Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
G |
1: 71,327,712 (GRCm39) |
H1456P |
possibly damaging |
Het |
Abcg1 |
C |
A |
17: 31,324,578 (GRCm39) |
H274Q |
probably damaging |
Het |
Adamts4 |
G |
A |
1: 171,078,512 (GRCm39) |
R44Q |
probably benign |
Het |
Amigo2 |
A |
T |
15: 97,143,494 (GRCm39) |
C309* |
probably null |
Het |
Ccdc88c |
A |
C |
12: 100,919,552 (GRCm39) |
S446A |
probably benign |
Het |
Cd9 |
A |
T |
6: 125,449,458 (GRCm39) |
V28E |
probably damaging |
Het |
Cops2 |
A |
T |
2: 125,678,163 (GRCm39) |
|
probably benign |
Het |
Csn1s1 |
C |
T |
5: 87,825,453 (GRCm39) |
|
probably benign |
Het |
Cul9 |
G |
T |
17: 46,851,302 (GRCm39) |
R373S |
possibly damaging |
Het |
D630045J12Rik |
G |
T |
6: 38,126,640 (GRCm39) |
H1457N |
probably damaging |
Het |
Dennd2b |
C |
A |
7: 109,155,442 (GRCm39) |
R436L |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 65,920,189 (GRCm39) |
S2235P |
probably damaging |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Fbxo10 |
A |
T |
4: 45,043,883 (GRCm39) |
W647R |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,930,919 (GRCm38) |
|
probably benign |
Het |
Flnc |
G |
T |
6: 29,440,684 (GRCm39) |
V301L |
probably damaging |
Het |
Hfm1 |
T |
C |
5: 107,049,627 (GRCm39) |
S445G |
probably benign |
Het |
Hif3a |
A |
G |
7: 16,773,603 (GRCm39) |
|
probably benign |
Het |
Hsd17b4 |
T |
C |
18: 50,288,220 (GRCm39) |
Y217H |
probably damaging |
Het |
Iba57 |
T |
C |
11: 59,049,772 (GRCm39) |
T192A |
probably benign |
Het |
Igkv5-48 |
A |
T |
6: 69,703,671 (GRCm39) |
I78N |
probably damaging |
Het |
Inhbe |
A |
T |
10: 127,186,797 (GRCm39) |
W128R |
probably damaging |
Het |
Ism1 |
T |
C |
2: 139,599,121 (GRCm39) |
C365R |
probably damaging |
Het |
Kif19a |
A |
T |
11: 114,670,470 (GRCm39) |
T127S |
probably damaging |
Het |
Kmt2d |
C |
A |
15: 98,755,439 (GRCm39) |
|
probably benign |
Het |
Mmp20 |
A |
G |
9: 7,654,042 (GRCm39) |
R321G |
probably damaging |
Het |
Nme9 |
T |
C |
9: 99,351,684 (GRCm39) |
C223R |
probably damaging |
Het |
Nucb1 |
G |
T |
7: 45,144,467 (GRCm39) |
|
probably benign |
Het |
Ocrl |
G |
A |
X: 47,022,315 (GRCm39) |
D262N |
probably benign |
Het |
Or13a18 |
A |
C |
7: 140,190,081 (GRCm39) |
M1L |
probably benign |
Het |
Or5b98 |
T |
A |
19: 12,931,556 (GRCm39) |
I201N |
possibly damaging |
Het |
Or6b1 |
A |
C |
6: 42,815,738 (GRCm39) |
I308L |
probably benign |
Het |
P4ha1 |
A |
G |
10: 59,206,824 (GRCm39) |
|
probably null |
Het |
Parp8 |
T |
C |
13: 116,998,838 (GRCm39) |
|
probably benign |
Het |
Pcdhb6 |
A |
G |
18: 37,468,507 (GRCm39) |
D476G |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,303,535 (GRCm39) |
E1685G |
possibly damaging |
Het |
Plod2 |
T |
A |
9: 92,489,147 (GRCm39) |
L714Q |
probably damaging |
Het |
Plscr2 |
A |
G |
9: 92,171,716 (GRCm39) |
I103V |
probably benign |
Het |
Plscr3 |
C |
A |
11: 69,738,209 (GRCm39) |
|
probably benign |
Het |
Pmaip1 |
A |
G |
18: 66,596,370 (GRCm39) |
R80G |
probably damaging |
Het |
Ppm1d |
C |
T |
11: 85,230,492 (GRCm39) |
P370L |
possibly damaging |
Het |
Prr36 |
C |
A |
8: 4,266,407 (GRCm39) |
E48* |
probably null |
Het |
Ptgir |
G |
A |
7: 16,641,409 (GRCm39) |
V234I |
possibly damaging |
Het |
Ptk7 |
A |
T |
17: 46,901,070 (GRCm39) |
V219E |
probably benign |
Het |
Rab39b |
T |
A |
X: 74,618,609 (GRCm39) |
I74F |
probably damaging |
Het |
Rasal2 |
A |
T |
1: 156,977,449 (GRCm39) |
M1075K |
possibly damaging |
Het |
Rpl37a |
G |
A |
1: 72,750,885 (GRCm39) |
A20T |
probably null |
Het |
Serpinb10 |
A |
C |
1: 107,466,155 (GRCm39) |
|
probably null |
Het |
Sipa1l1 |
T |
A |
12: 82,471,868 (GRCm39) |
Y1283N |
probably damaging |
Het |
Slc22a23 |
T |
A |
13: 34,528,468 (GRCm39) |
I105F |
possibly damaging |
Het |
Slc25a20 |
T |
A |
9: 108,559,599 (GRCm39) |
I221N |
probably damaging |
Het |
Smarcal1 |
A |
T |
1: 72,659,247 (GRCm39) |
H691L |
probably damaging |
Het |
Smo |
A |
C |
6: 29,758,480 (GRCm39) |
T542P |
probably damaging |
Het |
Spats2 |
T |
A |
15: 99,071,329 (GRCm39) |
I51N |
probably damaging |
Het |
Spon1 |
G |
T |
7: 113,635,897 (GRCm39) |
V704L |
probably benign |
Het |
Tex9 |
T |
A |
9: 72,389,774 (GRCm39) |
Q112L |
probably benign |
Het |
Tgfbr2 |
T |
C |
9: 115,919,486 (GRCm39) |
E580G |
probably benign |
Het |
Top2b |
T |
A |
14: 16,387,335 (GRCm38) |
V141E |
probably benign |
Het |
Trhde |
A |
T |
10: 114,636,466 (GRCm39) |
L247* |
probably null |
Het |
Umodl1 |
G |
T |
17: 31,217,628 (GRCm39) |
V1145F |
probably damaging |
Het |
Vasp |
C |
A |
7: 18,992,748 (GRCm39) |
|
probably benign |
Het |
Vmn1r8 |
G |
T |
6: 57,013,556 (GRCm39) |
L202F |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,787,837 (GRCm39) |
T505A |
probably benign |
Het |
Wdr27 |
A |
G |
17: 15,112,693 (GRCm39) |
|
probably benign |
Het |
Wfdc1 |
T |
G |
8: 120,406,909 (GRCm39) |
V109G |
probably damaging |
Het |
Zan |
C |
A |
5: 137,463,056 (GRCm39) |
E708* |
probably null |
Het |
Zbtb1 |
T |
A |
12: 76,432,169 (GRCm39) |
F52I |
possibly damaging |
Het |
Zfp236 |
A |
G |
18: 82,648,117 (GRCm39) |
S1015P |
probably damaging |
Het |
Zfp532 |
T |
C |
18: 65,757,113 (GRCm39) |
S349P |
probably damaging |
Het |
Znfx1 |
A |
T |
2: 166,889,550 (GRCm39) |
C731S |
possibly damaging |
Het |
|
Other mutations in Msl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00543:Msl2
|
APN |
9 |
100,978,269 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02798:Msl2
|
APN |
9 |
100,957,430 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03235:Msl2
|
APN |
9 |
100,977,967 (GRCm39) |
missense |
probably benign |
0.03 |
anguished
|
UTSW |
9 |
100,979,174 (GRCm39) |
missense |
possibly damaging |
0.66 |
Appalled
|
UTSW |
9 |
100,978,042 (GRCm39) |
missense |
probably benign |
|
Crestfallen
|
UTSW |
9 |
100,978,290 (GRCm39) |
nonsense |
probably null |
|
R0497:Msl2
|
UTSW |
9 |
100,978,493 (GRCm39) |
missense |
probably benign |
0.00 |
R1288:Msl2
|
UTSW |
9 |
100,979,308 (GRCm39) |
missense |
probably benign |
0.01 |
R2015:Msl2
|
UTSW |
9 |
100,957,304 (GRCm39) |
start gained |
probably benign |
|
R2038:Msl2
|
UTSW |
9 |
100,979,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R2238:Msl2
|
UTSW |
9 |
100,978,569 (GRCm39) |
missense |
probably benign |
0.41 |
R4393:Msl2
|
UTSW |
9 |
100,978,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Msl2
|
UTSW |
9 |
100,979,350 (GRCm39) |
missense |
probably benign |
0.00 |
R5290:Msl2
|
UTSW |
9 |
100,978,606 (GRCm39) |
splice site |
probably null |
|
R5567:Msl2
|
UTSW |
9 |
100,978,936 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5934:Msl2
|
UTSW |
9 |
100,979,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:Msl2
|
UTSW |
9 |
100,978,290 (GRCm39) |
nonsense |
probably null |
|
R6339:Msl2
|
UTSW |
9 |
100,978,949 (GRCm39) |
missense |
probably benign |
|
R6736:Msl2
|
UTSW |
9 |
100,978,201 (GRCm39) |
missense |
probably damaging |
0.99 |
R6950:Msl2
|
UTSW |
9 |
100,979,174 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6971:Msl2
|
UTSW |
9 |
100,978,042 (GRCm39) |
missense |
probably benign |
|
R7022:Msl2
|
UTSW |
9 |
100,957,335 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7408:Msl2
|
UTSW |
9 |
100,979,316 (GRCm39) |
missense |
probably benign |
0.08 |
R7955:Msl2
|
UTSW |
9 |
100,979,354 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8069:Msl2
|
UTSW |
9 |
100,978,159 (GRCm39) |
missense |
probably benign |
|
R8281:Msl2
|
UTSW |
9 |
100,978,894 (GRCm39) |
missense |
probably benign |
0.10 |
R8437:Msl2
|
UTSW |
9 |
100,978,167 (GRCm39) |
missense |
probably benign |
0.25 |
R9162:Msl2
|
UTSW |
9 |
100,978,928 (GRCm39) |
missense |
probably benign |
|
R9675:Msl2
|
UTSW |
9 |
100,978,555 (GRCm39) |
missense |
probably benign |
|
|