Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Cdh23 |
T |
C |
10: 60,228,802 (GRCm39) |
T1125A |
possibly damaging |
Het |
Cplane1 |
T |
A |
15: 8,233,171 (GRCm39) |
N1165K |
probably benign |
Het |
Ctf1 |
A |
T |
7: 127,316,174 (GRCm39) |
|
probably null |
Het |
Defb26 |
T |
C |
2: 152,350,122 (GRCm39) |
N53D |
possibly damaging |
Het |
Dhtkd1 |
T |
C |
2: 5,907,825 (GRCm39) |
T787A |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fbxl7 |
A |
G |
15: 26,552,979 (GRCm39) |
L96P |
probably damaging |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Gpr65 |
A |
T |
12: 98,241,361 (GRCm39) |
S5C |
probably damaging |
Het |
Greb1l |
G |
A |
18: 10,542,427 (GRCm39) |
E1341K |
probably damaging |
Het |
Itga8 |
G |
A |
2: 12,115,898 (GRCm39) |
S76L |
probably damaging |
Het |
Mpdz |
A |
T |
4: 81,205,931 (GRCm39) |
F1810Y |
probably damaging |
Het |
Nfrkb |
T |
C |
9: 31,306,038 (GRCm39) |
L126P |
probably damaging |
Het |
Or4a77 |
T |
C |
2: 89,487,299 (GRCm39) |
Y162C |
probably benign |
Het |
Primpol |
A |
G |
8: 47,034,677 (GRCm39) |
V417A |
probably damaging |
Het |
Pus1 |
C |
T |
5: 110,925,584 (GRCm39) |
E79K |
probably damaging |
Het |
Rspo2 |
C |
T |
15: 43,033,210 (GRCm39) |
C4Y |
probably benign |
Het |
Serpina12 |
T |
C |
12: 104,004,563 (GRCm39) |
D23G |
probably benign |
Het |
Serpind1 |
A |
T |
16: 17,157,696 (GRCm39) |
R297S |
probably benign |
Het |
Skint8 |
C |
A |
4: 111,807,390 (GRCm39) |
L359M |
probably damaging |
Het |
Slc17a6 |
C |
T |
7: 51,275,145 (GRCm39) |
P68L |
probably damaging |
Het |
Slc6a5 |
C |
T |
7: 49,606,264 (GRCm39) |
P724L |
possibly damaging |
Het |
Spaca7 |
A |
G |
8: 12,649,004 (GRCm39) |
E166G |
possibly damaging |
Het |
Supt5 |
A |
G |
7: 28,021,993 (GRCm39) |
S345P |
probably damaging |
Het |
Syne2 |
G |
A |
12: 76,014,441 (GRCm39) |
D3211N |
probably benign |
Het |
Tmem132e |
G |
A |
11: 82,333,276 (GRCm39) |
|
probably null |
Het |
Trappc14 |
A |
G |
5: 138,261,964 (GRCm39) |
V44A |
probably benign |
Het |
Zfp384 |
T |
C |
6: 125,013,587 (GRCm39) |
S536P |
probably benign |
Het |
|
Other mutations in Arhgef10l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01420:Arhgef10l
|
APN |
4 |
140,297,649 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01732:Arhgef10l
|
APN |
4 |
140,307,726 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01988:Arhgef10l
|
APN |
4 |
140,305,672 (GRCm39) |
splice site |
probably benign |
|
IGL02031:Arhgef10l
|
APN |
4 |
140,302,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Arhgef10l
|
APN |
4 |
140,271,595 (GRCm39) |
nonsense |
probably null |
|
IGL02445:Arhgef10l
|
APN |
4 |
140,274,318 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02619:Arhgef10l
|
APN |
4 |
140,321,504 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02798:Arhgef10l
|
APN |
4 |
140,292,441 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03064:Arhgef10l
|
APN |
4 |
140,306,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03178:Arhgef10l
|
APN |
4 |
140,271,739 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03236:Arhgef10l
|
APN |
4 |
140,338,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03352:Arhgef10l
|
APN |
4 |
140,311,242 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
PIT4494001:Arhgef10l
|
UTSW |
4 |
140,292,522 (GRCm39) |
missense |
probably damaging |
0.98 |
R0057:Arhgef10l
|
UTSW |
4 |
140,338,529 (GRCm39) |
splice site |
probably benign |
|
R0062:Arhgef10l
|
UTSW |
4 |
140,279,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Arhgef10l
|
UTSW |
4 |
140,305,605 (GRCm39) |
missense |
probably benign |
0.02 |
R0109:Arhgef10l
|
UTSW |
4 |
140,305,605 (GRCm39) |
missense |
probably benign |
0.02 |
R0114:Arhgef10l
|
UTSW |
4 |
140,311,194 (GRCm39) |
missense |
probably benign |
0.17 |
R0334:Arhgef10l
|
UTSW |
4 |
140,311,237 (GRCm39) |
nonsense |
probably null |
|
R0742:Arhgef10l
|
UTSW |
4 |
140,264,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R1017:Arhgef10l
|
UTSW |
4 |
140,242,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R1166:Arhgef10l
|
UTSW |
4 |
140,302,581 (GRCm39) |
unclassified |
probably benign |
|
R1397:Arhgef10l
|
UTSW |
4 |
140,271,754 (GRCm39) |
missense |
probably damaging |
0.98 |
R1521:Arhgef10l
|
UTSW |
4 |
140,242,749 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1707:Arhgef10l
|
UTSW |
4 |
140,291,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Arhgef10l
|
UTSW |
4 |
140,242,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R2018:Arhgef10l
|
UTSW |
4 |
140,271,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Arhgef10l
|
UTSW |
4 |
140,297,601 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2098:Arhgef10l
|
UTSW |
4 |
140,306,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R2310:Arhgef10l
|
UTSW |
4 |
140,320,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R2879:Arhgef10l
|
UTSW |
4 |
140,242,598 (GRCm39) |
missense |
probably benign |
0.09 |
R2883:Arhgef10l
|
UTSW |
4 |
140,244,113 (GRCm39) |
missense |
probably benign |
0.02 |
R3732:Arhgef10l
|
UTSW |
4 |
140,308,930 (GRCm39) |
small deletion |
probably benign |
|
R3732:Arhgef10l
|
UTSW |
4 |
140,308,930 (GRCm39) |
small deletion |
probably benign |
|
R3861:Arhgef10l
|
UTSW |
4 |
140,242,798 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4049:Arhgef10l
|
UTSW |
4 |
140,242,762 (GRCm39) |
missense |
probably benign |
0.05 |
R4322:Arhgef10l
|
UTSW |
4 |
140,270,037 (GRCm39) |
missense |
probably benign |
0.07 |
R4707:Arhgef10l
|
UTSW |
4 |
140,264,194 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5395:Arhgef10l
|
UTSW |
4 |
140,297,601 (GRCm39) |
missense |
probably benign |
0.16 |
R6066:Arhgef10l
|
UTSW |
4 |
140,304,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Arhgef10l
|
UTSW |
4 |
140,270,073 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6464:Arhgef10l
|
UTSW |
4 |
140,314,126 (GRCm39) |
missense |
probably benign |
0.05 |
R6476:Arhgef10l
|
UTSW |
4 |
140,338,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Arhgef10l
|
UTSW |
4 |
140,270,068 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6483:Arhgef10l
|
UTSW |
4 |
140,344,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R6631:Arhgef10l
|
UTSW |
4 |
140,245,058 (GRCm39) |
intron |
probably benign |
|
R6721:Arhgef10l
|
UTSW |
4 |
140,297,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6890:Arhgef10l
|
UTSW |
4 |
140,271,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Arhgef10l
|
UTSW |
4 |
140,308,222 (GRCm39) |
missense |
probably benign |
0.01 |
R7100:Arhgef10l
|
UTSW |
4 |
140,244,126 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7117:Arhgef10l
|
UTSW |
4 |
140,291,497 (GRCm39) |
critical splice donor site |
probably null |
|
R7195:Arhgef10l
|
UTSW |
4 |
140,338,721 (GRCm39) |
missense |
probably benign |
|
R7222:Arhgef10l
|
UTSW |
4 |
140,248,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7397:Arhgef10l
|
UTSW |
4 |
140,290,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Arhgef10l
|
UTSW |
4 |
140,302,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R7801:Arhgef10l
|
UTSW |
4 |
140,271,578 (GRCm39) |
missense |
probably benign |
0.00 |
R7811:Arhgef10l
|
UTSW |
4 |
140,242,335 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7832:Arhgef10l
|
UTSW |
4 |
140,305,616 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7849:Arhgef10l
|
UTSW |
4 |
140,311,245 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7963:Arhgef10l
|
UTSW |
4 |
140,306,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R8434:Arhgef10l
|
UTSW |
4 |
140,291,582 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8943:Arhgef10l
|
UTSW |
4 |
140,292,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R9004:Arhgef10l
|
UTSW |
4 |
140,279,921 (GRCm39) |
missense |
probably damaging |
0.98 |
R9006:Arhgef10l
|
UTSW |
4 |
140,271,659 (GRCm39) |
missense |
probably benign |
0.04 |
R9033:Arhgef10l
|
UTSW |
4 |
140,321,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R9302:Arhgef10l
|
UTSW |
4 |
140,242,548 (GRCm39) |
missense |
probably benign |
0.04 |
R9337:Arhgef10l
|
UTSW |
4 |
140,338,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R9375:Arhgef10l
|
UTSW |
4 |
140,319,265 (GRCm39) |
missense |
probably benign |
|
R9454:Arhgef10l
|
UTSW |
4 |
140,308,236 (GRCm39) |
nonsense |
probably null |
|
Z1088:Arhgef10l
|
UTSW |
4 |
140,309,046 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1177:Arhgef10l
|
UTSW |
4 |
140,244,083 (GRCm39) |
missense |
probably benign |
0.28 |
|