Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
A |
G |
5: 64,055,696 (GRCm39) |
D144G |
probably damaging |
Het |
Adgrg1 |
G |
T |
8: 95,730,139 (GRCm39) |
D114Y |
probably damaging |
Het |
Ago4 |
T |
A |
4: 126,405,325 (GRCm39) |
N416I |
probably benign |
Het |
Aoc1 |
C |
T |
6: 48,882,843 (GRCm39) |
Q240* |
probably null |
Het |
Atl1 |
G |
A |
12: 69,972,799 (GRCm39) |
V40I |
probably benign |
Het |
Cdh2 |
T |
C |
18: 16,757,810 (GRCm39) |
I591V |
probably benign |
Het |
Cic |
C |
A |
7: 24,990,375 (GRCm39) |
Q1959K |
probably damaging |
Het |
Cmya5 |
C |
T |
13: 93,229,194 (GRCm39) |
E1965K |
possibly damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cspp1 |
T |
C |
1: 10,153,781 (GRCm39) |
S397P |
probably damaging |
Het |
D130043K22Rik |
T |
C |
13: 25,059,907 (GRCm39) |
Y593H |
probably damaging |
Het |
Dck |
A |
G |
5: 88,921,964 (GRCm39) |
Y142C |
probably damaging |
Het |
Eea1 |
A |
T |
10: 95,854,046 (GRCm39) |
E568V |
probably damaging |
Het |
Gabra3 |
A |
G |
X: 71,544,683 (GRCm39) |
|
probably null |
Het |
Gucy2f |
A |
G |
X: 140,962,984 (GRCm39) |
S342P |
probably benign |
Het |
Hbb-bh1 |
T |
A |
7: 103,492,032 (GRCm39) |
I61F |
possibly damaging |
Het |
Hook1 |
T |
C |
4: 95,889,488 (GRCm39) |
S235P |
possibly damaging |
Het |
Hoxd12 |
G |
A |
2: 74,506,278 (GRCm39) |
R230H |
probably damaging |
Het |
Iglc2 |
C |
T |
16: 19,017,483 (GRCm39) |
A41T |
probably benign |
Het |
Il1r1 |
A |
G |
1: 40,352,518 (GRCm39) |
K566E |
probably damaging |
Het |
Kcns3 |
A |
T |
12: 11,142,093 (GRCm39) |
M202K |
probably damaging |
Het |
Krt7 |
C |
A |
15: 101,325,497 (GRCm39) |
A442D |
probably benign |
Het |
Ltk |
C |
T |
2: 119,589,054 (GRCm39) |
R200H |
probably benign |
Het |
Macf1 |
G |
T |
4: 123,403,619 (GRCm39) |
D582E |
probably damaging |
Het |
Mbnl3 |
A |
T |
X: 50,228,218 (GRCm39) |
Y69N |
probably damaging |
Het |
Mpp1 |
T |
C |
X: 74,165,034 (GRCm39) |
|
probably benign |
Het |
Myo18b |
A |
G |
5: 113,025,976 (GRCm39) |
S25P |
unknown |
Het |
Nsd3 |
A |
G |
8: 26,200,775 (GRCm39) |
N1289S |
probably damaging |
Het |
Or8d1 |
T |
A |
9: 38,766,712 (GRCm39) |
M118K |
possibly damaging |
Het |
Pacs2 |
A |
G |
12: 113,020,420 (GRCm39) |
|
probably benign |
Het |
Sva |
T |
A |
6: 42,019,156 (GRCm39) |
C109S |
probably damaging |
Het |
Taf3 |
T |
C |
2: 9,957,645 (GRCm39) |
N174S |
probably damaging |
Het |
Tbc1d5 |
A |
T |
17: 51,159,628 (GRCm39) |
M393K |
probably damaging |
Het |
Tmem242 |
A |
T |
17: 5,461,682 (GRCm39) |
S129T |
probably benign |
Het |
Ttn |
A |
T |
2: 76,701,513 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Rab3gap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01359:Rab3gap2
|
APN |
1 |
184,971,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01620:Rab3gap2
|
APN |
1 |
184,936,523 (GRCm39) |
missense |
probably benign |
|
IGL01977:Rab3gap2
|
APN |
1 |
184,999,220 (GRCm39) |
nonsense |
probably null |
|
IGL02183:Rab3gap2
|
APN |
1 |
185,003,665 (GRCm39) |
nonsense |
probably null |
|
IGL02231:Rab3gap2
|
APN |
1 |
184,999,095 (GRCm39) |
splice site |
probably benign |
|
IGL02506:Rab3gap2
|
APN |
1 |
184,984,221 (GRCm39) |
splice site |
probably benign |
|
IGL02618:Rab3gap2
|
APN |
1 |
184,983,938 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02643:Rab3gap2
|
APN |
1 |
184,999,197 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03239:Rab3gap2
|
APN |
1 |
184,982,091 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4498001:Rab3gap2
|
UTSW |
1 |
185,013,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0173:Rab3gap2
|
UTSW |
1 |
184,982,104 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0372:Rab3gap2
|
UTSW |
1 |
184,994,891 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0492:Rab3gap2
|
UTSW |
1 |
184,984,589 (GRCm39) |
splice site |
probably benign |
|
R0510:Rab3gap2
|
UTSW |
1 |
184,992,705 (GRCm39) |
splice site |
probably benign |
|
R0708:Rab3gap2
|
UTSW |
1 |
184,982,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R0711:Rab3gap2
|
UTSW |
1 |
184,982,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R1135:Rab3gap2
|
UTSW |
1 |
185,008,140 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1428:Rab3gap2
|
UTSW |
1 |
184,980,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1599:Rab3gap2
|
UTSW |
1 |
184,983,223 (GRCm39) |
missense |
probably benign |
0.07 |
R1758:Rab3gap2
|
UTSW |
1 |
185,016,081 (GRCm39) |
missense |
probably benign |
0.13 |
R1903:Rab3gap2
|
UTSW |
1 |
184,954,099 (GRCm39) |
missense |
probably benign |
|
R1929:Rab3gap2
|
UTSW |
1 |
185,015,739 (GRCm39) |
critical splice donor site |
probably null |
|
R1994:Rab3gap2
|
UTSW |
1 |
184,968,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Rab3gap2
|
UTSW |
1 |
185,010,478 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2102:Rab3gap2
|
UTSW |
1 |
185,014,586 (GRCm39) |
missense |
probably benign |
0.00 |
R2120:Rab3gap2
|
UTSW |
1 |
184,993,564 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2219:Rab3gap2
|
UTSW |
1 |
185,008,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Rab3gap2
|
UTSW |
1 |
184,954,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R2270:Rab3gap2
|
UTSW |
1 |
185,015,739 (GRCm39) |
critical splice donor site |
probably null |
|
R2272:Rab3gap2
|
UTSW |
1 |
185,015,739 (GRCm39) |
critical splice donor site |
probably null |
|
R3083:Rab3gap2
|
UTSW |
1 |
184,936,466 (GRCm39) |
missense |
probably benign |
0.00 |
R3776:Rab3gap2
|
UTSW |
1 |
185,009,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R4050:Rab3gap2
|
UTSW |
1 |
185,004,840 (GRCm39) |
critical splice donor site |
probably null |
|
R4130:Rab3gap2
|
UTSW |
1 |
184,936,494 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4176:Rab3gap2
|
UTSW |
1 |
184,978,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R4296:Rab3gap2
|
UTSW |
1 |
184,988,034 (GRCm39) |
critical splice donor site |
probably null |
|
R4416:Rab3gap2
|
UTSW |
1 |
185,014,544 (GRCm39) |
missense |
probably benign |
0.00 |
R4426:Rab3gap2
|
UTSW |
1 |
184,967,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R4516:Rab3gap2
|
UTSW |
1 |
184,999,265 (GRCm39) |
missense |
probably benign |
|
R4518:Rab3gap2
|
UTSW |
1 |
184,999,265 (GRCm39) |
missense |
probably benign |
|
R4891:Rab3gap2
|
UTSW |
1 |
184,991,563 (GRCm39) |
missense |
probably benign |
0.00 |
R4913:Rab3gap2
|
UTSW |
1 |
184,995,026 (GRCm39) |
missense |
probably benign |
0.12 |
R4955:Rab3gap2
|
UTSW |
1 |
184,999,352 (GRCm39) |
intron |
probably benign |
|
R5411:Rab3gap2
|
UTSW |
1 |
185,009,342 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5516:Rab3gap2
|
UTSW |
1 |
184,967,684 (GRCm39) |
missense |
probably benign |
0.02 |
R5670:Rab3gap2
|
UTSW |
1 |
185,009,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R5670:Rab3gap2
|
UTSW |
1 |
184,954,096 (GRCm39) |
missense |
probably benign |
|
R6380:Rab3gap2
|
UTSW |
1 |
184,968,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6533:Rab3gap2
|
UTSW |
1 |
184,965,151 (GRCm39) |
splice site |
probably null |
|
R6655:Rab3gap2
|
UTSW |
1 |
184,982,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R6676:Rab3gap2
|
UTSW |
1 |
185,015,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R6726:Rab3gap2
|
UTSW |
1 |
184,980,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R6969:Rab3gap2
|
UTSW |
1 |
184,968,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:Rab3gap2
|
UTSW |
1 |
184,980,250 (GRCm39) |
missense |
probably benign |
0.00 |
R7168:Rab3gap2
|
UTSW |
1 |
184,936,494 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7196:Rab3gap2
|
UTSW |
1 |
185,013,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Rab3gap2
|
UTSW |
1 |
184,999,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R7371:Rab3gap2
|
UTSW |
1 |
184,983,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R7573:Rab3gap2
|
UTSW |
1 |
185,014,579 (GRCm39) |
missense |
probably benign |
|
R7779:Rab3gap2
|
UTSW |
1 |
184,991,641 (GRCm39) |
missense |
probably damaging |
0.98 |
R7913:Rab3gap2
|
UTSW |
1 |
184,995,013 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7922:Rab3gap2
|
UTSW |
1 |
184,982,117 (GRCm39) |
missense |
probably benign |
0.00 |
R8115:Rab3gap2
|
UTSW |
1 |
184,999,447 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8203:Rab3gap2
|
UTSW |
1 |
184,999,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R8242:Rab3gap2
|
UTSW |
1 |
184,954,050 (GRCm39) |
missense |
probably benign |
|
R8322:Rab3gap2
|
UTSW |
1 |
184,978,877 (GRCm39) |
missense |
probably benign |
0.42 |
R8360:Rab3gap2
|
UTSW |
1 |
184,999,270 (GRCm39) |
intron |
probably benign |
|
R8515:Rab3gap2
|
UTSW |
1 |
184,995,017 (GRCm39) |
missense |
probably benign |
0.15 |
R8678:Rab3gap2
|
UTSW |
1 |
184,983,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Rab3gap2
|
UTSW |
1 |
184,990,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9175:Rab3gap2
|
UTSW |
1 |
185,009,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Rab3gap2
|
UTSW |
1 |
184,983,331 (GRCm39) |
missense |
probably damaging |
0.99 |
R9312:Rab3gap2
|
UTSW |
1 |
185,015,684 (GRCm39) |
missense |
probably benign |
0.00 |
R9443:Rab3gap2
|
UTSW |
1 |
184,967,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Rab3gap2
|
UTSW |
1 |
185,014,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Rab3gap2
|
UTSW |
1 |
184,967,692 (GRCm39) |
missense |
probably benign |
0.28 |
Z1088:Rab3gap2
|
UTSW |
1 |
185,013,874 (GRCm39) |
missense |
probably damaging |
1.00 |
|