Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700022I11Rik |
A |
G |
4: 42,971,864 (GRCm38) |
N399S |
probably benign |
Het |
Aasdh |
A |
G |
5: 76,888,782 (GRCm38) |
V304A |
probably benign |
Het |
Angptl3 |
G |
A |
4: 99,034,465 (GRCm38) |
A248T |
probably benign |
Het |
Ap2b1 |
T |
A |
11: 83,324,565 (GRCm38) |
C112S |
possibly damaging |
Het |
Aqr |
A |
T |
2: 114,136,887 (GRCm38) |
I549N |
probably damaging |
Het |
Barhl1 |
C |
T |
2: 28,911,550 (GRCm38) |
D161N |
possibly damaging |
Het |
Col28a1 |
A |
G |
6: 8,014,942 (GRCm38) |
V821A |
probably damaging |
Het |
Dclk2 |
G |
A |
3: 86,920,035 (GRCm38) |
P46S |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 31,315,148 (GRCm38) |
L247P |
possibly damaging |
Het |
Dpysl2 |
T |
A |
14: 66,834,370 (GRCm38) |
H107L |
probably damaging |
Het |
Dzip3 |
A |
G |
16: 48,937,063 (GRCm38) |
L869S |
probably damaging |
Het |
Efs |
T |
C |
14: 54,920,095 (GRCm38) |
Y160C |
probably damaging |
Het |
Enam |
A |
T |
5: 88,504,447 (GRCm38) |
N1197Y |
possibly damaging |
Het |
Espl1 |
A |
G |
15: 102,312,989 (GRCm38) |
I944V |
probably damaging |
Het |
Fam184b |
A |
G |
5: 45,582,815 (GRCm38) |
V343A |
possibly damaging |
Het |
Fbxw26 |
A |
T |
9: 109,743,760 (GRCm38) |
Y105* |
probably null |
Het |
Fiz1 |
A |
G |
7: 5,008,172 (GRCm38) |
L449P |
probably benign |
Het |
Foxi2 |
T |
A |
7: 135,410,451 (GRCm38) |
C23S |
possibly damaging |
Het |
Gdf2 |
G |
A |
14: 33,944,957 (GRCm38) |
R212Q |
probably damaging |
Het |
Gm5105 |
C |
A |
3: 138,049,688 (GRCm38) |
A46S |
unknown |
Het |
Gm597 |
T |
C |
1: 28,776,575 (GRCm38) |
D792G |
probably benign |
Het |
Grik5 |
C |
T |
7: 25,022,571 (GRCm38) |
A581T |
probably benign |
Het |
Gse1 |
C |
G |
8: 120,572,742 (GRCm38) |
|
probably benign |
Het |
Hsp90aa1 |
T |
A |
12: 110,695,680 (GRCm38) |
M1L |
possibly damaging |
Het |
Hsp90aa1 |
C |
A |
12: 110,695,681 (GRCm38) |
|
probably null |
Het |
Kif1b |
A |
T |
4: 149,262,283 (GRCm38) |
|
probably benign |
Het |
Krt25 |
A |
C |
11: 99,317,298 (GRCm38) |
V368G |
possibly damaging |
Het |
Lacc1 |
A |
G |
14: 77,033,287 (GRCm38) |
V269A |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,251,150 (GRCm38) |
K417E |
probably damaging |
Het |
Miip |
A |
G |
4: 147,865,914 (GRCm38) |
M75T |
probably benign |
Het |
Nlrp10 |
A |
G |
7: 108,924,476 (GRCm38) |
F599S |
probably benign |
Het |
Nlrp12 |
T |
A |
7: 3,240,575 (GRCm38) |
M436L |
probably benign |
Het |
Olfr142 |
T |
C |
2: 90,252,409 (GRCm38) |
E193G |
possibly damaging |
Het |
Pafah1b1 |
G |
A |
11: 74,690,232 (GRCm38) |
S57F |
probably damaging |
Het |
Pard6b |
T |
C |
2: 168,087,339 (GRCm38) |
|
probably benign |
Het |
Pla2g2e |
G |
A |
4: 138,880,374 (GRCm38) |
V22I |
probably benign |
Het |
Plekhd1 |
A |
G |
12: 80,717,270 (GRCm38) |
E202G |
probably damaging |
Het |
Prss21 |
A |
G |
17: 23,872,831 (GRCm38) |
T258A |
probably benign |
Het |
Prss34 |
A |
G |
17: 25,298,846 (GRCm38) |
E65G |
probably benign |
Het |
Psap |
A |
G |
10: 60,294,603 (GRCm38) |
N149S |
probably benign |
Het |
Ptprf |
C |
T |
4: 118,237,883 (GRCm38) |
A275T |
probably benign |
Het |
Sem1 |
A |
G |
6: 6,578,520 (GRCm38) |
L12P |
probably damaging |
Het |
Sf3b3 |
A |
G |
8: 110,844,523 (GRCm38) |
Y4H |
probably damaging |
Het |
Sh3bp4 |
G |
T |
1: 89,137,705 (GRCm38) |
R7L |
probably damaging |
Het |
Slc16a1 |
T |
A |
3: 104,653,570 (GRCm38) |
L397Q |
probably damaging |
Het |
Smg5 |
A |
G |
3: 88,336,451 (GRCm38) |
S10G |
possibly damaging |
Het |
Smr2 |
AT |
ATT |
5: 88,108,824 (GRCm38) |
|
probably null |
Het |
Tas2r102 |
C |
T |
6: 132,762,818 (GRCm38) |
Q230* |
probably null |
Het |
Tdo2 |
A |
G |
3: 81,975,428 (GRCm38) |
Y13H |
possibly damaging |
Het |
Tmem231 |
C |
T |
8: 111,918,313 (GRCm38) |
R187H |
possibly damaging |
Het |
Tmem30b |
A |
G |
12: 73,545,579 (GRCm38) |
M254T |
probably damaging |
Het |
Trpm1 |
G |
A |
7: 64,243,570 (GRCm38) |
G1057R |
probably damaging |
Het |
Tusc3 |
A |
T |
8: 39,164,838 (GRCm38) |
K347N |
probably damaging |
Het |
Usp36 |
C |
T |
11: 118,276,759 (GRCm38) |
|
probably null |
Het |
Vash2 |
T |
C |
1: 190,970,419 (GRCm38) |
Y117C |
probably damaging |
Het |
Vrk2 |
A |
G |
11: 26,489,866 (GRCm38) |
I235T |
possibly damaging |
Het |
Wdr20 |
A |
G |
12: 110,793,939 (GRCm38) |
T420A |
probably benign |
Het |
|
Other mutations in A2ml1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00513:A2ml1
|
APN |
6 |
128,578,156 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL00596:A2ml1
|
APN |
6 |
128,570,067 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL00912:A2ml1
|
APN |
6 |
128,552,307 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01320:A2ml1
|
APN |
6 |
128,575,588 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01470:A2ml1
|
APN |
6 |
128,580,412 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01576:A2ml1
|
APN |
6 |
128,554,330 (GRCm38) |
splice site |
probably benign |
|
IGL01761:A2ml1
|
APN |
6 |
128,546,337 (GRCm38) |
missense |
possibly damaging |
0.61 |
IGL01792:A2ml1
|
APN |
6 |
128,560,679 (GRCm38) |
missense |
probably benign |
0.04 |
IGL01843:A2ml1
|
APN |
6 |
128,553,338 (GRCm38) |
splice site |
probably benign |
|
IGL01946:A2ml1
|
APN |
6 |
128,570,479 (GRCm38) |
missense |
possibly damaging |
0.81 |
IGL02016:A2ml1
|
APN |
6 |
128,558,335 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02170:A2ml1
|
APN |
6 |
128,547,210 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL02269:A2ml1
|
APN |
6 |
128,553,338 (GRCm38) |
splice site |
probably benign |
|
IGL02589:A2ml1
|
APN |
6 |
128,581,500 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02959:A2ml1
|
APN |
6 |
128,567,060 (GRCm38) |
missense |
probably benign |
0.04 |
IGL02970:A2ml1
|
APN |
6 |
128,569,979 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03206:A2ml1
|
APN |
6 |
128,553,276 (GRCm38) |
missense |
possibly damaging |
0.50 |
IGL03298:A2ml1
|
APN |
6 |
128,543,960 (GRCm38) |
missense |
probably benign |
0.00 |
1mM(1):A2ml1
|
UTSW |
6 |
128,580,960 (GRCm38) |
missense |
probably benign |
0.02 |
R0055:A2ml1
|
UTSW |
6 |
128,570,094 (GRCm38) |
splice site |
probably benign |
|
R0055:A2ml1
|
UTSW |
6 |
128,570,094 (GRCm38) |
splice site |
probably benign |
|
R0069:A2ml1
|
UTSW |
6 |
128,561,562 (GRCm38) |
missense |
probably damaging |
1.00 |
R0069:A2ml1
|
UTSW |
6 |
128,561,562 (GRCm38) |
missense |
probably damaging |
1.00 |
R0128:A2ml1
|
UTSW |
6 |
128,575,639 (GRCm38) |
splice site |
probably benign |
|
R0299:A2ml1
|
UTSW |
6 |
128,553,232 (GRCm38) |
splice site |
probably benign |
|
R0523:A2ml1
|
UTSW |
6 |
128,558,326 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0565:A2ml1
|
UTSW |
6 |
128,568,743 (GRCm38) |
nonsense |
probably null |
|
R0599:A2ml1
|
UTSW |
6 |
128,552,245 (GRCm38) |
missense |
probably damaging |
1.00 |
R0626:A2ml1
|
UTSW |
6 |
128,550,773 (GRCm38) |
missense |
probably damaging |
0.99 |
R0732:A2ml1
|
UTSW |
6 |
128,546,448 (GRCm38) |
missense |
probably damaging |
1.00 |
R0880:A2ml1
|
UTSW |
6 |
128,560,646 (GRCm38) |
missense |
possibly damaging |
0.49 |
R1070:A2ml1
|
UTSW |
6 |
128,543,300 (GRCm38) |
missense |
probably damaging |
1.00 |
R1166:A2ml1
|
UTSW |
6 |
128,570,917 (GRCm38) |
missense |
probably benign |
0.00 |
R1278:A2ml1
|
UTSW |
6 |
128,558,507 (GRCm38) |
missense |
probably damaging |
1.00 |
R1421:A2ml1
|
UTSW |
6 |
128,543,960 (GRCm38) |
missense |
probably benign |
0.00 |
R1536:A2ml1
|
UTSW |
6 |
128,547,233 (GRCm38) |
nonsense |
probably null |
|
R1786:A2ml1
|
UTSW |
6 |
128,576,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R1808:A2ml1
|
UTSW |
6 |
128,543,299 (GRCm38) |
missense |
probably damaging |
1.00 |
R1813:A2ml1
|
UTSW |
6 |
128,566,273 (GRCm38) |
missense |
probably benign |
0.34 |
R1863:A2ml1
|
UTSW |
6 |
128,550,783 (GRCm38) |
missense |
probably damaging |
0.99 |
R2007:A2ml1
|
UTSW |
6 |
128,542,892 (GRCm38) |
missense |
probably benign |
0.13 |
R2062:A2ml1
|
UTSW |
6 |
128,552,308 (GRCm38) |
missense |
probably benign |
0.08 |
R2127:A2ml1
|
UTSW |
6 |
128,558,437 (GRCm38) |
missense |
probably damaging |
1.00 |
R2130:A2ml1
|
UTSW |
6 |
128,576,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R2131:A2ml1
|
UTSW |
6 |
128,576,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R2201:A2ml1
|
UTSW |
6 |
128,547,305 (GRCm38) |
missense |
probably null |
0.34 |
R2319:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2321:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2322:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2369:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2370:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2371:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2372:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2375:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2893:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R2894:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R3438:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R3615:A2ml1
|
UTSW |
6 |
128,558,294 (GRCm38) |
missense |
probably benign |
0.07 |
R3773:A2ml1
|
UTSW |
6 |
128,555,083 (GRCm38) |
missense |
probably benign |
0.02 |
R3785:A2ml1
|
UTSW |
6 |
128,544,924 (GRCm38) |
critical splice donor site |
probably null |
|
R3803:A2ml1
|
UTSW |
6 |
128,545,070 (GRCm38) |
missense |
probably benign |
0.17 |
R3824:A2ml1
|
UTSW |
6 |
128,568,763 (GRCm38) |
missense |
probably damaging |
0.99 |
R3878:A2ml1
|
UTSW |
6 |
128,554,361 (GRCm38) |
missense |
probably benign |
0.05 |
R4176:A2ml1
|
UTSW |
6 |
128,545,037 (GRCm38) |
missense |
possibly damaging |
0.68 |
R4229:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R4230:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R4348:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R4351:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R4352:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R4353:A2ml1
|
UTSW |
6 |
128,580,386 (GRCm38) |
missense |
probably benign |
0.01 |
R4427:A2ml1
|
UTSW |
6 |
128,545,046 (GRCm38) |
missense |
probably benign |
0.00 |
R4971:A2ml1
|
UTSW |
6 |
128,547,227 (GRCm38) |
missense |
probably damaging |
0.98 |
R5014:A2ml1
|
UTSW |
6 |
128,543,933 (GRCm38) |
missense |
probably benign |
0.00 |
R5369:A2ml1
|
UTSW |
6 |
128,568,833 (GRCm38) |
missense |
probably damaging |
0.97 |
R5532:A2ml1
|
UTSW |
6 |
128,553,330 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5860:A2ml1
|
UTSW |
6 |
128,541,061 (GRCm38) |
missense |
probably benign |
0.15 |
R5872:A2ml1
|
UTSW |
6 |
128,561,526 (GRCm38) |
missense |
probably damaging |
1.00 |
R5926:A2ml1
|
UTSW |
6 |
128,560,645 (GRCm38) |
missense |
probably benign |
|
R5977:A2ml1
|
UTSW |
6 |
128,581,122 (GRCm38) |
missense |
probably damaging |
1.00 |
R5980:A2ml1
|
UTSW |
6 |
128,567,055 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6014:A2ml1
|
UTSW |
6 |
128,571,985 (GRCm38) |
missense |
probably damaging |
1.00 |
R6032:A2ml1
|
UTSW |
6 |
128,549,836 (GRCm38) |
nonsense |
probably null |
|
R6032:A2ml1
|
UTSW |
6 |
128,549,836 (GRCm38) |
nonsense |
probably null |
|
R6061:A2ml1
|
UTSW |
6 |
128,568,712 (GRCm38) |
missense |
probably damaging |
1.00 |
R6327:A2ml1
|
UTSW |
6 |
128,558,692 (GRCm38) |
splice site |
probably null |
|
R6331:A2ml1
|
UTSW |
6 |
128,552,236 (GRCm38) |
missense |
probably damaging |
0.96 |
R6465:A2ml1
|
UTSW |
6 |
128,541,078 (GRCm38) |
missense |
probably damaging |
1.00 |
R6640:A2ml1
|
UTSW |
6 |
128,553,285 (GRCm38) |
missense |
probably benign |
0.41 |
R6792:A2ml1
|
UTSW |
6 |
128,546,329 (GRCm38) |
nonsense |
probably null |
|
R6793:A2ml1
|
UTSW |
6 |
128,546,329 (GRCm38) |
nonsense |
probably null |
|
R7207:A2ml1
|
UTSW |
6 |
128,550,771 (GRCm38) |
missense |
probably benign |
0.04 |
R7378:A2ml1
|
UTSW |
6 |
128,546,247 (GRCm38) |
critical splice donor site |
probably null |
|
R7556:A2ml1
|
UTSW |
6 |
128,569,964 (GRCm38) |
missense |
probably damaging |
1.00 |
R8010:A2ml1
|
UTSW |
6 |
128,580,340 (GRCm38) |
missense |
probably benign |
0.08 |
R8017:A2ml1
|
UTSW |
6 |
128,581,447 (GRCm38) |
critical splice donor site |
probably null |
|
R8019:A2ml1
|
UTSW |
6 |
128,581,447 (GRCm38) |
critical splice donor site |
probably null |
|
R8035:A2ml1
|
UTSW |
6 |
128,553,280 (GRCm38) |
missense |
probably damaging |
0.99 |
R8094:A2ml1
|
UTSW |
6 |
128,572,082 (GRCm38) |
missense |
probably damaging |
1.00 |
R8144:A2ml1
|
UTSW |
6 |
128,569,999 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8365:A2ml1
|
UTSW |
6 |
128,580,955 (GRCm38) |
nonsense |
probably null |
|
R8382:A2ml1
|
UTSW |
6 |
128,560,682 (GRCm38) |
missense |
probably benign |
0.01 |
R8388:A2ml1
|
UTSW |
6 |
128,571,974 (GRCm38) |
missense |
probably benign |
0.03 |
R8717:A2ml1
|
UTSW |
6 |
128,566,995 (GRCm38) |
missense |
probably benign |
0.00 |
R8947:A2ml1
|
UTSW |
6 |
128,552,256 (GRCm38) |
missense |
probably damaging |
1.00 |
R8970:A2ml1
|
UTSW |
6 |
128,568,763 (GRCm38) |
missense |
probably damaging |
0.99 |
R9025:A2ml1
|
UTSW |
6 |
128,557,582 (GRCm38) |
missense |
possibly damaging |
0.49 |
R9083:A2ml1
|
UTSW |
6 |
128,557,561 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9129:A2ml1
|
UTSW |
6 |
128,546,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R9145:A2ml1
|
UTSW |
6 |
128,559,069 (GRCm38) |
missense |
probably benign |
|
R9165:A2ml1
|
UTSW |
6 |
128,560,669 (GRCm38) |
missense |
probably benign |
|
R9285:A2ml1
|
UTSW |
6 |
128,549,793 (GRCm38) |
missense |
probably benign |
|
R9408:A2ml1
|
UTSW |
6 |
128,545,067 (GRCm38) |
missense |
probably damaging |
0.98 |
R9486:A2ml1
|
UTSW |
6 |
128,569,979 (GRCm38) |
missense |
probably damaging |
0.99 |
R9781:A2ml1
|
UTSW |
6 |
128,542,897 (GRCm38) |
missense |
probably benign |
0.01 |
RF014:A2ml1
|
UTSW |
6 |
128,570,068 (GRCm38) |
missense |
probably damaging |
0.96 |
X0063:A2ml1
|
UTSW |
6 |
128,572,012 (GRCm38) |
missense |
probably benign |
|
Z1176:A2ml1
|
UTSW |
6 |
128,571,977 (GRCm38) |
missense |
probably benign |
0.09 |
Z1177:A2ml1
|
UTSW |
6 |
128,575,607 (GRCm38) |
missense |
possibly damaging |
0.80 |
Z1177:A2ml1
|
UTSW |
6 |
128,561,616 (GRCm38) |
nonsense |
probably null |
|
Z1177:A2ml1
|
UTSW |
6 |
128,545,076 (GRCm38) |
missense |
probably benign |
|
|