Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aff4 |
T |
A |
11: 53,259,522 (GRCm39) |
M11K |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,722,324 (GRCm39) |
D88G |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,170,727 (GRCm39) |
E1169G |
probably benign |
Het |
Atp7b |
A |
T |
8: 22,496,403 (GRCm39) |
V865E |
probably damaging |
Het |
Bcl2l13 |
T |
A |
6: 120,825,504 (GRCm39) |
Y13* |
probably null |
Het |
Birc6 |
A |
G |
17: 74,886,751 (GRCm39) |
Q693R |
possibly damaging |
Het |
Ccdc15 |
A |
T |
9: 37,188,773 (GRCm39) |
Y770* |
probably null |
Het |
Cenpf |
T |
C |
1: 189,386,460 (GRCm39) |
E1940G |
probably benign |
Het |
Cep295 |
C |
T |
9: 15,252,179 (GRCm39) |
E397K |
probably damaging |
Het |
Cmya5 |
A |
G |
13: 93,233,825 (GRCm39) |
V421A |
probably benign |
Het |
Cnnm1 |
A |
T |
19: 43,460,352 (GRCm39) |
Y698F |
possibly damaging |
Het |
Cnst |
C |
T |
1: 179,437,957 (GRCm39) |
T507I |
probably benign |
Het |
Coq8a |
T |
C |
1: 180,009,794 (GRCm39) |
M4V |
probably benign |
Het |
Csmd3 |
A |
G |
15: 48,485,485 (GRCm39) |
L140P |
probably damaging |
Het |
Cul2 |
A |
T |
18: 3,426,851 (GRCm39) |
I431F |
probably damaging |
Het |
Dnah8 |
G |
T |
17: 30,988,625 (GRCm39) |
E3198D |
probably benign |
Het |
Dnai3 |
C |
A |
3: 145,803,017 (GRCm39) |
R58L |
possibly damaging |
Het |
Epn2 |
T |
A |
11: 61,437,237 (GRCm39) |
I112F |
possibly damaging |
Het |
Ext2 |
T |
C |
2: 93,560,570 (GRCm39) |
E532G |
probably damaging |
Het |
Fndc3a |
A |
T |
14: 72,889,521 (GRCm39) |
V37E |
probably damaging |
Het |
Gabbr2 |
A |
G |
4: 46,677,603 (GRCm39) |
F759S |
possibly damaging |
Het |
Ghr |
G |
A |
15: 3,349,723 (GRCm39) |
P485L |
probably benign |
Het |
Glipr1l2 |
G |
T |
10: 111,928,470 (GRCm39) |
V122L |
probably benign |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably benign |
Het |
Gm6871 |
G |
T |
7: 41,195,876 (GRCm39) |
T287K |
probably damaging |
Het |
Gm7275 |
A |
G |
16: 47,894,120 (GRCm39) |
|
noncoding transcript |
Het |
Hephl1 |
C |
T |
9: 15,001,364 (GRCm39) |
V254I |
probably damaging |
Het |
Hnf4a |
C |
A |
2: 163,408,259 (GRCm39) |
Q362K |
possibly damaging |
Het |
Kcne3 |
C |
T |
7: 99,833,631 (GRCm39) |
R83C |
probably damaging |
Het |
Klb |
C |
A |
5: 65,533,204 (GRCm39) |
N504K |
probably damaging |
Het |
Loxl2 |
T |
A |
14: 69,929,851 (GRCm39) |
I743N |
possibly damaging |
Het |
Lrrc9 |
A |
T |
12: 72,502,891 (GRCm39) |
L287F |
probably damaging |
Het |
Mcm3ap |
C |
T |
10: 76,320,508 (GRCm39) |
P822L |
possibly damaging |
Het |
Nacc2 |
T |
C |
2: 25,950,155 (GRCm39) |
N527S |
probably benign |
Het |
Ncam1 |
G |
T |
9: 49,468,445 (GRCm39) |
P338H |
probably damaging |
Het |
Nfkbiz |
G |
T |
16: 55,636,757 (GRCm39) |
Q515K |
possibly damaging |
Het |
Nipsnap2 |
T |
C |
5: 129,834,149 (GRCm39) |
L263P |
probably damaging |
Het |
Nlrp1a |
A |
T |
11: 71,015,032 (GRCm39) |
S73T |
probably benign |
Het |
Nomo1 |
G |
A |
7: 45,719,461 (GRCm39) |
|
probably null |
Het |
Nos3 |
G |
A |
5: 24,582,310 (GRCm39) |
G594D |
probably benign |
Het |
Oprm1 |
A |
G |
10: 6,780,105 (GRCm39) |
I256V |
probably damaging |
Het |
Or10ak16 |
A |
G |
4: 118,750,723 (GRCm39) |
T148A |
probably benign |
Het |
Or10n1 |
A |
T |
9: 39,524,916 (GRCm39) |
T18S |
possibly damaging |
Het |
Or2b2 |
A |
G |
13: 21,887,620 (GRCm39) |
I150V |
probably benign |
Het |
Oxct2a |
A |
T |
4: 123,217,309 (GRCm39) |
L24Q |
possibly damaging |
Het |
Pcdhb14 |
T |
G |
18: 37,581,231 (GRCm39) |
S112R |
probably benign |
Het |
Polr2a |
A |
G |
11: 69,630,329 (GRCm39) |
I1246T |
probably damaging |
Het |
Ppil4 |
A |
T |
10: 7,683,145 (GRCm39) |
K327N |
probably damaging |
Het |
Pramel30 |
T |
C |
4: 144,059,575 (GRCm39) |
S429P |
probably benign |
Het |
Pstpip1 |
T |
C |
9: 56,033,214 (GRCm39) |
Y249H |
probably damaging |
Het |
Qrsl1 |
A |
T |
10: 43,757,511 (GRCm39) |
V369E |
probably damaging |
Het |
Ranbp10 |
G |
T |
8: 106,506,610 (GRCm39) |
P237T |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,567,110 (GRCm39) |
N1097S |
probably damaging |
Het |
Repin1 |
T |
A |
6: 48,574,684 (GRCm39) |
S538T |
probably damaging |
Het |
Rims2 |
A |
T |
15: 39,543,046 (GRCm39) |
M1151L |
probably benign |
Het |
Rin3 |
T |
A |
12: 102,356,355 (GRCm39) |
D965E |
possibly damaging |
Het |
Sdc2 |
A |
G |
15: 33,028,224 (GRCm39) |
D114G |
probably benign |
Het |
Slc25a30 |
C |
A |
14: 76,012,523 (GRCm39) |
A42S |
probably benign |
Het |
Sphkap |
G |
A |
1: 83,255,236 (GRCm39) |
R838* |
probably null |
Het |
Ssh2 |
T |
A |
11: 77,328,582 (GRCm39) |
F383I |
probably damaging |
Het |
St8sia1 |
A |
T |
6: 142,774,742 (GRCm39) |
V279E |
probably damaging |
Het |
Tacc2 |
C |
A |
7: 130,228,328 (GRCm39) |
S1690* |
probably null |
Het |
Taf1b |
A |
G |
12: 24,597,177 (GRCm39) |
D372G |
possibly damaging |
Het |
Timm21 |
G |
C |
18: 84,967,387 (GRCm39) |
L130V |
probably damaging |
Het |
Tmem165 |
G |
T |
5: 76,355,673 (GRCm39) |
G272C |
probably damaging |
Het |
Tsc22d2 |
TCAGTTAACACCTATGAACAGT |
TCAGT |
3: 58,324,960 (GRCm39) |
|
probably null |
Het |
Tssk4 |
C |
A |
14: 55,888,488 (GRCm39) |
A119D |
probably damaging |
Het |
Usp9y |
A |
G |
Y: 1,316,727 (GRCm39) |
Y1941H |
probably damaging |
Het |
Vmn2r42 |
A |
T |
7: 8,187,264 (GRCm39) |
M786K |
probably benign |
Het |
Wdfy3 |
G |
T |
5: 101,991,931 (GRCm39) |
T3470K |
probably benign |
Het |
Zc3h14 |
T |
C |
12: 98,745,448 (GRCm39) |
V479A |
probably benign |
Het |
Zfp821 |
G |
A |
8: 110,450,796 (GRCm39) |
R263Q |
probably damaging |
Het |
|
Other mutations in Bub1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00765:Bub1
|
APN |
2 |
127,671,392 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00795:Bub1
|
APN |
2 |
127,663,735 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00966:Bub1
|
APN |
2 |
127,652,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01807:Bub1
|
APN |
2 |
127,654,897 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02212:Bub1
|
APN |
2 |
127,647,271 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02537:Bub1
|
APN |
2 |
127,643,267 (GRCm39) |
nonsense |
probably null |
|
IGL02935:Bub1
|
APN |
2 |
127,643,215 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03064:Bub1
|
APN |
2 |
127,659,373 (GRCm39) |
missense |
probably benign |
0.00 |
R0052:Bub1
|
UTSW |
2 |
127,650,959 (GRCm39) |
missense |
probably benign |
0.10 |
R0052:Bub1
|
UTSW |
2 |
127,650,959 (GRCm39) |
missense |
probably benign |
0.10 |
R0325:Bub1
|
UTSW |
2 |
127,643,314 (GRCm39) |
nonsense |
probably null |
|
R1502:Bub1
|
UTSW |
2 |
127,669,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R1627:Bub1
|
UTSW |
2 |
127,650,933 (GRCm39) |
missense |
probably benign |
0.01 |
R1778:Bub1
|
UTSW |
2 |
127,645,042 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2043:Bub1
|
UTSW |
2 |
127,646,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Bub1
|
UTSW |
2 |
127,661,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R2165:Bub1
|
UTSW |
2 |
127,643,201 (GRCm39) |
missense |
probably benign |
0.01 |
R2190:Bub1
|
UTSW |
2 |
127,652,645 (GRCm39) |
missense |
probably benign |
0.06 |
R2507:Bub1
|
UTSW |
2 |
127,643,343 (GRCm39) |
missense |
probably benign |
0.04 |
R2508:Bub1
|
UTSW |
2 |
127,643,343 (GRCm39) |
missense |
probably benign |
0.04 |
R3836:Bub1
|
UTSW |
2 |
127,656,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R3862:Bub1
|
UTSW |
2 |
127,656,676 (GRCm39) |
splice site |
probably benign |
|
R3904:Bub1
|
UTSW |
2 |
127,663,862 (GRCm39) |
missense |
probably benign |
0.08 |
R4373:Bub1
|
UTSW |
2 |
127,647,156 (GRCm39) |
intron |
probably benign |
|
R4580:Bub1
|
UTSW |
2 |
127,671,596 (GRCm39) |
critical splice donor site |
probably null |
|
R4751:Bub1
|
UTSW |
2 |
127,665,858 (GRCm39) |
intron |
probably benign |
|
R5239:Bub1
|
UTSW |
2 |
127,663,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Bub1
|
UTSW |
2 |
127,656,629 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5591:Bub1
|
UTSW |
2 |
127,661,263 (GRCm39) |
missense |
probably benign |
0.16 |
R5672:Bub1
|
UTSW |
2 |
127,646,800 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5907:Bub1
|
UTSW |
2 |
127,661,142 (GRCm39) |
missense |
probably benign |
0.02 |
R6714:Bub1
|
UTSW |
2 |
127,656,652 (GRCm39) |
missense |
probably benign |
0.08 |
R6781:Bub1
|
UTSW |
2 |
127,649,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R6931:Bub1
|
UTSW |
2 |
127,643,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7057:Bub1
|
UTSW |
2 |
127,671,447 (GRCm39) |
missense |
probably benign |
|
R7094:Bub1
|
UTSW |
2 |
127,663,681 (GRCm39) |
missense |
probably null |
0.99 |
R8197:Bub1
|
UTSW |
2 |
127,643,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Bub1
|
UTSW |
2 |
127,649,750 (GRCm39) |
missense |
probably benign |
0.00 |
R8463:Bub1
|
UTSW |
2 |
127,659,353 (GRCm39) |
missense |
probably benign |
0.30 |
R8725:Bub1
|
UTSW |
2 |
127,646,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Bub1
|
UTSW |
2 |
127,646,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8840:Bub1
|
UTSW |
2 |
127,649,927 (GRCm39) |
missense |
probably benign |
0.01 |
R8904:Bub1
|
UTSW |
2 |
127,671,622 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9187:Bub1
|
UTSW |
2 |
127,656,856 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9624:Bub1
|
UTSW |
2 |
127,646,766 (GRCm39) |
missense |
probably damaging |
0.96 |
R9727:Bub1
|
UTSW |
2 |
127,652,609 (GRCm39) |
missense |
possibly damaging |
0.61 |
Z1176:Bub1
|
UTSW |
2 |
127,671,485 (GRCm39) |
missense |
probably damaging |
1.00 |
|