Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg8 |
A |
G |
17: 84,999,308 (GRCm39) |
N135D |
probably damaging |
Het |
Ak4 |
T |
C |
4: 101,277,148 (GRCm39) |
L44P |
probably damaging |
Het |
Angpt1 |
C |
A |
15: 42,339,818 (GRCm39) |
G298* |
probably null |
Het |
Appl2 |
C |
T |
10: 83,457,623 (GRCm39) |
|
probably benign |
Het |
Arhgap19 |
T |
A |
19: 41,769,760 (GRCm39) |
H341L |
probably benign |
Het |
Chmp5 |
T |
C |
4: 40,952,438 (GRCm39) |
S98P |
probably benign |
Het |
Chp1 |
A |
T |
2: 119,415,081 (GRCm39) |
Q161L |
probably benign |
Het |
Clgn |
T |
C |
8: 84,150,769 (GRCm39) |
V478A |
probably benign |
Het |
Cplane1 |
G |
A |
15: 8,242,279 (GRCm39) |
|
probably benign |
Het |
Cyp2b19 |
A |
T |
7: 26,461,809 (GRCm39) |
M210L |
probably benign |
Het |
Eif4g3 |
T |
A |
4: 137,853,166 (GRCm39) |
V244D |
probably damaging |
Het |
Ftcd |
T |
C |
10: 76,417,461 (GRCm39) |
I300T |
probably damaging |
Het |
Gm12886 |
C |
T |
4: 121,272,697 (GRCm39) |
|
probably benign |
Het |
Klrb1f |
A |
T |
6: 129,030,765 (GRCm39) |
E92V |
probably null |
Het |
Krt23 |
A |
G |
11: 99,374,700 (GRCm39) |
|
probably benign |
Het |
Mib2 |
T |
G |
4: 155,743,900 (GRCm39) |
R47S |
probably benign |
Het |
Mindy4 |
A |
G |
6: 55,286,315 (GRCm39) |
T728A |
probably damaging |
Het |
Myh15 |
A |
G |
16: 48,916,901 (GRCm39) |
N407S |
probably benign |
Het |
Nlrp4f |
A |
G |
13: 65,342,412 (GRCm39) |
V411A |
probably benign |
Het |
Or10ag56 |
T |
C |
2: 87,140,056 (GRCm39) |
*328Q |
probably null |
Het |
Or4c12b |
A |
C |
2: 89,647,486 (GRCm39) |
D266A |
probably damaging |
Het |
Otud4 |
T |
G |
8: 80,400,087 (GRCm39) |
S934A |
probably damaging |
Het |
P3h1 |
C |
T |
4: 119,093,983 (GRCm39) |
R213W |
probably damaging |
Het |
Phrf1 |
A |
T |
7: 140,834,881 (GRCm39) |
K19* |
probably null |
Het |
Prl3b1 |
A |
T |
13: 27,429,759 (GRCm39) |
M66L |
probably benign |
Het |
Psmd7 |
T |
C |
8: 108,309,099 (GRCm39) |
T149A |
probably benign |
Het |
Samd4b |
T |
C |
7: 28,105,868 (GRCm39) |
D450G |
probably damaging |
Het |
Scn3a |
G |
A |
2: 65,367,016 (GRCm39) |
A2V |
probably damaging |
Het |
Snrpa |
G |
A |
7: 26,891,186 (GRCm39) |
T95I |
probably benign |
Het |
Traip |
A |
G |
9: 107,840,125 (GRCm39) |
|
probably benign |
Het |
Trbc1 |
T |
A |
6: 41,515,383 (GRCm39) |
|
probably benign |
Het |
Trim72 |
A |
T |
7: 127,607,013 (GRCm39) |
M181L |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,594,212 (GRCm39) |
Y882H |
probably damaging |
Het |
Vmn2r9 |
G |
T |
5: 108,996,173 (GRCm39) |
|
probably benign |
Het |
Vps13a |
A |
G |
19: 16,688,246 (GRCm39) |
S854P |
probably benign |
Het |
Wdfy1 |
T |
C |
1: 79,692,622 (GRCm39) |
K232E |
possibly damaging |
Het |
Xpr1 |
A |
T |
1: 155,156,774 (GRCm39) |
D625E |
possibly damaging |
Het |
Zbbx |
T |
A |
3: 74,989,153 (GRCm39) |
T317S |
possibly damaging |
Het |
|
Other mutations in Vmn1r191 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Vmn1r191
|
APN |
13 |
22,362,890 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01645:Vmn1r191
|
APN |
13 |
22,363,614 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02224:Vmn1r191
|
APN |
13 |
22,363,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02321:Vmn1r191
|
APN |
13 |
22,363,068 (GRCm39) |
nonsense |
probably null |
|
IGL02516:Vmn1r191
|
APN |
13 |
22,363,710 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02602:Vmn1r191
|
APN |
13 |
22,363,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02630:Vmn1r191
|
APN |
13 |
22,363,431 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03380:Vmn1r191
|
APN |
13 |
22,363,055 (GRCm39) |
missense |
probably damaging |
0.99 |
R0571:Vmn1r191
|
UTSW |
13 |
22,363,217 (GRCm39) |
missense |
probably damaging |
0.96 |
R0981:Vmn1r191
|
UTSW |
13 |
22,363,389 (GRCm39) |
missense |
probably benign |
0.00 |
R1672:Vmn1r191
|
UTSW |
13 |
22,363,262 (GRCm39) |
missense |
probably benign |
0.01 |
R1955:Vmn1r191
|
UTSW |
13 |
22,362,985 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1969:Vmn1r191
|
UTSW |
13 |
22,362,952 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5059:Vmn1r191
|
UTSW |
13 |
22,363,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R6484:Vmn1r191
|
UTSW |
13 |
22,362,918 (GRCm39) |
missense |
probably benign |
0.00 |
R6736:Vmn1r191
|
UTSW |
13 |
22,363,720 (GRCm39) |
missense |
probably benign |
0.14 |
R7063:Vmn1r191
|
UTSW |
13 |
22,362,864 (GRCm39) |
missense |
probably benign |
0.08 |
R7475:Vmn1r191
|
UTSW |
13 |
22,362,942 (GRCm39) |
missense |
probably benign |
0.00 |
R9699:Vmn1r191
|
UTSW |
13 |
22,363,355 (GRCm39) |
missense |
probably benign |
0.25 |
|