Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
T |
11: 84,151,573 (GRCm39) |
K824* |
probably null |
Het |
Acot12 |
A |
G |
13: 91,908,106 (GRCm39) |
D96G |
probably damaging |
Het |
Acvr2b |
C |
T |
9: 119,257,064 (GRCm39) |
Q98* |
probably null |
Het |
Aldh8a1 |
T |
C |
10: 21,271,474 (GRCm39) |
V400A |
probably benign |
Het |
Aox1 |
C |
A |
1: 58,104,499 (GRCm39) |
H559N |
probably benign |
Het |
Atad5 |
A |
G |
11: 79,985,009 (GRCm39) |
D32G |
probably damaging |
Het |
Cgas |
T |
C |
9: 78,350,362 (GRCm39) |
|
probably null |
Het |
Cmtm8 |
T |
C |
9: 114,672,967 (GRCm39) |
H10R |
probably benign |
Het |
Cnn1 |
T |
G |
9: 22,015,674 (GRCm39) |
|
probably benign |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Defb23 |
C |
A |
2: 152,306,455 (GRCm39) |
E20* |
probably null |
Het |
Dennd2a |
A |
T |
6: 39,500,383 (GRCm39) |
S61T |
probably damaging |
Het |
Fam13a |
A |
T |
6: 58,964,204 (GRCm39) |
I76K |
probably benign |
Het |
Fgd5 |
A |
G |
6: 91,964,239 (GRCm39) |
|
probably benign |
Het |
Flt4 |
A |
T |
11: 49,521,217 (GRCm39) |
R409W |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,211,328 (GRCm39) |
T652A |
probably benign |
Het |
Grik1 |
C |
T |
16: 87,732,808 (GRCm39) |
G703D |
probably damaging |
Het |
Impg2 |
A |
G |
16: 56,079,960 (GRCm39) |
E479G |
possibly damaging |
Het |
Itpr1 |
A |
G |
6: 108,526,781 (GRCm39) |
N2743S |
probably damaging |
Het |
Klc1 |
A |
G |
12: 111,744,550 (GRCm39) |
|
probably benign |
Het |
Ndufa9 |
G |
A |
6: 126,821,366 (GRCm39) |
R75* |
probably null |
Het |
Neurl4 |
A |
G |
11: 69,801,166 (GRCm39) |
N1181S |
probably damaging |
Het |
Or5an9 |
T |
C |
19: 12,187,824 (GRCm39) |
I298T |
probably damaging |
Het |
Phf1 |
A |
G |
17: 27,155,843 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,376,245 (GRCm39) |
I969T |
probably benign |
Het |
Pprc1 |
G |
A |
19: 46,060,190 (GRCm39) |
R1538Q |
probably damaging |
Het |
Rasd1 |
C |
T |
11: 59,854,778 (GRCm39) |
G234D |
possibly damaging |
Het |
Rnf152 |
T |
C |
1: 105,212,549 (GRCm39) |
T3A |
probably benign |
Het |
Rrh |
C |
T |
3: 129,605,346 (GRCm39) |
V115I |
probably benign |
Het |
Rundc3a |
G |
T |
11: 102,290,460 (GRCm39) |
E217* |
probably null |
Het |
Sae1 |
A |
T |
7: 16,064,581 (GRCm39) |
V306E |
possibly damaging |
Het |
Serpinb7 |
T |
C |
1: 107,363,102 (GRCm39) |
S89P |
possibly damaging |
Het |
Serpinb9h |
A |
G |
13: 33,588,182 (GRCm39) |
T256A |
probably damaging |
Het |
Sgo2b |
T |
A |
8: 64,394,118 (GRCm39) |
T74S |
possibly damaging |
Het |
Slc5a7 |
T |
C |
17: 54,604,022 (GRCm39) |
D48G |
probably damaging |
Het |
Stn1 |
T |
C |
19: 47,504,612 (GRCm39) |
M177V |
possibly damaging |
Het |
Tgm1 |
T |
C |
14: 55,942,392 (GRCm39) |
E653G |
possibly damaging |
Het |
Thsd4 |
T |
C |
9: 60,301,398 (GRCm39) |
K299R |
probably benign |
Het |
Ttc22 |
A |
G |
4: 106,493,186 (GRCm39) |
T278A |
probably damaging |
Het |
Ubl4b |
G |
T |
3: 107,462,141 (GRCm39) |
Q40K |
possibly damaging |
Het |
Zfp677 |
A |
G |
17: 21,613,499 (GRCm39) |
D31G |
probably damaging |
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 |
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 |
R6617:Arhgef18
|
UTSW |
8 |
3,489,592 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|