Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
G |
11: 109,865,471 (GRCm39) |
T329P |
probably damaging |
Het |
Adamts4 |
C |
A |
1: 171,086,559 (GRCm39) |
P784T |
probably damaging |
Het |
Adamts6 |
T |
C |
13: 104,630,145 (GRCm39) |
L1096P |
probably damaging |
Het |
Ap1b1 |
A |
G |
11: 4,990,290 (GRCm39) |
S849G |
probably benign |
Het |
Arap2 |
T |
C |
5: 62,761,747 (GRCm39) |
S1660G |
probably benign |
Het |
Atp10b |
A |
C |
11: 43,121,174 (GRCm39) |
T946P |
probably damaging |
Het |
Brpf1 |
A |
G |
6: 113,299,381 (GRCm39) |
D1103G |
probably damaging |
Het |
Ccdc182 |
A |
G |
11: 88,185,193 (GRCm39) |
E91G |
probably benign |
Het |
Cd200r4 |
C |
T |
16: 44,653,803 (GRCm39) |
T154M |
probably damaging |
Het |
Cdh20 |
A |
G |
1: 104,881,755 (GRCm39) |
T407A |
probably benign |
Het |
Col6a2 |
T |
C |
10: 76,450,512 (GRCm39) |
I140V |
probably benign |
Het |
Csn3 |
C |
A |
5: 88,077,983 (GRCm39) |
T163K |
probably damaging |
Het |
Dars2 |
A |
T |
1: 160,874,375 (GRCm39) |
L438* |
probably null |
Het |
Dbr1 |
T |
C |
9: 99,464,440 (GRCm39) |
L289P |
probably damaging |
Het |
Ddx46 |
A |
G |
13: 55,811,122 (GRCm39) |
R573G |
possibly damaging |
Het |
Defb10 |
T |
C |
8: 22,348,972 (GRCm39) |
I10T |
possibly damaging |
Het |
Dis3l |
T |
C |
9: 64,233,069 (GRCm39) |
E136G |
possibly damaging |
Het |
Dnajb13 |
T |
C |
7: 100,156,668 (GRCm39) |
Q136R |
probably benign |
Het |
Dse |
A |
T |
10: 34,029,214 (GRCm39) |
S625R |
probably damaging |
Het |
Dvl3 |
A |
G |
16: 20,342,209 (GRCm39) |
D94G |
probably damaging |
Het |
Dynlt2a2 |
A |
G |
17: 15,187,876 (GRCm39) |
F133L |
probably benign |
Het |
E130311K13Rik |
A |
C |
3: 63,822,968 (GRCm39) |
Y225* |
probably null |
Het |
Etnppl |
A |
G |
3: 130,422,438 (GRCm39) |
I222V |
probably benign |
Het |
Evc2 |
T |
C |
5: 37,550,440 (GRCm39) |
L818P |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,205,626 (GRCm39) |
C1083* |
probably null |
Het |
Flnc |
G |
A |
6: 29,438,693 (GRCm39) |
V196I |
probably benign |
Het |
Fscn3 |
A |
G |
6: 28,435,622 (GRCm39) |
D415G |
probably benign |
Het |
Gm4861 |
A |
C |
3: 137,256,381 (GRCm39) |
V75G |
probably damaging |
Het |
Gpld1 |
A |
T |
13: 25,155,399 (GRCm39) |
T345S |
probably benign |
Het |
Grik4 |
T |
C |
9: 42,432,169 (GRCm39) |
S943G |
probably damaging |
Het |
Grik4 |
C |
T |
9: 42,502,743 (GRCm39) |
R460Q |
probably benign |
Het |
Ifi207 |
A |
C |
1: 173,556,872 (GRCm39) |
L629R |
possibly damaging |
Het |
Ift52 |
G |
A |
2: 162,871,782 (GRCm39) |
|
probably null |
Het |
Insl3 |
A |
G |
8: 72,142,876 (GRCm39) |
D79G |
probably damaging |
Het |
Kif5a |
A |
T |
10: 127,081,310 (GRCm39) |
I208N |
probably damaging |
Het |
Lag3 |
T |
C |
6: 124,886,206 (GRCm39) |
Y249C |
probably damaging |
Het |
Lipe |
T |
C |
7: 25,097,572 (GRCm39) |
N124D |
possibly damaging |
Het |
Lnpep |
A |
G |
17: 17,791,906 (GRCm39) |
Y412H |
probably damaging |
Het |
Lrtm2 |
A |
G |
6: 119,294,235 (GRCm39) |
Y299H |
probably benign |
Het |
Lypd4 |
T |
C |
7: 24,566,253 (GRCm39) |
T24A |
probably benign |
Het |
Magi1 |
T |
A |
6: 93,671,151 (GRCm39) |
I805F |
probably damaging |
Het |
Mfap3 |
T |
C |
11: 57,418,975 (GRCm39) |
L45P |
probably benign |
Het |
Nbea |
G |
A |
3: 55,912,310 (GRCm39) |
P1159L |
probably benign |
Het |
Ndst4 |
A |
T |
3: 125,231,407 (GRCm39) |
|
probably benign |
Het |
Notch1 |
A |
T |
2: 26,374,335 (GRCm39) |
N229K |
possibly damaging |
Het |
Nova1 |
A |
G |
12: 46,767,615 (GRCm39) |
I102T |
unknown |
Het |
Npepps |
T |
C |
11: 97,109,401 (GRCm39) |
E725G |
possibly damaging |
Het |
Or11g27 |
A |
T |
14: 50,771,234 (GRCm39) |
M122L |
possibly damaging |
Het |
Or13a1 |
T |
C |
6: 116,471,242 (GRCm39) |
I224T |
probably damaging |
Het |
Or5l14 |
T |
C |
2: 87,792,379 (GRCm39) |
N286D |
probably damaging |
Het |
Or6c69c |
T |
C |
10: 129,910,741 (GRCm39) |
I154T |
probably damaging |
Het |
Pappa2 |
A |
T |
1: 158,784,858 (GRCm39) |
W51R |
probably damaging |
Het |
Pde8a |
T |
C |
7: 80,942,007 (GRCm39) |
S149P |
probably damaging |
Het |
Pgap6 |
A |
G |
17: 26,339,290 (GRCm39) |
T535A |
possibly damaging |
Het |
Phkb |
T |
A |
8: 86,785,968 (GRCm39) |
L1052Q |
possibly damaging |
Het |
Pou5f2 |
T |
A |
13: 78,173,370 (GRCm39) |
L104Q |
probably benign |
Het |
Pramel32 |
T |
A |
4: 88,546,269 (GRCm39) |
I358F |
probably benign |
Het |
Psme2b |
A |
T |
11: 48,836,576 (GRCm39) |
W124R |
probably damaging |
Het |
Ptk2b |
G |
A |
14: 66,400,529 (GRCm39) |
S762L |
possibly damaging |
Het |
Ptprs |
T |
C |
17: 56,744,992 (GRCm39) |
N248S |
probably benign |
Het |
Rgs22 |
G |
A |
15: 36,080,997 (GRCm39) |
T705I |
probably damaging |
Het |
Rnf123 |
T |
C |
9: 107,945,709 (GRCm39) |
|
probably null |
Het |
Sel1l2 |
A |
T |
2: 140,231,515 (GRCm39) |
I13N |
probably damaging |
Het |
Slc39a4 |
T |
C |
15: 76,500,793 (GRCm39) |
T57A |
probably benign |
Het |
Smpdl3a |
T |
G |
10: 57,685,187 (GRCm39) |
V319G |
probably damaging |
Het |
Syt9 |
T |
C |
7: 107,035,694 (GRCm39) |
L237P |
probably damaging |
Het |
Tbc1d16 |
G |
T |
11: 119,044,830 (GRCm39) |
A536E |
probably damaging |
Het |
Tcf20 |
T |
C |
15: 82,739,777 (GRCm39) |
D558G |
probably damaging |
Het |
Tdpoz2 |
A |
T |
3: 93,559,453 (GRCm39) |
M173K |
probably benign |
Het |
Tek |
A |
G |
4: 94,669,339 (GRCm39) |
I113M |
probably damaging |
Het |
Tmem50a |
A |
T |
4: 134,636,980 (GRCm39) |
D50E |
probably benign |
Het |
Trappc11 |
A |
T |
8: 47,983,862 (GRCm39) |
V10E |
possibly damaging |
Het |
Vmn1r172 |
C |
T |
7: 23,359,681 (GRCm39) |
R189* |
probably null |
Het |
Vmn2r63 |
A |
T |
7: 42,578,015 (GRCm39) |
D174E |
possibly damaging |
Het |
Zc3h10 |
A |
T |
10: 128,380,151 (GRCm39) |
M402K |
probably damaging |
Het |
Zfp109 |
T |
C |
7: 23,927,588 (GRCm39) |
H615R |
probably damaging |
Het |
Zfp982 |
A |
C |
4: 147,597,126 (GRCm39) |
H161P |
probably benign |
Het |
Zhx1 |
A |
G |
15: 57,917,992 (GRCm39) |
F85L |
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 |
|
R1627:Bub1
|
UTSW |
2 |
127,650,933 (GRCm39) |
missense |
probably benign |
0.01 |
R1743:Bub1
|
UTSW |
2 |
127,655,770 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|