Het |
Dcdc2b |
T |
C |
4: 129,507,936 (GRCm39) |
T39A |
probably damaging |
Het |
Ddx55 |
A |
T |
5: 124,705,997 (GRCm39) |
D474V |
probably benign |
Het |
Dipk2a |
A |
T |
9: 94,402,457 (GRCm39) |
C402S |
probably damaging |
Het |
Dnah17 |
A |
G |
11: 118,010,640 (GRCm39) |
L521P |
probably damaging |
Het |
Exoc1 |
A |
G |
5: 76,707,010 (GRCm39) |
D497G |
probably null |
Het |
Fam151a |
A |
G |
4: 106,605,456 (GRCm39) |
E606G |
possibly damaging |
Het |
Fbxw11 |
T |
A |
11: 32,692,535 (GRCm39) |
L502* |
probably null |
Het |
Fcrl1 |
A |
G |
3: 87,297,563 (GRCm39) |
S337G |
possibly damaging |
Het |
G6pc1 |
C |
A |
11: 101,267,439 (GRCm39) |
F296L |
probably benign |
Het |
Gm17472 |
C |
A |
6: 42,957,809 (GRCm39) |
T26N |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,751,870 (GRCm39) |
V564A |
probably benign |
Het |
H2-Ob |
T |
C |
17: 34,461,618 (GRCm39) |
I119T |
probably benign |
Het |
Hhip |
A |
G |
8: 80,771,726 (GRCm39) |
Y195H |
probably damaging |
Het |
Igkc |
A |
T |
6: 70,703,662 (GRCm39) |
|
probably benign |
Het |
Islr |
A |
T |
9: 58,064,642 (GRCm39) |
D288E |
probably damaging |
Het |
Kdelr1 |
A |
G |
7: 45,523,197 (GRCm39) |
S36G |
probably benign |
Het |
Lama5 |
G |
T |
2: 179,821,159 (GRCm39) |
H3134Q |
possibly damaging |
Het |
Loricrin |
A |
G |
3: 91,989,050 (GRCm39) |
Y79H |
unknown |
Het |
Lrp1b |
A |
G |
2: 40,691,496 (GRCm39) |
F3327S |
probably damaging |
Het |
Lrrc41 |
C |
T |
4: 115,952,332 (GRCm39) |
H637Y |
probably benign |
Het |
Map2k6 |
C |
T |
11: 110,290,220 (GRCm39) |
|
probably benign |
Het |
Mcm3ap |
T |
G |
10: 76,306,404 (GRCm39) |
F172L |
probably damaging |
Het |
Muc19 |
G |
A |
15: 91,772,411 (GRCm39) |
|
noncoding transcript |
Het |
Muc21 |
T |
A |
17: 35,930,599 (GRCm39) |
|
probably benign |
Het |
Muc6 |
T |
A |
7: 141,224,212 (GRCm39) |
|
probably benign |
Het |
Nek1 |
A |
T |
8: 61,481,840 (GRCm39) |
I252L |
probably damaging |
Het |
Nrg2 |
A |
T |
18: 36,154,152 (GRCm39) |
H588Q |
possibly damaging |
Het |
Nt5dc2 |
T |
C |
14: 30,860,878 (GRCm39) |
V351A |
possibly damaging |
Het |
Or1j12 |
A |
G |
2: 36,343,062 (GRCm39) |
N155S |
probably benign |
Het |
Or51b17 |
T |
C |
7: 103,542,615 (GRCm39) |
E109G |
probably damaging |
Het |
Or5m5 |
A |
G |
2: 85,814,315 (GRCm39) |
T44A |
possibly damaging |
Het |
Or8k1 |
A |
T |
2: 86,048,032 (GRCm39) |
S7R |
probably benign |
Het |
Pde3a |
A |
G |
6: 141,411,865 (GRCm39) |
N480D |
probably benign |
Het |
Pde6c |
A |
G |
19: 38,145,833 (GRCm39) |
K374E |
probably damaging |
Het |
Pdhx |
G |
A |
2: 102,903,811 (GRCm39) |
|
probably null |
Het |
Pi4ka |
A |
G |
16: 17,100,237 (GRCm39) |
Y1888H |
probably damaging |
Het |
Pnpla2 |
T |
A |
7: 141,038,356 (GRCm39) |
M203K |
probably damaging |
Het |
Prrc2c |
C |
T |
1: 162,532,748 (GRCm39) |
|
probably benign |
Het |
Ptcd3 |
G |
T |
6: 71,870,498 (GRCm39) |
H321N |
probably benign |
Het |
Ptprt |
A |
G |
2: 161,743,366 (GRCm39) |
|
probably null |
Het |
Ptx4 |
A |
G |
17: 25,342,100 (GRCm39) |
T192A |
probably benign |
Het |
Qars1 |
A |
G |
9: 108,386,889 (GRCm39) |
|
probably benign |
Het |
Ralgapa2 |
G |
A |
2: 146,187,387 (GRCm39) |
P1372S |
possibly damaging |
Het |
Rps6ka4 |
G |
T |
19: 6,816,854 (GRCm39) |
T107K |
probably damaging |
Het |
Rsf1 |
A |
G |
7: 97,329,980 (GRCm39) |
T1169A |
possibly damaging |
Het |
Ryr2 |
C |
A |
13: 11,721,553 (GRCm39) |
W2626L |
probably damaging |
Het |
Scn4a |
C |
T |
11: 106,214,788 (GRCm39) |
V1270I |
probably damaging |
Het |
Serpinb9b |
T |
C |
13: 33,223,806 (GRCm39) |
S333P |
probably damaging |
Het |
Sned1 |
A |
G |
1: 93,224,019 (GRCm39) |
|
probably benign |
Het |
Sult1c2 |
C |
T |
17: 54,137,137 (GRCm39) |
V262M |
possibly damaging |
Het |
Tll1 |
A |
T |
8: 64,504,411 (GRCm39) |
F662I |
probably benign |
Het |
Tmem161a |
A |
T |
8: 70,633,597 (GRCm39) |
|
probably null |
Het |
Top1mt |
A |
C |
15: 75,535,907 (GRCm39) |
V465G |
possibly damaging |
Het |
Trcg1 |
A |
G |
9: 57,153,144 (GRCm39) |
K596E |
possibly damaging |
Het |
Trim27 |
T |
A |
13: 21,365,086 (GRCm39) |
|
probably null |
Het |
Trpm3 |
A |
G |
19: 22,964,752 (GRCm39) |
I1406V |
possibly damaging |
Het |
Tssc4 |
T |
A |
7: 142,624,246 (GRCm39) |
S254T |
probably damaging |
Het |
Ttc7 |
C |
A |
17: 87,678,163 (GRCm39) |
|
probably benign |
Het |
Usp48 |
C |
A |
4: 137,343,692 (GRCm39) |
R441S |
probably benign |
Het |
Vmn1r29 |
T |
C |
6: 58,284,285 (GRCm39) |
S2P |
probably benign |
Het |
Vmn2r65 |
T |
A |
7: 84,613,082 (GRCm39) |
I46L |
possibly damaging |
Het |
Zeb1 |
A |
T |
18: 5,766,775 (GRCm39) |
I429F |
probably damaging |
Het |
Zfp943 |
A |
G |
17: 22,212,176 (GRCm39) |
R421G |
probably benign |
Het |
|
Other mutations in Usp30 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03353:Usp30
|
APN |
5 |
114,259,119 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03384:Usp30
|
APN |
5 |
114,259,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:Usp30
|
UTSW |
5 |
114,243,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Usp30
|
UTSW |
5 |
114,249,925 (GRCm39) |
splice site |
probably benign |
|
R1184:Usp30
|
UTSW |
5 |
114,241,888 (GRCm39) |
critical splice donor site |
probably null |
|
R1589:Usp30
|
UTSW |
5 |
114,251,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Usp30
|
UTSW |
5 |
114,259,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Usp30
|
UTSW |
5 |
114,249,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Usp30
|
UTSW |
5 |
114,249,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R2341:Usp30
|
UTSW |
5 |
114,249,241 (GRCm39) |
nonsense |
probably null |
|
R5191:Usp30
|
UTSW |
5 |
114,203,755 (GRCm39) |
start gained |
probably benign |
|
R5956:Usp30
|
UTSW |
5 |
114,257,682 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6730:Usp30
|
UTSW |
5 |
114,241,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Usp30
|
UTSW |
5 |
114,241,821 (GRCm39) |
missense |
probably benign |
0.01 |
R7572:Usp30
|
UTSW |
5 |
114,258,308 (GRCm39) |
missense |
probably benign |
0.15 |
R7653:Usp30
|
UTSW |
5 |
114,259,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Usp30
|
UTSW |
5 |
114,240,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Usp30
|
UTSW |
5 |
114,251,033 (GRCm39) |
nonsense |
probably null |
|
R8063:Usp30
|
UTSW |
5 |
114,238,524 (GRCm39) |
missense |
probably benign |
0.01 |
R8100:Usp30
|
UTSW |
5 |
114,249,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R8393:Usp30
|
UTSW |
5 |
114,259,826 (GRCm39) |
nonsense |
probably null |
|
R9035:Usp30
|
UTSW |
5 |
114,243,877 (GRCm39) |
missense |
probably benign |
0.13 |
|