Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl4 |
A |
G |
3: 95,584,556 (GRCm39) |
S947P |
probably damaging |
Het |
Agl |
T |
A |
3: 116,574,672 (GRCm39) |
H709L |
probably damaging |
Het |
Alpi |
T |
A |
1: 87,027,830 (GRCm39) |
D250V |
probably benign |
Het |
Anapc4 |
A |
G |
5: 53,023,740 (GRCm39) |
S735G |
probably benign |
Het |
Ank1 |
A |
T |
8: 23,594,848 (GRCm39) |
I611L |
probably benign |
Het |
Canx |
A |
G |
11: 50,195,309 (GRCm39) |
V253A |
possibly damaging |
Het |
Cbfa2t3 |
A |
T |
8: 123,361,873 (GRCm39) |
I383N |
probably damaging |
Het |
Ccn3 |
C |
T |
15: 54,612,680 (GRCm39) |
R230C |
possibly damaging |
Het |
Cdc23 |
T |
C |
18: 34,767,513 (GRCm39) |
Y519C |
probably damaging |
Het |
Celsr3 |
T |
A |
9: 108,703,806 (GRCm39) |
N96K |
probably benign |
Het |
Clptm1 |
A |
G |
7: 19,371,072 (GRCm39) |
Y355H |
probably damaging |
Het |
Col6a5 |
C |
T |
9: 105,811,038 (GRCm39) |
S827N |
unknown |
Het |
Cyp21a1 |
G |
T |
17: 35,022,420 (GRCm39) |
|
probably null |
Het |
Cyp24a1 |
T |
G |
2: 170,327,886 (GRCm39) |
H452P |
probably damaging |
Het |
Cyp2c39 |
T |
A |
19: 39,552,295 (GRCm39) |
H329Q |
probably benign |
Het |
D630003M21Rik |
C |
T |
2: 158,058,664 (GRCm39) |
R412Q |
probably benign |
Het |
Dennd1b |
G |
A |
1: 139,029,767 (GRCm39) |
R308Q |
possibly damaging |
Het |
Deup1 |
T |
C |
9: 15,519,096 (GRCm39) |
S137G |
possibly damaging |
Het |
Dmbt1 |
T |
A |
7: 130,712,778 (GRCm39) |
I1583N |
probably damaging |
Het |
Dvl1 |
G |
A |
4: 155,939,609 (GRCm39) |
V320M |
probably damaging |
Het |
Elmod3 |
A |
G |
6: 72,546,299 (GRCm39) |
S254P |
probably damaging |
Het |
Emsy |
G |
A |
7: 98,286,473 (GRCm39) |
Q226* |
probably null |
Het |
Ephb6 |
C |
A |
6: 41,591,108 (GRCm39) |
D88E |
probably damaging |
Het |
Exoc1 |
A |
G |
5: 76,690,005 (GRCm39) |
M182V |
possibly damaging |
Het |
Fbxw4 |
T |
G |
19: 45,580,160 (GRCm39) |
|
probably benign |
Het |
Fgr |
A |
G |
4: 132,713,577 (GRCm39) |
D35G |
probably damaging |
Het |
Gm20547 |
A |
T |
17: 35,080,008 (GRCm39) |
D366E |
probably damaging |
Het |
Gucy1a1 |
T |
C |
3: 82,004,988 (GRCm39) |
N599S |
probably damaging |
Het |
Ighg2b |
G |
A |
12: 113,270,298 (GRCm39) |
P240L |
probably damaging |
Het |
Jak3 |
A |
G |
8: 72,138,727 (GRCm39) |
D975G |
probably benign |
Het |
Klhl26 |
A |
T |
8: 70,908,283 (GRCm39) |
N24K |
probably benign |
Het |
Letm1 |
T |
A |
5: 33,918,202 (GRCm39) |
E314D |
probably damaging |
Het |
Lin54 |
A |
T |
5: 100,598,852 (GRCm39) |
F319L |
probably damaging |
Het |
Lrp5 |
A |
T |
19: 3,670,314 (GRCm39) |
|
probably null |
Het |
Lvrn |
T |
C |
18: 47,013,776 (GRCm39) |
F486S |
probably damaging |
Het |
Or1e19 |
T |
C |
11: 73,316,009 (GRCm39) |
T267A |
probably benign |
Het |
Or2h1b |
A |
G |
17: 37,462,534 (GRCm39) |
C110R |
probably damaging |
Het |
Or4c113 |
T |
C |
2: 88,885,357 (GRCm39) |
R138G |
probably benign |
Het |
Or51m1 |
A |
C |
7: 103,578,329 (GRCm39) |
I100L |
probably benign |
Het |
Or8g54 |
A |
T |
9: 39,706,977 (GRCm39) |
Y102F |
probably benign |
Het |
Pramel24 |
A |
G |
4: 143,452,703 (GRCm39) |
T45A |
probably benign |
Het |
Sap30bp |
T |
A |
11: 115,848,214 (GRCm39) |
M112K |
possibly damaging |
Het |
Sbno1 |
A |
G |
5: 124,525,374 (GRCm39) |
|
probably benign |
Het |
Slc30a5 |
T |
C |
13: 100,950,338 (GRCm39) |
I307V |
probably benign |
Het |
Trim37 |
T |
A |
11: 87,080,963 (GRCm39) |
D21E |
probably damaging |
Het |
Usp34 |
T |
C |
11: 23,396,958 (GRCm39) |
F614S |
possibly damaging |
Het |
Vipas39 |
C |
T |
12: 87,300,028 (GRCm39) |
C149Y |
probably damaging |
Het |
Vmn2r107 |
C |
A |
17: 20,595,974 (GRCm39) |
H842Q |
probably benign |
Het |
Vps18 |
T |
A |
2: 119,123,658 (GRCm39) |
V195E |
probably benign |
Het |
Vsx1 |
A |
G |
2: 150,527,510 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Usp39 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00654:Usp39
|
APN |
6 |
72,305,607 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01065:Usp39
|
APN |
6 |
72,316,958 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01669:Usp39
|
APN |
6 |
72,315,476 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03397:Usp39
|
APN |
6 |
72,313,296 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0561:Usp39
|
UTSW |
6 |
72,313,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Usp39
|
UTSW |
6 |
72,315,372 (GRCm39) |
splice site |
probably benign |
|
R3552:Usp39
|
UTSW |
6 |
72,314,815 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4010:Usp39
|
UTSW |
6 |
72,313,468 (GRCm39) |
missense |
probably benign |
0.44 |
R4854:Usp39
|
UTSW |
6 |
72,302,665 (GRCm39) |
missense |
probably benign |
0.29 |
R5502:Usp39
|
UTSW |
6 |
72,305,670 (GRCm39) |
missense |
probably benign |
|
R6868:Usp39
|
UTSW |
6 |
72,314,734 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6887:Usp39
|
UTSW |
6 |
72,310,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Usp39
|
UTSW |
6 |
72,313,413 (GRCm39) |
missense |
probably benign |
0.00 |
R7429:Usp39
|
UTSW |
6 |
72,319,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Usp39
|
UTSW |
6 |
72,319,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Usp39
|
UTSW |
6 |
72,313,251 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7544:Usp39
|
UTSW |
6 |
72,319,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R7548:Usp39
|
UTSW |
6 |
72,321,996 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7741:Usp39
|
UTSW |
6 |
72,315,521 (GRCm39) |
splice site |
probably benign |
|
R8377:Usp39
|
UTSW |
6 |
72,305,657 (GRCm39) |
missense |
probably benign |
0.00 |
R8405:Usp39
|
UTSW |
6 |
72,305,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9333:Usp39
|
UTSW |
6 |
72,314,710 (GRCm39) |
missense |
probably benign |
0.16 |
R9496:Usp39
|
UTSW |
6 |
72,302,759 (GRCm39) |
missense |
probably benign |
0.03 |
|