Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930516K23Rik |
T |
C |
7: 103,708,470 (GRCm39) |
E113G |
probably damaging |
Het |
Adamts8 |
A |
G |
9: 30,870,360 (GRCm39) |
E650G |
probably damaging |
Het |
Adgrg7 |
G |
A |
16: 56,570,792 (GRCm39) |
T412M |
probably damaging |
Het |
Ank2 |
C |
T |
3: 126,781,808 (GRCm39) |
V7I |
possibly damaging |
Het |
Bpifb1 |
G |
A |
2: 154,055,031 (GRCm39) |
V308M |
probably damaging |
Het |
C3 |
A |
G |
17: 57,513,220 (GRCm39) |
S1476P |
probably benign |
Het |
Dgkb |
A |
T |
12: 38,031,789 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
A |
G |
2: 113,359,655 (GRCm39) |
|
probably null |
Het |
Foxb1 |
G |
A |
9: 69,667,141 (GRCm39) |
Q130* |
probably null |
Het |
Gemin5 |
C |
T |
11: 58,021,228 (GRCm39) |
|
probably null |
Het |
Ghr |
T |
A |
15: 3,349,396 (GRCm39) |
D594V |
possibly damaging |
Het |
Gm10272 |
A |
C |
10: 77,542,460 (GRCm39) |
M1L |
unknown |
Het |
Gpr161 |
G |
A |
1: 165,146,404 (GRCm39) |
V447M |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,268,751 (GRCm39) |
S2157T |
possibly damaging |
Het |
Irs1 |
A |
G |
1: 82,265,723 (GRCm39) |
V831A |
not run |
Het |
Iws1 |
T |
A |
18: 32,213,536 (GRCm39) |
S321R |
possibly damaging |
Het |
Kctd19 |
G |
T |
8: 106,113,567 (GRCm39) |
P702Q |
probably benign |
Het |
Man2c1 |
G |
A |
9: 57,047,559 (GRCm39) |
D739N |
probably damaging |
Het |
Mboat4 |
T |
A |
8: 34,591,178 (GRCm39) |
L205Q |
probably damaging |
Het |
Meis3 |
C |
A |
7: 15,911,418 (GRCm39) |
Y38* |
probably null |
Het |
Mroh7 |
G |
T |
4: 106,577,595 (GRCm39) |
T361K |
possibly damaging |
Het |
Msantd5f2 |
C |
T |
4: 73,586,648 (GRCm39) |
|
probably benign |
Het |
Myl6b |
T |
A |
10: 128,332,149 (GRCm39) |
K106* |
probably null |
Het |
Naaa |
T |
A |
5: 92,411,583 (GRCm39) |
T241S |
probably benign |
Het |
Neurog3 |
T |
G |
10: 61,969,756 (GRCm39) |
I172S |
probably benign |
Het |
Nub1 |
T |
G |
5: 24,906,527 (GRCm39) |
I351R |
probably damaging |
Het |
Or2t47 |
C |
A |
11: 58,442,457 (GRCm39) |
V203L |
possibly damaging |
Het |
Or3a1c |
A |
T |
11: 74,046,414 (GRCm39) |
R145W |
probably benign |
Het |
Or6c207 |
A |
T |
10: 129,105,003 (GRCm39) |
F63Y |
probably benign |
Het |
Osbp2 |
T |
C |
11: 3,667,944 (GRCm39) |
K18E |
probably damaging |
Het |
Pcdh8 |
A |
T |
14: 80,008,543 (GRCm39) |
W7R |
probably benign |
Het |
Pcsk7 |
G |
T |
9: 45,838,971 (GRCm39) |
|
probably null |
Het |
Plin4 |
G |
A |
17: 56,411,883 (GRCm39) |
T716I |
probably damaging |
Het |
Prkcb |
G |
A |
7: 122,167,357 (GRCm39) |
V356I |
probably damaging |
Het |
Pus7 |
G |
A |
5: 23,965,244 (GRCm39) |
T304I |
probably damaging |
Het |
Rmnd1 |
A |
G |
10: 4,353,989 (GRCm39) |
V402A |
probably damaging |
Het |
Slmap |
T |
C |
14: 26,181,346 (GRCm39) |
E329G |
probably damaging |
Het |
Sytl3 |
T |
C |
17: 6,949,346 (GRCm39) |
|
probably benign |
Het |
Tg |
A |
G |
15: 66,561,776 (GRCm39) |
I1087V |
probably benign |
Het |
Tmco1 |
A |
G |
1: 167,153,572 (GRCm39) |
T162A |
|
Het |
Tti1 |
G |
A |
2: 157,849,916 (GRCm39) |
T441I |
probably benign |
Het |
Tubgcp6 |
G |
T |
15: 88,986,526 (GRCm39) |
Q1366K |
possibly damaging |
Het |
Ush1g |
T |
C |
11: 115,209,399 (GRCm39) |
K265R |
probably benign |
Het |
Zdhhc8 |
A |
G |
16: 18,045,674 (GRCm39) |
V209A |
probably damaging |
Het |
Zfp160 |
T |
A |
17: 21,245,922 (GRCm39) |
Y157* |
probably null |
Het |
Zfp423 |
A |
T |
8: 88,414,695 (GRCm39) |
C1208S |
possibly damaging |
Het |
Zfyve26 |
A |
T |
12: 79,315,450 (GRCm39) |
V1342E |
probably damaging |
Het |
Zmym1 |
A |
T |
4: 126,942,550 (GRCm39) |
C613S |
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 |
|
R0356:Itga8
|
UTSW |
2 |
12,187,532 (GRCm39) |
missense |
possibly damaging |
0.73 |
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 |
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 |
|