Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd11 |
G |
A |
5: 135,038,654 (GRCm39) |
C30Y |
probably benign |
Het |
Akr1c20 |
C |
T |
13: 4,562,671 (GRCm39) |
V95M |
probably damaging |
Het |
Ano7 |
A |
G |
1: 93,322,195 (GRCm39) |
D401G |
probably benign |
Het |
Arhgef10l |
G |
A |
4: 140,305,616 (GRCm39) |
T176I |
possibly damaging |
Het |
Armc2 |
A |
C |
10: 41,842,792 (GRCm39) |
V337G |
probably damaging |
Het |
Atp6v0d2 |
T |
A |
4: 19,922,400 (GRCm39) |
Y33F |
probably benign |
Het |
Banp |
A |
G |
8: 122,747,291 (GRCm39) |
S447G |
probably benign |
Het |
Car8 |
T |
A |
4: 8,238,860 (GRCm39) |
Y32F |
possibly damaging |
Het |
Ccdc188 |
C |
T |
16: 18,036,539 (GRCm39) |
P124S |
probably damaging |
Het |
Cdc23 |
A |
T |
18: 34,780,072 (GRCm39) |
D85E |
probably benign |
Het |
Cnot6l |
T |
C |
5: 96,242,084 (GRCm39) |
E213G |
possibly damaging |
Het |
Cntnap4 |
A |
G |
8: 113,484,113 (GRCm39) |
T389A |
probably benign |
Het |
Cramp1 |
A |
T |
17: 25,202,196 (GRCm39) |
C429S |
probably damaging |
Het |
Crygn |
T |
C |
5: 24,961,072 (GRCm39) |
H78R |
probably benign |
Het |
D630003M21Rik |
T |
A |
2: 158,059,588 (GRCm39) |
D104V |
probably damaging |
Het |
Dcaf10 |
T |
G |
4: 45,348,196 (GRCm39) |
H217Q |
probably damaging |
Het |
Dmrtb1 |
C |
T |
4: 107,541,179 (GRCm39) |
V61M |
probably benign |
Het |
Dnai1 |
A |
G |
4: 41,605,823 (GRCm39) |
E271G |
probably benign |
Het |
Efr3a |
G |
A |
15: 65,701,679 (GRCm39) |
V198I |
probably benign |
Het |
Emsy |
G |
A |
7: 98,289,060 (GRCm39) |
T79M |
probably damaging |
Het |
Ergic1 |
A |
G |
17: 26,853,449 (GRCm39) |
D145G |
probably damaging |
Het |
Fah |
A |
G |
7: 84,244,686 (GRCm39) |
V229A |
probably damaging |
Het |
Fam76a |
G |
A |
4: 132,629,342 (GRCm39) |
T270I |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,055,353 (GRCm39) |
M4191L |
probably benign |
Het |
Fbxl22 |
G |
T |
9: 66,418,999 (GRCm39) |
R213S |
probably benign |
Het |
Fktn |
T |
C |
4: 53,734,859 (GRCm39) |
F127L |
probably benign |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
A |
T |
4: 46,734,096 (GRCm39) |
S541T |
probably benign |
Het |
Gm7489 |
A |
G |
15: 53,749,402 (GRCm39) |
H158R |
unknown |
Het |
Greb1l |
G |
C |
18: 10,542,056 (GRCm39) |
E1268Q |
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,482,848 (GRCm39) |
D126G |
probably damaging |
Het |
Ikzf3 |
T |
A |
11: 98,409,525 (GRCm39) |
T13S |
probably benign |
Het |
Il23r |
T |
C |
6: 67,400,846 (GRCm39) |
T495A |
probably benign |
Het |
Insyn2b |
A |
G |
11: 34,353,034 (GRCm39) |
T359A |
probably benign |
Het |
Irf5 |
A |
G |
6: 29,535,461 (GRCm39) |
T230A |
probably benign |
Het |
Itga2b |
A |
T |
11: 102,348,108 (GRCm39) |
I831N |
probably damaging |
Het |
Itgb4 |
A |
G |
11: 115,891,087 (GRCm39) |
D1168G |
probably damaging |
Het |
Kcnma1 |
G |
T |
14: 23,440,991 (GRCm39) |
P605Q |
probably benign |
Het |
Larp7 |
A |
T |
3: 127,337,916 (GRCm39) |
M381K |
possibly damaging |
Het |
Lfng |
G |
A |
5: 140,598,588 (GRCm39) |
G269D |
probably benign |
Het |
Liph |
T |
C |
16: 21,780,986 (GRCm39) |
I335V |
probably benign |
Het |
Map2k2 |
A |
T |
10: 80,954,040 (GRCm39) |
I169F |
possibly damaging |
Het |
Mmrn1 |
T |
A |
6: 60,964,044 (GRCm39) |
|
probably null |
Het |
Nod2 |
A |
G |
8: 89,387,425 (GRCm39) |
|
probably null |
Het |
Or51ag1 |
A |
C |
7: 103,155,586 (GRCm39) |
L189R |
probably damaging |
Het |
Or5b101 |
T |
A |
19: 13,005,360 (GRCm39) |
Y111F |
probably benign |
Het |
Or9s23 |
T |
C |
1: 92,501,219 (GRCm39) |
F109L |
probably benign |
Het |
Pcdh20 |
G |
T |
14: 88,707,143 (GRCm39) |
F52L |
probably null |
Het |
Pkhd1 |
A |
T |
1: 20,573,223 (GRCm39) |
N1894K |
probably damaging |
Het |
Pla2r1 |
T |
A |
2: 60,334,536 (GRCm39) |
D412V |
possibly damaging |
Het |
Pole |
T |
G |
5: 110,465,663 (GRCm39) |
M1197R |
probably benign |
Het |
Pom121l2 |
C |
T |
13: 22,168,048 (GRCm39) |
T773I |
possibly damaging |
Het |
Ppp2r5d |
A |
T |
17: 46,995,472 (GRCm39) |
M497K |
probably benign |
Het |
Rbm45 |
G |
T |
2: 76,206,797 (GRCm39) |
V270F |
possibly damaging |
Het |
Ros1 |
A |
T |
10: 52,020,957 (GRCm39) |
F673I |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,691,048 (GRCm39) |
L1113* |
probably null |
Het |
Scn4a |
A |
G |
11: 106,212,841 (GRCm39) |
I1388T |
probably benign |
Het |
Sema3c |
G |
A |
5: 17,899,845 (GRCm39) |
V446I |
probably damaging |
Het |
Six4 |
T |
C |
12: 73,159,408 (GRCm39) |
Y176C |
probably damaging |
Het |
Slc35a5 |
T |
A |
16: 44,964,570 (GRCm39) |
K221M |
possibly damaging |
Het |
Slc6a19 |
A |
G |
13: 73,841,182 (GRCm39) |
I76T |
probably damaging |
Het |
Slfn4 |
A |
G |
11: 83,077,419 (GRCm39) |
D69G |
probably damaging |
Het |
Smc6 |
T |
C |
12: 11,367,844 (GRCm39) |
F1085L |
probably benign |
Het |
Spatc1l |
A |
G |
10: 76,398,224 (GRCm39) |
S9G |
probably benign |
Het |
Stx8 |
T |
A |
11: 68,000,106 (GRCm39) |
I182N |
probably damaging |
Het |
Sult2a8 |
A |
T |
7: 14,147,596 (GRCm39) |
C232S |
probably benign |
Het |
Susd4 |
G |
A |
1: 182,686,070 (GRCm39) |
A207T |
probably benign |
Het |
Svep1 |
G |
A |
4: 58,054,539 (GRCm39) |
P3350S |
probably benign |
Het |
Tbx20 |
A |
T |
9: 24,685,108 (GRCm39) |
S12T |
probably damaging |
Het |
Tfrc |
A |
G |
16: 32,437,985 (GRCm39) |
K346R |
probably benign |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Umodl1 |
A |
T |
17: 31,192,666 (GRCm39) |
|
probably null |
Het |
Vmn1r201 |
T |
C |
13: 22,659,538 (GRCm39) |
F251L |
possibly damaging |
Het |
Vmn1r230 |
A |
G |
17: 21,066,933 (GRCm39) |
T41A |
probably benign |
Het |
Vmn2r20 |
A |
G |
6: 123,362,882 (GRCm39) |
L634P |
probably damaging |
Het |
Wdr41 |
A |
T |
13: 95,151,701 (GRCm39) |
N287I |
probably benign |
Het |
Zfp202 |
A |
G |
9: 40,121,758 (GRCm39) |
D285G |
possibly damaging |
Het |
|
Other mutations in Vmn2r81 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01111:Vmn2r81
|
APN |
10 |
79,083,831 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02255:Vmn2r81
|
APN |
10 |
79,083,806 (GRCm39) |
nonsense |
probably null |
|
IGL02901:Vmn2r81
|
APN |
10 |
79,106,564 (GRCm39) |
missense |
probably damaging |
0.98 |
R0383:Vmn2r81
|
UTSW |
10 |
79,129,281 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0555:Vmn2r81
|
UTSW |
10 |
79,129,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0715:Vmn2r81
|
UTSW |
10 |
79,104,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Vmn2r81
|
UTSW |
10 |
79,083,857 (GRCm39) |
splice site |
probably benign |
|
R1438:Vmn2r81
|
UTSW |
10 |
79,129,691 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Vmn2r81
|
UTSW |
10 |
79,129,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Vmn2r81
|
UTSW |
10 |
79,129,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Vmn2r81
|
UTSW |
10 |
79,128,858 (GRCm39) |
missense |
probably damaging |
0.99 |
R1671:Vmn2r81
|
UTSW |
10 |
79,103,265 (GRCm39) |
missense |
probably benign |
0.04 |
R1672:Vmn2r81
|
UTSW |
10 |
79,104,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R1728:Vmn2r81
|
UTSW |
10 |
79,106,489 (GRCm39) |
missense |
probably benign |
0.08 |
R1784:Vmn2r81
|
UTSW |
10 |
79,106,489 (GRCm39) |
missense |
probably benign |
0.08 |
R1931:Vmn2r81
|
UTSW |
10 |
79,129,328 (GRCm39) |
missense |
probably damaging |
0.98 |
R1934:Vmn2r81
|
UTSW |
10 |
79,083,628 (GRCm39) |
start codon destroyed |
probably null |
0.71 |
R1944:Vmn2r81
|
UTSW |
10 |
79,129,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Vmn2r81
|
UTSW |
10 |
79,129,334 (GRCm39) |
missense |
probably damaging |
0.97 |
R2190:Vmn2r81
|
UTSW |
10 |
79,104,085 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2392:Vmn2r81
|
UTSW |
10 |
79,110,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R3770:Vmn2r81
|
UTSW |
10 |
79,106,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4551:Vmn2r81
|
UTSW |
10 |
79,104,241 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4629:Vmn2r81
|
UTSW |
10 |
79,103,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R4691:Vmn2r81
|
UTSW |
10 |
79,129,211 (GRCm39) |
nonsense |
probably null |
|
R4829:Vmn2r81
|
UTSW |
10 |
79,083,635 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4914:Vmn2r81
|
UTSW |
10 |
79,106,357 (GRCm39) |
missense |
probably null |
1.00 |
R4996:Vmn2r81
|
UTSW |
10 |
79,129,247 (GRCm39) |
missense |
probably benign |
0.04 |
R5242:Vmn2r81
|
UTSW |
10 |
79,129,309 (GRCm39) |
nonsense |
probably null |
|
R5253:Vmn2r81
|
UTSW |
10 |
79,083,820 (GRCm39) |
missense |
probably benign |
0.00 |
R5925:Vmn2r81
|
UTSW |
10 |
79,083,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Vmn2r81
|
UTSW |
10 |
79,104,382 (GRCm39) |
missense |
probably benign |
|
R6270:Vmn2r81
|
UTSW |
10 |
79,129,649 (GRCm39) |
missense |
probably benign |
|
R6525:Vmn2r81
|
UTSW |
10 |
79,129,560 (GRCm39) |
missense |
probably benign |
0.11 |
R6813:Vmn2r81
|
UTSW |
10 |
79,104,439 (GRCm39) |
missense |
probably benign |
0.00 |
R6886:Vmn2r81
|
UTSW |
10 |
79,103,988 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7200:Vmn2r81
|
UTSW |
10 |
79,106,570 (GRCm39) |
critical splice donor site |
probably null |
|
R7350:Vmn2r81
|
UTSW |
10 |
79,104,219 (GRCm39) |
missense |
probably benign |
0.03 |
R7504:Vmn2r81
|
UTSW |
10 |
79,104,166 (GRCm39) |
missense |
probably benign |
|
R8130:Vmn2r81
|
UTSW |
10 |
79,110,538 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8362:Vmn2r81
|
UTSW |
10 |
79,103,283 (GRCm39) |
missense |
probably benign |
0.17 |
R8407:Vmn2r81
|
UTSW |
10 |
79,104,028 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8540:Vmn2r81
|
UTSW |
10 |
79,129,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R8558:Vmn2r81
|
UTSW |
10 |
79,106,467 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8700:Vmn2r81
|
UTSW |
10 |
79,129,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8779:Vmn2r81
|
UTSW |
10 |
79,103,218 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8987:Vmn2r81
|
UTSW |
10 |
79,129,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Vmn2r81
|
UTSW |
10 |
79,104,104 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9055:Vmn2r81
|
UTSW |
10 |
79,110,441 (GRCm39) |
missense |
probably benign |
|
R9145:Vmn2r81
|
UTSW |
10 |
79,104,028 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9151:Vmn2r81
|
UTSW |
10 |
79,103,905 (GRCm39) |
missense |
|
|
R9253:Vmn2r81
|
UTSW |
10 |
79,129,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R9255:Vmn2r81
|
UTSW |
10 |
79,103,166 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9370:Vmn2r81
|
UTSW |
10 |
79,104,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Vmn2r81
|
UTSW |
10 |
79,129,205 (GRCm39) |
missense |
possibly damaging |
0.46 |
X0067:Vmn2r81
|
UTSW |
10 |
79,128,877 (GRCm39) |
missense |
possibly damaging |
0.46 |
|