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 |
Sgip1 |
A |
T |
4: 102,786,097 (GRCm39) |
T351S |
possibly damaging |
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 |
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 Tent4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00502:Tent4b
|
APN |
8 |
88,978,886 (GRCm39) |
nonsense |
probably null |
|
R0079:Tent4b
|
UTSW |
8 |
88,926,631 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0158:Tent4b
|
UTSW |
8 |
88,977,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Tent4b
|
UTSW |
8 |
88,978,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1351:Tent4b
|
UTSW |
8 |
88,927,002 (GRCm39) |
nonsense |
probably null |
|
R1381:Tent4b
|
UTSW |
8 |
88,969,937 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1541:Tent4b
|
UTSW |
8 |
88,972,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Tent4b
|
UTSW |
8 |
88,977,416 (GRCm39) |
missense |
probably benign |
0.25 |
R1994:Tent4b
|
UTSW |
8 |
88,973,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Tent4b
|
UTSW |
8 |
88,972,223 (GRCm39) |
splice site |
probably null |
|
R2290:Tent4b
|
UTSW |
8 |
88,978,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R3791:Tent4b
|
UTSW |
8 |
88,969,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R3845:Tent4b
|
UTSW |
8 |
88,977,292 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3886:Tent4b
|
UTSW |
8 |
88,927,043 (GRCm39) |
missense |
probably benign |
0.03 |
R5041:Tent4b
|
UTSW |
8 |
88,981,878 (GRCm39) |
small deletion |
probably benign |
|
R5253:Tent4b
|
UTSW |
8 |
88,926,651 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6881:Tent4b
|
UTSW |
8 |
88,977,416 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7792:Tent4b
|
UTSW |
8 |
88,979,182 (GRCm39) |
missense |
probably benign |
|
R8054:Tent4b
|
UTSW |
8 |
88,974,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R8997:Tent4b
|
UTSW |
8 |
88,979,023 (GRCm39) |
missense |
probably benign |
0.12 |
R8998:Tent4b
|
UTSW |
8 |
88,977,350 (GRCm39) |
missense |
probably benign |
0.09 |
X0024:Tent4b
|
UTSW |
8 |
88,973,103 (GRCm39) |
missense |
probably damaging |
1.00 |
|