Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
T |
C |
11: 7,117,054 (GRCm39) |
|
probably benign |
Het |
Asb5 |
T |
C |
8: 55,038,098 (GRCm39) |
V207A |
probably benign |
Het |
Atxn3 |
G |
T |
12: 101,912,181 (GRCm39) |
|
probably benign |
Het |
Brwd1 |
T |
C |
16: 95,839,100 (GRCm39) |
D857G |
probably benign |
Het |
Cacna1i |
A |
G |
15: 80,239,917 (GRCm39) |
N322S |
probably benign |
Het |
Ccn6 |
T |
C |
10: 39,029,163 (GRCm39) |
N255S |
probably benign |
Het |
Dcun1d1 |
A |
T |
3: 35,973,220 (GRCm39) |
W92R |
probably damaging |
Het |
Dnah7a |
A |
C |
1: 53,561,368 (GRCm39) |
|
probably null |
Het |
Enpep |
T |
C |
3: 129,086,896 (GRCm39) |
D581G |
probably benign |
Het |
Fam135a |
G |
A |
1: 24,092,357 (GRCm39) |
L201F |
probably damaging |
Het |
Gm14496 |
T |
G |
2: 181,642,329 (GRCm39) |
L667V |
probably damaging |
Het |
Grk4 |
T |
A |
5: 34,909,553 (GRCm39) |
M539K |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,081,742 (GRCm39) |
V2261A |
probably benign |
Het |
Krtap5-2 |
A |
G |
7: 141,728,751 (GRCm39) |
S310P |
unknown |
Het |
Mme |
A |
T |
3: 63,237,111 (GRCm39) |
Y232F |
possibly damaging |
Het |
Mtmr4 |
T |
C |
11: 87,488,519 (GRCm39) |
Y58H |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,244,411 (GRCm39) |
S983P |
possibly damaging |
Het |
Nbas |
A |
G |
12: 13,381,111 (GRCm39) |
|
probably benign |
Het |
Neb |
C |
T |
2: 52,049,560 (GRCm39) |
G6428R |
probably damaging |
Het |
Neb |
T |
A |
2: 52,087,856 (GRCm39) |
T5448S |
possibly damaging |
Het |
Or2ag17 |
T |
A |
7: 106,389,552 (GRCm39) |
I219L |
probably benign |
Het |
Or2t1 |
A |
T |
14: 14,328,284 (GRCm38) |
M58L |
probably damaging |
Het |
Or52ab7 |
G |
T |
7: 102,977,873 (GRCm39) |
S60I |
possibly damaging |
Het |
Or5l13 |
T |
A |
2: 87,780,415 (GRCm39) |
Q54L |
probably benign |
Het |
Or5p52 |
T |
C |
7: 107,502,173 (GRCm39) |
M83T |
probably benign |
Het |
Otx2 |
A |
G |
14: 48,898,781 (GRCm39) |
I75T |
probably damaging |
Het |
Phex |
A |
T |
X: 155,960,500 (GRCm39) |
N681K |
probably damaging |
Het |
Plekha8 |
C |
A |
6: 54,612,755 (GRCm39) |
A454E |
probably damaging |
Het |
Rbfa |
C |
A |
18: 80,240,506 (GRCm39) |
K152N |
probably benign |
Het |
Satb2 |
C |
A |
1: 56,884,739 (GRCm39) |
S513I |
probably damaging |
Het |
Slc4a2 |
G |
T |
5: 24,639,879 (GRCm39) |
R520L |
probably benign |
Het |
Slfn14 |
T |
C |
11: 83,169,826 (GRCm39) |
H606R |
probably benign |
Het |
Smc1b |
G |
A |
15: 84,982,147 (GRCm39) |
Q716* |
probably null |
Het |
Syncrip |
C |
T |
9: 88,346,696 (GRCm39) |
|
probably benign |
Het |
Vps13c |
C |
T |
9: 67,804,477 (GRCm39) |
A762V |
probably null |
Het |
Wdr64 |
C |
A |
1: 175,571,201 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn2r30 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01797:Vmn2r30
|
APN |
7 |
7,337,195 (GRCm39) |
missense |
probably benign |
|
IGL02114:Vmn2r30
|
APN |
7 |
7,340,408 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02429:Vmn2r30
|
APN |
7 |
7,337,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1723:Vmn2r30
|
UTSW |
7 |
7,337,259 (GRCm39) |
missense |
probably benign |
0.00 |
R4472:Vmn2r30
|
UTSW |
7 |
7,320,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5409:Vmn2r30
|
UTSW |
7 |
7,315,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Vmn2r30
|
UTSW |
7 |
7,315,334 (GRCm39) |
missense |
probably damaging |
0.99 |
R6035:Vmn2r30
|
UTSW |
7 |
7,337,350 (GRCm39) |
missense |
probably benign |
0.34 |
R6035:Vmn2r30
|
UTSW |
7 |
7,337,350 (GRCm39) |
missense |
probably benign |
0.34 |
R6336:Vmn2r30
|
UTSW |
7 |
7,337,307 (GRCm39) |
missense |
probably benign |
0.03 |
R6904:Vmn2r30
|
UTSW |
7 |
7,315,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Vmn2r30
|
UTSW |
7 |
7,337,183 (GRCm39) |
missense |
probably benign |
0.05 |
R8415:Vmn2r30
|
UTSW |
7 |
7,315,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R8558:Vmn2r30
|
UTSW |
7 |
7,315,655 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9267:Vmn2r30
|
UTSW |
7 |
7,340,432 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9744:Vmn2r30
|
UTSW |
7 |
7,315,284 (GRCm39) |
missense |
possibly damaging |
0.91 |
V8831:Vmn2r30
|
UTSW |
7 |
7,337,148 (GRCm39) |
missense |
probably benign |
0.00 |
|