Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg1 |
T |
A |
9: 54,530,004 (GRCm39) |
I231L |
probably benign |
Het |
Adcyap1 |
T |
A |
17: 93,507,506 (GRCm39) |
V22D |
probably damaging |
Het |
Adgra3 |
T |
C |
5: 50,164,272 (GRCm39) |
T236A |
possibly damaging |
Het |
Adipor2 |
A |
T |
6: 119,338,887 (GRCm39) |
L122H |
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,074,291 (GRCm39) |
I321V |
probably benign |
Het |
Bhmt2 |
A |
T |
13: 93,799,661 (GRCm39) |
Y258* |
probably null |
Het |
C230029F24Rik |
T |
A |
1: 49,377,253 (GRCm39) |
|
noncoding transcript |
Het |
Ccpg1 |
T |
A |
9: 72,913,159 (GRCm39) |
F232I |
probably damaging |
Het |
Cd83 |
A |
T |
13: 43,955,153 (GRCm39) |
T195S |
probably benign |
Het |
Cdcp3 |
G |
T |
7: 130,848,386 (GRCm39) |
G847* |
probably null |
Het |
Cfap70 |
G |
A |
14: 20,453,186 (GRCm39) |
T897M |
probably damaging |
Het |
Cyp3a11 |
T |
A |
5: 145,805,475 (GRCm39) |
M181L |
probably benign |
Het |
Frem2 |
C |
T |
3: 53,457,083 (GRCm39) |
V2090I |
probably benign |
Het |
Gm45234 |
A |
G |
6: 124,723,571 (GRCm39) |
|
probably benign |
Het |
Igsf9 |
T |
A |
1: 172,319,738 (GRCm39) |
C39* |
probably null |
Het |
Il1rap |
A |
T |
16: 26,541,463 (GRCm39) |
D568V |
probably damaging |
Het |
Ints7 |
C |
T |
1: 191,345,331 (GRCm39) |
|
probably benign |
Het |
Lsamp |
C |
T |
16: 41,964,375 (GRCm39) |
R250* |
probably null |
Het |
Oit3 |
T |
A |
10: 59,274,731 (GRCm39) |
D23V |
probably damaging |
Het |
Pcdh17 |
T |
A |
14: 84,684,442 (GRCm39) |
L303Q |
probably damaging |
Het |
Pcdhb1 |
T |
A |
18: 37,400,450 (GRCm39) |
N800K |
probably benign |
Het |
Plce1 |
A |
G |
19: 38,513,331 (GRCm39) |
D210G |
probably benign |
Het |
Plekhb2 |
T |
A |
1: 34,908,411 (GRCm39) |
Y152N |
probably damaging |
Het |
Rbp3 |
T |
C |
14: 33,678,088 (GRCm39) |
S679P |
probably benign |
Het |
Rps6kc1 |
T |
C |
1: 190,643,854 (GRCm39) |
T2A |
possibly damaging |
Het |
Tmem167 |
T |
A |
13: 90,246,504 (GRCm39) |
S9R |
probably damaging |
Het |
Xpnpep1 |
A |
T |
19: 52,985,463 (GRCm39) |
S522T |
probably benign |
Het |
|
Other mutations in Gm7964 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01691:Gm7964
|
APN |
7 |
83,405,344 (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 |
|