Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
A |
17: 24,621,385 (GRCm39) |
C1082S |
probably benign |
Het |
Akt2 |
G |
T |
7: 27,328,806 (GRCm39) |
R176L |
probably benign |
Het |
Aldh16a1 |
A |
G |
7: 44,795,018 (GRCm39) |
Y484H |
probably damaging |
Het |
Apeh |
A |
G |
9: 107,969,209 (GRCm39) |
S280P |
possibly damaging |
Het |
Atp1a4 |
T |
C |
1: 172,071,653 (GRCm39) |
M481V |
probably benign |
Het |
Atraid |
G |
A |
5: 31,210,214 (GRCm39) |
S135N |
probably damaging |
Het |
Camta2 |
C |
T |
11: 70,566,484 (GRCm39) |
G677D |
possibly damaging |
Het |
Ccdc18 |
A |
G |
5: 108,319,614 (GRCm39) |
N545S |
probably benign |
Het |
Cic |
A |
G |
7: 24,985,069 (GRCm39) |
D1105G |
probably damaging |
Het |
Crisp1 |
A |
T |
17: 40,623,957 (GRCm39) |
M4K |
unknown |
Het |
Crnkl1 |
C |
T |
2: 145,772,532 (GRCm39) |
E182K |
possibly damaging |
Het |
Dnmt1 |
A |
T |
9: 20,847,847 (GRCm39) |
C114S |
probably benign |
Het |
Dsc2 |
A |
T |
18: 20,174,788 (GRCm39) |
Y496N |
probably damaging |
Het |
Dst |
T |
C |
1: 34,309,910 (GRCm39) |
V1528A |
probably damaging |
Het |
Fbxl8 |
C |
T |
8: 105,994,752 (GRCm39) |
T88M |
probably benign |
Het |
Fbxo10 |
T |
C |
4: 45,041,928 (GRCm39) |
N767S |
probably benign |
Het |
Gm1527 |
A |
G |
3: 28,949,829 (GRCm39) |
T30A |
unknown |
Het |
Gorasp2 |
C |
A |
2: 70,509,838 (GRCm39) |
Y166* |
probably null |
Het |
Gucy2c |
T |
A |
6: 136,690,146 (GRCm39) |
Q744L |
probably damaging |
Het |
Heg1 |
A |
T |
16: 33,546,992 (GRCm39) |
N593I |
probably damaging |
Het |
Ice1 |
T |
A |
13: 70,757,278 (GRCm39) |
S236C |
possibly damaging |
Het |
Il12b |
T |
C |
11: 44,298,808 (GRCm39) |
Y88H |
probably damaging |
Het |
Izumo3 |
C |
T |
4: 92,035,200 (GRCm39) |
V6I |
probably benign |
Het |
Kcna6 |
A |
G |
6: 126,715,515 (GRCm39) |
V458A |
probably damaging |
Het |
Kif13b |
G |
A |
14: 65,040,889 (GRCm39) |
R1659Q |
probably benign |
Het |
Klk1b1 |
A |
G |
7: 43,619,789 (GRCm39) |
D116G |
possibly damaging |
Het |
Lama2 |
T |
C |
10: 26,917,227 (GRCm39) |
T2233A |
possibly damaging |
Het |
Lin9 |
A |
T |
1: 180,479,444 (GRCm39) |
K59N |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,838,709 (GRCm39) |
E1083G |
probably damaging |
Het |
Mfsd11 |
T |
A |
11: 116,750,177 (GRCm39) |
S105T |
probably damaging |
Het |
Mga |
T |
A |
2: 119,776,770 (GRCm39) |
I1768N |
possibly damaging |
Het |
Mical3 |
C |
A |
6: 120,984,270 (GRCm39) |
G202V |
probably damaging |
Het |
Mylk |
A |
T |
16: 34,806,911 (GRCm39) |
I1719F |
probably benign |
Het |
Nusap1 |
T |
A |
2: 119,460,867 (GRCm39) |
F120Y |
possibly damaging |
Het |
Or52e8 |
T |
A |
7: 104,624,596 (GRCm39) |
M203L |
probably benign |
Het |
Or8b56 |
T |
A |
9: 38,739,511 (GRCm39) |
C175S |
probably damaging |
Het |
Or8k32 |
T |
C |
2: 86,368,492 (GRCm39) |
T256A |
possibly damaging |
Het |
Pidd1 |
T |
C |
7: 141,023,021 (GRCm39) |
Y57C |
probably benign |
Het |
Pik3cd |
T |
A |
4: 149,739,028 (GRCm39) |
M671L |
probably benign |
Het |
Ppp5c |
A |
G |
7: 16,740,885 (GRCm39) |
V361A |
probably benign |
Het |
Prune2 |
T |
C |
19: 17,096,725 (GRCm39) |
V743A |
probably benign |
Het |
Siglec1 |
C |
A |
2: 130,917,889 (GRCm39) |
S996I |
possibly damaging |
Het |
Slc12a7 |
A |
G |
13: 73,957,206 (GRCm39) |
R948G |
possibly damaging |
Het |
Slc40a1 |
A |
T |
1: 45,948,668 (GRCm39) |
Y537* |
probably null |
Het |
Smarca4 |
T |
A |
9: 21,584,638 (GRCm39) |
|
probably benign |
Het |
Smg6 |
C |
T |
11: 74,944,760 (GRCm39) |
P1109S |
probably damaging |
Het |
Sorl1 |
T |
A |
9: 41,975,070 (GRCm39) |
N513Y |
probably damaging |
Het |
Trim58 |
C |
T |
11: 58,531,292 (GRCm39) |
|
probably benign |
Het |
Trim72 |
T |
C |
7: 127,603,704 (GRCm39) |
C17R |
probably damaging |
Het |
Ttc3 |
T |
C |
16: 94,268,785 (GRCm39) |
C1956R |
probably damaging |
Het |
Vmn2r66 |
A |
T |
7: 84,644,623 (GRCm39) |
S596T |
probably benign |
Het |
Zfp609 |
A |
G |
9: 65,611,602 (GRCm39) |
S454P |
possibly damaging |
Het |
|
Other mutations in Vmn1r211 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Vmn1r211
|
APN |
13 |
23,036,272 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01583:Vmn1r211
|
APN |
13 |
23,036,571 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02735:Vmn1r211
|
APN |
13 |
23,036,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,377 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Vmn1r211
|
APN |
13 |
23,036,376 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03292:Vmn1r211
|
APN |
13 |
23,036,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Vmn1r211
|
UTSW |
13 |
23,036,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Vmn1r211
|
UTSW |
13 |
23,035,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R1868:Vmn1r211
|
UTSW |
13 |
23,035,779 (GRCm39) |
missense |
probably benign |
0.07 |
R2002:Vmn1r211
|
UTSW |
13 |
23,035,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Vmn1r211
|
UTSW |
13 |
23,036,134 (GRCm39) |
missense |
probably damaging |
0.98 |
R2655:Vmn1r211
|
UTSW |
13 |
23,036,586 (GRCm39) |
missense |
probably benign |
0.42 |
R4837:Vmn1r211
|
UTSW |
13 |
23,036,296 (GRCm39) |
missense |
probably benign |
0.41 |
R6284:Vmn1r211
|
UTSW |
13 |
23,036,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R6701:Vmn1r211
|
UTSW |
13 |
23,035,779 (GRCm39) |
missense |
probably benign |
0.07 |
R6715:Vmn1r211
|
UTSW |
13 |
23,035,949 (GRCm39) |
missense |
probably benign |
0.00 |
R7058:Vmn1r211
|
UTSW |
13 |
23,036,063 (GRCm39) |
missense |
probably benign |
0.15 |
R7465:Vmn1r211
|
UTSW |
13 |
23,036,086 (GRCm39) |
missense |
probably benign |
0.13 |
R8085:Vmn1r211
|
UTSW |
13 |
23,035,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8720:Vmn1r211
|
UTSW |
13 |
23,036,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8730:Vmn1r211
|
UTSW |
13 |
23,035,838 (GRCm39) |
nonsense |
probably null |
|
R9120:Vmn1r211
|
UTSW |
13 |
23,035,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9725:Vmn1r211
|
UTSW |
13 |
23,036,506 (GRCm39) |
missense |
probably benign |
0.03 |
|