Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12 |
C |
T |
2: 150,700,413 (GRCm39) |
|
probably benign |
Het |
Adarb1 |
G |
A |
10: 77,131,588 (GRCm39) |
P624S |
probably benign |
Het |
Afg3l2 |
A |
T |
18: 67,562,110 (GRCm39) |
F322I |
possibly damaging |
Het |
Arhgap23 |
A |
G |
11: 97,381,831 (GRCm39) |
|
probably benign |
Het |
Atp13a1 |
A |
G |
8: 70,259,751 (GRCm39) |
N1114S |
probably damaging |
Het |
C3ar1 |
T |
C |
6: 122,826,838 (GRCm39) |
N460D |
probably benign |
Het |
Cacna1e |
A |
G |
1: 154,279,493 (GRCm39) |
Y1988H |
probably damaging |
Het |
Calr |
T |
C |
8: 85,569,415 (GRCm39) |
|
probably benign |
Het |
D5Ertd579e |
A |
G |
5: 36,773,529 (GRCm39) |
S289P |
probably damaging |
Het |
Erbb4 |
G |
A |
1: 68,081,596 (GRCm39) |
|
probably benign |
Het |
Fam98a |
A |
G |
17: 75,845,936 (GRCm39) |
|
probably benign |
Het |
Gm3739 |
A |
T |
14: 18,505,274 (GRCm39) |
D83E |
possibly damaging |
Het |
Gm5420 |
A |
T |
10: 21,567,071 (GRCm39) |
|
noncoding transcript |
Het |
Heatr5b |
A |
G |
17: 79,135,396 (GRCm39) |
V245A |
probably damaging |
Het |
Kptn |
C |
A |
7: 15,861,038 (GRCm39) |
|
probably benign |
Het |
Llgl2 |
T |
C |
11: 115,735,661 (GRCm39) |
C86R |
probably damaging |
Het |
Lrr1 |
T |
A |
12: 69,215,665 (GRCm39) |
C12* |
probably null |
Het |
Mcf2 |
T |
C |
X: 59,180,812 (GRCm39) |
D255G |
probably damaging |
Het |
Med13 |
A |
T |
11: 86,174,771 (GRCm39) |
|
probably benign |
Het |
Mthfd1 |
C |
T |
12: 76,364,406 (GRCm39) |
T735M |
probably damaging |
Het |
Nlrp2 |
C |
T |
7: 5,331,809 (GRCm39) |
A196T |
probably damaging |
Het |
Nnmt |
T |
C |
9: 48,514,838 (GRCm39) |
I60V |
probably damaging |
Het |
Odad2 |
G |
T |
18: 7,285,719 (GRCm39) |
Q215K |
probably benign |
Het |
Or4c110 |
T |
A |
2: 88,832,507 (GRCm39) |
T42S |
probably benign |
Het |
Or6ae1 |
A |
T |
7: 139,742,513 (GRCm39) |
S117T |
probably benign |
Het |
P2rx3 |
T |
C |
2: 84,853,571 (GRCm39) |
I140V |
probably benign |
Het |
Patj |
A |
G |
4: 98,480,173 (GRCm39) |
N1293D |
probably damaging |
Het |
Pitpnm2 |
G |
A |
5: 124,278,821 (GRCm39) |
|
probably benign |
Het |
Ppp1r26 |
T |
G |
2: 28,343,292 (GRCm39) |
V974G |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,116,973 (GRCm39) |
L1376* |
probably null |
Het |
Rab33a |
T |
A |
X: 47,608,584 (GRCm39) |
I36N |
probably damaging |
Het |
Rab3gap1 |
A |
T |
1: 127,855,840 (GRCm39) |
N493I |
possibly damaging |
Het |
Scara3 |
C |
A |
14: 66,170,559 (GRCm39) |
G107* |
probably null |
Het |
Siglec1 |
T |
C |
2: 130,913,098 (GRCm39) |
E1606G |
probably benign |
Het |
Skint9 |
A |
T |
4: 112,246,447 (GRCm39) |
Y222N |
possibly damaging |
Het |
Slc47a1 |
A |
T |
11: 61,253,884 (GRCm39) |
I185N |
probably damaging |
Het |
Slc47a2 |
C |
A |
11: 61,193,020 (GRCm39) |
|
probably benign |
Het |
Slc4a2 |
A |
G |
5: 24,639,711 (GRCm39) |
I506V |
probably damaging |
Het |
Slc9a4 |
A |
C |
1: 40,639,942 (GRCm39) |
I245L |
probably benign |
Het |
Smarcb1 |
T |
C |
10: 75,733,328 (GRCm39) |
T357A |
probably damaging |
Het |
Spata31d1d |
A |
G |
13: 59,877,954 (GRCm39) |
|
probably benign |
Het |
Stox2 |
T |
A |
8: 47,639,573 (GRCm39) |
I874F |
probably damaging |
Het |
Taar7b |
A |
T |
10: 23,876,050 (GRCm39) |
I72F |
probably damaging |
Het |
Tacc2 |
G |
A |
7: 130,225,129 (GRCm39) |
V605I |
probably benign |
Het |
Tef |
T |
C |
15: 81,699,301 (GRCm39) |
L34P |
probably damaging |
Het |
Trak2 |
A |
G |
1: 58,949,204 (GRCm39) |
V532A |
probably benign |
Het |
Usp13 |
T |
A |
3: 32,973,209 (GRCm39) |
D795E |
probably damaging |
Het |
Vmn1r32 |
T |
A |
6: 66,529,913 (GRCm39) |
I288F |
probably benign |
Het |
Zfp871 |
A |
T |
17: 32,993,329 (GRCm39) |
F615L |
probably benign |
Het |
Zfp941 |
G |
A |
7: 140,392,612 (GRCm39) |
T249M |
probably benign |
Het |
Zhx1 |
T |
C |
15: 57,917,137 (GRCm39) |
I370V |
probably damaging |
Het |
|
Other mutations in Vmn1r75 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01901:Vmn1r75
|
APN |
7 |
11,614,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02175:Vmn1r75
|
APN |
7 |
11,614,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02648:Vmn1r75
|
APN |
7 |
11,615,091 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03372:Vmn1r75
|
APN |
7 |
11,614,496 (GRCm39) |
missense |
probably benign |
0.29 |
R0538:Vmn1r75
|
UTSW |
7 |
11,614,797 (GRCm39) |
missense |
probably damaging |
0.97 |
R0599:Vmn1r75
|
UTSW |
7 |
11,615,189 (GRCm39) |
splice site |
probably null |
|
R3910:Vmn1r75
|
UTSW |
7 |
11,614,757 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4491:Vmn1r75
|
UTSW |
7 |
11,614,909 (GRCm39) |
missense |
probably damaging |
0.97 |
R5566:Vmn1r75
|
UTSW |
7 |
11,614,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Vmn1r75
|
UTSW |
7 |
11,614,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6230:Vmn1r75
|
UTSW |
7 |
11,614,966 (GRCm39) |
missense |
probably damaging |
0.98 |
R6490:Vmn1r75
|
UTSW |
7 |
11,615,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R6570:Vmn1r75
|
UTSW |
7 |
11,614,883 (GRCm39) |
missense |
probably damaging |
0.98 |
R7184:Vmn1r75
|
UTSW |
7 |
11,614,915 (GRCm39) |
nonsense |
probably null |
|
R7189:Vmn1r75
|
UTSW |
7 |
11,614,475 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7501:Vmn1r75
|
UTSW |
7 |
11,614,997 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7973:Vmn1r75
|
UTSW |
7 |
11,614,961 (GRCm39) |
missense |
probably benign |
0.04 |
R7997:Vmn1r75
|
UTSW |
7 |
11,614,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Vmn1r75
|
UTSW |
7 |
11,614,657 (GRCm39) |
missense |
probably benign |
0.10 |
R8812:Vmn1r75
|
UTSW |
7 |
11,614,630 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8932:Vmn1r75
|
UTSW |
7 |
11,614,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R9089:Vmn1r75
|
UTSW |
7 |
11,614,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R9129:Vmn1r75
|
UTSW |
7 |
11,614,513 (GRCm39) |
missense |
probably benign |
0.15 |
|