Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap28 |
G |
A |
17: 68,165,195 (GRCm39) |
T516I |
probably benign |
Het |
Birc6 |
T |
C |
17: 74,955,192 (GRCm39) |
C3486R |
probably benign |
Het |
Camk2g |
G |
A |
14: 20,797,922 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,300,194 (GRCm39) |
E3167G |
unknown |
Het |
Dmxl1 |
T |
A |
18: 50,095,272 (GRCm39) |
H2950Q |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,800,870 (GRCm39) |
S379T |
probably benign |
Het |
Epb41l3 |
C |
T |
17: 69,555,704 (GRCm39) |
H13Y |
probably damaging |
Het |
Fam149a |
A |
T |
8: 45,803,479 (GRCm39) |
D337E |
probably damaging |
Het |
Galnt14 |
T |
A |
17: 73,842,361 (GRCm39) |
|
probably benign |
Het |
Hspg2 |
G |
A |
4: 137,266,494 (GRCm39) |
R1885H |
probably damaging |
Het |
Jag1 |
T |
A |
2: 136,941,971 (GRCm39) |
|
probably benign |
Het |
Nalcn |
A |
T |
14: 123,809,503 (GRCm39) |
N216K |
probably benign |
Het |
Ndst1 |
T |
C |
18: 60,846,198 (GRCm39) |
Y37C |
probably damaging |
Het |
Nr2c2 |
A |
G |
6: 92,139,019 (GRCm39) |
N486S |
probably benign |
Het |
Obscn |
A |
T |
11: 58,890,506 (GRCm39) |
L7342Q |
unknown |
Het |
Or13l2 |
A |
T |
3: 97,318,036 (GRCm39) |
C154S |
probably damaging |
Het |
Or56b2 |
A |
G |
7: 104,338,052 (GRCm39) |
I277V |
probably benign |
Het |
Or8k20 |
C |
A |
2: 86,106,085 (GRCm39) |
V249F |
probably damaging |
Het |
Pou4f2 |
A |
C |
8: 79,162,284 (GRCm39) |
D106E |
probably damaging |
Het |
Ppic |
G |
A |
18: 53,551,001 (GRCm39) |
P10S |
unknown |
Het |
Psd2 |
A |
G |
18: 36,112,838 (GRCm39) |
T178A |
probably damaging |
Het |
Ro60 |
A |
T |
1: 143,637,038 (GRCm39) |
N391K |
probably damaging |
Het |
Slc25a34 |
G |
T |
4: 141,349,821 (GRCm39) |
|
probably null |
Het |
Stap2 |
A |
G |
17: 56,304,623 (GRCm39) |
S360P |
probably benign |
Het |
Stx3 |
T |
C |
19: 11,763,969 (GRCm39) |
E129G |
probably damaging |
Het |
Sun3 |
T |
A |
11: 8,979,436 (GRCm39) |
E28D |
probably damaging |
Het |
Tmem126a |
C |
T |
7: 90,100,750 (GRCm39) |
|
probably null |
Het |
Trpc6 |
A |
T |
9: 8,634,058 (GRCm39) |
H379L |
probably damaging |
Het |
Ttf2 |
A |
G |
3: 100,863,511 (GRCm39) |
S608P |
possibly damaging |
Het |
Tubgcp3 |
T |
C |
8: 12,711,297 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Gm6489 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1957:Gm6489
|
UTSW |
1 |
31,326,452 (GRCm39) |
exon |
noncoding transcript |
|
R3740:Gm6489
|
UTSW |
1 |
31,326,764 (GRCm39) |
unclassified |
noncoding transcript |
|
R3741:Gm6489
|
UTSW |
1 |
31,326,764 (GRCm39) |
unclassified |
noncoding transcript |
|
R3742:Gm6489
|
UTSW |
1 |
31,326,764 (GRCm39) |
unclassified |
noncoding transcript |
|
R4489:Gm6489
|
UTSW |
1 |
31,326,320 (GRCm39) |
exon |
noncoding transcript |
|
R5239:Gm6489
|
UTSW |
1 |
31,326,351 (GRCm39) |
exon |
noncoding transcript |
|
|