Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,849,913 (GRCm39) |
H380R |
probably benign |
Het |
Aff3 |
A |
T |
1: 38,249,649 (GRCm39) |
I486N |
probably benign |
Het |
Bltp1 |
T |
A |
3: 36,929,611 (GRCm39) |
F76Y |
probably damaging |
Het |
Cfap44 |
A |
C |
16: 44,230,832 (GRCm39) |
D271A |
probably benign |
Het |
Dbndd2 |
T |
A |
2: 164,330,270 (GRCm39) |
V34D |
probably damaging |
Het |
Erc2 |
T |
A |
14: 27,733,732 (GRCm39) |
|
probably null |
Het |
Fcgbp |
T |
C |
7: 27,774,838 (GRCm39) |
|
probably benign |
Het |
Frem3 |
T |
C |
8: 81,417,402 (GRCm39) |
S2036P |
probably damaging |
Het |
Golph3l |
A |
G |
3: 95,499,024 (GRCm39) |
|
probably benign |
Het |
Grm7 |
G |
T |
6: 110,623,309 (GRCm39) |
V161F |
probably damaging |
Het |
Ifrd2 |
G |
A |
9: 107,467,221 (GRCm39) |
G60S |
probably null |
Het |
Ints9 |
T |
A |
14: 65,187,727 (GRCm39) |
W3R |
probably benign |
Het |
Jmjd1c |
A |
G |
10: 66,993,711 (GRCm39) |
E64G |
probably damaging |
Het |
Katnip |
T |
A |
7: 125,465,512 (GRCm39) |
H1321Q |
probably damaging |
Het |
Matn3 |
A |
C |
12: 9,002,217 (GRCm39) |
Q143P |
probably damaging |
Het |
Myo18a |
A |
T |
11: 77,749,846 (GRCm39) |
|
probably benign |
Het |
Nop9 |
T |
C |
14: 55,988,631 (GRCm39) |
S358P |
probably benign |
Het |
Pard3b |
T |
C |
1: 62,384,037 (GRCm39) |
S801P |
probably damaging |
Het |
Pax2 |
T |
C |
19: 44,804,463 (GRCm39) |
F268L |
probably damaging |
Het |
Pik3r1 |
A |
G |
13: 101,823,771 (GRCm39) |
I538T |
probably damaging |
Het |
Plekha8 |
T |
C |
6: 54,599,107 (GRCm39) |
S214P |
probably benign |
Het |
Ppme1 |
T |
C |
7: 99,981,084 (GRCm39) |
H352R |
probably damaging |
Het |
Ppp1r26 |
A |
C |
2: 28,342,314 (GRCm39) |
D648A |
probably damaging |
Het |
Prom1 |
C |
A |
5: 44,191,733 (GRCm39) |
V337F |
probably damaging |
Het |
Rapgef4 |
T |
C |
2: 72,028,717 (GRCm39) |
I378T |
probably damaging |
Het |
Rnf115 |
T |
C |
3: 96,661,675 (GRCm39) |
S43P |
probably damaging |
Het |
Rnf216 |
A |
G |
5: 143,061,480 (GRCm39) |
|
probably null |
Het |
Scn7a |
G |
T |
2: 66,530,240 (GRCm39) |
Q702K |
probably benign |
Het |
Shisal2b |
T |
A |
13: 104,994,899 (GRCm39) |
I83F |
possibly damaging |
Het |
Slc2a1 |
T |
A |
4: 118,989,340 (GRCm39) |
N13K |
probably damaging |
Het |
Tnr |
A |
G |
1: 159,715,829 (GRCm39) |
I864V |
probably benign |
Het |
Tspyl3 |
A |
T |
2: 153,066,650 (GRCm39) |
M196K |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Umod |
T |
C |
7: 119,071,763 (GRCm39) |
D326G |
probably damaging |
Het |
Upf2 |
A |
G |
2: 5,980,890 (GRCm39) |
D492G |
unknown |
Het |
Vsig10l |
T |
A |
7: 43,116,881 (GRCm39) |
I574K |
possibly damaging |
Het |
|
Other mutations in Vash1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00478:Vash1
|
APN |
12 |
86,727,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2289:Vash1
|
UTSW |
12 |
86,726,952 (GRCm39) |
missense |
probably damaging |
0.98 |
R4896:Vash1
|
UTSW |
12 |
86,726,916 (GRCm39) |
missense |
probably benign |
0.04 |
R5471:Vash1
|
UTSW |
12 |
86,735,902 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5540:Vash1
|
UTSW |
12 |
86,726,831 (GRCm39) |
small deletion |
probably benign |
|
R6684:Vash1
|
UTSW |
12 |
86,735,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R7714:Vash1
|
UTSW |
12 |
86,738,614 (GRCm39) |
missense |
probably benign |
0.02 |
R7767:Vash1
|
UTSW |
12 |
86,733,767 (GRCm39) |
missense |
probably damaging |
0.98 |
R7976:Vash1
|
UTSW |
12 |
86,726,758 (GRCm39) |
start gained |
probably benign |
|
R8411:Vash1
|
UTSW |
12 |
86,726,952 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8692:Vash1
|
UTSW |
12 |
86,735,863 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9495:Vash1
|
UTSW |
12 |
86,738,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R9549:Vash1
|
UTSW |
12 |
86,735,870 (GRCm39) |
missense |
probably damaging |
0.98 |
|