Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430097D07Rik |
T |
C |
2: 32,464,418 (GRCm39) |
|
probably benign |
Het |
Adgrg6 |
C |
T |
10: 14,302,642 (GRCm39) |
V924M |
possibly damaging |
Het |
Anxa9 |
A |
G |
3: 95,215,387 (GRCm39) |
|
probably benign |
Het |
Ap3d1 |
G |
T |
10: 80,563,812 (GRCm39) |
S122R |
probably damaging |
Het |
Arhgap5 |
T |
C |
12: 52,563,091 (GRCm39) |
S21P |
probably damaging |
Het |
Atp13a5 |
A |
G |
16: 29,167,573 (GRCm39) |
|
probably benign |
Het |
AU040320 |
A |
T |
4: 126,731,155 (GRCm39) |
D618V |
probably damaging |
Het |
Cbfa2t2 |
T |
A |
2: 154,373,269 (GRCm39) |
D475E |
probably benign |
Het |
Ccdc202 |
T |
A |
14: 96,119,801 (GRCm39) |
V186E |
possibly damaging |
Het |
Ccdc62 |
G |
A |
5: 124,092,811 (GRCm39) |
V599I |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,786,953 (GRCm39) |
E917G |
probably damaging |
Het |
Cog5 |
T |
C |
12: 31,887,180 (GRCm39) |
|
probably benign |
Het |
Col9a1 |
T |
A |
1: 24,224,328 (GRCm39) |
L170* |
probably null |
Het |
Daxx |
T |
A |
17: 34,132,867 (GRCm39) |
V627D |
probably benign |
Het |
Dnah9 |
A |
G |
11: 66,021,388 (GRCm39) |
|
probably null |
Het |
Drg2 |
T |
A |
11: 60,352,407 (GRCm39) |
V203E |
probably damaging |
Het |
Fbxl17 |
G |
A |
17: 63,663,846 (GRCm39) |
R67C |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,865,930 (GRCm39) |
Y1586C |
probably damaging |
Het |
Gp6 |
A |
T |
7: 4,373,141 (GRCm39) |
|
probably benign |
Het |
Hhip |
T |
C |
8: 80,724,121 (GRCm39) |
I374V |
probably benign |
Het |
Hspa12b |
G |
T |
2: 130,986,719 (GRCm39) |
V547L |
possibly damaging |
Het |
Iars1 |
G |
A |
13: 49,856,709 (GRCm39) |
V321I |
probably benign |
Het |
Lcn5 |
T |
C |
2: 25,550,705 (GRCm39) |
I131T |
probably damaging |
Het |
Mki67 |
G |
A |
7: 135,306,135 (GRCm39) |
T614M |
probably benign |
Het |
Mmp3 |
G |
A |
9: 7,451,768 (GRCm39) |
E369K |
probably benign |
Het |
Myt1l |
A |
G |
12: 29,861,500 (GRCm39) |
D94G |
unknown |
Het |
Neil1 |
T |
C |
9: 57,054,180 (GRCm39) |
I47V |
possibly damaging |
Het |
Nr5a2 |
T |
C |
1: 136,773,430 (GRCm39) |
N424S |
possibly damaging |
Het |
Or1e21 |
A |
T |
11: 73,344,906 (GRCm39) |
I44N |
possibly damaging |
Het |
Or51f5 |
A |
T |
7: 102,424,286 (GRCm39) |
D185V |
probably damaging |
Het |
Or5b120 |
A |
G |
19: 13,480,441 (GRCm39) |
T245A |
possibly damaging |
Het |
Or7e166 |
G |
T |
9: 19,624,743 (GRCm39) |
G207C |
probably damaging |
Het |
Pakap |
C |
A |
4: 57,855,628 (GRCm39) |
T360K |
possibly damaging |
Het |
Pde8b |
G |
T |
13: 95,182,962 (GRCm39) |
N265K |
probably damaging |
Het |
Prpf40b |
T |
C |
15: 99,203,080 (GRCm39) |
|
probably null |
Het |
Samd9l |
T |
C |
6: 3,375,107 (GRCm39) |
D718G |
possibly damaging |
Het |
Sirpb1c |
T |
C |
3: 15,887,309 (GRCm39) |
N175D |
possibly damaging |
Het |
Srgap1 |
A |
T |
10: 121,691,441 (GRCm39) |
|
probably null |
Het |
Tgm5 |
T |
A |
2: 120,884,055 (GRCm39) |
T313S |
probably damaging |
Het |
Tigar |
A |
G |
6: 127,068,145 (GRCm39) |
|
probably null |
Het |
Tmprss11b |
A |
G |
5: 86,808,326 (GRCm39) |
*417Q |
probably null |
Het |
Trim32 |
G |
A |
4: 65,531,491 (GRCm39) |
R16Q |
probably damaging |
Het |
Ttll11 |
T |
C |
2: 35,792,688 (GRCm39) |
D385G |
possibly damaging |
Het |
Zfp426 |
T |
C |
9: 20,382,541 (GRCm39) |
T135A |
probably benign |
Het |
|
Other mutations in Itga8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00806:Itga8
|
APN |
2 |
12,260,777 (GRCm39) |
nonsense |
probably null |
|
IGL00820:Itga8
|
APN |
2 |
12,237,703 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01409:Itga8
|
APN |
2 |
12,196,525 (GRCm39) |
missense |
probably benign |
|
IGL01508:Itga8
|
APN |
2 |
12,237,613 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01585:Itga8
|
APN |
2 |
12,165,123 (GRCm39) |
splice site |
probably benign |
|
IGL01590:Itga8
|
APN |
2 |
12,165,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01743:Itga8
|
APN |
2 |
12,270,144 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02634:Itga8
|
APN |
2 |
12,145,289 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02805:Itga8
|
APN |
2 |
12,194,291 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03200:Itga8
|
APN |
2 |
12,196,010 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03218:Itga8
|
APN |
2 |
12,115,836 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03248:Itga8
|
APN |
2 |
12,137,327 (GRCm39) |
missense |
probably benign |
0.20 |
PIT4576001:Itga8
|
UTSW |
2 |
12,234,903 (GRCm39) |
missense |
probably benign |
0.19 |
R0196:Itga8
|
UTSW |
2 |
12,209,540 (GRCm39) |
critical splice donor site |
probably null |
|
R0466:Itga8
|
UTSW |
2 |
12,237,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R0530:Itga8
|
UTSW |
2 |
12,196,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R0715:Itga8
|
UTSW |
2 |
12,196,053 (GRCm39) |
splice site |
probably benign |
|
R0800:Itga8
|
UTSW |
2 |
12,198,362 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0881:Itga8
|
UTSW |
2 |
12,267,003 (GRCm39) |
splice site |
probably null |
|
R1675:Itga8
|
UTSW |
2 |
12,204,974 (GRCm39) |
missense |
probably damaging |
0.99 |
R1758:Itga8
|
UTSW |
2 |
12,270,144 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1939:Itga8
|
UTSW |
2 |
12,305,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R2187:Itga8
|
UTSW |
2 |
12,199,231 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2295:Itga8
|
UTSW |
2 |
12,187,520 (GRCm39) |
missense |
probably benign |
0.38 |
R2356:Itga8
|
UTSW |
2 |
12,204,952 (GRCm39) |
missense |
probably benign |
|
R2371:Itga8
|
UTSW |
2 |
12,258,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R2412:Itga8
|
UTSW |
2 |
12,306,526 (GRCm39) |
missense |
probably benign |
|
R2440:Itga8
|
UTSW |
2 |
12,183,491 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2848:Itga8
|
UTSW |
2 |
12,165,215 (GRCm39) |
missense |
probably damaging |
0.98 |
R3730:Itga8
|
UTSW |
2 |
12,198,321 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3933:Itga8
|
UTSW |
2 |
12,194,330 (GRCm39) |
missense |
probably benign |
|
R3982:Itga8
|
UTSW |
2 |
12,305,774 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4513:Itga8
|
UTSW |
2 |
12,187,547 (GRCm39) |
missense |
probably benign |
0.01 |
R4514:Itga8
|
UTSW |
2 |
12,187,547 (GRCm39) |
missense |
probably benign |
0.01 |
R4660:Itga8
|
UTSW |
2 |
12,270,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Itga8
|
UTSW |
2 |
12,198,102 (GRCm39) |
splice site |
probably benign |
|
R5533:Itga8
|
UTSW |
2 |
12,165,161 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5619:Itga8
|
UTSW |
2 |
12,270,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R5720:Itga8
|
UTSW |
2 |
12,115,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R5749:Itga8
|
UTSW |
2 |
12,266,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R5930:Itga8
|
UTSW |
2 |
12,235,019 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5954:Itga8
|
UTSW |
2 |
12,137,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R6035:Itga8
|
UTSW |
2 |
12,196,525 (GRCm39) |
missense |
probably benign |
|
R6035:Itga8
|
UTSW |
2 |
12,196,525 (GRCm39) |
missense |
probably benign |
|
R6211:Itga8
|
UTSW |
2 |
12,198,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R6337:Itga8
|
UTSW |
2 |
12,258,280 (GRCm39) |
nonsense |
probably null |
|
R6442:Itga8
|
UTSW |
2 |
12,234,954 (GRCm39) |
missense |
probably benign |
0.00 |
R6491:Itga8
|
UTSW |
2 |
12,209,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R6543:Itga8
|
UTSW |
2 |
12,306,455 (GRCm39) |
missense |
probably damaging |
0.99 |
R6574:Itga8
|
UTSW |
2 |
12,234,972 (GRCm39) |
missense |
probably benign |
0.17 |
R6760:Itga8
|
UTSW |
2 |
12,306,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Itga8
|
UTSW |
2 |
12,204,892 (GRCm39) |
missense |
probably benign |
0.00 |
R6943:Itga8
|
UTSW |
2 |
12,160,182 (GRCm39) |
critical splice donor site |
probably null |
|
R7048:Itga8
|
UTSW |
2 |
12,115,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R7203:Itga8
|
UTSW |
2 |
12,234,906 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7266:Itga8
|
UTSW |
2 |
12,237,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7323:Itga8
|
UTSW |
2 |
12,266,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R7540:Itga8
|
UTSW |
2 |
12,115,848 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7637:Itga8
|
UTSW |
2 |
12,113,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Itga8
|
UTSW |
2 |
12,235,050 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7848:Itga8
|
UTSW |
2 |
12,196,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R8031:Itga8
|
UTSW |
2 |
12,160,297 (GRCm39) |
missense |
probably benign |
|
R8077:Itga8
|
UTSW |
2 |
12,247,244 (GRCm39) |
missense |
probably benign |
0.09 |
R8757:Itga8
|
UTSW |
2 |
12,266,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Itga8
|
UTSW |
2 |
12,266,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Itga8
|
UTSW |
2 |
12,187,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8773:Itga8
|
UTSW |
2 |
12,187,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Itga8
|
UTSW |
2 |
12,187,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Itga8
|
UTSW |
2 |
12,187,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8775:Itga8
|
UTSW |
2 |
12,187,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8775-TAIL:Itga8
|
UTSW |
2 |
12,187,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8808:Itga8
|
UTSW |
2 |
12,137,328 (GRCm39) |
nonsense |
probably null |
|
R8898:Itga8
|
UTSW |
2 |
12,145,206 (GRCm39) |
missense |
probably benign |
0.05 |
R8962:Itga8
|
UTSW |
2 |
12,196,045 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9056:Itga8
|
UTSW |
2 |
12,235,019 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9155:Itga8
|
UTSW |
2 |
12,194,330 (GRCm39) |
missense |
probably benign |
|
R9354:Itga8
|
UTSW |
2 |
12,237,668 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9563:Itga8
|
UTSW |
2 |
12,165,219 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9589:Itga8
|
UTSW |
2 |
12,237,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Itga8
|
UTSW |
2 |
12,196,580 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Itga8
|
UTSW |
2 |
12,306,643 (GRCm39) |
start gained |
probably benign |
|
Z1176:Itga8
|
UTSW |
2 |
12,266,947 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Itga8
|
UTSW |
2 |
12,252,329 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Itga8
|
UTSW |
2 |
12,305,744 (GRCm39) |
missense |
possibly damaging |
0.89 |
|