Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agap2 |
A |
G |
10: 126,918,911 (GRCm39) |
E429G |
probably damaging |
Het |
Akap12 |
T |
A |
10: 4,307,405 (GRCm39) |
V1405D |
probably damaging |
Het |
Akap7 |
C |
T |
10: 25,159,880 (GRCm39) |
D107N |
possibly damaging |
Het |
Arfgef1 |
A |
G |
1: 10,269,952 (GRCm39) |
|
probably null |
Het |
Cacna1s |
T |
A |
1: 136,026,113 (GRCm39) |
|
probably null |
Het |
Ctsd |
T |
C |
7: 141,931,070 (GRCm39) |
Q274R |
probably benign |
Het |
Dysf |
G |
A |
6: 84,163,453 (GRCm39) |
R1575Q |
probably damaging |
Het |
Erich6b |
A |
T |
14: 75,896,274 (GRCm39) |
L53F |
possibly damaging |
Het |
Exoc6 |
A |
C |
19: 37,582,218 (GRCm39) |
|
probably null |
Het |
Fbxw19 |
A |
T |
9: 109,315,133 (GRCm39) |
V143E |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Fndc1 |
A |
G |
17: 7,991,608 (GRCm39) |
F696S |
unknown |
Het |
Foxa3 |
G |
T |
7: 18,748,940 (GRCm39) |
Y102* |
probably null |
Het |
Foxn1 |
A |
G |
11: 78,256,792 (GRCm39) |
M301T |
probably damaging |
Het |
Foxp2 |
C |
T |
6: 15,197,119 (GRCm39) |
Q54* |
probably null |
Het |
Glra1 |
T |
C |
11: 55,423,208 (GRCm39) |
E117G |
possibly damaging |
Het |
Glt1d1 |
A |
T |
5: 127,768,095 (GRCm39) |
D234V |
probably damaging |
Het |
Golm2 |
AGATGGTGATGGTG |
AGATGGTG |
2: 121,756,178 (GRCm39) |
|
probably benign |
Het |
Gulp1 |
T |
C |
1: 44,812,441 (GRCm39) |
I137T |
probably damaging |
Het |
Itga8 |
A |
G |
2: 12,165,161 (GRCm39) |
V816A |
possibly damaging |
Het |
Kdm4c |
G |
A |
4: 74,233,886 (GRCm39) |
|
probably benign |
Het |
Krtap19-2 |
A |
G |
16: 88,670,996 (GRCm39) |
|
probably benign |
Het |
Lcorl |
T |
C |
5: 45,891,219 (GRCm39) |
N378S |
possibly damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Mocos |
T |
C |
18: 24,807,357 (GRCm39) |
L363P |
probably damaging |
Het |
Mycbp2 |
G |
T |
14: 103,520,081 (GRCm39) |
Y745* |
probably null |
Het |
Nav3 |
A |
C |
10: 109,719,539 (GRCm39) |
N141K |
possibly damaging |
Het |
Ncor1 |
T |
C |
11: 62,233,837 (GRCm39) |
N779S |
probably benign |
Het |
Nebl |
G |
T |
2: 17,398,079 (GRCm39) |
Y414* |
probably null |
Het |
Nf1 |
T |
G |
11: 79,336,615 (GRCm39) |
C1065G |
probably damaging |
Het |
Nfib |
A |
G |
4: 82,278,004 (GRCm39) |
V216A |
probably damaging |
Het |
Nub1 |
A |
T |
5: 24,907,379 (GRCm39) |
N354I |
possibly damaging |
Het |
Nyap1 |
C |
T |
5: 137,733,726 (GRCm39) |
V436I |
probably benign |
Het |
Or5m11b |
A |
G |
2: 85,805,797 (GRCm39) |
D70G |
possibly damaging |
Het |
Or5p73 |
T |
C |
7: 108,065,469 (GRCm39) |
F313L |
probably benign |
Het |
Pde2a |
T |
A |
7: 101,155,187 (GRCm39) |
M570K |
probably damaging |
Het |
Pfas |
T |
C |
11: 68,882,296 (GRCm39) |
S856G |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,794,855 (GRCm39) |
E368G |
probably benign |
Het |
Ptf1a |
G |
A |
2: 19,451,969 (GRCm39) |
V323M |
probably damaging |
Het |
Ptprh |
T |
C |
7: 4,552,504 (GRCm39) |
Y920C |
probably damaging |
Het |
Sergef |
T |
A |
7: 46,264,200 (GRCm39) |
D229V |
possibly damaging |
Het |
Slc1a4 |
T |
C |
11: 20,254,417 (GRCm39) |
K483R |
probably benign |
Het |
Slc26a6 |
G |
A |
9: 108,735,155 (GRCm39) |
R351H |
probably damaging |
Het |
Slc6a19 |
G |
A |
13: 73,833,948 (GRCm39) |
T370I |
possibly damaging |
Het |
Smpd5 |
T |
C |
15: 76,178,757 (GRCm39) |
S42P |
possibly damaging |
Het |
Snx13 |
G |
A |
12: 35,173,025 (GRCm39) |
|
probably null |
Het |
Sox10 |
G |
A |
15: 79,040,502 (GRCm39) |
S185L |
probably benign |
Het |
Spata31e5 |
T |
A |
1: 28,817,163 (GRCm39) |
I290F |
probably damaging |
Het |
Srpk1 |
T |
C |
17: 28,821,733 (GRCm39) |
Y227C |
probably damaging |
Het |
Stambpl1 |
T |
A |
19: 34,211,316 (GRCm39) |
|
probably null |
Het |
Stk36 |
A |
G |
1: 74,665,750 (GRCm39) |
R698G |
possibly damaging |
Het |
Tas2r122 |
T |
A |
6: 132,688,393 (GRCm39) |
T167S |
probably damaging |
Het |
Tlr12 |
A |
G |
4: 128,509,656 (GRCm39) |
S865P |
probably damaging |
Het |
Trp53bp1 |
A |
G |
2: 121,038,227 (GRCm39) |
L1537P |
probably damaging |
Het |
Xpo7 |
A |
T |
14: 70,931,407 (GRCm39) |
F304I |
probably damaging |
Het |
Zfp286 |
T |
C |
11: 62,671,796 (GRCm39) |
|
probably benign |
Het |
Zfp985 |
A |
T |
4: 147,667,440 (GRCm39) |
K103* |
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 |
R2251:Vstm2a
|
UTSW |
11 |
16,318,273 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|
|