Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg3 |
T |
A |
8: 95,760,084 (GRCm39) |
V101D |
possibly damaging |
Het |
Brca1 |
T |
C |
11: 101,380,738 (GRCm39) |
D1765G |
probably benign |
Het |
Cadps2 |
T |
C |
6: 23,496,808 (GRCm39) |
K450R |
probably benign |
Het |
Cc2d2a |
A |
T |
5: 43,885,636 (GRCm39) |
|
probably null |
Het |
Dbh |
A |
G |
2: 27,058,321 (GRCm39) |
Y163C |
probably damaging |
Het |
Drc7 |
T |
A |
8: 95,800,925 (GRCm39) |
I649N |
probably damaging |
Het |
Dst |
G |
A |
1: 34,328,668 (GRCm39) |
A7097T |
probably benign |
Het |
Fbxo46 |
A |
G |
7: 18,869,537 (GRCm39) |
H52R |
probably benign |
Het |
Gm9944 |
T |
C |
4: 144,179,709 (GRCm39) |
|
probably benign |
Het |
Lsm14a |
G |
T |
7: 34,070,596 (GRCm39) |
S100* |
probably null |
Het |
Mrc2 |
C |
T |
11: 105,231,997 (GRCm39) |
R850C |
probably damaging |
Het |
Musk |
A |
G |
4: 58,373,364 (GRCm39) |
D763G |
probably damaging |
Het |
Ncan |
C |
T |
8: 70,562,735 (GRCm39) |
V508I |
probably benign |
Het |
Or4k35 |
A |
T |
2: 111,100,073 (GRCm39) |
L213Q |
probably damaging |
Het |
Pgls |
C |
T |
8: 72,046,741 (GRCm39) |
S18L |
probably damaging |
Het |
Phf20l1 |
A |
G |
15: 66,467,000 (GRCm39) |
T98A |
probably damaging |
Het |
Ppp1r36dn |
A |
C |
12: 76,497,944 (GRCm39) |
|
noncoding transcript |
Het |
Prdm13 |
T |
A |
4: 21,683,421 (GRCm39) |
K180* |
probably null |
Het |
Rai1 |
T |
C |
11: 60,077,844 (GRCm39) |
V636A |
probably benign |
Het |
Setd5 |
T |
C |
6: 113,091,899 (GRCm39) |
F240S |
possibly damaging |
Het |
Slco1a5 |
A |
G |
6: 142,187,731 (GRCm39) |
L536P |
probably damaging |
Het |
Stk39 |
C |
T |
2: 68,051,243 (GRCm39) |
|
probably null |
Het |
Tenm2 |
T |
C |
11: 35,932,471 (GRCm39) |
T1707A |
probably damaging |
Het |
Tlr2 |
A |
T |
3: 83,743,781 (GRCm39) |
D767E |
probably benign |
Het |
Tlr7 |
C |
T |
X: 166,090,830 (GRCm39) |
V219I |
probably benign |
Het |
Tmprss7 |
A |
G |
16: 45,476,818 (GRCm39) |
S815P |
probably damaging |
Het |
Trav12-1 |
T |
A |
14: 53,776,017 (GRCm39) |
W57R |
probably damaging |
Het |
Uxt |
T |
C |
X: 20,826,025 (GRCm39) |
E66G |
possibly damaging |
Het |
Vmn2r45 |
A |
T |
7: 8,475,369 (GRCm39) |
M553K |
probably damaging |
Het |
Vmn2r67 |
A |
G |
7: 84,785,951 (GRCm39) |
W685R |
probably benign |
Het |
Zfp592 |
A |
G |
7: 80,674,575 (GRCm39) |
H513R |
probably damaging |
Het |
Zfp830 |
T |
A |
11: 82,656,295 (GRCm39) |
|
probably benign |
Het |
Zfp990 |
A |
G |
4: 145,261,492 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vstm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01597:Vstm5
|
APN |
9 |
15,168,675 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Vstm5
|
APN |
9 |
15,168,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R1155:Vstm5
|
UTSW |
9 |
15,168,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Vstm5
|
UTSW |
9 |
15,168,663 (GRCm39) |
missense |
probably benign |
0.13 |
R2368:Vstm5
|
UTSW |
9 |
15,169,027 (GRCm39) |
missense |
probably benign |
0.00 |
R3160:Vstm5
|
UTSW |
9 |
15,168,594 (GRCm39) |
missense |
probably benign |
0.02 |
R3161:Vstm5
|
UTSW |
9 |
15,168,594 (GRCm39) |
missense |
probably benign |
0.02 |
R3162:Vstm5
|
UTSW |
9 |
15,168,594 (GRCm39) |
missense |
probably benign |
0.02 |
R4612:Vstm5
|
UTSW |
9 |
15,168,789 (GRCm39) |
missense |
probably benign |
0.22 |
R4692:Vstm5
|
UTSW |
9 |
15,168,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R4950:Vstm5
|
UTSW |
9 |
15,169,090 (GRCm39) |
splice site |
probably null |
|
R5088:Vstm5
|
UTSW |
9 |
15,168,601 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6351:Vstm5
|
UTSW |
9 |
15,168,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Vstm5
|
UTSW |
9 |
15,150,549 (GRCm39) |
start gained |
probably benign |
|
R7720:Vstm5
|
UTSW |
9 |
15,150,652 (GRCm39) |
missense |
probably benign |
0.08 |
R9300:Vstm5
|
UTSW |
9 |
15,168,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R9491:Vstm5
|
UTSW |
9 |
15,168,586 (GRCm39) |
missense |
probably damaging |
0.99 |
|