Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
A |
G |
1: 58,398,228 (GRCm39) |
D1323G |
probably null |
Het |
Asxl2 |
A |
G |
12: 3,550,094 (GRCm39) |
D612G |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,718,864 (GRCm39) |
F395L |
probably damaging |
Het |
Cct8 |
A |
G |
16: 87,283,198 (GRCm39) |
S380P |
probably damaging |
Het |
Cltb |
T |
C |
13: 54,746,883 (GRCm39) |
E31G |
probably damaging |
Het |
Cobl |
T |
C |
11: 12,203,364 (GRCm39) |
M1031V |
probably benign |
Het |
Colgalt1 |
C |
A |
8: 72,075,731 (GRCm39) |
|
probably null |
Het |
Dcstamp |
A |
G |
15: 39,617,620 (GRCm39) |
I10V |
probably benign |
Het |
Diaph3 |
T |
C |
14: 87,310,738 (GRCm39) |
I138V |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,945,804 (GRCm39) |
V1827A |
probably damaging |
Het |
Dpf1 |
T |
A |
7: 29,015,986 (GRCm39) |
|
probably benign |
Het |
Dscam |
A |
T |
16: 96,621,969 (GRCm39) |
L494Q |
probably benign |
Het |
Eif2ak4 |
C |
T |
2: 118,252,693 (GRCm39) |
H422Y |
probably damaging |
Het |
Galnt10 |
T |
C |
11: 57,662,326 (GRCm39) |
V324A |
probably damaging |
Het |
Hcfc1 |
T |
C |
X: 72,999,220 (GRCm39) |
I309V |
probably benign |
Het |
Il24 |
T |
C |
1: 130,812,584 (GRCm39) |
T96A |
probably benign |
Het |
Itga2 |
T |
C |
13: 114,973,020 (GRCm39) |
|
probably benign |
Het |
Lrrc32 |
A |
G |
7: 98,147,454 (GRCm39) |
H78R |
possibly damaging |
Het |
Lrrk1 |
T |
C |
7: 65,909,707 (GRCm39) |
E2001G |
probably damaging |
Het |
Lztr1 |
T |
A |
16: 17,336,392 (GRCm39) |
M199K |
probably damaging |
Het |
Mcm8 |
A |
G |
2: 132,663,362 (GRCm39) |
Y160C |
possibly damaging |
Het |
Msh4 |
G |
A |
3: 153,575,245 (GRCm39) |
T710M |
probably damaging |
Het |
Pilrb1 |
A |
T |
5: 137,853,227 (GRCm39) |
L192Q |
probably damaging |
Het |
Pim1 |
T |
A |
17: 29,712,693 (GRCm39) |
|
probably benign |
Het |
Slc12a1 |
A |
T |
2: 125,048,009 (GRCm39) |
Q817L |
possibly damaging |
Het |
Trip11 |
T |
C |
12: 101,865,184 (GRCm39) |
D163G |
probably damaging |
Het |
Tsc2 |
A |
T |
17: 24,847,028 (GRCm39) |
V179E |
probably damaging |
Het |
Zfp641 |
C |
T |
15: 98,186,568 (GRCm39) |
V352M |
probably damaging |
Het |
|
Other mutations in Pate8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01455:Pate8
|
APN |
9 |
36,492,659 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01693:Pate8
|
APN |
9 |
36,492,662 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02268:Pate8
|
APN |
9 |
36,493,166 (GRCm39) |
missense |
possibly damaging |
0.71 |
PIT4354001:Pate8
|
UTSW |
9 |
36,492,597 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0401:Pate8
|
UTSW |
9 |
36,493,924 (GRCm39) |
missense |
unknown |
|
R0743:Pate8
|
UTSW |
9 |
36,492,597 (GRCm39) |
missense |
probably benign |
0.03 |
R1483:Pate8
|
UTSW |
9 |
36,492,620 (GRCm39) |
missense |
probably benign |
0.00 |
R1701:Pate8
|
UTSW |
9 |
36,493,114 (GRCm39) |
critical splice donor site |
probably benign |
|
R2258:Pate8
|
UTSW |
9 |
36,493,161 (GRCm39) |
missense |
probably benign |
0.03 |
R3764:Pate8
|
UTSW |
9 |
36,493,114 (GRCm39) |
critical splice donor site |
probably null |
|
R5143:Pate8
|
UTSW |
9 |
36,493,200 (GRCm39) |
missense |
probably benign |
0.31 |
R6783:Pate8
|
UTSW |
9 |
36,492,631 (GRCm39) |
splice site |
probably null |
|
R7013:Pate8
|
UTSW |
9 |
36,493,854 (GRCm39) |
missense |
unknown |
|
R7014:Pate8
|
UTSW |
9 |
36,493,854 (GRCm39) |
missense |
unknown |
|
|