Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Epha8 |
G |
T |
4: 136,659,051 (GRCm39) |
Q868K |
possibly damaging |
Het |
Erc1 |
T |
A |
6: 119,760,355 (GRCm39) |
M386L |
probably damaging |
Het |
Gfpt2 |
T |
A |
11: 49,715,150 (GRCm39) |
|
probably null |
Het |
Gpr142 |
T |
A |
11: 114,695,152 (GRCm39) |
L39Q |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,474,148 (GRCm39) |
W4765R |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,314,264 (GRCm39) |
E3603V |
possibly damaging |
Het |
Hsp90b1 |
C |
T |
10: 86,540,234 (GRCm39) |
D26N |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,486,274 (GRCm39) |
T4760A |
probably damaging |
Het |
Lmo7 |
C |
A |
14: 102,163,576 (GRCm39) |
|
probably benign |
Het |
Mup4 |
A |
T |
4: 59,960,120 (GRCm39) |
I48K |
probably damaging |
Het |
Mylk3 |
T |
A |
8: 86,091,718 (GRCm39) |
D29V |
probably damaging |
Het |
Myo1b |
A |
G |
1: 51,823,690 (GRCm39) |
F405S |
probably damaging |
Het |
Nbea |
T |
C |
3: 55,712,669 (GRCm39) |
D2136G |
possibly damaging |
Het |
Or1l4b |
A |
T |
2: 37,036,986 (GRCm39) |
Y254F |
probably damaging |
Het |
Or52a20 |
T |
G |
7: 103,366,204 (GRCm39) |
H134Q |
probably damaging |
Het |
Or5g27 |
T |
A |
2: 85,409,875 (GRCm39) |
C97* |
probably null |
Het |
Or7e175 |
A |
T |
9: 20,048,750 (GRCm39) |
T113S |
probably damaging |
Het |
Psmg2 |
G |
A |
18: 67,786,293 (GRCm39) |
V218I |
probably benign |
Het |
Rpp40 |
T |
C |
13: 36,090,183 (GRCm39) |
|
probably null |
Het |
Samd7 |
T |
A |
3: 30,819,399 (GRCm39) |
S383T |
probably damaging |
Het |
Tbc1d10c |
T |
C |
19: 4,234,823 (GRCm39) |
T413A |
probably damaging |
Het |
Tlr12 |
A |
G |
4: 128,509,535 (GRCm39) |
L905P |
probably damaging |
Het |
Tnr |
A |
G |
1: 159,701,828 (GRCm39) |
K643R |
probably benign |
Het |
Vmn2r124 |
T |
C |
17: 18,283,617 (GRCm39) |
|
probably null |
Het |
Vwf |
A |
T |
6: 125,656,252 (GRCm39) |
I2606F |
probably benign |
Het |
Wbp4 |
T |
C |
14: 79,703,774 (GRCm39) |
T258A |
probably benign |
Het |
Zfp1005 |
T |
A |
2: 150,108,363 (GRCm39) |
|
probably benign |
Het |
Zfp758 |
T |
C |
17: 22,594,021 (GRCm39) |
L137S |
probably damaging |
Het |
|
Other mutations in 4930556J24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
P4717OSA:4930556J24Rik
|
UTSW |
11 |
3,888,178 (GRCm39) |
splice site |
probably null |
|
P4748:4930556J24Rik
|
UTSW |
11 |
3,888,178 (GRCm39) |
splice site |
probably null |
|
R0478:4930556J24Rik
|
UTSW |
11 |
3,926,259 (GRCm39) |
intron |
probably benign |
|
R5593:4930556J24Rik
|
UTSW |
11 |
3,888,027 (GRCm39) |
missense |
unknown |
|
R5594:4930556J24Rik
|
UTSW |
11 |
3,888,027 (GRCm39) |
missense |
unknown |
|
R5698:4930556J24Rik
|
UTSW |
11 |
3,926,366 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6081:4930556J24Rik
|
UTSW |
11 |
3,888,140 (GRCm39) |
missense |
unknown |
|
R6169:4930556J24Rik
|
UTSW |
11 |
3,888,005 (GRCm39) |
missense |
unknown |
|
R6626:4930556J24Rik
|
UTSW |
11 |
3,888,056 (GRCm39) |
missense |
unknown |
|
R8695:4930556J24Rik
|
UTSW |
11 |
3,926,192 (GRCm39) |
critical splice donor site |
probably benign |
|
T0975:4930556J24Rik
|
UTSW |
11 |
3,926,324 (GRCm39) |
missense |
unknown |
|
T0975:4930556J24Rik
|
UTSW |
11 |
3,887,945 (GRCm39) |
frame shift |
probably null |
|
|