Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp1b2 |
T |
C |
11: 69,496,102 (GRCm39) |
T33A |
probably benign |
Het |
Brd2 |
A |
T |
17: 34,331,590 (GRCm39) |
|
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,208,299 (GRCm39) |
|
probably benign |
Het |
Cdh9 |
A |
T |
15: 16,856,318 (GRCm39) |
D786V |
probably damaging |
Het |
Cep128 |
A |
C |
12: 91,233,504 (GRCm39) |
|
probably benign |
Het |
Cep85 |
T |
C |
4: 133,883,038 (GRCm39) |
T284A |
probably benign |
Het |
Chrna1 |
C |
T |
2: 73,398,450 (GRCm39) |
E330K |
probably benign |
Het |
Clec2l |
T |
C |
6: 38,653,785 (GRCm39) |
Y104H |
probably damaging |
Het |
Clybl |
G |
T |
14: 122,616,664 (GRCm39) |
K226N |
probably damaging |
Het |
Cmip |
T |
A |
8: 118,172,067 (GRCm39) |
D467E |
probably benign |
Het |
Cpne3 |
A |
T |
4: 19,543,340 (GRCm39) |
|
probably null |
Het |
Crisp4 |
A |
G |
1: 18,204,324 (GRCm39) |
V46A |
probably damaging |
Het |
Csnk2a1 |
T |
C |
2: 152,116,070 (GRCm39) |
Y261H |
probably damaging |
Het |
Cul5 |
C |
A |
9: 53,569,973 (GRCm39) |
G86V |
probably benign |
Het |
Czib |
T |
G |
4: 107,752,065 (GRCm39) |
|
probably benign |
Het |
Depdc7 |
T |
C |
2: 104,560,626 (GRCm39) |
T123A |
probably benign |
Het |
Edem2 |
T |
C |
2: 155,547,661 (GRCm39) |
T384A |
probably damaging |
Het |
F8 |
C |
T |
X: 74,376,247 (GRCm39) |
M377I |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,021,367 (GRCm39) |
|
probably null |
Het |
Fez2 |
T |
C |
17: 78,689,051 (GRCm39) |
D366G |
probably damaging |
Het |
Gm4841 |
A |
C |
18: 60,404,037 (GRCm39) |
S19A |
probably benign |
Het |
Gm4862 |
T |
A |
3: 138,834,396 (GRCm39) |
|
noncoding transcript |
Het |
Hk3 |
T |
A |
13: 55,162,908 (GRCm39) |
Q44L |
probably damaging |
Het |
Irgm1 |
C |
A |
11: 48,757,642 (GRCm39) |
L56F |
probably damaging |
Het |
Ldlr |
A |
G |
9: 21,644,795 (GRCm39) |
T108A |
probably benign |
Het |
Lgr4 |
T |
A |
2: 109,841,635 (GRCm39) |
M516K |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,587,537 (GRCm39) |
N3906S |
probably null |
Het |
Lrrtm4 |
A |
G |
6: 79,998,845 (GRCm39) |
N86D |
possibly damaging |
Het |
Map3k2 |
A |
G |
18: 32,340,587 (GRCm39) |
D198G |
probably damaging |
Het |
Mapkapk3 |
C |
T |
9: 107,139,621 (GRCm39) |
|
probably null |
Het |
Myo3a |
T |
C |
2: 22,404,776 (GRCm39) |
S711P |
probably benign |
Het |
Myom3 |
A |
G |
4: 135,497,986 (GRCm39) |
K189E |
probably damaging |
Het |
Naip1 |
T |
A |
13: 100,563,304 (GRCm39) |
K620N |
probably benign |
Het |
Nlrp10 |
T |
C |
7: 108,524,709 (GRCm39) |
E257G |
probably damaging |
Het |
Nptn |
T |
G |
9: 58,548,012 (GRCm39) |
M139R |
possibly damaging |
Het |
Nrk |
T |
G |
X: 137,889,544 (GRCm39) |
M1105R |
possibly damaging |
Het |
Or10a3n |
A |
T |
7: 108,493,046 (GRCm39) |
C189* |
probably null |
Het |
Or10d4 |
T |
G |
9: 39,580,374 (GRCm39) |
V7G |
probably damaging |
Het |
Or1q1 |
T |
A |
2: 36,887,477 (GRCm39) |
Y218* |
probably null |
Het |
Pcdhb16 |
A |
G |
18: 37,612,248 (GRCm39) |
T403A |
probably benign |
Het |
Pcyt1b |
A |
G |
X: 92,745,722 (GRCm39) |
E50G |
possibly damaging |
Het |
Pigg |
C |
T |
5: 108,492,190 (GRCm39) |
T892I |
probably damaging |
Het |
Ppig |
T |
G |
2: 69,566,327 (GRCm39) |
|
probably null |
Het |
Prr12 |
A |
G |
7: 44,699,429 (GRCm39) |
|
probably benign |
Het |
Slc5a5 |
G |
T |
8: 71,345,073 (GRCm39) |
A78E |
possibly damaging |
Het |
Slc7a2 |
T |
G |
8: 41,364,095 (GRCm39) |
M436R |
probably benign |
Het |
Sp7 |
T |
A |
15: 102,267,690 (GRCm39) |
M39L |
probably benign |
Het |
Spag8 |
T |
A |
4: 43,653,134 (GRCm39) |
|
probably benign |
Het |
Svep1 |
A |
G |
4: 58,068,556 (GRCm39) |
S3077P |
probably benign |
Het |
Tmem30a |
A |
T |
9: 79,681,371 (GRCm39) |
|
probably benign |
Het |
Tmem63a |
C |
T |
1: 180,800,353 (GRCm39) |
T714I |
probably benign |
Het |
Trank1 |
T |
C |
9: 111,193,028 (GRCm39) |
L535P |
probably damaging |
Het |
Tuba8 |
A |
C |
6: 121,197,470 (GRCm39) |
N44T |
probably benign |
Het |
Wnk1 |
A |
G |
6: 119,926,039 (GRCm39) |
|
probably benign |
Het |
Zfp654 |
A |
T |
16: 64,605,391 (GRCm39) |
I396K |
probably benign |
Het |
|
Other mutations in Mvp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01090:Mvp
|
APN |
7 |
126,588,859 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01503:Mvp
|
APN |
7 |
126,601,133 (GRCm39) |
splice site |
probably benign |
|
IGL03412:Mvp
|
APN |
7 |
126,592,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Mvp
|
UTSW |
7 |
126,589,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R0458:Mvp
|
UTSW |
7 |
126,597,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R0811:Mvp
|
UTSW |
7 |
126,586,728 (GRCm39) |
missense |
probably benign |
|
R0812:Mvp
|
UTSW |
7 |
126,586,728 (GRCm39) |
missense |
probably benign |
|
R1625:Mvp
|
UTSW |
7 |
126,600,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R1707:Mvp
|
UTSW |
7 |
126,600,744 (GRCm39) |
missense |
probably benign |
|
R1711:Mvp
|
UTSW |
7 |
126,594,907 (GRCm39) |
critical splice donor site |
probably null |
|
R1776:Mvp
|
UTSW |
7 |
126,591,933 (GRCm39) |
missense |
probably benign |
0.27 |
R3814:Mvp
|
UTSW |
7 |
126,586,801 (GRCm39) |
missense |
probably benign |
|
R4065:Mvp
|
UTSW |
7 |
126,595,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Mvp
|
UTSW |
7 |
126,588,875 (GRCm39) |
missense |
probably benign |
0.16 |
R4471:Mvp
|
UTSW |
7 |
126,601,130 (GRCm39) |
start codon destroyed |
probably null |
|
R4652:Mvp
|
UTSW |
7 |
126,592,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R4693:Mvp
|
UTSW |
7 |
126,597,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R4972:Mvp
|
UTSW |
7 |
126,588,970 (GRCm39) |
missense |
probably damaging |
0.99 |
R5031:Mvp
|
UTSW |
7 |
126,592,788 (GRCm39) |
nonsense |
probably null |
|
R5530:Mvp
|
UTSW |
7 |
126,595,095 (GRCm39) |
missense |
probably benign |
0.45 |
R7053:Mvp
|
UTSW |
7 |
126,586,776 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7324:Mvp
|
UTSW |
7 |
126,592,781 (GRCm39) |
missense |
probably benign |
|
R7580:Mvp
|
UTSW |
7 |
126,591,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R8146:Mvp
|
UTSW |
7 |
126,586,171 (GRCm39) |
missense |
probably benign |
0.15 |
R9180:Mvp
|
UTSW |
7 |
126,591,822 (GRCm39) |
missense |
probably benign |
0.04 |
R9197:Mvp
|
UTSW |
7 |
126,588,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R9351:Mvp
|
UTSW |
7 |
126,595,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R9727:Mvp
|
UTSW |
7 |
126,595,040 (GRCm39) |
missense |
probably damaging |
1.00 |
|