Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
T |
A |
7: 41,275,516 (GRCm39) |
Y406* |
probably null |
Het |
Acadvl |
T |
C |
11: 69,905,159 (GRCm39) |
D109G |
probably benign |
Het |
Adam24 |
G |
A |
8: 41,134,542 (GRCm39) |
G670E |
probably damaging |
Het |
Angpt1 |
T |
C |
15: 42,323,136 (GRCm39) |
M378V |
probably benign |
Het |
Ankrd33 |
G |
A |
15: 101,014,993 (GRCm39) |
|
probably null |
Het |
Apol7b |
G |
A |
15: 77,307,625 (GRCm39) |
T290I |
probably benign |
Het |
Atg4a-ps |
A |
G |
3: 103,553,180 (GRCm39) |
W54R |
probably damaging |
Het |
B3glct |
A |
G |
5: 149,663,069 (GRCm39) |
|
probably null |
Het |
Bmp7 |
A |
G |
2: 172,714,706 (GRCm39) |
S368P |
probably damaging |
Het |
Boc |
A |
G |
16: 44,312,154 (GRCm39) |
V636A |
probably damaging |
Het |
Cacna1i |
G |
A |
15: 80,259,002 (GRCm39) |
R1237H |
probably damaging |
Het |
Cdcp1 |
T |
C |
9: 123,002,980 (GRCm39) |
D697G |
probably benign |
Het |
Cep85l |
T |
C |
10: 53,225,194 (GRCm39) |
T132A |
probably benign |
Het |
Ces1b |
T |
A |
8: 93,787,038 (GRCm39) |
Y447F |
probably damaging |
Het |
Cfhr4 |
T |
G |
1: 139,659,391 (GRCm39) |
N642H |
possibly damaging |
Het |
Cntn4 |
A |
T |
6: 106,674,544 (GRCm39) |
T1015S |
probably benign |
Het |
Eea1 |
T |
G |
10: 95,838,741 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
C |
T |
7: 27,836,638 (GRCm39) |
R186C |
probably damaging |
Het |
Hipk1 |
A |
T |
3: 103,684,828 (GRCm39) |
N262K |
possibly damaging |
Het |
Jmjd8 |
G |
A |
17: 26,048,026 (GRCm39) |
R41H |
possibly damaging |
Het |
Klhl3 |
T |
A |
13: 58,178,259 (GRCm39) |
T344S |
probably damaging |
Het |
Krt39 |
T |
C |
11: 99,410,647 (GRCm39) |
D175G |
probably damaging |
Het |
Map4k1 |
A |
G |
7: 28,686,227 (GRCm39) |
Y81C |
probably damaging |
Het |
Mpdu1 |
T |
A |
11: 69,549,411 (GRCm39) |
T95S |
probably benign |
Het |
Myl12b |
A |
T |
17: 71,284,135 (GRCm39) |
I31N |
probably damaging |
Het |
Ndufaf5 |
T |
A |
2: 140,030,700 (GRCm39) |
Y195* |
probably null |
Het |
Or4c119 |
G |
A |
2: 88,987,157 (GRCm39) |
R121C |
possibly damaging |
Het |
Or4d5 |
T |
C |
9: 40,012,652 (GRCm39) |
I45V |
probably benign |
Het |
Or51v15-ps1 |
A |
T |
7: 103,278,790 (GRCm39) |
F126I |
probably benign |
Het |
Or52z12 |
T |
A |
7: 103,233,727 (GRCm39) |
I166N |
possibly damaging |
Het |
Or5w17 |
A |
G |
2: 87,584,223 (GRCm39) |
V38A |
probably benign |
Het |
Oxgr1 |
T |
A |
14: 120,259,431 (GRCm39) |
I259F |
possibly damaging |
Het |
Pcdhb9 |
T |
A |
18: 37,534,970 (GRCm39) |
D321E |
probably benign |
Het |
Pi4kb |
G |
T |
3: 94,900,461 (GRCm39) |
R392L |
probably damaging |
Het |
Pramel18 |
G |
A |
4: 101,767,291 (GRCm39) |
C180Y |
possibly damaging |
Het |
Prss41 |
T |
C |
17: 24,056,622 (GRCm39) |
K151R |
probably benign |
Het |
Rev3l |
T |
A |
10: 39,697,477 (GRCm39) |
V658D |
probably benign |
Het |
Snx4 |
A |
G |
16: 33,115,108 (GRCm39) |
I430V |
probably damaging |
Het |
Tanc2 |
C |
T |
11: 105,726,056 (GRCm39) |
H407Y |
possibly damaging |
Het |
Tcf25 |
G |
A |
8: 124,127,437 (GRCm39) |
|
probably null |
Het |
Tsc22d1 |
A |
T |
14: 76,743,923 (GRCm39) |
K24* |
probably null |
Het |
Xrcc6 |
A |
G |
15: 81,913,323 (GRCm39) |
T319A |
probably benign |
Het |
Zbtb1 |
C |
T |
12: 76,432,985 (GRCm39) |
R324* |
probably null |
Het |
Zc3h7a |
A |
G |
16: 10,963,535 (GRCm39) |
Y729H |
probably damaging |
Het |
Zfp329 |
C |
A |
7: 12,540,457 (GRCm39) |
|
probably benign |
Het |
Zfp456 |
A |
T |
13: 67,514,384 (GRCm39) |
S441T |
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 |
IGL03214:Vmn2r30
|
APN |
7 |
7,337,259 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|