Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
G |
1: 130,668,740 (GRCm39) |
S36G |
probably damaging |
Het |
Aarsd1 |
T |
C |
11: 101,301,203 (GRCm39) |
N280D |
probably benign |
Het |
Abca2 |
T |
A |
2: 25,335,686 (GRCm39) |
M2099K |
probably damaging |
Het |
Abcb5 |
T |
A |
12: 118,875,278 (GRCm39) |
E631D |
probably benign |
Het |
Acss2 |
T |
A |
2: 155,415,149 (GRCm39) |
L682Q |
probably null |
Het |
Adamts14 |
G |
A |
10: 61,034,267 (GRCm39) |
P1207L |
probably benign |
Het |
Adora1 |
G |
A |
1: 134,130,748 (GRCm39) |
R308* |
probably null |
Het |
Arcn1 |
A |
T |
9: 44,668,444 (GRCm39) |
V264E |
probably benign |
Het |
B3galt1 |
G |
A |
2: 67,949,112 (GRCm39) |
G276S |
probably damaging |
Het |
Bnip3l |
T |
C |
14: 67,225,180 (GRCm39) |
Y218C |
probably damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,390,805 (GRCm39) |
E379G |
probably null |
Het |
Cacng6 |
G |
A |
7: 3,483,376 (GRCm39) |
G235R |
probably damaging |
Het |
Capn8 |
A |
T |
1: 182,456,169 (GRCm39) |
T640S |
probably benign |
Het |
Ccdc106 |
T |
C |
7: 5,063,159 (GRCm39) |
|
probably benign |
Het |
Ccdc33 |
A |
T |
9: 57,993,860 (GRCm39) |
N95K |
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,719,907 (GRCm39) |
|
probably benign |
Het |
Cemip |
A |
T |
7: 83,604,509 (GRCm39) |
N844K |
probably damaging |
Het |
Chrdl2 |
A |
T |
7: 99,677,948 (GRCm39) |
T284S |
probably damaging |
Het |
Ckm |
A |
G |
7: 19,154,090 (GRCm39) |
Y279C |
probably damaging |
Het |
Clvs1 |
A |
T |
4: 9,424,261 (GRCm39) |
I236F |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,234,620 (GRCm39) |
|
probably null |
Het |
Csmd1 |
T |
C |
8: 17,266,728 (GRCm39) |
E66G |
possibly damaging |
Het |
Ctdsp2 |
A |
G |
10: 126,831,923 (GRCm39) |
D26G |
probably damaging |
Het |
Ctsll3 |
C |
A |
13: 60,946,721 (GRCm39) |
|
probably null |
Het |
Cyp2d12 |
A |
T |
15: 82,439,423 (GRCm39) |
M26L |
probably benign |
Het |
Cyp8b1 |
C |
T |
9: 121,743,950 (GRCm39) |
D461N |
probably damaging |
Het |
Dbt |
A |
T |
3: 116,322,220 (GRCm39) |
|
probably benign |
Het |
Dnah7c |
A |
G |
1: 46,704,728 (GRCm39) |
D2247G |
probably benign |
Het |
Dsg1c |
A |
G |
18: 20,400,994 (GRCm39) |
I166V |
possibly damaging |
Het |
Duoxa1 |
T |
A |
2: 122,134,361 (GRCm39) |
E252D |
probably damaging |
Het |
Ezr |
T |
A |
17: 7,020,448 (GRCm39) |
K211M |
probably damaging |
Het |
Faap100 |
T |
A |
11: 120,268,458 (GRCm39) |
E105V |
possibly damaging |
Het |
Fahd2a |
T |
C |
2: 127,283,878 (GRCm39) |
D54G |
possibly damaging |
Het |
Fbxo9 |
A |
T |
9: 78,003,146 (GRCm39) |
|
probably null |
Het |
Fndc1 |
A |
G |
17: 7,991,540 (GRCm39) |
S719P |
unknown |
Het |
Gas7 |
G |
T |
11: 67,552,916 (GRCm39) |
G159C |
probably damaging |
Het |
Gba2 |
T |
C |
4: 43,574,063 (GRCm39) |
D130G |
probably damaging |
Het |
Gli3 |
T |
G |
13: 15,723,092 (GRCm39) |
S78A |
probably damaging |
Het |
Gtpbp6 |
A |
G |
5: 110,254,770 (GRCm39) |
F101S |
probably damaging |
Het |
Gzme |
G |
A |
14: 56,355,224 (GRCm39) |
H236Y |
probably benign |
Het |
Hira |
T |
C |
16: 18,773,508 (GRCm39) |
Y943H |
probably damaging |
Het |
Hmbox1 |
G |
A |
14: 65,134,144 (GRCm39) |
S152L |
possibly damaging |
Het |
Ibtk |
A |
G |
9: 85,619,519 (GRCm39) |
|
probably null |
Het |
Jade1 |
T |
C |
3: 41,568,413 (GRCm39) |
I827T |
possibly damaging |
Het |
Jakmip3 |
A |
T |
7: 138,627,164 (GRCm39) |
E389D |
possibly damaging |
Het |
Klhdc8b |
A |
T |
9: 108,326,241 (GRCm39) |
|
probably benign |
Het |
Lama2 |
T |
C |
10: 27,014,942 (GRCm39) |
T1589A |
probably benign |
Het |
Lbx2 |
A |
C |
6: 83,064,784 (GRCm39) |
K107T |
probably damaging |
Het |
Ldha |
A |
G |
7: 46,503,522 (GRCm39) |
M259V |
probably benign |
Het |
Lrrtm4 |
A |
G |
6: 79,999,620 (GRCm39) |
K344R |
probably damaging |
Het |
Ltb |
A |
T |
17: 35,414,935 (GRCm39) |
E245V |
probably damaging |
Het |
Macf1 |
GCCCCC |
GCCCCCC |
4: 123,244,784 (GRCm39) |
|
probably null |
Het |
Map3k13 |
T |
A |
16: 21,740,397 (GRCm39) |
S575T |
possibly damaging |
Het |
Mcpt2 |
A |
T |
14: 56,280,833 (GRCm39) |
I74F |
probably damaging |
Het |
Mpeg1 |
T |
A |
19: 12,439,013 (GRCm39) |
V157D |
probably damaging |
Het |
Mrpl21 |
A |
T |
19: 3,337,009 (GRCm39) |
|
probably null |
Het |
Nagpa |
T |
C |
16: 5,017,877 (GRCm39) |
T99A |
possibly damaging |
Het |
Nphs1 |
A |
T |
7: 30,163,250 (GRCm39) |
I469F |
probably benign |
Het |
Nyap2 |
A |
G |
1: 81,169,756 (GRCm39) |
E171G |
possibly damaging |
Het |
Oas1e |
A |
G |
5: 120,930,006 (GRCm39) |
Y171H |
probably damaging |
Het |
Or10ag59 |
T |
A |
2: 87,406,043 (GRCm39) |
V205D |
probably damaging |
Het |
Or2y1f |
T |
C |
11: 49,184,493 (GRCm39) |
L115P |
probably damaging |
Het |
Or5ac23 |
T |
C |
16: 59,149,461 (GRCm39) |
K137R |
probably benign |
Het |
Or5h26 |
T |
C |
16: 58,987,983 (GRCm39) |
I174M |
possibly damaging |
Het |
Otud7b |
C |
A |
3: 96,063,055 (GRCm39) |
Q765K |
probably benign |
Het |
Pdzd7 |
A |
G |
19: 45,017,216 (GRCm39) |
V851A |
probably benign |
Het |
Pi4ka |
T |
G |
16: 17,143,277 (GRCm39) |
K794T |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,410,258 (GRCm39) |
N2588K |
probably damaging |
Het |
Pla2g6 |
A |
T |
15: 79,186,837 (GRCm39) |
M471K |
probably benign |
Het |
Plagl2 |
T |
C |
2: 153,077,759 (GRCm39) |
H74R |
possibly damaging |
Het |
Prf1 |
T |
A |
10: 61,136,037 (GRCm39) |
N104K |
probably benign |
Het |
Ptprf |
A |
T |
4: 118,093,586 (GRCm39) |
I358N |
probably damaging |
Het |
Rcsd1 |
A |
G |
1: 165,482,872 (GRCm39) |
|
probably null |
Het |
Rev1 |
G |
A |
1: 38,147,532 (GRCm39) |
R3* |
probably null |
Het |
Rp1 |
T |
C |
1: 4,419,583 (GRCm39) |
|
probably null |
Het |
Rrp12 |
G |
A |
19: 41,881,035 (GRCm39) |
T132I |
probably damaging |
Het |
Sema3a |
T |
C |
5: 13,649,357 (GRCm39) |
V702A |
probably benign |
Het |
Serpinb12 |
A |
G |
1: 106,884,174 (GRCm39) |
N307D |
probably damaging |
Het |
Slc35d1 |
A |
G |
4: 103,070,383 (GRCm39) |
L103P |
probably damaging |
Het |
Smyd4 |
T |
C |
11: 75,281,765 (GRCm39) |
C413R |
probably damaging |
Het |
Stab1 |
G |
A |
14: 30,883,793 (GRCm39) |
Q255* |
probably null |
Het |
Synpo |
T |
A |
18: 60,736,918 (GRCm39) |
I343F |
possibly damaging |
Het |
Tcirg1 |
A |
G |
19: 3,952,342 (GRCm39) |
|
probably null |
Het |
Tmem132c |
A |
G |
5: 127,640,816 (GRCm39) |
T996A |
possibly damaging |
Het |
Trim10 |
A |
G |
17: 37,181,081 (GRCm39) |
E104G |
probably damaging |
Het |
Trpc1 |
T |
C |
9: 95,603,524 (GRCm39) |
|
probably null |
Het |
Tspo2 |
A |
T |
17: 48,756,887 (GRCm39) |
|
probably benign |
Het |
Ugt2a3 |
A |
T |
5: 87,479,174 (GRCm39) |
I258N |
probably damaging |
Het |
Usp34 |
T |
C |
11: 23,418,846 (GRCm39) |
L2998P |
probably damaging |
Het |
Vmn1r45 |
A |
C |
6: 89,910,123 (GRCm39) |
D162E |
possibly damaging |
Het |
Vmn2r117 |
A |
T |
17: 23,696,848 (GRCm39) |
Y186* |
probably null |
Het |
Vmn2r67 |
A |
G |
7: 84,785,698 (GRCm39) |
F769S |
probably damaging |
Het |
Zbtb17 |
A |
G |
4: 141,192,942 (GRCm39) |
I514V |
probably benign |
Het |
Zfp329 |
A |
C |
7: 12,545,421 (GRCm39) |
D34E |
probably benign |
Het |
|
Other mutations in Bms1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Bms1
|
APN |
6 |
118,381,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00763:Bms1
|
APN |
6 |
118,395,363 (GRCm39) |
splice site |
probably benign |
|
IGL00839:Bms1
|
APN |
6 |
118,382,252 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02005:Bms1
|
APN |
6 |
118,381,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02271:Bms1
|
APN |
6 |
118,366,290 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02403:Bms1
|
APN |
6 |
118,382,185 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02474:Bms1
|
APN |
6 |
118,393,480 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03230:Bms1
|
APN |
6 |
118,395,522 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03277:Bms1
|
APN |
6 |
118,382,083 (GRCm39) |
missense |
probably benign |
|
PIT4508001:Bms1
|
UTSW |
6 |
118,360,767 (GRCm39) |
missense |
probably benign |
0.03 |
R0028:Bms1
|
UTSW |
6 |
118,393,480 (GRCm39) |
missense |
probably benign |
0.00 |
R0056:Bms1
|
UTSW |
6 |
118,382,190 (GRCm39) |
missense |
probably benign |
0.00 |
R0056:Bms1
|
UTSW |
6 |
118,382,190 (GRCm39) |
missense |
probably benign |
0.00 |
R0276:Bms1
|
UTSW |
6 |
118,385,095 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0295:Bms1
|
UTSW |
6 |
118,366,298 (GRCm39) |
missense |
probably benign |
0.04 |
R0360:Bms1
|
UTSW |
6 |
118,382,251 (GRCm39) |
missense |
probably benign |
0.13 |
R0556:Bms1
|
UTSW |
6 |
118,390,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Bms1
|
UTSW |
6 |
118,382,182 (GRCm39) |
missense |
probably benign |
0.00 |
R1583:Bms1
|
UTSW |
6 |
118,366,350 (GRCm39) |
splice site |
probably benign |
|
R1815:Bms1
|
UTSW |
6 |
118,360,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Bms1
|
UTSW |
6 |
118,369,939 (GRCm39) |
missense |
probably damaging |
0.98 |
R2045:Bms1
|
UTSW |
6 |
118,369,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Bms1
|
UTSW |
6 |
118,368,114 (GRCm39) |
splice site |
probably null |
|
R4293:Bms1
|
UTSW |
6 |
118,382,308 (GRCm39) |
splice site |
probably null |
|
R4296:Bms1
|
UTSW |
6 |
118,381,960 (GRCm39) |
missense |
probably damaging |
0.96 |
R4467:Bms1
|
UTSW |
6 |
118,360,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R4688:Bms1
|
UTSW |
6 |
118,369,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R4718:Bms1
|
UTSW |
6 |
118,380,196 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5015:Bms1
|
UTSW |
6 |
118,381,224 (GRCm39) |
nonsense |
probably null |
|
R5489:Bms1
|
UTSW |
6 |
118,390,706 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5511:Bms1
|
UTSW |
6 |
118,365,848 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5636:Bms1
|
UTSW |
6 |
118,365,786 (GRCm39) |
missense |
probably benign |
0.00 |
R5815:Bms1
|
UTSW |
6 |
118,381,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R6245:Bms1
|
UTSW |
6 |
118,373,797 (GRCm39) |
missense |
probably damaging |
0.96 |
R6299:Bms1
|
UTSW |
6 |
118,395,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R6389:Bms1
|
UTSW |
6 |
118,380,196 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6838:Bms1
|
UTSW |
6 |
118,393,455 (GRCm39) |
missense |
probably benign |
0.00 |
R7129:Bms1
|
UTSW |
6 |
118,380,122 (GRCm39) |
nonsense |
probably null |
|
R7414:Bms1
|
UTSW |
6 |
118,360,706 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7811:Bms1
|
UTSW |
6 |
118,380,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R7883:Bms1
|
UTSW |
6 |
118,365,735 (GRCm39) |
missense |
probably benign |
0.04 |
R8046:Bms1
|
UTSW |
6 |
118,385,105 (GRCm39) |
missense |
probably benign |
|
R8068:Bms1
|
UTSW |
6 |
118,390,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Bms1
|
UTSW |
6 |
118,361,219 (GRCm39) |
missense |
probably damaging |
0.98 |
R8176:Bms1
|
UTSW |
6 |
118,395,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Bms1
|
UTSW |
6 |
118,365,721 (GRCm39) |
missense |
probably benign |
0.24 |
R8728:Bms1
|
UTSW |
6 |
118,369,331 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8793:Bms1
|
UTSW |
6 |
118,360,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Bms1
|
UTSW |
6 |
118,369,292 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9234:Bms1
|
UTSW |
6 |
118,375,044 (GRCm39) |
missense |
probably damaging |
0.96 |
R9440:Bms1
|
UTSW |
6 |
118,382,217 (GRCm39) |
missense |
probably benign |
|
R9701:Bms1
|
UTSW |
6 |
118,368,147 (GRCm39) |
missense |
probably damaging |
0.98 |
R9802:Bms1
|
UTSW |
6 |
118,368,147 (GRCm39) |
missense |
probably damaging |
0.98 |
X0067:Bms1
|
UTSW |
6 |
118,381,795 (GRCm39) |
missense |
probably benign |
0.26 |
|