Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6b |
T |
A |
12: 113,454,152 (GRCm39) |
I323K |
possibly damaging |
Het |
Agbl4 |
T |
A |
4: 110,437,332 (GRCm39) |
V81D |
probably damaging |
Het |
Akap13 |
A |
G |
7: 75,380,111 (GRCm39) |
D2147G |
possibly damaging |
Het |
Akap9 |
C |
G |
5: 4,018,745 (GRCm39) |
H1109D |
probably benign |
Het |
Atad2b |
C |
A |
12: 5,074,668 (GRCm39) |
L1076I |
probably benign |
Het |
Chp2 |
T |
C |
7: 121,819,917 (GRCm39) |
V59A |
probably benign |
Het |
Cped1 |
T |
A |
6: 22,215,546 (GRCm39) |
C555* |
probably null |
Het |
Crebbp |
C |
T |
16: 3,937,670 (GRCm39) |
A698T |
possibly damaging |
Het |
Crispld1 |
G |
A |
1: 17,798,886 (GRCm39) |
M2I |
probably benign |
Het |
Cul3 |
T |
C |
1: 80,254,156 (GRCm39) |
N540S |
probably damaging |
Het |
Dll4 |
A |
G |
2: 119,158,412 (GRCm39) |
T134A |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,186,931 (GRCm39) |
T1305I |
probably benign |
Het |
Fbxw8 |
A |
G |
5: 118,280,731 (GRCm39) |
|
probably null |
Het |
Gm9195 |
A |
T |
14: 72,669,215 (GRCm39) |
L2649H |
probably damaging |
Het |
Gprc5c |
A |
G |
11: 114,754,931 (GRCm39) |
I203V |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,619,547 (GRCm39) |
D1189G |
probably benign |
Het |
Hnrnpl |
C |
A |
7: 28,518,009 (GRCm39) |
|
probably benign |
Het |
Homer1 |
T |
A |
13: 93,478,370 (GRCm39) |
Y38N |
probably damaging |
Het |
Itgb5 |
A |
G |
16: 33,766,962 (GRCm39) |
T707A |
probably benign |
Het |
Lmbrd1 |
G |
A |
1: 24,724,509 (GRCm39) |
R31Q |
probably damaging |
Het |
Mbtps1 |
G |
A |
8: 120,264,876 (GRCm39) |
P341S |
probably damaging |
Het |
Mlxip |
A |
G |
5: 123,580,512 (GRCm39) |
|
probably null |
Het |
Myh13 |
A |
T |
11: 67,252,226 (GRCm39) |
T1445S |
probably benign |
Het |
Ncapg |
C |
T |
5: 45,827,474 (GRCm39) |
A37V |
probably benign |
Het |
Neb |
A |
G |
2: 52,097,759 (GRCm39) |
F4909L |
probably damaging |
Het |
Nrcam |
T |
A |
12: 44,587,746 (GRCm39) |
W141R |
probably damaging |
Het |
Or6k4 |
T |
G |
1: 173,964,814 (GRCm39) |
F168C |
probably damaging |
Het |
Phykpl |
A |
G |
11: 51,484,781 (GRCm39) |
E247G |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,873,715 (GRCm39) |
I333M |
possibly damaging |
Het |
Sorcs2 |
A |
G |
5: 36,235,310 (GRCm39) |
F69L |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,467,980 (GRCm39) |
T349K |
possibly damaging |
Het |
Stap2 |
A |
G |
17: 56,306,746 (GRCm39) |
S276P |
probably benign |
Het |
Tle1 |
A |
G |
4: 72,059,517 (GRCm39) |
S275P |
probably damaging |
Het |
Topors |
G |
A |
4: 40,261,896 (GRCm39) |
Q463* |
probably null |
Het |
Tsc1 |
A |
G |
2: 28,577,001 (GRCm39) |
D1101G |
possibly damaging |
Het |
Tyrp1 |
G |
A |
4: 80,764,984 (GRCm39) |
A54T |
probably benign |
Het |
Vcam1 |
A |
G |
3: 115,919,711 (GRCm39) |
V185A |
possibly damaging |
Het |
Vmn2r19 |
T |
A |
6: 123,313,494 (GRCm39) |
*855R |
probably null |
Het |
|
Other mutations in Arhgef18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00790:Arhgef18
|
APN |
8 |
3,479,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01629:Arhgef18
|
APN |
8 |
3,431,942 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01649:Arhgef18
|
APN |
8 |
3,491,211 (GRCm39) |
splice site |
probably benign |
|
IGL01736:Arhgef18
|
APN |
8 |
3,501,624 (GRCm39) |
splice site |
probably benign |
|
IGL01743:Arhgef18
|
APN |
8 |
3,414,697 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02206:Arhgef18
|
APN |
8 |
3,495,034 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02401:Arhgef18
|
APN |
8 |
3,487,078 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Arhgef18
|
APN |
8 |
3,500,802 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02943:Arhgef18
|
APN |
8 |
3,498,553 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02990:Arhgef18
|
APN |
8 |
3,494,904 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03162:Arhgef18
|
APN |
8 |
3,491,301 (GRCm39) |
splice site |
probably null |
|
IGL03334:Arhgef18
|
APN |
8 |
3,438,023 (GRCm39) |
missense |
probably benign |
0.04 |
R0417:Arhgef18
|
UTSW |
8 |
3,438,957 (GRCm39) |
utr 3 prime |
probably benign |
|
R0646:Arhgef18
|
UTSW |
8 |
3,436,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0759:Arhgef18
|
UTSW |
8 |
3,438,822 (GRCm39) |
utr 3 prime |
probably benign |
|
R0880:Arhgef18
|
UTSW |
8 |
3,439,032 (GRCm39) |
utr 3 prime |
probably benign |
|
R0980:Arhgef18
|
UTSW |
8 |
3,439,095 (GRCm39) |
utr 3 prime |
probably benign |
|
R1175:Arhgef18
|
UTSW |
8 |
3,439,023 (GRCm39) |
utr 3 prime |
probably benign |
|
R1622:Arhgef18
|
UTSW |
8 |
3,491,272 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1649:Arhgef18
|
UTSW |
8 |
3,439,094 (GRCm39) |
utr 3 prime |
probably benign |
|
R1681:Arhgef18
|
UTSW |
8 |
3,489,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Arhgef18
|
UTSW |
8 |
3,504,228 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1781:Arhgef18
|
UTSW |
8 |
3,430,495 (GRCm39) |
missense |
probably damaging |
0.98 |
R2126:Arhgef18
|
UTSW |
8 |
3,501,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R2161:Arhgef18
|
UTSW |
8 |
3,489,575 (GRCm39) |
nonsense |
probably null |
|
R2211:Arhgef18
|
UTSW |
8 |
3,437,680 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2843:Arhgef18
|
UTSW |
8 |
3,414,634 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2878:Arhgef18
|
UTSW |
8 |
3,482,759 (GRCm39) |
missense |
probably benign |
|
R3916:Arhgef18
|
UTSW |
8 |
3,504,197 (GRCm39) |
missense |
probably benign |
|
R4231:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4233:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4234:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4235:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4236:Arhgef18
|
UTSW |
8 |
3,500,317 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4450:Arhgef18
|
UTSW |
8 |
3,487,097 (GRCm39) |
missense |
probably damaging |
0.97 |
R4539:Arhgef18
|
UTSW |
8 |
3,497,070 (GRCm39) |
missense |
probably benign |
|
R4670:Arhgef18
|
UTSW |
8 |
3,484,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R4753:Arhgef18
|
UTSW |
8 |
3,494,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Arhgef18
|
UTSW |
8 |
3,494,979 (GRCm39) |
missense |
probably benign |
|
R5313:Arhgef18
|
UTSW |
8 |
3,501,629 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5319:Arhgef18
|
UTSW |
8 |
3,435,010 (GRCm39) |
critical splice donor site |
probably null |
|
R5415:Arhgef18
|
UTSW |
8 |
3,438,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R5588:Arhgef18
|
UTSW |
8 |
3,438,878 (GRCm39) |
utr 3 prime |
probably benign |
|
R5698:Arhgef18
|
UTSW |
8 |
3,489,499 (GRCm39) |
missense |
probably damaging |
0.99 |
R5781:Arhgef18
|
UTSW |
8 |
3,489,439 (GRCm39) |
splice site |
probably null |
|
R5851:Arhgef18
|
UTSW |
8 |
3,484,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5897:Arhgef18
|
UTSW |
8 |
3,489,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Arhgef18
|
UTSW |
8 |
3,503,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R6123:Arhgef18
|
UTSW |
8 |
3,487,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R6136:Arhgef18
|
UTSW |
8 |
3,504,507 (GRCm39) |
missense |
probably benign |
|
R6240:Arhgef18
|
UTSW |
8 |
3,489,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Arhgef18
|
UTSW |
8 |
3,438,753 (GRCm39) |
missense |
probably benign |
0.16 |
R7573:Arhgef18
|
UTSW |
8 |
3,434,918 (GRCm39) |
missense |
probably damaging |
0.96 |
R7575:Arhgef18
|
UTSW |
8 |
3,501,635 (GRCm39) |
missense |
probably damaging |
0.99 |
R7664:Arhgef18
|
UTSW |
8 |
3,436,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R7731:Arhgef18
|
UTSW |
8 |
3,434,936 (GRCm39) |
missense |
probably damaging |
0.99 |
R7845:Arhgef18
|
UTSW |
8 |
3,436,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R7851:Arhgef18
|
UTSW |
8 |
3,498,409 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7947:Arhgef18
|
UTSW |
8 |
3,482,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Arhgef18
|
UTSW |
8 |
3,489,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R8167:Arhgef18
|
UTSW |
8 |
3,403,636 (GRCm39) |
start gained |
probably benign |
|
R8681:Arhgef18
|
UTSW |
8 |
3,439,074 (GRCm39) |
missense |
unknown |
|
R8798:Arhgef18
|
UTSW |
8 |
3,414,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8815:Arhgef18
|
UTSW |
8 |
3,430,410 (GRCm39) |
missense |
probably benign |
0.01 |
R8825:Arhgef18
|
UTSW |
8 |
3,436,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R8848:Arhgef18
|
UTSW |
8 |
3,477,481 (GRCm39) |
missense |
probably benign |
0.00 |
R9038:Arhgef18
|
UTSW |
8 |
3,503,257 (GRCm39) |
missense |
probably benign |
0.30 |
R9131:Arhgef18
|
UTSW |
8 |
3,487,007 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9162:Arhgef18
|
UTSW |
8 |
3,414,645 (GRCm39) |
missense |
probably benign |
0.18 |
R9229:Arhgef18
|
UTSW |
8 |
3,479,314 (GRCm39) |
missense |
probably benign |
0.01 |
R9599:Arhgef18
|
UTSW |
8 |
3,482,718 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9794:Arhgef18
|
UTSW |
8 |
3,501,634 (GRCm39) |
missense |
probably benign |
0.03 |
X0021:Arhgef18
|
UTSW |
8 |
3,484,942 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Arhgef18
|
UTSW |
8 |
3,489,628 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arhgef18
|
UTSW |
8 |
3,503,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|