Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
C |
17: 48,348,059 (GRCm39) |
N82D |
probably benign |
Het |
Aadacl4fm2 |
A |
G |
4: 144,281,652 (GRCm39) |
V380A |
probably benign |
Het |
Acadm |
C |
T |
3: 153,638,755 (GRCm39) |
R206H |
possibly damaging |
Het |
Acly |
T |
A |
11: 100,414,372 (GRCm39) |
Y18F |
probably benign |
Het |
Acnat2 |
G |
T |
4: 49,380,452 (GRCm39) |
Q291K |
probably benign |
Het |
Agtpbp1 |
T |
C |
13: 59,648,453 (GRCm39) |
I456V |
probably benign |
Het |
Ankrd7 |
A |
G |
6: 18,868,076 (GRCm39) |
N114S |
possibly damaging |
Het |
Arfgef1 |
A |
T |
1: 10,275,132 (GRCm39) |
L307I |
probably benign |
Het |
Arhgef2 |
A |
T |
3: 88,542,956 (GRCm39) |
I383F |
probably damaging |
Het |
Cbs |
C |
T |
17: 31,843,198 (GRCm39) |
|
probably null |
Het |
Cep135 |
T |
C |
5: 76,763,624 (GRCm39) |
V538A |
probably benign |
Het |
Dennd5a |
T |
C |
7: 109,532,936 (GRCm39) |
E254G |
probably damaging |
Het |
Drc7 |
T |
C |
8: 95,788,345 (GRCm39) |
V236A |
probably benign |
Het |
Dtna |
C |
T |
18: 23,723,302 (GRCm39) |
Q169* |
probably null |
Het |
Egfem1 |
G |
A |
3: 29,411,345 (GRCm39) |
|
probably null |
Het |
Eif2ak3 |
T |
C |
6: 70,835,462 (GRCm39) |
S130P |
possibly damaging |
Het |
Ewsr1 |
T |
C |
11: 5,032,355 (GRCm39) |
N297S |
unknown |
Het |
F13a1 |
T |
G |
13: 37,156,037 (GRCm39) |
D192A |
probably damaging |
Het |
Fam120a |
A |
G |
13: 49,034,411 (GRCm39) |
V1067A |
probably benign |
Het |
Gm17490 |
T |
C |
2: 11,631,062 (GRCm39) |
Y5C |
unknown |
Het |
Gm57859 |
T |
C |
11: 113,579,654 (GRCm39) |
S350P |
possibly damaging |
Het |
Gm8587 |
C |
T |
12: 88,056,556 (GRCm39) |
|
noncoding transcript |
Het |
H2-Ab1 |
C |
T |
17: 34,488,352 (GRCm39) |
|
probably benign |
Het |
Hoxd12 |
T |
C |
2: 74,505,447 (GRCm39) |
L6P |
probably damaging |
Het |
Ifi204 |
C |
T |
1: 173,576,910 (GRCm39) |
D564N |
possibly damaging |
Het |
Irak2 |
T |
C |
6: 113,667,751 (GRCm39) |
V444A |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,921,748 (GRCm39) |
A199T |
probably damaging |
Het |
Lrba |
A |
C |
3: 86,235,526 (GRCm39) |
N877H |
probably damaging |
Het |
Mylk3 |
T |
C |
8: 86,079,495 (GRCm39) |
I388V |
probably benign |
Het |
Myo9b |
C |
T |
8: 71,801,733 (GRCm39) |
A1286V |
probably benign |
Het |
Myt1l |
A |
C |
12: 29,861,647 (GRCm39) |
D143A |
unknown |
Het |
Ngfr |
T |
C |
11: 95,471,808 (GRCm39) |
N63S |
probably benign |
Het |
Or2ag16 |
A |
T |
7: 106,352,426 (GRCm39) |
H56Q |
probably benign |
Het |
Or4c3 |
T |
A |
2: 89,851,870 (GRCm39) |
Y180F |
probably damaging |
Het |
Or51a7 |
A |
G |
7: 102,615,071 (GRCm39) |
I255V |
probably benign |
Het |
Or6c70 |
C |
T |
10: 129,709,967 (GRCm39) |
V220I |
probably benign |
Het |
Or6z6 |
A |
G |
7: 6,491,519 (GRCm39) |
L118P |
probably damaging |
Het |
P2rx7 |
T |
C |
5: 122,811,858 (GRCm39) |
S390P |
probably benign |
Het |
Pcdhga4 |
A |
C |
18: 37,820,794 (GRCm39) |
Q781P |
probably benign |
Het |
Phip |
G |
A |
9: 82,790,915 (GRCm39) |
S677F |
probably benign |
Het |
Ptpdc1 |
C |
A |
13: 48,740,265 (GRCm39) |
V389F |
possibly damaging |
Het |
Rab2a |
T |
A |
4: 8,604,381 (GRCm39) |
I161N |
probably benign |
Het |
Rnf113a2 |
T |
A |
12: 84,464,111 (GRCm39) |
M1K |
probably null |
Het |
Schip1 |
T |
C |
3: 68,402,205 (GRCm39) |
V122A |
probably benign |
Het |
Sdr16c5 |
C |
A |
4: 4,006,663 (GRCm39) |
A210S |
probably benign |
Het |
Sh3bp1 |
A |
G |
15: 78,787,301 (GRCm39) |
K83E |
probably damaging |
Het |
Slc22a21 |
T |
C |
11: 53,870,673 (GRCm39) |
Y4C |
probably damaging |
Het |
Smco1 |
C |
T |
16: 32,092,592 (GRCm39) |
H88Y |
probably damaging |
Het |
Tll2 |
T |
C |
19: 41,084,336 (GRCm39) |
D697G |
probably damaging |
Het |
Trim34a |
A |
G |
7: 103,910,200 (GRCm39) |
N334S |
possibly damaging |
Het |
Ubqln1 |
A |
G |
13: 58,346,847 (GRCm39) |
I64T |
probably benign |
Het |
Vstm2b |
T |
A |
7: 40,551,912 (GRCm39) |
|
probably null |
Het |
Wdr17 |
A |
G |
8: 55,140,639 (GRCm39) |
F238L |
probably damaging |
Het |
Wiz |
T |
C |
17: 32,596,822 (GRCm39) |
|
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,579,434 (GRCm39) |
S560G |
probably benign |
Het |
|
Other mutations in Sipa1l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00534:Sipa1l2
|
APN |
8 |
126,218,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00939:Sipa1l2
|
APN |
8 |
126,191,174 (GRCm39) |
splice site |
probably benign |
|
IGL00965:Sipa1l2
|
APN |
8 |
126,174,613 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01321:Sipa1l2
|
APN |
8 |
126,218,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01450:Sipa1l2
|
APN |
8 |
126,149,316 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01753:Sipa1l2
|
APN |
8 |
126,180,031 (GRCm39) |
splice site |
probably benign |
|
IGL01930:Sipa1l2
|
APN |
8 |
126,145,978 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02041:Sipa1l2
|
APN |
8 |
126,218,558 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02215:Sipa1l2
|
APN |
8 |
126,174,576 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02272:Sipa1l2
|
APN |
8 |
126,218,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02370:Sipa1l2
|
APN |
8 |
126,207,008 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Sipa1l2
|
APN |
8 |
126,178,716 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02633:Sipa1l2
|
APN |
8 |
126,174,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03394:Sipa1l2
|
APN |
8 |
126,218,398 (GRCm39) |
missense |
possibly damaging |
0.67 |
Rebellious
|
UTSW |
8 |
126,195,078 (GRCm39) |
missense |
probably benign |
0.01 |
R0144:Sipa1l2
|
UTSW |
8 |
126,176,615 (GRCm39) |
splice site |
probably null |
|
R0153:Sipa1l2
|
UTSW |
8 |
126,148,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R0276:Sipa1l2
|
UTSW |
8 |
126,148,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0318:Sipa1l2
|
UTSW |
8 |
126,174,436 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0373:Sipa1l2
|
UTSW |
8 |
126,191,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R0427:Sipa1l2
|
UTSW |
8 |
126,207,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0634:Sipa1l2
|
UTSW |
8 |
126,149,363 (GRCm39) |
nonsense |
probably null |
|
R1377:Sipa1l2
|
UTSW |
8 |
126,218,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1404:Sipa1l2
|
UTSW |
8 |
126,176,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1404:Sipa1l2
|
UTSW |
8 |
126,176,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Sipa1l2
|
UTSW |
8 |
126,195,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R1523:Sipa1l2
|
UTSW |
8 |
126,174,352 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1577:Sipa1l2
|
UTSW |
8 |
126,219,001 (GRCm39) |
missense |
probably benign |
0.00 |
R1581:Sipa1l2
|
UTSW |
8 |
126,218,356 (GRCm39) |
missense |
probably damaging |
0.96 |
R1583:Sipa1l2
|
UTSW |
8 |
126,148,634 (GRCm39) |
missense |
probably damaging |
0.97 |
R1719:Sipa1l2
|
UTSW |
8 |
126,171,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R1730:Sipa1l2
|
UTSW |
8 |
126,206,880 (GRCm39) |
splice site |
probably null |
|
R1940:Sipa1l2
|
UTSW |
8 |
126,206,887 (GRCm39) |
splice site |
probably benign |
|
R2007:Sipa1l2
|
UTSW |
8 |
126,166,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Sipa1l2
|
UTSW |
8 |
126,218,230 (GRCm39) |
missense |
probably benign |
0.07 |
R2203:Sipa1l2
|
UTSW |
8 |
126,218,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R2764:Sipa1l2
|
UTSW |
8 |
126,219,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R3722:Sipa1l2
|
UTSW |
8 |
126,200,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Sipa1l2
|
UTSW |
8 |
126,177,122 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3787:Sipa1l2
|
UTSW |
8 |
126,149,944 (GRCm39) |
missense |
probably benign |
|
R4106:Sipa1l2
|
UTSW |
8 |
126,219,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R4117:Sipa1l2
|
UTSW |
8 |
126,195,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R4194:Sipa1l2
|
UTSW |
8 |
126,218,411 (GRCm39) |
missense |
probably benign |
0.00 |
R4237:Sipa1l2
|
UTSW |
8 |
126,218,395 (GRCm39) |
missense |
probably benign |
0.44 |
R4240:Sipa1l2
|
UTSW |
8 |
126,218,395 (GRCm39) |
missense |
probably benign |
0.44 |
R4448:Sipa1l2
|
UTSW |
8 |
126,219,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R4515:Sipa1l2
|
UTSW |
8 |
126,218,965 (GRCm39) |
missense |
probably benign |
0.00 |
R4519:Sipa1l2
|
UTSW |
8 |
126,218,965 (GRCm39) |
missense |
probably benign |
0.00 |
R4523:Sipa1l2
|
UTSW |
8 |
126,219,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Sipa1l2
|
UTSW |
8 |
126,191,154 (GRCm39) |
missense |
probably damaging |
0.98 |
R4667:Sipa1l2
|
UTSW |
8 |
126,180,209 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4687:Sipa1l2
|
UTSW |
8 |
126,217,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:Sipa1l2
|
UTSW |
8 |
126,200,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Sipa1l2
|
UTSW |
8 |
126,218,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R5065:Sipa1l2
|
UTSW |
8 |
126,218,324 (GRCm39) |
missense |
probably benign |
0.19 |
R5266:Sipa1l2
|
UTSW |
8 |
126,218,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R5475:Sipa1l2
|
UTSW |
8 |
126,218,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R5718:Sipa1l2
|
UTSW |
8 |
126,217,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Sipa1l2
|
UTSW |
8 |
126,218,423 (GRCm39) |
missense |
probably benign |
0.42 |
R5916:Sipa1l2
|
UTSW |
8 |
126,195,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Sipa1l2
|
UTSW |
8 |
126,200,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R6083:Sipa1l2
|
UTSW |
8 |
126,195,212 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6185:Sipa1l2
|
UTSW |
8 |
126,194,992 (GRCm39) |
nonsense |
probably null |
|
R6235:Sipa1l2
|
UTSW |
8 |
126,201,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Sipa1l2
|
UTSW |
8 |
126,196,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Sipa1l2
|
UTSW |
8 |
126,180,203 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6374:Sipa1l2
|
UTSW |
8 |
126,171,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Sipa1l2
|
UTSW |
8 |
126,171,223 (GRCm39) |
critical splice donor site |
probably null |
|
R6462:Sipa1l2
|
UTSW |
8 |
126,217,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Sipa1l2
|
UTSW |
8 |
126,176,633 (GRCm39) |
missense |
probably benign |
0.00 |
R6543:Sipa1l2
|
UTSW |
8 |
126,177,101 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7154:Sipa1l2
|
UTSW |
8 |
126,195,078 (GRCm39) |
missense |
probably benign |
0.01 |
R7192:Sipa1l2
|
UTSW |
8 |
126,149,348 (GRCm39) |
missense |
probably benign |
0.09 |
R7240:Sipa1l2
|
UTSW |
8 |
126,196,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Sipa1l2
|
UTSW |
8 |
126,180,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R7383:Sipa1l2
|
UTSW |
8 |
126,174,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:Sipa1l2
|
UTSW |
8 |
126,208,845 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7604:Sipa1l2
|
UTSW |
8 |
126,146,011 (GRCm39) |
missense |
probably benign |
0.45 |
R7658:Sipa1l2
|
UTSW |
8 |
126,219,029 (GRCm39) |
missense |
probably benign |
0.00 |
R7743:Sipa1l2
|
UTSW |
8 |
126,190,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R7781:Sipa1l2
|
UTSW |
8 |
126,218,566 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7812:Sipa1l2
|
UTSW |
8 |
126,218,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7829:Sipa1l2
|
UTSW |
8 |
126,178,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R7880:Sipa1l2
|
UTSW |
8 |
126,191,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Sipa1l2
|
UTSW |
8 |
126,174,337 (GRCm39) |
missense |
probably benign |
|
R8057:Sipa1l2
|
UTSW |
8 |
126,195,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Sipa1l2
|
UTSW |
8 |
126,218,548 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8092:Sipa1l2
|
UTSW |
8 |
126,145,907 (GRCm39) |
missense |
probably benign |
0.03 |
R8247:Sipa1l2
|
UTSW |
8 |
126,149,372 (GRCm39) |
missense |
probably benign |
0.29 |
R8252:Sipa1l2
|
UTSW |
8 |
126,195,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R8386:Sipa1l2
|
UTSW |
8 |
126,218,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R8466:Sipa1l2
|
UTSW |
8 |
126,218,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R8697:Sipa1l2
|
UTSW |
8 |
126,208,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Sipa1l2
|
UTSW |
8 |
126,177,125 (GRCm39) |
missense |
probably benign |
0.28 |
R8727:Sipa1l2
|
UTSW |
8 |
126,177,125 (GRCm39) |
missense |
probably benign |
0.28 |
R9048:Sipa1l2
|
UTSW |
8 |
126,174,465 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9224:Sipa1l2
|
UTSW |
8 |
126,218,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Sipa1l2
|
UTSW |
8 |
126,208,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R9392:Sipa1l2
|
UTSW |
8 |
126,194,960 (GRCm39) |
missense |
probably benign |
|
R9574:Sipa1l2
|
UTSW |
8 |
126,169,453 (GRCm39) |
missense |
probably benign |
|
R9591:Sipa1l2
|
UTSW |
8 |
126,219,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R9614:Sipa1l2
|
UTSW |
8 |
126,196,565 (GRCm39) |
missense |
probably null |
0.01 |
R9690:Sipa1l2
|
UTSW |
8 |
126,218,996 (GRCm39) |
missense |
probably benign |
|
X0027:Sipa1l2
|
UTSW |
8 |
126,218,875 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sipa1l2
|
UTSW |
8 |
126,174,295 (GRCm39) |
missense |
possibly damaging |
0.72 |
|