Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bpifb9b |
A |
T |
2: 154,311,659 (GRCm38) |
D215V |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,368,671 (GRCm38) |
E625G |
probably damaging |
Het |
Cage1 |
C |
T |
13: 38,023,326 (GRCm38) |
S181N |
possibly damaging |
Het |
Ccdc36 |
A |
C |
9: 108,421,510 (GRCm38) |
S36R |
probably damaging |
Het |
Ccdc73 |
A |
C |
2: 104,992,366 (GRCm38) |
I887L |
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,906,336 (GRCm38) |
K1408* |
probably null |
Het |
Cngb1 |
C |
A |
8: 95,248,507 (GRCm38) |
G654W |
probably damaging |
Het |
Cxcl15 |
A |
T |
5: 90,795,245 (GRCm38) |
E35D |
possibly damaging |
Het |
Ddi1 |
A |
G |
9: 6,266,073 (GRCm38) |
S99P |
probably benign |
Het |
Disp3 |
A |
T |
4: 148,258,126 (GRCm38) |
D622E |
possibly damaging |
Het |
Dnajc22 |
G |
A |
15: 99,101,734 (GRCm38) |
V267I |
probably benign |
Het |
Dph5 |
G |
A |
3: 115,928,643 (GRCm38) |
G257S |
probably benign |
Het |
Elmo2 |
A |
T |
2: 165,314,813 (GRCm38) |
|
probably null |
Het |
Fam186a |
T |
C |
15: 99,941,653 (GRCm38) |
R2237G |
unknown |
Het |
Fez1 |
G |
A |
9: 36,867,882 (GRCm38) |
R285Q |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,946,932 (GRCm38) |
H101L |
probably damaging |
Het |
Fsip2 |
G |
A |
2: 82,977,414 (GRCm38) |
C1359Y |
probably benign |
Het |
Fxyd7 |
G |
A |
7: 31,047,390 (GRCm38) |
T15I |
probably benign |
Het |
Gpr155 |
A |
T |
2: 73,382,185 (GRCm38) |
D31E |
probably benign |
Het |
Irx6 |
A |
T |
8: 92,678,800 (GRCm38) |
Y432F |
probably damaging |
Het |
Itih5 |
A |
C |
2: 10,235,081 (GRCm38) |
I340L |
probably damaging |
Het |
Lao1 |
T |
C |
4: 118,965,375 (GRCm38) |
L164S |
probably damaging |
Het |
Mcoln3 |
T |
C |
3: 146,139,519 (GRCm38) |
I490T |
probably damaging |
Het |
Mef2b |
T |
C |
8: 70,167,196 (GRCm38) |
Y311H |
probably damaging |
Het |
Mras |
A |
T |
9: 99,394,484 (GRCm38) |
L111Q |
probably damaging |
Het |
Mrc1 |
A |
G |
2: 14,271,280 (GRCm38) |
D475G |
probably damaging |
Het |
Nrcam |
T |
C |
12: 44,598,490 (GRCm38) |
I1155T |
probably damaging |
Het |
Ntrk1 |
A |
G |
3: 87,789,611 (GRCm38) |
|
probably null |
Het |
Olfr58 |
G |
A |
9: 19,783,731 (GRCm38) |
M199I |
probably benign |
Het |
Olfr885 |
T |
C |
9: 38,062,001 (GRCm38) |
I227T |
probably damaging |
Het |
Parp9 |
A |
T |
16: 35,948,007 (GRCm38) |
I186F |
probably damaging |
Het |
Pcdhac2 |
T |
A |
18: 37,145,230 (GRCm38) |
V421E |
probably benign |
Het |
Pck1 |
T |
A |
2: 173,154,827 (GRCm38) |
I178K |
probably benign |
Het |
Pde6b |
A |
G |
5: 108,430,703 (GRCm38) |
K836E |
probably benign |
Het |
Ptprd |
T |
A |
4: 76,140,515 (GRCm38) |
|
probably null |
Het |
Pwp2 |
A |
G |
10: 78,183,006 (GRCm38) |
Y56H |
probably benign |
Het |
Rarb |
G |
A |
14: 16,432,085 (GRCm38) |
|
probably benign |
Het |
Rpain |
C |
G |
11: 70,970,921 (GRCm38) |
H50Q |
probably benign |
Het |
Rps9 |
CTGTTTG |
CTG |
7: 3,704,759 (GRCm38) |
|
probably null |
Het |
Rubcn |
A |
T |
16: 32,843,193 (GRCm38) |
S358T |
probably damaging |
Het |
Ryr2 |
G |
A |
13: 11,742,011 (GRCm38) |
R1586C |
probably damaging |
Het |
Slfn9 |
T |
C |
11: 82,981,904 (GRCm38) |
I669V |
probably benign |
Het |
Slx1b |
T |
C |
7: 126,691,767 (GRCm38) |
|
probably benign |
Het |
Spsb3 |
T |
A |
17: 24,887,511 (GRCm38) |
|
probably benign |
Het |
Tbx15 |
A |
G |
3: 99,326,384 (GRCm38) |
I288V |
possibly damaging |
Het |
Tlr2 |
C |
A |
3: 83,837,332 (GRCm38) |
E481D |
probably damaging |
Het |
Trim17 |
A |
T |
11: 58,970,428 (GRCm38) |
D253V |
probably damaging |
Het |
Trim69 |
A |
G |
2: 122,178,746 (GRCm38) |
D429G |
probably damaging |
Het |
Vwa3b |
A |
G |
1: 37,085,332 (GRCm38) |
Q337R |
probably benign |
Het |
Zfp113 |
T |
C |
5: 138,145,472 (GRCm38) |
N172S |
probably benign |
Het |
Zfp607a |
T |
A |
7: 27,878,751 (GRCm38) |
H415Q |
probably damaging |
Het |
Zfp87 |
G |
A |
13: 67,517,899 (GRCm38) |
T148I |
probably benign |
Het |
|
Other mutations in Vstm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01597:Vstm5
|
APN |
9 |
15,257,379 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01781:Vstm5
|
APN |
9 |
15,257,672 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02940:Vstm5
|
APN |
9 |
15,257,666 (GRCm38) |
missense |
probably damaging |
1.00 |
R1155:Vstm5
|
UTSW |
9 |
15,257,553 (GRCm38) |
missense |
probably damaging |
1.00 |
R1721:Vstm5
|
UTSW |
9 |
15,257,367 (GRCm38) |
missense |
probably benign |
0.13 |
R2368:Vstm5
|
UTSW |
9 |
15,257,731 (GRCm38) |
missense |
probably benign |
0.00 |
R3160:Vstm5
|
UTSW |
9 |
15,257,298 (GRCm38) |
missense |
probably benign |
0.02 |
R3161:Vstm5
|
UTSW |
9 |
15,257,298 (GRCm38) |
missense |
probably benign |
0.02 |
R3162:Vstm5
|
UTSW |
9 |
15,257,298 (GRCm38) |
missense |
probably benign |
0.02 |
R4612:Vstm5
|
UTSW |
9 |
15,257,493 (GRCm38) |
missense |
probably benign |
0.22 |
R4692:Vstm5
|
UTSW |
9 |
15,257,422 (GRCm38) |
missense |
probably damaging |
0.99 |
R5088:Vstm5
|
UTSW |
9 |
15,257,305 (GRCm38) |
missense |
possibly damaging |
0.87 |
R6351:Vstm5
|
UTSW |
9 |
15,257,533 (GRCm38) |
missense |
probably damaging |
1.00 |
R7063:Vstm5
|
UTSW |
9 |
15,239,253 (GRCm38) |
start gained |
probably benign |
|
R7720:Vstm5
|
UTSW |
9 |
15,239,356 (GRCm38) |
missense |
probably benign |
0.08 |
R9300:Vstm5
|
UTSW |
9 |
15,257,289 (GRCm38) |
missense |
probably damaging |
1.00 |
R9491:Vstm5
|
UTSW |
9 |
15,257,290 (GRCm38) |
missense |
probably damaging |
0.99 |
|