Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
A |
G |
9: 114,108,452 (GRCm39) |
|
noncoding transcript |
Het |
Alas1 |
A |
T |
9: 106,115,451 (GRCm39) |
|
probably null |
Het |
Arf5 |
A |
G |
6: 28,426,075 (GRCm39) |
Y154C |
probably damaging |
Het |
Arhgap20 |
T |
A |
9: 51,750,272 (GRCm39) |
I344N |
probably damaging |
Het |
Arhgap30 |
A |
C |
1: 171,235,516 (GRCm39) |
E630A |
possibly damaging |
Het |
B4galt5 |
A |
G |
2: 167,151,154 (GRCm39) |
L118P |
probably damaging |
Het |
Bdp1 |
A |
G |
13: 100,177,962 (GRCm39) |
I1969T |
probably benign |
Het |
Bysl |
C |
T |
17: 47,921,867 (GRCm39) |
R77Q |
probably benign |
Het |
Cap1 |
A |
T |
4: 122,756,868 (GRCm39) |
H272Q |
possibly damaging |
Het |
Ccdc146 |
T |
C |
5: 21,527,754 (GRCm39) |
I187M |
possibly damaging |
Het |
Ccdc192 |
G |
A |
18: 57,727,214 (GRCm39) |
|
probably benign |
Het |
Cdhr18 |
A |
G |
14: 13,899,571 (GRCm38) |
V117A |
probably damaging |
Het |
Cdk13 |
C |
A |
13: 17,894,079 (GRCm39) |
A1123S |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,228,811 (GRCm39) |
M473K |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,474,663 (GRCm39) |
S123P |
probably benign |
Het |
Cwc22 |
G |
A |
2: 77,738,455 (GRCm39) |
A497V |
probably damaging |
Het |
Cwh43 |
T |
C |
5: 73,575,370 (GRCm39) |
S296P |
probably damaging |
Het |
Cyp2c50 |
T |
A |
19: 40,080,837 (GRCm39) |
|
probably benign |
Het |
Dlg1 |
C |
A |
16: 31,624,508 (GRCm39) |
Y399* |
probably null |
Het |
Drosha |
A |
T |
15: 12,846,216 (GRCm39) |
E92D |
probably benign |
Het |
Fanca |
C |
T |
8: 123,995,278 (GRCm39) |
G1408D |
probably benign |
Het |
Frem1 |
T |
A |
4: 82,854,406 (GRCm39) |
D1621V |
possibly damaging |
Het |
Frem2 |
G |
A |
3: 53,563,629 (GRCm39) |
R293C |
probably damaging |
Het |
Fut8 |
T |
A |
12: 77,495,334 (GRCm39) |
V308D |
probably damaging |
Het |
Glipr1 |
A |
G |
10: 111,829,446 (GRCm39) |
I105T |
probably benign |
Het |
Glmn |
A |
T |
5: 107,708,800 (GRCm39) |
S385T |
probably benign |
Het |
Gon4l |
T |
A |
3: 88,802,989 (GRCm39) |
V1200D |
probably damaging |
Het |
Gpc1 |
G |
A |
1: 92,785,221 (GRCm39) |
D387N |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,675,486 (GRCm39) |
Y110H |
probably damaging |
Het |
Gucy1b1 |
T |
A |
3: 81,941,698 (GRCm39) |
H586L |
probably benign |
Het |
Gucy2e |
A |
G |
11: 69,127,458 (GRCm39) |
L5P |
unknown |
Het |
Hectd4 |
A |
G |
5: 121,433,569 (GRCm39) |
|
probably benign |
Het |
Hmcn1 |
T |
A |
1: 150,684,398 (GRCm39) |
I391F |
possibly damaging |
Het |
Hsf4 |
A |
T |
8: 105,999,336 (GRCm39) |
|
probably null |
Het |
I830077J02Rik |
G |
A |
3: 105,833,886 (GRCm39) |
T90M |
probably damaging |
Het |
Ino80 |
A |
T |
2: 119,261,497 (GRCm39) |
H722Q |
probably damaging |
Het |
Kcnma1 |
C |
A |
14: 23,364,243 (GRCm39) |
R980L |
probably damaging |
Het |
Kif1a |
A |
G |
1: 92,974,500 (GRCm39) |
|
probably benign |
Het |
Klhdc7b |
A |
G |
15: 89,272,724 (GRCm39) |
H1202R |
probably benign |
Het |
Lig3 |
A |
G |
11: 82,684,761 (GRCm39) |
D559G |
probably damaging |
Het |
Lyst |
T |
C |
13: 13,852,537 (GRCm39) |
V2179A |
probably benign |
Het |
Mab21l4 |
A |
T |
1: 93,087,447 (GRCm39) |
S135R |
possibly damaging |
Het |
Mansc4 |
A |
G |
6: 146,976,725 (GRCm39) |
I297T |
possibly damaging |
Het |
Marchf6 |
A |
T |
15: 31,475,958 (GRCm39) |
F633I |
probably benign |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Megf10 |
G |
T |
18: 57,392,874 (GRCm39) |
V424L |
possibly damaging |
Het |
Mfsd13a |
C |
T |
19: 46,354,943 (GRCm39) |
T40I |
probably benign |
Het |
Mib2 |
A |
G |
4: 155,740,519 (GRCm39) |
|
probably benign |
Het |
Mmut |
C |
T |
17: 41,267,118 (GRCm39) |
T564M |
probably damaging |
Het |
Myh8 |
A |
G |
11: 67,197,090 (GRCm39) |
|
probably benign |
Het |
Mypn |
T |
C |
10: 63,028,159 (GRCm39) |
|
probably benign |
Het |
Nf1 |
G |
A |
11: 79,359,702 (GRCm39) |
|
probably null |
Het |
Notch3 |
T |
A |
17: 32,352,436 (GRCm39) |
T1866S |
possibly damaging |
Het |
Or1e30 |
A |
G |
11: 73,678,141 (GRCm39) |
I126V |
possibly damaging |
Het |
Or1o11 |
C |
T |
17: 37,756,670 (GRCm39) |
A86V |
probably benign |
Het |
Or4c102 |
A |
T |
2: 88,422,999 (GRCm39) |
I284F |
probably damaging |
Het |
Or4k51 |
T |
A |
2: 111,584,930 (GRCm39) |
M112K |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,420,714 (GRCm39) |
I2464N |
probably damaging |
Het |
Pkn1 |
A |
G |
8: 84,397,658 (GRCm39) |
S817P |
probably damaging |
Het |
Prkg2 |
A |
T |
5: 99,142,514 (GRCm39) |
|
probably null |
Het |
Prl8a6 |
T |
C |
13: 27,617,084 (GRCm39) |
D201G |
probably benign |
Het |
Psmd1 |
C |
T |
1: 86,010,993 (GRCm39) |
T356I |
possibly damaging |
Het |
Ptk6 |
G |
A |
2: 180,844,320 (GRCm39) |
|
probably benign |
Het |
Ptprn2 |
T |
C |
12: 117,175,466 (GRCm39) |
|
probably benign |
Het |
Rbm42 |
G |
A |
7: 30,347,200 (GRCm39) |
T106I |
probably damaging |
Het |
Rims4 |
A |
T |
2: 163,706,040 (GRCm39) |
V198E |
probably damaging |
Het |
Ripk1 |
T |
C |
13: 34,193,733 (GRCm39) |
S32P |
probably damaging |
Het |
Rorc |
T |
C |
3: 94,284,916 (GRCm39) |
|
probably benign |
Het |
Rpl22l1 |
T |
C |
3: 28,860,685 (GRCm39) |
F15L |
probably damaging |
Het |
Slc6a20a |
C |
A |
9: 123,507,823 (GRCm39) |
A17S |
possibly damaging |
Het |
Sorcs1 |
A |
G |
19: 50,624,891 (GRCm39) |
|
probably benign |
Het |
Sp100 |
A |
G |
1: 85,577,852 (GRCm39) |
|
probably benign |
Het |
Ssc5d |
G |
A |
7: 4,930,880 (GRCm39) |
|
probably benign |
Het |
Taf11 |
A |
G |
17: 28,126,635 (GRCm39) |
L4P |
probably benign |
Het |
Tm2d3 |
A |
G |
7: 65,345,082 (GRCm39) |
|
probably benign |
Het |
Tmub2 |
T |
C |
11: 102,179,201 (GRCm39) |
|
probably null |
Het |
Trim34a |
T |
A |
7: 103,897,109 (GRCm39) |
C58S |
probably damaging |
Het |
Trpc3 |
T |
C |
3: 36,678,566 (GRCm39) |
I840V |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,807,316 (GRCm39) |
V1020A |
probably damaging |
Het |
Vmn1r214 |
T |
A |
13: 23,219,464 (GRCm39) |
Y319* |
probably null |
Het |
Vmn2r74 |
T |
C |
7: 85,606,564 (GRCm39) |
M261V |
probably benign |
Het |
Vmn2r89 |
T |
C |
14: 51,693,577 (GRCm39) |
F309S |
probably damaging |
Het |
Wdr95 |
A |
T |
5: 149,487,855 (GRCm39) |
D163V |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,340,253 (GRCm39) |
F831L |
possibly damaging |
Het |
Ythdc2 |
C |
T |
18: 44,974,490 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn1r59 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01684:Vmn1r59
|
APN |
7 |
5,457,299 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02035:Vmn1r59
|
APN |
7 |
5,457,208 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02039:Vmn1r59
|
APN |
7 |
5,457,380 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02812:Vmn1r59
|
APN |
7 |
5,457,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R0033:Vmn1r59
|
UTSW |
7 |
5,457,433 (GRCm39) |
missense |
probably benign |
0.08 |
R1164:Vmn1r59
|
UTSW |
7 |
5,457,410 (GRCm39) |
missense |
probably benign |
0.00 |
R1629:Vmn1r59
|
UTSW |
7 |
5,457,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Vmn1r59
|
UTSW |
7 |
5,457,553 (GRCm39) |
missense |
probably benign |
0.03 |
R1969:Vmn1r59
|
UTSW |
7 |
5,457,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Vmn1r59
|
UTSW |
7 |
5,457,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Vmn1r59
|
UTSW |
7 |
5,457,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Vmn1r59
|
UTSW |
7 |
5,457,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R3712:Vmn1r59
|
UTSW |
7 |
5,457,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R4580:Vmn1r59
|
UTSW |
7 |
5,457,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R4593:Vmn1r59
|
UTSW |
7 |
5,457,686 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4697:Vmn1r59
|
UTSW |
7 |
5,457,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Vmn1r59
|
UTSW |
7 |
5,457,532 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4873:Vmn1r59
|
UTSW |
7 |
5,457,108 (GRCm39) |
missense |
probably benign |
|
R4875:Vmn1r59
|
UTSW |
7 |
5,457,108 (GRCm39) |
missense |
probably benign |
|
R4925:Vmn1r59
|
UTSW |
7 |
5,457,115 (GRCm39) |
missense |
probably benign |
0.07 |
R5319:Vmn1r59
|
UTSW |
7 |
5,457,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R6239:Vmn1r59
|
UTSW |
7 |
5,457,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R6533:Vmn1r59
|
UTSW |
7 |
5,457,463 (GRCm39) |
missense |
probably benign |
0.00 |
R6912:Vmn1r59
|
UTSW |
7 |
5,457,599 (GRCm39) |
missense |
probably benign |
0.01 |
R7023:Vmn1r59
|
UTSW |
7 |
5,457,477 (GRCm39) |
missense |
probably benign |
0.37 |
R7205:Vmn1r59
|
UTSW |
7 |
5,457,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7374:Vmn1r59
|
UTSW |
7 |
5,457,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R7390:Vmn1r59
|
UTSW |
7 |
5,456,986 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7776:Vmn1r59
|
UTSW |
7 |
5,457,634 (GRCm39) |
missense |
probably damaging |
0.97 |
R8306:Vmn1r59
|
UTSW |
7 |
5,456,966 (GRCm39) |
missense |
probably benign |
0.01 |
R8473:Vmn1r59
|
UTSW |
7 |
5,457,064 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8499:Vmn1r59
|
UTSW |
7 |
5,457,750 (GRCm39) |
missense |
probably benign |
0.00 |
R8523:Vmn1r59
|
UTSW |
7 |
5,457,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R8706:Vmn1r59
|
UTSW |
7 |
5,457,715 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9104:Vmn1r59
|
UTSW |
7 |
5,457,166 (GRCm39) |
missense |
probably benign |
0.00 |
|