Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1 |
A |
G |
2: 58,390,558 (GRCm39) |
V2A |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,760,903 (GRCm39) |
Q866L |
probably benign |
Het |
Ankrd13a |
A |
G |
5: 114,935,914 (GRCm39) |
E295G |
probably benign |
Het |
Arid1a |
T |
C |
4: 133,408,348 (GRCm39) |
D2053G |
unknown |
Het |
Calr4 |
A |
G |
4: 109,111,071 (GRCm39) |
E272G |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,225,714 (GRCm39) |
S3125G |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,165,948 (GRCm39) |
Y538H |
probably damaging |
Het |
Eri3 |
T |
C |
4: 117,446,356 (GRCm39) |
|
probably null |
Het |
Fmo6 |
T |
A |
1: 162,757,580 (GRCm39) |
R63* |
probably null |
Het |
Gm7168 |
G |
A |
17: 14,169,169 (GRCm39) |
D179N |
probably benign |
Het |
Got1l1 |
T |
C |
8: 27,688,019 (GRCm39) |
T337A |
probably damaging |
Het |
Gvin-ps3 |
T |
C |
7: 105,682,962 (GRCm39) |
I98V |
probably benign |
Het |
Igf2r |
A |
G |
17: 12,923,236 (GRCm39) |
M1191T |
probably benign |
Het |
Ighv1-54 |
A |
G |
12: 115,157,557 (GRCm39) |
L30P |
probably damaging |
Het |
Igkv8-30 |
A |
G |
6: 70,094,331 (GRCm39) |
S27P |
probably benign |
Het |
Kcnab2 |
A |
T |
4: 152,478,254 (GRCm39) |
V335E |
possibly damaging |
Het |
Klf12 |
A |
T |
14: 100,387,193 (GRCm39) |
I3N |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,063,174 (GRCm39) |
V2510A |
probably benign |
Het |
Mme |
A |
G |
3: 63,269,467 (GRCm39) |
D592G |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,112,127 (GRCm39) |
N1727S |
probably benign |
Het |
Ncor1 |
A |
G |
11: 62,231,420 (GRCm39) |
S796P |
probably damaging |
Het |
Nlrp14 |
A |
G |
7: 106,797,120 (GRCm39) |
|
probably benign |
Het |
Or51f23 |
T |
A |
7: 102,453,061 (GRCm39) |
Y125* |
probably null |
Het |
Or5b95 |
T |
A |
19: 12,658,167 (GRCm39) |
Y232N |
probably benign |
Het |
Or5p80 |
C |
T |
7: 108,229,885 (GRCm39) |
R229C |
probably benign |
Het |
Plekhm2 |
A |
G |
4: 141,369,737 (GRCm39) |
V86A |
probably damaging |
Het |
Popdc2 |
G |
T |
16: 38,194,493 (GRCm39) |
V305L |
probably benign |
Het |
Rttn |
C |
T |
18: 89,013,737 (GRCm39) |
H469Y |
probably benign |
Het |
Slc2a12 |
T |
C |
10: 22,540,583 (GRCm39) |
V146A |
probably damaging |
Het |
Sptlc3 |
A |
G |
2: 139,388,341 (GRCm39) |
E111G |
possibly damaging |
Het |
Zfp108 |
T |
C |
7: 23,957,872 (GRCm39) |
|
probably benign |
Het |
Zfp719 |
T |
A |
7: 43,240,554 (GRCm39) |
F714Y |
probably damaging |
Het |
|
Other mutations in Prb1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02259:Prb1b
|
APN |
6 |
132,289,637 (GRCm39) |
missense |
unknown |
|
IGL02434:Prb1b
|
APN |
6 |
132,289,339 (GRCm39) |
missense |
unknown |
|
IGL03238:Prb1b
|
APN |
6 |
132,289,308 (GRCm39) |
missense |
unknown |
|
R0971:Prb1b
|
UTSW |
6 |
132,290,618 (GRCm39) |
missense |
unknown |
|
R1900:Prb1b
|
UTSW |
6 |
132,291,661 (GRCm39) |
missense |
unknown |
|
R3800:Prb1b
|
UTSW |
6 |
132,289,657 (GRCm39) |
missense |
unknown |
|
R3951:Prb1b
|
UTSW |
6 |
132,289,657 (GRCm39) |
missense |
unknown |
|
R3952:Prb1b
|
UTSW |
6 |
132,289,657 (GRCm39) |
missense |
unknown |
|
R3981:Prb1b
|
UTSW |
6 |
132,289,657 (GRCm39) |
missense |
unknown |
|
R4083:Prb1b
|
UTSW |
6 |
132,289,657 (GRCm39) |
missense |
unknown |
|
R4348:Prb1b
|
UTSW |
6 |
132,290,624 (GRCm39) |
missense |
unknown |
|
R4351:Prb1b
|
UTSW |
6 |
132,290,624 (GRCm39) |
missense |
unknown |
|
R4352:Prb1b
|
UTSW |
6 |
132,290,624 (GRCm39) |
missense |
unknown |
|
R4353:Prb1b
|
UTSW |
6 |
132,290,624 (GRCm39) |
missense |
unknown |
|
R6190:Prb1b
|
UTSW |
6 |
132,289,692 (GRCm39) |
missense |
unknown |
|
R7001:Prb1b
|
UTSW |
6 |
132,289,527 (GRCm39) |
missense |
unknown |
|
R9023:Prb1b
|
UTSW |
6 |
132,289,174 (GRCm39) |
frame shift |
probably null |
|
R9028:Prb1b
|
UTSW |
6 |
132,289,618 (GRCm39) |
missense |
unknown |
|
R9193:Prb1b
|
UTSW |
6 |
132,288,996 (GRCm39) |
missense |
unknown |
|
R9256:Prb1b
|
UTSW |
6 |
132,288,972 (GRCm39) |
missense |
unknown |
|
R9388:Prb1b
|
UTSW |
6 |
132,289,437 (GRCm39) |
missense |
unknown |
|
R9644:Prb1b
|
UTSW |
6 |
132,289,218 (GRCm39) |
missense |
unknown |
|
|