Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930558K02Rik |
C |
T |
1: 161,795,565 (GRCm39) |
A8T |
probably benign |
Het |
Acacb |
T |
C |
5: 114,351,441 (GRCm39) |
V1130A |
probably damaging |
Het |
Ackr1 |
A |
G |
1: 173,159,775 (GRCm39) |
F248S |
probably damaging |
Het |
Alx4 |
G |
A |
2: 93,505,657 (GRCm39) |
R253Q |
probably damaging |
Het |
Ap3b2 |
T |
C |
7: 81,122,783 (GRCm39) |
I485V |
possibly damaging |
Het |
Aqp7 |
T |
C |
4: 41,045,305 (GRCm39) |
E25G |
probably damaging |
Het |
Cacna1g |
T |
C |
11: 94,307,524 (GRCm39) |
N1753D |
probably benign |
Het |
Cacna2d1 |
T |
A |
5: 16,570,865 (GRCm39) |
N1063K |
possibly damaging |
Het |
Cad |
T |
C |
5: 31,231,945 (GRCm39) |
V1801A |
probably benign |
Het |
Ccdc171 |
T |
C |
4: 83,600,577 (GRCm39) |
W868R |
probably damaging |
Het |
Cecr2 |
T |
C |
6: 120,710,779 (GRCm39) |
Y165H |
probably damaging |
Het |
Clip4 |
G |
T |
17: 72,163,270 (GRCm39) |
G614V |
possibly damaging |
Het |
Ctnnal1 |
T |
A |
4: 56,838,986 (GRCm39) |
M236L |
probably damaging |
Het |
Ctps1 |
T |
C |
4: 120,399,947 (GRCm39) |
D470G |
probably benign |
Het |
Dmwd |
A |
C |
7: 18,812,113 (GRCm39) |
Q189P |
probably damaging |
Het |
Dnah17 |
A |
G |
11: 117,976,985 (GRCm39) |
I1869T |
possibly damaging |
Het |
Eepd1 |
A |
G |
9: 25,497,998 (GRCm39) |
N361S |
probably benign |
Het |
Ephb6 |
C |
T |
6: 41,591,157 (GRCm39) |
H105Y |
probably damaging |
Het |
Fkbp15 |
A |
T |
4: 62,239,295 (GRCm39) |
Y603* |
probably null |
Het |
Flt3 |
T |
C |
5: 147,294,811 (GRCm39) |
Y420C |
possibly damaging |
Het |
Frem2 |
T |
A |
3: 53,433,249 (GRCm39) |
T2692S |
probably damaging |
Het |
Gna12 |
T |
A |
5: 140,771,200 (GRCm39) |
R157S |
probably benign |
Het |
Gsdmc |
A |
T |
15: 63,651,883 (GRCm39) |
S243T |
probably benign |
Het |
Hectd1 |
A |
G |
12: 51,819,320 (GRCm39) |
|
probably benign |
Het |
Hoxd11 |
G |
A |
2: 74,513,013 (GRCm39) |
G93R |
unknown |
Het |
Hydin |
A |
G |
8: 111,259,515 (GRCm39) |
I2496V |
probably benign |
Het |
Igsf10 |
A |
G |
3: 59,226,308 (GRCm39) |
I2455T |
probably benign |
Het |
Ilvbl |
A |
T |
10: 78,419,196 (GRCm39) |
R482* |
probably null |
Het |
Itpr1 |
A |
G |
6: 108,500,327 (GRCm39) |
Y2640C |
probably damaging |
Het |
Kif20a |
C |
G |
18: 34,761,584 (GRCm39) |
Q326E |
probably benign |
Het |
Lamp1 |
A |
T |
8: 13,224,448 (GRCm39) |
M371L |
possibly damaging |
Het |
Lcn6 |
A |
G |
2: 25,567,166 (GRCm39) |
N56D |
probably benign |
Het |
Map3k10 |
A |
G |
7: 27,362,784 (GRCm39) |
V434A |
probably benign |
Het |
Mdga1 |
T |
C |
17: 30,065,615 (GRCm39) |
N331S |
probably damaging |
Het |
Mndal |
C |
A |
1: 173,700,558 (GRCm39) |
E138* |
probably null |
Het |
Morc3 |
T |
C |
16: 93,667,908 (GRCm39) |
V762A |
probably benign |
Het |
Ngef |
A |
T |
1: 87,417,459 (GRCm39) |
F279Y |
probably damaging |
Het |
Or10ac1 |
A |
G |
6: 42,515,629 (GRCm39) |
V109A |
probably damaging |
Het |
Or5m13b |
A |
T |
2: 85,754,200 (GRCm39) |
K196I |
possibly damaging |
Het |
Padi4 |
GGAGCTCCTGA |
GGA |
4: 140,485,230 (GRCm39) |
|
probably null |
Het |
Pcdhb4 |
G |
A |
18: 37,441,832 (GRCm39) |
V381M |
probably benign |
Het |
Ppm1d |
T |
C |
11: 85,227,986 (GRCm39) |
Y301H |
possibly damaging |
Het |
Rasgrf1 |
A |
G |
9: 89,877,055 (GRCm39) |
T807A |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Skic3 |
A |
G |
13: 76,328,274 (GRCm39) |
S1441G |
probably damaging |
Het |
Slc52a3 |
A |
G |
2: 151,846,396 (GRCm39) |
D119G |
probably damaging |
Het |
Srsf4 |
C |
T |
4: 131,628,042 (GRCm39) |
H379Y |
unknown |
Het |
Ssr1 |
G |
T |
13: 38,167,425 (GRCm39) |
S246* |
probably null |
Het |
Tars2 |
C |
T |
3: 95,653,374 (GRCm39) |
E509K |
possibly damaging |
Het |
Tepsin |
G |
T |
11: 119,988,354 (GRCm39) |
Y34* |
probably null |
Het |
Tmtc2 |
A |
G |
10: 105,205,831 (GRCm39) |
I488T |
probably damaging |
Het |
Trgc2 |
A |
T |
13: 19,491,514 (GRCm39) |
M69K |
|
Het |
Ttn |
A |
G |
2: 76,575,120 (GRCm39) |
W25258R |
probably damaging |
Het |
Utp14b |
T |
C |
1: 78,644,244 (GRCm39) |
M714T |
probably benign |
Het |
Vwa3b |
T |
A |
1: 37,115,461 (GRCm39) |
H308Q |
probably benign |
Het |
Washc2 |
A |
G |
6: 116,206,220 (GRCm39) |
D480G |
probably benign |
Het |
Xcl1 |
C |
T |
1: 164,763,008 (GRCm39) |
V18I |
unknown |
Het |
Zcchc2 |
C |
A |
1: 105,958,494 (GRCm39) |
N988K |
probably damaging |
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 |
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 |
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 |
|