Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
A |
T |
19: 43,772,674 (GRCm39) |
Q28L |
probably damaging |
Het |
Abtb3 |
G |
A |
10: 85,223,418 (GRCm39) |
D76N |
unknown |
Het |
Afg1l |
A |
G |
10: 42,330,376 (GRCm39) |
V97A |
probably damaging |
Het |
Akap6 |
A |
C |
12: 53,187,436 (GRCm39) |
S1617R |
probably damaging |
Het |
Aldh1a3 |
T |
C |
7: 66,057,579 (GRCm39) |
N285D |
probably damaging |
Het |
Arhgap20 |
A |
T |
9: 51,757,490 (GRCm39) |
N494I |
possibly damaging |
Het |
Atg9a |
G |
T |
1: 75,159,748 (GRCm39) |
Q712K |
possibly damaging |
Het |
Cdcp2 |
G |
A |
4: 106,964,386 (GRCm39) |
|
probably benign |
Het |
Cds2 |
T |
A |
2: 132,136,363 (GRCm39) |
I84N |
possibly damaging |
Het |
Clcn3 |
T |
C |
8: 61,376,187 (GRCm39) |
I596V |
probably damaging |
Het |
Ctxn1 |
A |
G |
8: 4,308,514 (GRCm39) |
L39P |
probably damaging |
Het |
Efhb |
A |
T |
17: 53,733,287 (GRCm39) |
V528D |
probably damaging |
Het |
Fmod |
T |
G |
1: 133,968,001 (GRCm39) |
S14A |
probably benign |
Het |
Foxh1 |
A |
G |
15: 76,553,120 (GRCm39) |
F198S |
probably damaging |
Het |
Gcc2 |
A |
G |
10: 58,105,103 (GRCm39) |
E77G |
probably damaging |
Het |
Gm5420 |
G |
T |
10: 21,566,933 (GRCm39) |
|
noncoding transcript |
Het |
Gm6434 |
T |
G |
7: 25,581,655 (GRCm39) |
|
noncoding transcript |
Het |
Il1b |
A |
T |
2: 129,211,662 (GRCm39) |
N19K |
possibly damaging |
Het |
Lama2 |
T |
A |
10: 26,860,322 (GRCm39) |
D3055V |
probably damaging |
Het |
Lcn3 |
G |
A |
2: 25,655,636 (GRCm39) |
V18I |
probably benign |
Het |
Lpcat2 |
A |
G |
8: 93,644,809 (GRCm39) |
S533G |
probably benign |
Het |
Map4k2 |
G |
A |
19: 6,401,348 (GRCm39) |
R606Q |
probably benign |
Het |
Mtnr1b |
T |
C |
9: 15,774,589 (GRCm39) |
T157A |
probably benign |
Het |
Myo15a |
G |
A |
11: 60,397,689 (GRCm39) |
E2705K |
probably damaging |
Het |
Ncf2 |
A |
G |
1: 152,711,871 (GRCm39) |
|
probably benign |
Het |
Nfkbil1 |
G |
A |
17: 35,439,934 (GRCm39) |
T193M |
probably benign |
Het |
Nmi |
T |
G |
2: 51,850,641 (GRCm39) |
K9T |
possibly damaging |
Het |
Or2d4 |
T |
C |
7: 106,543,320 (GRCm39) |
D296G |
possibly damaging |
Het |
Or5p69 |
T |
C |
7: 107,966,742 (GRCm39) |
F15S |
probably damaging |
Het |
Or6c6c |
A |
G |
10: 129,541,104 (GRCm39) |
D119G |
probably damaging |
Het |
Osbpl7 |
T |
A |
11: 96,951,334 (GRCm39) |
C502S |
probably benign |
Het |
Pex5 |
A |
T |
6: 124,382,240 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,356,452 (GRCm39) |
|
probably null |
Het |
Prmt3 |
C |
T |
7: 49,478,711 (GRCm39) |
T424M |
possibly damaging |
Het |
Rapgef4 |
G |
A |
2: 72,029,140 (GRCm39) |
G404D |
probably damaging |
Het |
Rbm5 |
C |
T |
9: 107,633,045 (GRCm39) |
|
probably benign |
Het |
Rfc2 |
T |
A |
5: 134,623,098 (GRCm39) |
F238L |
probably benign |
Het |
Rsl1 |
A |
G |
13: 67,324,612 (GRCm39) |
E46G |
probably damaging |
Het |
Sall1 |
A |
G |
8: 89,758,097 (GRCm39) |
F669S |
probably damaging |
Het |
Slc26a8 |
A |
G |
17: 28,861,225 (GRCm39) |
Y820H |
probably damaging |
Het |
Tas2r115 |
A |
G |
6: 132,714,430 (GRCm39) |
F174L |
probably benign |
Het |
Terb1 |
A |
C |
8: 105,221,746 (GRCm39) |
C185G |
probably damaging |
Het |
Vmn2r108 |
A |
T |
17: 20,683,398 (GRCm39) |
V602E |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,514,703 (GRCm39) |
I89F |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,423,391 (GRCm39) |
R237L |
probably damaging |
Het |
Zfp865 |
T |
C |
7: 5,034,372 (GRCm39) |
S786P |
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 |
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 |
R5194:Sipa1l2
|
UTSW |
8 |
126,166,012 (GRCm39) |
missense |
possibly damaging |
0.48 |
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 |
|