Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra3 |
C |
T |
5: 50,016,867 (GRCm38) |
A110T |
probably benign |
Het |
Adra1a |
A |
C |
14: 66,637,935 (GRCm38) |
I120L |
probably damaging |
Het |
Ahnak2 |
C |
T |
12: 112,774,405 (GRCm38) |
V1078I |
possibly damaging |
Het |
Ccser1 |
A |
G |
6: 61,570,723 (GRCm38) |
H590R |
probably benign |
Het |
Cdh12 |
T |
G |
15: 21,583,765 (GRCm38) |
L564V |
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,836,622 (GRCm38) |
H1900Q |
probably benign |
Het |
Clasp1 |
T |
A |
1: 118,545,434 (GRCm38) |
M918K |
probably benign |
Het |
Cmtm6 |
A |
G |
9: 114,731,240 (GRCm38) |
E2G |
probably damaging |
Het |
Ctsg |
A |
G |
14: 56,100,541 (GRCm38) |
|
probably null |
Het |
Cylc2 |
T |
A |
4: 51,229,256 (GRCm38) |
|
probably null |
Het |
Dna2 |
A |
G |
10: 62,971,993 (GRCm38) |
|
probably null |
Het |
Dnaic1 |
G |
A |
4: 41,614,323 (GRCm38) |
R333H |
probably benign |
Het |
Egln3 |
T |
C |
12: 54,180,628 (GRCm38) |
D239G |
probably benign |
Het |
Fam13a |
A |
T |
6: 58,987,284 (GRCm38) |
D54E |
probably damaging |
Het |
Fn1 |
A |
G |
1: 71,597,516 (GRCm38) |
V2159A |
probably benign |
Het |
Gcnt2 |
T |
A |
13: 40,887,681 (GRCm38) |
F105L |
probably benign |
Het |
Gm5788 |
T |
C |
12: 87,494,842 (GRCm38) |
M41T |
possibly damaging |
Het |
Gpd1 |
G |
A |
15: 99,722,086 (GRCm38) |
S255N |
probably damaging |
Het |
Hacd4 |
A |
G |
4: 88,437,478 (GRCm38) |
F57L |
probably benign |
Het |
Helb |
T |
C |
10: 120,105,283 (GRCm38) |
D500G |
probably benign |
Het |
Ighv1-26 |
G |
A |
12: 114,788,442 (GRCm38) |
S94F |
probably damaging |
Het |
Kirrel |
T |
C |
3: 87,083,439 (GRCm38) |
D692G |
possibly damaging |
Het |
Klra7 |
A |
T |
6: 130,230,091 (GRCm38) |
|
probably null |
Het |
Lyl1 |
T |
C |
8: 84,704,300 (GRCm38) |
V277A |
probably benign |
Het |
Mon2 |
A |
C |
10: 123,023,939 (GRCm38) |
W811G |
probably damaging |
Het |
Myo9b |
T |
C |
8: 71,354,801 (GRCm38) |
L1627P |
probably benign |
Het |
Neurl1b |
C |
G |
17: 26,438,746 (GRCm38) |
H219Q |
probably benign |
Het |
Odf4 |
A |
T |
11: 68,922,423 (GRCm38) |
C218S |
possibly damaging |
Het |
Olfr1038-ps |
A |
G |
2: 86,121,938 (GRCm38) |
N5S |
possibly damaging |
Het |
Olfr11 |
T |
A |
13: 21,638,609 (GRCm38) |
I305F |
probably benign |
Het |
Pde5a |
A |
G |
3: 122,818,030 (GRCm38) |
D571G |
probably damaging |
Het |
Pgc |
A |
G |
17: 47,734,186 (GRCm38) |
E343G |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,654,583 (GRCm38) |
F667L |
possibly damaging |
Het |
Prf1 |
G |
A |
10: 61,300,155 (GRCm38) |
R70H |
possibly damaging |
Het |
Ptprb |
C |
T |
10: 116,353,991 (GRCm38) |
Q1565* |
probably null |
Het |
Rapgef4 |
T |
A |
2: 72,205,733 (GRCm38) |
N523K |
probably benign |
Het |
Rbm25 |
T |
C |
12: 83,672,877 (GRCm38) |
L557P |
probably damaging |
Het |
Rhobtb3 |
C |
T |
13: 75,878,857 (GRCm38) |
V466I |
probably benign |
Het |
Rnpep |
A |
G |
1: 135,278,858 (GRCm38) |
V166A |
probably benign |
Het |
Sgo2a |
A |
G |
1: 58,017,795 (GRCm38) |
K1046R |
probably benign |
Het |
Slc12a2 |
T |
C |
18: 57,904,393 (GRCm38) |
V525A |
probably benign |
Het |
Slc1a4 |
A |
T |
11: 20,306,487 (GRCm38) |
I448N |
probably damaging |
Het |
Slc29a4 |
C |
T |
5: 142,718,506 (GRCm38) |
P305L |
probably benign |
Het |
Slc9a5 |
T |
A |
8: 105,363,253 (GRCm38) |
|
probably null |
Het |
Spag16 |
A |
T |
1: 69,887,520 (GRCm38) |
N258I |
possibly damaging |
Het |
Sspo |
T |
A |
6: 48,466,699 (GRCm38) |
L2076Q |
probably damaging |
Het |
Taok1 |
T |
A |
11: 77,545,326 (GRCm38) |
H704L |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,145,120 (GRCm38) |
F148L |
probably damaging |
Het |
Tm4sf1 |
A |
G |
3: 57,294,755 (GRCm38) |
Y12H |
probably benign |
Het |
Traj6 |
C |
T |
14: 54,212,714 (GRCm38) |
T9M |
|
Het |
Ttll4 |
A |
G |
1: 74,687,259 (GRCm38) |
N672S |
possibly damaging |
Het |
Ube3a |
T |
A |
7: 59,303,689 (GRCm38) |
H790Q |
possibly damaging |
Het |
Usp49 |
G |
A |
17: 47,672,280 (GRCm38) |
R70Q |
probably benign |
Het |
Wars |
A |
G |
12: 108,882,875 (GRCm38) |
S49P |
probably benign |
Het |
Zbp1 |
T |
A |
2: 173,207,811 (GRCm38) |
Q386L |
possibly damaging |
Het |
Zfp369 |
T |
C |
13: 65,279,273 (GRCm38) |
F10S |
unknown |
Het |
Zfp512 |
C |
G |
5: 31,473,539 (GRCm38) |
I408M |
possibly damaging |
Het |
Zfp952 |
A |
G |
17: 33,003,782 (GRCm38) |
I412V |
probably benign |
Het |
|
Other mutations in Vmn2r32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Vmn2r32
|
APN |
7 |
7,476,697 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02333:Vmn2r32
|
APN |
7 |
7,464,144 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02406:Vmn2r32
|
APN |
7 |
7,476,710 (GRCm38) |
missense |
probably benign |
|
IGL02428:Vmn2r32
|
APN |
7 |
7,474,284 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02484:Vmn2r32
|
APN |
7 |
7,464,117 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03277:Vmn2r32
|
APN |
7 |
7,474,252 (GRCm38) |
missense |
probably benign |
0.23 |
IGL03366:Vmn2r32
|
APN |
7 |
7,464,030 (GRCm38) |
missense |
probably damaging |
0.99 |
R1055:Vmn2r32
|
UTSW |
7 |
7,474,327 (GRCm38) |
nonsense |
probably null |
|
R1695:Vmn2r32
|
UTSW |
7 |
7,463,992 (GRCm38) |
missense |
probably benign |
0.01 |
R2172:Vmn2r32
|
UTSW |
7 |
7,474,615 (GRCm38) |
missense |
probably damaging |
0.99 |
R2262:Vmn2r32
|
UTSW |
7 |
7,474,619 (GRCm38) |
missense |
probably benign |
|
R3150:Vmn2r32
|
UTSW |
7 |
7,472,555 (GRCm38) |
missense |
probably benign |
|
R4362:Vmn2r32
|
UTSW |
7 |
7,479,858 (GRCm38) |
nonsense |
probably null |
|
R4432:Vmn2r32
|
UTSW |
7 |
7,479,919 (GRCm38) |
missense |
probably damaging |
0.98 |
R4851:Vmn2r32
|
UTSW |
7 |
7,479,954 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4949:Vmn2r32
|
UTSW |
7 |
7,464,084 (GRCm38) |
missense |
probably benign |
0.22 |
R5990:Vmn2r32
|
UTSW |
7 |
7,479,810 (GRCm38) |
missense |
probably damaging |
0.97 |
R6083:Vmn2r32
|
UTSW |
7 |
7,464,210 (GRCm38) |
missense |
probably benign |
0.15 |
R6084:Vmn2r32
|
UTSW |
7 |
7,464,210 (GRCm38) |
missense |
probably benign |
0.15 |
R6116:Vmn2r32
|
UTSW |
7 |
7,464,093 (GRCm38) |
missense |
probably damaging |
1.00 |
R6263:Vmn2r32
|
UTSW |
7 |
7,476,692 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6889:Vmn2r32
|
UTSW |
7 |
7,472,574 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7286:Vmn2r32
|
UTSW |
7 |
7,479,808 (GRCm38) |
missense |
probably benign |
0.21 |
R7390:Vmn2r32
|
UTSW |
7 |
7,479,852 (GRCm38) |
missense |
probably benign |
0.00 |
R7412:Vmn2r32
|
UTSW |
7 |
7,474,213 (GRCm38) |
missense |
possibly damaging |
0.53 |
R8812:Vmn2r32
|
UTSW |
7 |
7,474,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R8968:Vmn2r32
|
UTSW |
7 |
7,474,205 (GRCm38) |
missense |
probably benign |
0.00 |
R9331:Vmn2r32
|
UTSW |
7 |
7,464,403 (GRCm38) |
nonsense |
probably null |
|
R9358:Vmn2r32
|
UTSW |
7 |
7,474,198 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Vmn2r32
|
UTSW |
7 |
7,474,161 (GRCm38) |
missense |
probably damaging |
0.98 |
|