Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
G |
A |
14: 59,380,061 (GRCm39) |
S79F |
probably damaging |
Het |
Abl1 |
T |
A |
2: 31,669,131 (GRCm39) |
V170E |
probably damaging |
Het |
Akap13 |
C |
T |
7: 75,389,225 (GRCm39) |
T2381M |
possibly damaging |
Het |
Armc8 |
T |
A |
9: 99,384,653 (GRCm39) |
|
probably null |
Het |
B3gnt3 |
A |
T |
8: 72,145,462 (GRCm39) |
M302K |
probably damaging |
Het |
Casp3 |
G |
T |
8: 47,090,990 (GRCm39) |
W214L |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 96,489,814 (GRCm39) |
V463A |
probably benign |
Het |
Cntn2 |
T |
C |
1: 132,453,059 (GRCm39) |
E411G |
probably damaging |
Het |
Dgkg |
A |
T |
16: 22,441,010 (GRCm39) |
M1K |
probably null |
Het |
Faap20 |
A |
C |
4: 155,335,010 (GRCm39) |
E37A |
possibly damaging |
Het |
Fam186a |
T |
C |
15: 99,842,978 (GRCm39) |
T1089A |
probably benign |
Het |
Fgb |
T |
G |
3: 82,950,591 (GRCm39) |
T388P |
probably damaging |
Het |
Fndc1 |
G |
A |
17: 7,972,439 (GRCm39) |
R1498W |
probably damaging |
Het |
Gch1 |
T |
C |
14: 47,426,798 (GRCm39) |
|
probably benign |
Het |
Gzf1 |
T |
C |
2: 148,525,856 (GRCm39) |
M109T |
probably damaging |
Het |
H2-M10.1 |
A |
C |
17: 36,636,498 (GRCm39) |
L102R |
probably damaging |
Het |
Kpna1 |
T |
C |
16: 35,841,939 (GRCm39) |
Y280H |
possibly damaging |
Het |
Mbtps2 |
A |
T |
X: 156,342,029 (GRCm39) |
F270L |
probably benign |
Het |
Mrpl40 |
T |
C |
16: 18,694,125 (GRCm39) |
H29R |
probably benign |
Het |
N4bp2 |
G |
A |
5: 65,964,071 (GRCm39) |
V707I |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,103,025 (GRCm39) |
K608E |
probably damaging |
Het |
Nfix |
T |
C |
8: 85,442,799 (GRCm39) |
D458G |
probably benign |
Het |
Ngdn |
T |
C |
14: 55,260,852 (GRCm39) |
|
probably null |
Het |
Nr3c1 |
G |
T |
18: 39,619,804 (GRCm39) |
T161K |
probably benign |
Het |
Or2n1e |
C |
T |
17: 38,585,794 (GRCm39) |
A44V |
probably benign |
Het |
Or4g16 |
A |
G |
2: 111,136,655 (GRCm39) |
Y35C |
probably damaging |
Het |
Or52e15 |
A |
T |
7: 104,645,802 (GRCm39) |
M103K |
probably damaging |
Het |
Or5ak20 |
A |
G |
2: 85,184,202 (GRCm39) |
S23P |
possibly damaging |
Het |
Pbld2 |
G |
T |
10: 62,860,384 (GRCm39) |
|
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,784,177 (GRCm39) |
Y700C |
probably damaging |
Het |
Plcb2 |
T |
C |
2: 118,554,246 (GRCm39) |
N69S |
probably benign |
Het |
Pwp2 |
T |
A |
10: 78,016,922 (GRCm39) |
Q266L |
probably benign |
Het |
Rnf133 |
T |
C |
6: 23,649,174 (GRCm39) |
M252V |
probably benign |
Het |
Scn8a |
A |
G |
15: 100,914,987 (GRCm39) |
I1184V |
probably benign |
Het |
Slc7a2 |
T |
C |
8: 41,358,658 (GRCm39) |
Y334H |
probably benign |
Het |
Smim11 |
T |
C |
16: 92,107,716 (GRCm39) |
Y14H |
probably benign |
Het |
Spata17 |
A |
T |
1: 186,780,670 (GRCm39) |
L359Q |
possibly damaging |
Het |
Spn |
T |
C |
7: 126,736,331 (GRCm39) |
K59E |
probably benign |
Het |
Tap2 |
A |
G |
17: 34,430,928 (GRCm39) |
S343G |
probably damaging |
Het |
Tcp11l2 |
T |
C |
10: 84,440,933 (GRCm39) |
|
probably null |
Het |
Tlr11 |
T |
A |
14: 50,598,249 (GRCm39) |
N78K |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,377,143 (GRCm39) |
S224T |
probably benign |
Het |
Trpm1 |
G |
A |
7: 63,859,724 (GRCm39) |
G261D |
probably damaging |
Het |
Tut4 |
T |
A |
4: 108,377,405 (GRCm39) |
D938E |
probably damaging |
Het |
Usp3 |
T |
C |
9: 66,469,860 (GRCm39) |
D87G |
probably damaging |
Het |
Vmn1r189 |
T |
C |
13: 22,286,718 (GRCm39) |
K40E |
probably damaging |
Het |
Vps45 |
A |
T |
3: 95,964,352 (GRCm39) |
D56E |
probably benign |
Het |
Zfp575 |
A |
T |
7: 24,285,015 (GRCm39) |
C209S |
probably damaging |
Het |
Zfp768 |
T |
C |
7: 126,943,550 (GRCm39) |
T193A |
probably benign |
Het |
Zfp867 |
T |
A |
11: 59,356,319 (GRCm39) |
R38* |
probably null |
Het |
|
Other mutations in Vstm2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Vstm2a
|
APN |
11 |
16,231,874 (GRCm39) |
missense |
possibly damaging |
0.51 |
popiah
|
UTSW |
11 |
16,213,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Vstm2a
|
UTSW |
11 |
16,208,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R0314:Vstm2a
|
UTSW |
11 |
16,318,388 (GRCm39) |
splice site |
probably benign |
|
R0480:Vstm2a
|
UTSW |
11 |
16,213,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R0533:Vstm2a
|
UTSW |
11 |
16,213,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:Vstm2a
|
UTSW |
11 |
16,213,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R0788:Vstm2a
|
UTSW |
11 |
16,209,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Vstm2a
|
UTSW |
11 |
16,213,166 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1934:Vstm2a
|
UTSW |
11 |
16,359,734 (GRCm39) |
missense |
unknown |
|
R2066:Vstm2a
|
UTSW |
11 |
16,211,483 (GRCm39) |
missense |
probably benign |
0.09 |
R2101:Vstm2a
|
UTSW |
11 |
16,213,191 (GRCm39) |
missense |
probably benign |
0.19 |
R4084:Vstm2a
|
UTSW |
11 |
16,213,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R4093:Vstm2a
|
UTSW |
11 |
16,209,884 (GRCm39) |
missense |
probably damaging |
0.98 |
R4745:Vstm2a
|
UTSW |
11 |
16,213,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4978:Vstm2a
|
UTSW |
11 |
16,211,460 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5533:Vstm2a
|
UTSW |
11 |
16,213,125 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5873:Vstm2a
|
UTSW |
11 |
16,208,044 (GRCm39) |
missense |
probably damaging |
0.99 |
R5894:Vstm2a
|
UTSW |
11 |
16,211,483 (GRCm39) |
missense |
probably benign |
0.09 |
R7094:Vstm2a
|
UTSW |
11 |
16,207,990 (GRCm39) |
unclassified |
probably benign |
|
R7753:Vstm2a
|
UTSW |
11 |
16,213,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8313:Vstm2a
|
UTSW |
11 |
16,231,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8336:Vstm2a
|
UTSW |
11 |
16,207,801 (GRCm39) |
unclassified |
probably benign |
|
|