Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
T |
A |
6: 91,900,445 (GRCm39) |
L438* |
probably null |
Het |
Adamts18 |
T |
A |
8: 114,493,760 (GRCm39) |
I460F |
probably damaging |
Het |
Api5 |
C |
T |
2: 94,268,392 (GRCm39) |
|
probably benign |
Het |
Arap2 |
A |
G |
5: 62,888,048 (GRCm39) |
S433P |
probably damaging |
Het |
Arhgap26 |
T |
C |
18: 39,338,340 (GRCm39) |
Y371H |
probably damaging |
Het |
Asf1b |
T |
C |
8: 84,695,848 (GRCm39) |
I163T |
probably benign |
Het |
Cacna2d2 |
A |
G |
9: 107,401,326 (GRCm39) |
N696S |
probably damaging |
Het |
Carns1 |
A |
C |
19: 4,216,152 (GRCm39) |
S677A |
probably benign |
Het |
Cd276 |
G |
A |
9: 58,448,113 (GRCm39) |
|
probably benign |
Het |
Cdk8 |
T |
A |
5: 146,236,644 (GRCm39) |
M353K |
possibly damaging |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Chsy3 |
A |
G |
18: 59,542,418 (GRCm39) |
I519V |
probably damaging |
Het |
Chtop |
T |
C |
3: 90,414,658 (GRCm39) |
|
probably benign |
Het |
Clstn3 |
T |
A |
6: 124,408,972 (GRCm39) |
D892V |
possibly damaging |
Het |
Col16a1 |
A |
T |
4: 129,990,664 (GRCm39) |
|
probably null |
Het |
Dnah5 |
A |
G |
15: 28,345,983 (GRCm39) |
E2441G |
possibly damaging |
Het |
Dpy19l2 |
T |
G |
9: 24,469,454 (GRCm39) |
D734A |
probably damaging |
Het |
Dusp2 |
T |
A |
2: 127,178,812 (GRCm39) |
Y172* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,890,524 (GRCm39) |
N4202S |
possibly damaging |
Het |
Efcab3 |
G |
A |
11: 104,937,385 (GRCm39) |
|
probably null |
Het |
Eml4 |
G |
A |
17: 83,781,115 (GRCm39) |
R771Q |
possibly damaging |
Het |
Fat2 |
T |
A |
11: 55,200,993 (GRCm39) |
M694L |
probably benign |
Het |
Fat2 |
C |
A |
11: 55,201,986 (GRCm39) |
E363* |
probably null |
Het |
Gdpgp1 |
A |
G |
7: 79,888,826 (GRCm39) |
I286V |
probably damaging |
Het |
Gps1 |
T |
A |
11: 120,677,199 (GRCm39) |
V166E |
probably damaging |
Het |
H60b |
T |
A |
10: 22,162,055 (GRCm39) |
N93K |
probably benign |
Het |
Imp4 |
C |
T |
1: 34,482,114 (GRCm39) |
T79I |
probably benign |
Het |
Kank3 |
A |
G |
17: 34,037,841 (GRCm39) |
S485G |
probably benign |
Het |
Kcnv2 |
A |
G |
19: 27,300,167 (GRCm39) |
N6S |
probably benign |
Het |
Krba1 |
A |
T |
6: 48,388,603 (GRCm39) |
Q534L |
probably damaging |
Het |
Lgr4 |
A |
G |
2: 109,836,863 (GRCm39) |
N399S |
probably damaging |
Het |
Lgr5 |
A |
G |
10: 115,288,952 (GRCm39) |
V564A |
probably damaging |
Het |
Lrtm2 |
A |
G |
6: 119,297,394 (GRCm39) |
F216L |
probably benign |
Het |
Lsm8 |
T |
A |
6: 18,849,658 (GRCm39) |
M22K |
probably benign |
Het |
Mboat2 |
C |
T |
12: 25,005,392 (GRCm39) |
T389M |
probably damaging |
Het |
Mcoln1 |
T |
G |
8: 3,555,924 (GRCm39) |
I73S |
probably damaging |
Het |
Myh7 |
T |
A |
14: 55,216,920 (GRCm39) |
I1146F |
possibly damaging |
Het |
Naa16 |
G |
A |
14: 79,578,486 (GRCm39) |
T666I |
possibly damaging |
Het |
Ncoa1 |
A |
G |
12: 4,385,873 (GRCm39) |
S88P |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,941,334 (GRCm39) |
T4496A |
possibly damaging |
Het |
Or13a28 |
T |
C |
7: 140,217,652 (GRCm39) |
F13L |
probably damaging |
Het |
Or7a35 |
T |
A |
10: 78,853,872 (GRCm39) |
F239I |
probably damaging |
Het |
Pdxk |
G |
T |
10: 78,277,012 (GRCm39) |
A262D |
possibly damaging |
Het |
Pebp4 |
T |
A |
14: 70,089,082 (GRCm39) |
L68Q |
probably damaging |
Het |
Pfdn5 |
C |
T |
15: 102,236,978 (GRCm39) |
H77Y |
possibly damaging |
Het |
Pld1 |
T |
C |
3: 28,130,651 (GRCm39) |
Y484H |
probably damaging |
Het |
Pou3f3 |
C |
A |
1: 42,736,560 (GRCm39) |
N85K |
unknown |
Het |
Ppm1m |
C |
A |
9: 106,075,144 (GRCm39) |
A134S |
probably damaging |
Het |
Prdm11 |
A |
T |
2: 92,806,106 (GRCm39) |
S281R |
possibly damaging |
Het |
Prdm2 |
C |
A |
4: 142,862,434 (GRCm39) |
L285F |
probably damaging |
Het |
Ptchd3 |
C |
T |
11: 121,721,939 (GRCm39) |
R271* |
probably null |
Het |
Ptprq |
A |
C |
10: 107,488,572 (GRCm39) |
V955G |
probably damaging |
Het |
Pygb |
A |
T |
2: 150,657,589 (GRCm39) |
M351L |
probably benign |
Het |
Rcl1 |
G |
A |
19: 29,095,805 (GRCm39) |
|
probably null |
Het |
Slc22a5 |
T |
C |
11: 53,760,215 (GRCm39) |
N367S |
probably damaging |
Het |
Sox6 |
A |
G |
7: 115,143,830 (GRCm39) |
V437A |
probably benign |
Het |
Spata16 |
T |
A |
3: 26,721,572 (GRCm39) |
M31K |
possibly damaging |
Het |
Stab1 |
C |
A |
14: 30,879,372 (GRCm39) |
V703F |
possibly damaging |
Het |
Tbc1d4 |
C |
T |
14: 101,703,190 (GRCm39) |
G752R |
probably damaging |
Het |
Tent4b |
G |
A |
8: 88,978,913 (GRCm39) |
G505R |
probably null |
Het |
Tes3-ps |
C |
T |
13: 49,647,460 (GRCm39) |
A112V |
probably benign |
Het |
Tnfrsf19 |
T |
C |
14: 61,208,382 (GRCm39) |
T380A |
probably benign |
Het |
Trim75 |
C |
T |
8: 65,435,190 (GRCm39) |
G420E |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,703,712 (GRCm39) |
D290G |
probably benign |
Het |
Unc5c |
T |
A |
3: 141,534,238 (GRCm39) |
F920I |
possibly damaging |
Het |
Vmn1r233 |
T |
A |
17: 21,214,237 (GRCm39) |
R238* |
probably null |
Het |
Vmn2r113 |
A |
G |
17: 23,176,917 (GRCm39) |
E567G |
probably benign |
Het |
Vmn2r97 |
T |
A |
17: 19,150,662 (GRCm39) |
I503K |
probably damaging |
Het |
Wdr62 |
A |
G |
7: 29,964,584 (GRCm39) |
W387R |
probably damaging |
Het |
Zfp36l2 |
A |
T |
17: 84,495,090 (GRCm39) |
D11E |
probably benign |
Het |
|
Other mutations in Sgip1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00847:Sgip1
|
APN |
4 |
102,786,118 (GRCm39) |
splice site |
probably benign |
|
IGL01348:Sgip1
|
APN |
4 |
102,772,353 (GRCm39) |
splice site |
probably null |
|
IGL01446:Sgip1
|
APN |
4 |
102,786,110 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01937:Sgip1
|
APN |
4 |
102,823,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01945:Sgip1
|
APN |
4 |
102,823,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Sgip1
|
APN |
4 |
102,768,667 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03232:Sgip1
|
APN |
4 |
102,772,251 (GRCm39) |
splice site |
probably benign |
|
3-1:Sgip1
|
UTSW |
4 |
102,824,860 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4378001:Sgip1
|
UTSW |
4 |
102,778,280 (GRCm39) |
missense |
unknown |
|
R0309:Sgip1
|
UTSW |
4 |
102,772,354 (GRCm39) |
splice site |
probably benign |
|
R0689:Sgip1
|
UTSW |
4 |
102,823,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Sgip1
|
UTSW |
4 |
102,823,457 (GRCm39) |
missense |
probably benign |
0.38 |
R1715:Sgip1
|
UTSW |
4 |
102,772,256 (GRCm39) |
missense |
probably benign |
0.09 |
R1899:Sgip1
|
UTSW |
4 |
102,825,534 (GRCm39) |
critical splice donor site |
probably null |
|
R2286:Sgip1
|
UTSW |
4 |
102,724,844 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2372:Sgip1
|
UTSW |
4 |
102,766,988 (GRCm39) |
critical splice donor site |
probably null |
|
R3836:Sgip1
|
UTSW |
4 |
102,724,897 (GRCm39) |
splice site |
probably null |
|
R4670:Sgip1
|
UTSW |
4 |
102,726,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Sgip1
|
UTSW |
4 |
102,791,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Sgip1
|
UTSW |
4 |
102,823,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R4892:Sgip1
|
UTSW |
4 |
102,823,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Sgip1
|
UTSW |
4 |
102,726,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R5236:Sgip1
|
UTSW |
4 |
102,784,784 (GRCm39) |
critical splice donor site |
probably null |
|
R5285:Sgip1
|
UTSW |
4 |
102,778,674 (GRCm39) |
unclassified |
probably benign |
|
R5323:Sgip1
|
UTSW |
4 |
102,823,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Sgip1
|
UTSW |
4 |
102,791,763 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5386:Sgip1
|
UTSW |
4 |
102,772,256 (GRCm39) |
missense |
probably benign |
0.09 |
R5682:Sgip1
|
UTSW |
4 |
102,824,847 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6226:Sgip1
|
UTSW |
4 |
102,823,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R6371:Sgip1
|
UTSW |
4 |
102,823,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6594:Sgip1
|
UTSW |
4 |
102,819,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R6656:Sgip1
|
UTSW |
4 |
102,762,765 (GRCm39) |
intron |
probably benign |
|
R6800:Sgip1
|
UTSW |
4 |
102,778,225 (GRCm39) |
unclassified |
probably benign |
|
R6855:Sgip1
|
UTSW |
4 |
102,819,573 (GRCm39) |
missense |
probably damaging |
0.99 |
R6917:Sgip1
|
UTSW |
4 |
102,825,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R7340:Sgip1
|
UTSW |
4 |
102,778,661 (GRCm39) |
missense |
unknown |
|
R7414:Sgip1
|
UTSW |
4 |
102,824,821 (GRCm39) |
nonsense |
probably null |
|
R7612:Sgip1
|
UTSW |
4 |
102,727,005 (GRCm39) |
missense |
probably benign |
0.28 |
R7944:Sgip1
|
UTSW |
4 |
102,772,298 (GRCm39) |
missense |
probably benign |
|
R7976:Sgip1
|
UTSW |
4 |
102,757,736 (GRCm39) |
critical splice donor site |
probably null |
|
R8508:Sgip1
|
UTSW |
4 |
102,772,268 (GRCm39) |
missense |
probably benign |
0.14 |
R8997:Sgip1
|
UTSW |
4 |
102,790,781 (GRCm39) |
missense |
|
|
|