Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aoc2 |
A |
T |
11: 101,220,102 (GRCm39) |
N696I |
probably damaging |
Het |
Ccr4 |
G |
T |
9: 114,321,350 (GRCm39) |
N238K |
probably benign |
Het |
Cd300e |
A |
C |
11: 114,952,849 (GRCm39) |
M1R |
probably null |
Het |
Cep95 |
A |
G |
11: 106,700,013 (GRCm39) |
|
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,834,918 (GRCm39) |
I1096V |
probably benign |
Het |
Clca4b |
C |
A |
3: 144,617,878 (GRCm39) |
V742L |
probably benign |
Het |
Diaph3 |
A |
T |
14: 86,893,892 (GRCm39) |
I39N |
possibly damaging |
Het |
Dll3 |
A |
T |
7: 27,993,520 (GRCm39) |
D566E |
possibly damaging |
Het |
Dmpk |
A |
G |
7: 18,826,944 (GRCm39) |
T579A |
probably benign |
Het |
E330034G19Rik |
A |
T |
14: 24,346,965 (GRCm39) |
Y84F |
possibly damaging |
Het |
Eya1 |
G |
A |
1: 14,374,691 (GRCm39) |
|
probably benign |
Het |
Fat4 |
A |
G |
3: 38,944,940 (GRCm39) |
T1278A |
possibly damaging |
Het |
Galnt12 |
A |
G |
4: 47,104,264 (GRCm39) |
D174G |
probably damaging |
Het |
Gm20939 |
T |
A |
17: 95,184,721 (GRCm39) |
H456Q |
probably damaging |
Het |
Gm7853 |
A |
G |
14: 35,811,358 (GRCm39) |
|
noncoding transcript |
Het |
Hsd3b5 |
G |
A |
3: 98,529,375 (GRCm39) |
A85V |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,676,560 (GRCm39) |
K916R |
probably benign |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Krt6a |
T |
C |
15: 101,599,801 (GRCm39) |
Y437C |
probably damaging |
Het |
Lrp5 |
A |
G |
19: 3,665,849 (GRCm39) |
S707P |
probably damaging |
Het |
Med14 |
G |
A |
X: 12,550,330 (GRCm39) |
|
probably benign |
Het |
Mmp11 |
C |
T |
10: 75,762,948 (GRCm39) |
|
probably benign |
Het |
Mtus2 |
A |
G |
5: 148,168,637 (GRCm39) |
H950R |
probably damaging |
Het |
Myo1g |
G |
T |
11: 6,464,527 (GRCm39) |
T511K |
possibly damaging |
Het |
Myo7a |
A |
G |
7: 97,701,499 (GRCm39) |
F2154S |
probably damaging |
Het |
Or11h4 |
A |
G |
14: 50,974,271 (GRCm39) |
V116A |
probably benign |
Het |
Or5b101 |
G |
C |
19: 13,005,411 (GRCm39) |
A94G |
probably benign |
Het |
Or8h8 |
C |
T |
2: 86,752,950 (GRCm39) |
E309K |
probably benign |
Het |
Prss52 |
G |
T |
14: 64,350,992 (GRCm39) |
W259L |
probably damaging |
Het |
Sbk2 |
G |
A |
7: 4,960,526 (GRCm39) |
R215* |
probably null |
Het |
Sectm1a |
A |
G |
11: 120,959,603 (GRCm39) |
I175T |
probably benign |
Het |
Smu1 |
T |
A |
4: 40,754,529 (GRCm39) |
R123S |
possibly damaging |
Het |
Stk3 |
A |
G |
15: 35,008,387 (GRCm39) |
S178P |
possibly damaging |
Het |
Tle6 |
T |
C |
10: 81,431,038 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn2r37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01346:Vmn2r37
|
APN |
7 |
9,209,680 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01909:Vmn2r37
|
APN |
7 |
9,219,032 (GRCm39) |
nonsense |
probably null |
|
IGL02281:Vmn2r37
|
APN |
7 |
9,220,881 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02282:Vmn2r37
|
APN |
7 |
9,209,761 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02513:Vmn2r37
|
APN |
7 |
9,220,934 (GRCm39) |
missense |
probably benign |
0.14 |
R0136:Vmn2r37
|
UTSW |
7 |
9,220,782 (GRCm39) |
nonsense |
probably null |
|
R2051:Vmn2r37
|
UTSW |
7 |
9,220,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R2262:Vmn2r37
|
UTSW |
7 |
9,220,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R4084:Vmn2r37
|
UTSW |
7 |
9,218,984 (GRCm39) |
missense |
probably benign |
|
R4114:Vmn2r37
|
UTSW |
7 |
9,213,092 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5231:Vmn2r37
|
UTSW |
7 |
9,209,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5462:Vmn2r37
|
UTSW |
7 |
9,220,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R6437:Vmn2r37
|
UTSW |
7 |
9,220,850 (GRCm39) |
missense |
probably damaging |
0.98 |
R7104:Vmn2r37
|
UTSW |
7 |
9,219,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Vmn2r37
|
UTSW |
7 |
9,220,898 (GRCm39) |
missense |
probably benign |
0.00 |
R7381:Vmn2r37
|
UTSW |
7 |
9,213,032 (GRCm39) |
missense |
probably benign |
0.21 |
R8775:Vmn2r37
|
UTSW |
7 |
9,218,991 (GRCm39) |
nonsense |
probably null |
|
R8775-TAIL:Vmn2r37
|
UTSW |
7 |
9,218,991 (GRCm39) |
nonsense |
probably null |
|
R8869:Vmn2r37
|
UTSW |
7 |
9,209,854 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8884:Vmn2r37
|
UTSW |
7 |
9,218,916 (GRCm39) |
missense |
probably benign |
|
RF004:Vmn2r37
|
UTSW |
7 |
9,220,686 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Vmn2r37
|
UTSW |
7 |
9,212,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|