Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl6a |
T |
A |
3: 32,774,349 (GRCm39) |
M282K |
possibly damaging |
Het |
Adam22 |
T |
C |
5: 8,142,742 (GRCm39) |
N831S |
probably damaging |
Het |
Adamdec1 |
C |
T |
14: 68,810,556 (GRCm39) |
R200Q |
probably damaging |
Het |
Asb15 |
A |
G |
6: 24,567,271 (GRCm39) |
I531V |
probably benign |
Het |
Btrc |
T |
A |
19: 45,501,117 (GRCm39) |
D223E |
probably benign |
Het |
Ccdc30 |
T |
A |
4: 119,250,761 (GRCm39) |
E161V |
probably damaging |
Het |
Cd38 |
G |
A |
5: 44,060,928 (GRCm39) |
|
probably benign |
Het |
Clec2d |
T |
C |
6: 129,161,185 (GRCm39) |
F94S |
probably damaging |
Het |
Cwf19l1 |
C |
T |
19: 44,109,311 (GRCm39) |
|
probably null |
Het |
Dnah2 |
A |
T |
11: 69,430,269 (GRCm39) |
N96K |
probably benign |
Het |
Ephb6 |
G |
A |
6: 41,591,449 (GRCm39) |
R202H |
probably benign |
Het |
Gm43191 |
T |
A |
3: 116,471,616 (GRCm39) |
I218L |
probably benign |
Het |
Gm7168 |
G |
A |
17: 14,169,140 (GRCm39) |
S169N |
probably damaging |
Het |
Kif20b |
T |
C |
19: 34,913,143 (GRCm39) |
|
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,702,089 (GRCm39) |
T906A |
probably benign |
Het |
Mboat2 |
A |
G |
12: 25,004,221 (GRCm39) |
N341D |
probably damaging |
Het |
Msh6 |
T |
C |
17: 88,292,907 (GRCm39) |
V554A |
probably benign |
Het |
Ndc80 |
T |
C |
17: 71,815,634 (GRCm39) |
T384A |
possibly damaging |
Het |
Or1af1 |
G |
T |
2: 37,110,038 (GRCm39) |
C179F |
probably damaging |
Het |
Or8g18 |
G |
A |
9: 39,149,315 (GRCm39) |
T135I |
probably benign |
Het |
Ptpn5 |
G |
T |
7: 46,732,906 (GRCm39) |
H312Q |
probably benign |
Het |
Rftn2 |
C |
T |
1: 55,253,445 (GRCm39) |
V53I |
probably damaging |
Het |
Rgs20 |
T |
C |
1: 4,987,145 (GRCm39) |
T124A |
probably benign |
Het |
Sox18 |
T |
C |
2: 181,313,143 (GRCm39) |
S58G |
possibly damaging |
Het |
Togaram2 |
A |
G |
17: 72,036,485 (GRCm39) |
M1012V |
probably null |
Het |
Usp48 |
A |
T |
4: 137,350,583 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gm7964 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01665:Gm7964
|
APN |
7 |
83,406,341 (GRCm39) |
exon |
noncoding transcript |
|
IGL02232:Gm7964
|
APN |
7 |
83,405,515 (GRCm39) |
exon |
noncoding transcript |
|
IGL02525:Gm7964
|
APN |
7 |
83,405,250 (GRCm39) |
exon |
noncoding transcript |
|
R0512:Gm7964
|
UTSW |
7 |
83,405,158 (GRCm39) |
exon |
noncoding transcript |
|
R0543:Gm7964
|
UTSW |
7 |
83,405,602 (GRCm39) |
exon |
noncoding transcript |
|
R0723:Gm7964
|
UTSW |
7 |
83,405,374 (GRCm39) |
exon |
noncoding transcript |
|
R1977:Gm7964
|
UTSW |
7 |
83,406,560 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2397:Gm7964
|
UTSW |
7 |
83,406,321 (GRCm39) |
exon |
noncoding transcript |
|
R3623:Gm7964
|
UTSW |
7 |
83,405,629 (GRCm39) |
missense |
probably benign |
0.02 |
R3769:Gm7964
|
UTSW |
7 |
83,405,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R4222:Gm7964
|
UTSW |
7 |
83,406,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R4224:Gm7964
|
UTSW |
7 |
83,406,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Gm7964
|
UTSW |
7 |
83,405,109 (GRCm39) |
splice site |
probably null |
|
R4869:Gm7964
|
UTSW |
7 |
83,405,350 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5086:Gm7964
|
UTSW |
7 |
83,406,560 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5944:Gm7964
|
UTSW |
7 |
83,405,743 (GRCm39) |
missense |
probably benign |
0.00 |
|