Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
A |
G |
4: 62,465,563 (GRCm39) |
E419G |
possibly damaging |
Het |
Abcg3 |
A |
G |
5: 105,122,631 (GRCm39) |
|
probably benign |
Het |
Adam17 |
T |
C |
12: 21,395,698 (GRCm39) |
D256G |
probably damaging |
Het |
Adgrb3 |
G |
A |
1: 25,570,978 (GRCm39) |
R500* |
probably null |
Het |
Aldh3a2 |
A |
G |
11: 61,149,665 (GRCm39) |
Y234H |
probably damaging |
Het |
Alpk3 |
A |
G |
7: 80,743,143 (GRCm39) |
T987A |
probably benign |
Het |
Amtn |
A |
G |
5: 88,532,828 (GRCm39) |
K148E |
possibly damaging |
Het |
Asap1 |
G |
A |
15: 64,032,123 (GRCm39) |
T237M |
probably damaging |
Het |
Ccdc124 |
A |
T |
8: 71,321,573 (GRCm39) |
|
probably null |
Het |
Cdon |
T |
C |
9: 35,389,255 (GRCm39) |
Y787H |
probably damaging |
Het |
Cimip4 |
T |
C |
15: 78,269,516 (GRCm39) |
D188G |
probably damaging |
Het |
Coro7 |
A |
G |
16: 4,453,246 (GRCm39) |
|
probably null |
Het |
Dram2 |
T |
A |
3: 106,462,490 (GRCm39) |
|
probably benign |
Het |
Drd5 |
T |
C |
5: 38,477,124 (GRCm39) |
V39A |
probably benign |
Het |
Ern1 |
A |
G |
11: 106,300,924 (GRCm39) |
L490P |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,483,160 (GRCm39) |
T3083A |
possibly damaging |
Het |
Irgm1 |
A |
G |
11: 48,757,094 (GRCm39) |
I239T |
probably damaging |
Het |
Klhl10 |
A |
T |
11: 100,347,758 (GRCm39) |
T605S |
probably benign |
Het |
Lcor |
T |
A |
19: 41,546,795 (GRCm39) |
S126R |
probably damaging |
Het |
Lgi4 |
G |
T |
7: 30,759,983 (GRCm39) |
V60F |
probably damaging |
Het |
Lin37 |
G |
A |
7: 30,256,585 (GRCm39) |
R84W |
probably damaging |
Het |
Lmf1 |
A |
G |
17: 25,804,624 (GRCm39) |
S97G |
possibly damaging |
Het |
Oasl2 |
A |
G |
5: 115,039,393 (GRCm39) |
T194A |
probably benign |
Het |
Or5ac17 |
A |
G |
16: 59,036,566 (GRCm39) |
S137P |
probably benign |
Het |
Pnpo |
A |
T |
11: 96,834,661 (GRCm39) |
F12I |
probably damaging |
Het |
Prdm4 |
T |
C |
10: 85,743,860 (GRCm39) |
T132A |
probably benign |
Het |
Ptbp2 |
T |
C |
3: 119,545,593 (GRCm39) |
T118A |
probably benign |
Het |
Ptf1a |
T |
A |
2: 19,451,456 (GRCm39) |
|
probably benign |
Het |
Rev3l |
T |
A |
10: 39,682,874 (GRCm39) |
F331I |
probably damaging |
Het |
Rfx6 |
C |
A |
10: 51,599,217 (GRCm39) |
S524* |
probably null |
Het |
Scube3 |
A |
G |
17: 28,386,032 (GRCm39) |
S758G |
possibly damaging |
Het |
Slc44a2 |
T |
C |
9: 21,254,496 (GRCm39) |
I257T |
probably benign |
Het |
Spon1 |
A |
T |
7: 113,629,579 (GRCm39) |
I408F |
probably damaging |
Het |
Srpk1 |
C |
A |
17: 28,811,240 (GRCm39) |
D541Y |
possibly damaging |
Het |
Tenm4 |
A |
T |
7: 96,522,969 (GRCm39) |
I1467F |
probably damaging |
Het |
Uggt1 |
A |
C |
1: 36,241,899 (GRCm39) |
V345G |
possibly damaging |
Het |
Whamm |
A |
G |
7: 81,239,280 (GRCm39) |
|
probably benign |
Het |
Zeb1 |
A |
G |
18: 5,770,511 (GRCm39) |
D888G |
probably damaging |
Het |
Zfp263 |
A |
G |
16: 3,564,744 (GRCm39) |
N253S |
possibly damaging |
Het |
Zfp446 |
C |
A |
7: 12,711,834 (GRCm39) |
A19E |
probably benign |
Het |
|
Other mutations in Vmn1r23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01563:Vmn1r23
|
APN |
6 |
57,903,061 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01980:Vmn1r23
|
APN |
6 |
57,903,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02934:Vmn1r23
|
APN |
6 |
57,902,914 (GRCm39) |
missense |
probably benign |
0.26 |
R0410:Vmn1r23
|
UTSW |
6 |
57,903,175 (GRCm39) |
missense |
probably benign |
0.11 |
R0452:Vmn1r23
|
UTSW |
6 |
57,903,469 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0590:Vmn1r23
|
UTSW |
6 |
57,903,349 (GRCm39) |
missense |
probably benign |
0.43 |
R0647:Vmn1r23
|
UTSW |
6 |
57,903,169 (GRCm39) |
missense |
probably benign |
|
R0692:Vmn1r23
|
UTSW |
6 |
57,903,110 (GRCm39) |
nonsense |
probably null |
|
R1674:Vmn1r23
|
UTSW |
6 |
57,903,046 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1744:Vmn1r23
|
UTSW |
6 |
57,902,910 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1774:Vmn1r23
|
UTSW |
6 |
57,903,675 (GRCm39) |
missense |
probably damaging |
0.97 |
R2101:Vmn1r23
|
UTSW |
6 |
57,903,437 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2202:Vmn1r23
|
UTSW |
6 |
57,903,604 (GRCm39) |
missense |
probably benign |
0.01 |
R2204:Vmn1r23
|
UTSW |
6 |
57,903,604 (GRCm39) |
missense |
probably benign |
0.01 |
R2205:Vmn1r23
|
UTSW |
6 |
57,903,604 (GRCm39) |
missense |
probably benign |
0.01 |
R4282:Vmn1r23
|
UTSW |
6 |
57,903,452 (GRCm39) |
missense |
probably benign |
0.27 |
R4408:Vmn1r23
|
UTSW |
6 |
57,903,353 (GRCm39) |
missense |
probably benign |
0.01 |
R4532:Vmn1r23
|
UTSW |
6 |
57,902,914 (GRCm39) |
missense |
probably benign |
0.21 |
R4690:Vmn1r23
|
UTSW |
6 |
57,903,010 (GRCm39) |
missense |
probably benign |
|
R4700:Vmn1r23
|
UTSW |
6 |
57,903,190 (GRCm39) |
missense |
probably benign |
0.17 |
R4894:Vmn1r23
|
UTSW |
6 |
57,903,310 (GRCm39) |
missense |
probably benign |
0.00 |
R6164:Vmn1r23
|
UTSW |
6 |
57,903,040 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6930:Vmn1r23
|
UTSW |
6 |
57,903,130 (GRCm39) |
missense |
probably benign |
|
R7129:Vmn1r23
|
UTSW |
6 |
57,903,061 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7731:Vmn1r23
|
UTSW |
6 |
57,903,319 (GRCm39) |
missense |
probably benign |
0.03 |
R7877:Vmn1r23
|
UTSW |
6 |
57,903,541 (GRCm39) |
missense |
probably benign |
|
R8751:Vmn1r23
|
UTSW |
6 |
57,903,452 (GRCm39) |
missense |
probably benign |
0.27 |
R8809:Vmn1r23
|
UTSW |
6 |
57,903,352 (GRCm39) |
missense |
probably damaging |
0.97 |
|