Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
G |
3: 59,659,444 (GRCm39) |
E299G |
probably damaging |
Het |
Adamtsl4 |
C |
A |
3: 95,587,473 (GRCm39) |
R701L |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,761,890 (GRCm39) |
V1195A |
probably damaging |
Het |
Agpat5 |
A |
G |
8: 18,931,878 (GRCm39) |
T333A |
possibly damaging |
Het |
Aspm |
G |
T |
1: 139,392,033 (GRCm39) |
G795C |
probably damaging |
Het |
Car4 |
C |
A |
11: 84,856,626 (GRCm39) |
Q305K |
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,894,672 (GRCm39) |
N612S |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,726,511 (GRCm39) |
R354W |
probably damaging |
Het |
Cdh9 |
G |
A |
15: 16,851,099 (GRCm39) |
V623I |
probably benign |
Het |
Cfap65 |
A |
G |
1: 74,964,061 (GRCm39) |
V629A |
probably benign |
Het |
Chd1 |
G |
A |
17: 15,956,005 (GRCm39) |
V535I |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,585,329 (GRCm39) |
V1316A |
probably damaging |
Het |
Col6a3 |
A |
T |
1: 90,712,965 (GRCm39) |
D1721E |
unknown |
Het |
Cop1 |
T |
A |
1: 159,154,734 (GRCm39) |
F647L |
probably damaging |
Het |
Corin |
A |
C |
5: 72,500,362 (GRCm39) |
S421A |
probably damaging |
Het |
Crb2 |
T |
C |
2: 37,680,833 (GRCm39) |
V587A |
probably damaging |
Het |
Ctc1 |
T |
A |
11: 68,920,636 (GRCm39) |
V646E |
possibly damaging |
Het |
Cyp2a12 |
A |
T |
7: 26,730,643 (GRCm39) |
M203L |
probably benign |
Het |
Dcdc2c |
T |
A |
12: 28,566,656 (GRCm39) |
K336M |
possibly damaging |
Het |
Ddx39a |
G |
A |
8: 84,448,950 (GRCm39) |
R275H |
probably benign |
Het |
Dennd2b |
A |
G |
7: 109,156,519 (GRCm39) |
L77P |
probably benign |
Het |
Des |
A |
G |
1: 75,339,572 (GRCm39) |
N310S |
possibly damaging |
Het |
Dlk1 |
C |
A |
12: 109,425,764 (GRCm39) |
S212R |
probably benign |
Het |
Dnajc5b |
A |
G |
3: 19,633,224 (GRCm39) |
E149G |
probably benign |
Het |
Dpep1 |
A |
T |
8: 123,920,828 (GRCm39) |
I3F |
probably benign |
Het |
Eml6 |
T |
A |
11: 29,753,108 (GRCm39) |
R934S |
probably benign |
Het |
Ercc6l2 |
T |
C |
13: 64,016,925 (GRCm39) |
L676P |
possibly damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,560,575 (GRCm39) |
I1311F |
probably damaging |
Het |
Gldc |
T |
A |
19: 30,123,125 (GRCm39) |
M257L |
probably damaging |
Het |
Gm8674 |
T |
G |
13: 50,055,390 (GRCm39) |
|
noncoding transcript |
Het |
Gnai3 |
C |
T |
3: 108,030,857 (GRCm39) |
|
probably null |
Het |
Gtf3a |
A |
G |
5: 146,891,965 (GRCm39) |
D300G |
probably damaging |
Het |
Haus3 |
A |
T |
5: 34,323,449 (GRCm39) |
V387D |
probably damaging |
Het |
Hpf1 |
T |
A |
8: 61,346,768 (GRCm39) |
F28I |
possibly damaging |
Het |
Iars1 |
A |
G |
13: 49,843,967 (GRCm39) |
D147G |
probably damaging |
Het |
Ibtk |
A |
T |
9: 85,625,743 (GRCm39) |
D2E |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,239,601 (GRCm39) |
I86K |
possibly damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,898,241 (GRCm39) |
I235F |
probably damaging |
Het |
Ighv3-8 |
G |
T |
12: 114,286,252 (GRCm39) |
A30E |
probably benign |
Het |
Kcnq5 |
T |
A |
1: 21,575,949 (GRCm39) |
T252S |
probably damaging |
Het |
Lrrc4b |
A |
T |
7: 44,110,787 (GRCm39) |
N220Y |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Mamdc4 |
T |
C |
2: 25,454,702 (GRCm39) |
T1037A |
possibly damaging |
Het |
Mbd5 |
A |
T |
2: 49,162,106 (GRCm39) |
I863F |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,570,484 (GRCm39) |
S515T |
possibly damaging |
Het |
Mylk4 |
T |
A |
13: 32,892,864 (GRCm39) |
|
probably null |
Het |
Neu4 |
G |
A |
1: 93,952,669 (GRCm39) |
R346H |
probably benign |
Het |
Nxpe5 |
T |
A |
5: 138,238,200 (GRCm39) |
Y253* |
probably null |
Het |
Olfml2b |
A |
T |
1: 170,477,330 (GRCm39) |
E155V |
probably damaging |
Het |
Or14a258 |
A |
G |
7: 86,034,867 (GRCm39) |
*334Q |
probably null |
Het |
Or6a2 |
T |
A |
7: 106,600,111 (GRCm39) |
N319Y |
probably benign |
Het |
Or8a1b |
T |
A |
9: 37,623,300 (GRCm39) |
I92F |
probably damaging |
Het |
Pamr1 |
G |
A |
2: 102,417,029 (GRCm39) |
A114T |
probably damaging |
Het |
Pdzd2 |
T |
A |
15: 12,592,263 (GRCm39) |
N127I |
probably damaging |
Het |
Pglyrp4 |
C |
T |
3: 90,634,271 (GRCm39) |
L5F |
probably damaging |
Het |
Plce1 |
T |
A |
19: 38,747,279 (GRCm39) |
S1667T |
possibly damaging |
Het |
Qser1 |
A |
T |
2: 104,617,776 (GRCm39) |
V1012E |
possibly damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
Rcn3 |
A |
T |
7: 44,736,203 (GRCm39) |
D168E |
probably damaging |
Het |
Rdh1 |
T |
G |
10: 127,595,832 (GRCm39) |
V9G |
possibly damaging |
Het |
Rin2 |
A |
G |
2: 145,686,680 (GRCm39) |
T70A |
probably benign |
Het |
Rnf207 |
T |
C |
4: 152,398,346 (GRCm39) |
D276G |
probably damaging |
Het |
Rtel1 |
C |
T |
2: 180,982,354 (GRCm39) |
S368L |
probably benign |
Het |
Slc15a5 |
C |
A |
6: 138,056,751 (GRCm39) |
C55F |
probably damaging |
Het |
Slc36a4 |
T |
C |
9: 15,638,212 (GRCm39) |
F213L |
possibly damaging |
Het |
Snhg16 |
G |
T |
11: 116,562,582 (GRCm39) |
M18I |
probably benign |
Het |
Spata25 |
C |
T |
2: 164,669,954 (GRCm39) |
G19D |
probably damaging |
Het |
Tas2r102 |
A |
T |
6: 132,739,360 (GRCm39) |
L89F |
probably damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,481,910 (GRCm39) |
K704E |
probably damaging |
Het |
Tert |
T |
G |
13: 73,775,473 (GRCm39) |
S75A |
probably damaging |
Het |
Tiparp |
T |
A |
3: 65,454,986 (GRCm39) |
L195Q |
possibly damaging |
Het |
Tmem205 |
A |
C |
9: 21,837,380 (GRCm39) |
Y57* |
probably null |
Het |
Tomm22 |
A |
G |
15: 79,555,428 (GRCm39) |
R5G |
probably benign |
Het |
Trav10 |
A |
T |
14: 53,743,515 (GRCm39) |
S39C |
probably benign |
Het |
Trav6-2 |
T |
A |
14: 52,905,205 (GRCm39) |
N75K |
probably benign |
Het |
Trio |
T |
C |
15: 27,748,372 (GRCm39) |
S2427G |
probably benign |
Het |
Ttc41 |
C |
A |
10: 86,580,342 (GRCm39) |
H763N |
possibly damaging |
Het |
Vmn1r204 |
G |
T |
13: 22,740,912 (GRCm39) |
W181L |
probably damaging |
Het |
Vmn2r76 |
G |
A |
7: 85,875,267 (GRCm39) |
T570M |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,069,819 (GRCm39) |
L1173P |
probably damaging |
Het |
Wnt9a |
T |
A |
11: 59,219,396 (GRCm39) |
C141S |
probably damaging |
Het |
Zfp462 |
A |
T |
4: 55,012,299 (GRCm39) |
I1422L |
probably benign |
Het |
|
Other mutations in Usp29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00659:Usp29
|
APN |
7 |
6,965,281 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01588:Usp29
|
APN |
7 |
6,965,610 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02032:Usp29
|
APN |
7 |
6,965,017 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02052:Usp29
|
APN |
7 |
6,965,525 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02331:Usp29
|
APN |
7 |
6,965,155 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02551:Usp29
|
APN |
7 |
6,966,352 (GRCm39) |
splice site |
probably null |
|
IGL02573:Usp29
|
APN |
7 |
6,965,617 (GRCm39) |
splice site |
probably null |
|
IGL02894:Usp29
|
APN |
7 |
6,964,633 (GRCm39) |
missense |
probably benign |
0.00 |
R0029:Usp29
|
UTSW |
7 |
6,964,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R0142:Usp29
|
UTSW |
7 |
6,965,334 (GRCm39) |
missense |
probably benign |
0.12 |
R0452:Usp29
|
UTSW |
7 |
6,966,181 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0680:Usp29
|
UTSW |
7 |
6,965,884 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1161:Usp29
|
UTSW |
7 |
6,964,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R2391:Usp29
|
UTSW |
7 |
6,966,770 (GRCm39) |
splice site |
probably null |
|
R3104:Usp29
|
UTSW |
7 |
6,965,052 (GRCm39) |
nonsense |
probably null |
|
R4119:Usp29
|
UTSW |
7 |
6,965,805 (GRCm39) |
missense |
probably benign |
0.03 |
R4490:Usp29
|
UTSW |
7 |
6,964,949 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4598:Usp29
|
UTSW |
7 |
6,965,479 (GRCm39) |
missense |
probably benign |
0.06 |
R4606:Usp29
|
UTSW |
7 |
6,966,356 (GRCm39) |
splice site |
probably null |
|
R4670:Usp29
|
UTSW |
7 |
6,965,914 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4777:Usp29
|
UTSW |
7 |
6,965,747 (GRCm39) |
missense |
probably benign |
0.07 |
R4783:Usp29
|
UTSW |
7 |
6,964,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Usp29
|
UTSW |
7 |
6,964,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4896:Usp29
|
UTSW |
7 |
6,965,158 (GRCm39) |
missense |
probably benign |
0.29 |
R4915:Usp29
|
UTSW |
7 |
6,964,504 (GRCm39) |
missense |
probably benign |
|
R4944:Usp29
|
UTSW |
7 |
6,964,927 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5004:Usp29
|
UTSW |
7 |
6,965,158 (GRCm39) |
missense |
probably benign |
0.29 |
R5171:Usp29
|
UTSW |
7 |
6,965,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R5572:Usp29
|
UTSW |
7 |
6,965,191 (GRCm39) |
missense |
probably benign |
0.12 |
R5933:Usp29
|
UTSW |
7 |
6,964,744 (GRCm39) |
missense |
probably benign |
|
R6694:Usp29
|
UTSW |
7 |
6,965,276 (GRCm39) |
missense |
probably benign |
0.03 |
R7389:Usp29
|
UTSW |
7 |
6,966,457 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7446:Usp29
|
UTSW |
7 |
6,964,219 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7447:Usp29
|
UTSW |
7 |
6,964,219 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7535:Usp29
|
UTSW |
7 |
6,964,219 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7537:Usp29
|
UTSW |
7 |
6,964,219 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8081:Usp29
|
UTSW |
7 |
6,966,629 (GRCm39) |
missense |
probably benign |
0.02 |
R8233:Usp29
|
UTSW |
7 |
6,965,406 (GRCm39) |
missense |
probably benign |
0.12 |
R8703:Usp29
|
UTSW |
7 |
6,964,321 (GRCm39) |
missense |
probably benign |
0.32 |
R8725:Usp29
|
UTSW |
7 |
6,965,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R8727:Usp29
|
UTSW |
7 |
6,965,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R8844:Usp29
|
UTSW |
7 |
6,964,891 (GRCm39) |
missense |
probably benign |
0.02 |
R9173:Usp29
|
UTSW |
7 |
6,964,636 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9616:Usp29
|
UTSW |
7 |
6,966,179 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9623:Usp29
|
UTSW |
7 |
6,964,396 (GRCm39) |
missense |
possibly damaging |
0.60 |
|