Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933415A04Rik |
GTGTGTATGTGT |
GTGTGT |
11: 43,478,241 (GRCm39) |
|
probably benign |
Het |
Ago4 |
A |
T |
4: 126,406,423 (GRCm39) |
C296S |
probably benign |
Het |
Apbb1 |
A |
G |
7: 105,215,807 (GRCm39) |
L401P |
probably damaging |
Het |
Cacnb2 |
C |
A |
2: 14,972,848 (GRCm39) |
P252T |
probably benign |
Het |
Ctnna2 |
C |
T |
6: 77,618,357 (GRCm39) |
V202I |
probably benign |
Het |
Dapk1 |
A |
T |
13: 60,873,153 (GRCm39) |
I352F |
probably benign |
Het |
Dexi |
T |
C |
16: 10,360,349 (GRCm39) |
D69G |
possibly damaging |
Het |
Dlg5 |
T |
C |
14: 24,215,388 (GRCm39) |
E645G |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,551,841 (GRCm39) |
I2826T |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,610,235 (GRCm39) |
W1734R |
probably damaging |
Het |
Dtna |
A |
G |
18: 23,728,666 (GRCm39) |
K287R |
probably damaging |
Het |
Elovl5 |
A |
G |
9: 77,887,105 (GRCm39) |
|
probably null |
Het |
Ess2 |
T |
A |
16: 17,729,031 (GRCm39) |
I47F |
probably damaging |
Het |
Fam222b |
C |
A |
11: 78,044,979 (GRCm39) |
P180Q |
probably benign |
Het |
Fat3 |
C |
T |
9: 15,901,888 (GRCm39) |
V3046I |
probably benign |
Het |
Fem1a |
A |
G |
17: 56,565,068 (GRCm39) |
D387G |
probably damaging |
Het |
Frmd5 |
A |
G |
2: 121,422,225 (GRCm39) |
Y33H |
probably damaging |
Het |
Gucy2g |
A |
T |
19: 55,216,584 (GRCm39) |
L464H |
probably benign |
Het |
Ints2 |
T |
C |
11: 86,103,489 (GRCm39) |
E1189G |
possibly damaging |
Het |
Lepr |
A |
T |
4: 101,639,783 (GRCm39) |
S750C |
probably damaging |
Het |
Lingo1 |
T |
C |
9: 56,526,798 (GRCm39) |
D603G |
probably benign |
Het |
Map4k3 |
A |
C |
17: 80,922,499 (GRCm39) |
V474G |
probably damaging |
Het |
Myl4 |
T |
A |
11: 104,475,787 (GRCm39) |
V167E |
probably damaging |
Het |
Naa25 |
T |
C |
5: 121,562,652 (GRCm39) |
V478A |
probably benign |
Het |
Neurl4 |
T |
A |
11: 69,796,700 (GRCm39) |
L487H |
probably benign |
Het |
Nkx2-9 |
C |
T |
12: 56,658,917 (GRCm39) |
R99H |
probably damaging |
Het |
Or4c110 |
C |
G |
2: 88,831,855 (GRCm39) |
R259P |
unknown |
Het |
Or52x1 |
A |
T |
7: 104,853,367 (GRCm39) |
M61K |
probably damaging |
Het |
Or6c76 |
A |
G |
10: 129,612,091 (GRCm39) |
I103V |
probably benign |
Het |
Pcdhga9 |
A |
G |
18: 37,871,132 (GRCm39) |
I320M |
probably damaging |
Het |
Pi15 |
T |
A |
1: 17,695,137 (GRCm39) |
C251* |
probably null |
Het |
Pkhd1l1 |
A |
T |
15: 44,460,534 (GRCm39) |
K4248* |
probably null |
Het |
Prkg1 |
C |
T |
19: 30,556,032 (GRCm39) |
V625I |
probably benign |
Het |
Prkg1 |
G |
A |
19: 30,602,170 (GRCm39) |
A362V |
possibly damaging |
Het |
Prol1 |
C |
T |
5: 88,476,264 (GRCm39) |
T218I |
unknown |
Het |
Ptpro |
G |
A |
6: 137,376,599 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
A |
10: 39,699,481 (GRCm39) |
I1326K |
probably benign |
Het |
Shank1 |
C |
A |
7: 43,962,308 (GRCm39) |
R60S |
unknown |
Het |
Slc24a2 |
A |
G |
4: 86,909,774 (GRCm39) |
V648A |
probably damaging |
Het |
Slc35d3 |
T |
C |
10: 19,725,116 (GRCm39) |
T247A |
probably damaging |
Het |
Specc1 |
C |
T |
11: 62,096,223 (GRCm39) |
T895I |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,023,471 (GRCm39) |
E626G |
possibly damaging |
Het |
Syngr2 |
C |
A |
11: 117,703,401 (GRCm39) |
S72R |
possibly damaging |
Het |
Synj2 |
T |
A |
17: 6,069,809 (GRCm39) |
L490Q |
unknown |
Het |
Tbc1d9 |
T |
C |
8: 83,963,341 (GRCm39) |
L351P |
possibly damaging |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Themis3 |
G |
A |
17: 66,862,605 (GRCm39) |
T451I |
probably benign |
Het |
Tia1 |
T |
C |
6: 86,401,364 (GRCm39) |
S146P |
probably benign |
Het |
Tpp2 |
T |
A |
1: 44,022,441 (GRCm39) |
N946K |
probably benign |
Het |
Tpr |
A |
T |
1: 150,308,310 (GRCm39) |
R1688S |
probably damaging |
Het |
Trav12-1 |
A |
G |
14: 53,775,988 (GRCm39) |
Q47R |
possibly damaging |
Het |
Ttll9 |
G |
A |
2: 152,844,278 (GRCm39) |
|
probably null |
Het |
Ttn |
G |
A |
2: 76,537,585 (GRCm39) |
T34781M |
possibly damaging |
Het |
V1ra8 |
A |
G |
6: 90,180,298 (GRCm39) |
Y167C |
probably damaging |
Het |
Vegfb |
T |
C |
19: 6,963,707 (GRCm39) |
D84G |
probably damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,368,324 (GRCm39) |
L223M |
probably benign |
Het |
Wdr26 |
A |
G |
1: 181,010,387 (GRCm39) |
I554T |
probably damaging |
Het |
|
Other mutations in Itgb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01360:Itgb4
|
APN |
11 |
115,881,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01391:Itgb4
|
APN |
11 |
115,881,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01431:Itgb4
|
APN |
11 |
115,897,283 (GRCm39) |
splice site |
probably benign |
|
IGL01750:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01752:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01756:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01766:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01769:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02188:Itgb4
|
APN |
11 |
115,894,213 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02262:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02293:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02318:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02319:Itgb4
|
APN |
11 |
115,879,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02338:Itgb4
|
APN |
11 |
115,898,795 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02734:Itgb4
|
APN |
11 |
115,896,792 (GRCm39) |
missense |
probably benign |
|
IGL02879:Itgb4
|
APN |
11 |
115,885,178 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02889:Itgb4
|
APN |
11 |
115,879,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Itgb4
|
APN |
11 |
115,879,550 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03054:Itgb4
|
UTSW |
11 |
115,891,166 (GRCm39) |
nonsense |
probably null |
|
R0021:Itgb4
|
UTSW |
11 |
115,870,453 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0092:Itgb4
|
UTSW |
11 |
115,869,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R0305:Itgb4
|
UTSW |
11 |
115,870,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R0408:Itgb4
|
UTSW |
11 |
115,898,428 (GRCm39) |
missense |
probably damaging |
0.99 |
R0465:Itgb4
|
UTSW |
11 |
115,870,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0499:Itgb4
|
UTSW |
11 |
115,870,521 (GRCm39) |
missense |
probably benign |
0.00 |
R0535:Itgb4
|
UTSW |
11 |
115,881,835 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0571:Itgb4
|
UTSW |
11 |
115,870,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0613:Itgb4
|
UTSW |
11 |
115,884,168 (GRCm39) |
missense |
probably damaging |
0.98 |
R0838:Itgb4
|
UTSW |
11 |
115,888,988 (GRCm39) |
intron |
probably benign |
|
R1381:Itgb4
|
UTSW |
11 |
115,885,163 (GRCm39) |
missense |
probably benign |
0.00 |
R1451:Itgb4
|
UTSW |
11 |
115,881,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Itgb4
|
UTSW |
11 |
115,869,937 (GRCm39) |
missense |
probably benign |
0.42 |
R1460:Itgb4
|
UTSW |
11 |
115,874,990 (GRCm39) |
missense |
probably damaging |
0.96 |
R1473:Itgb4
|
UTSW |
11 |
115,874,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1484:Itgb4
|
UTSW |
11 |
115,890,625 (GRCm39) |
missense |
probably benign |
0.01 |
R1593:Itgb4
|
UTSW |
11 |
115,871,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Itgb4
|
UTSW |
11 |
115,882,142 (GRCm39) |
nonsense |
probably null |
|
R1633:Itgb4
|
UTSW |
11 |
115,898,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Itgb4
|
UTSW |
11 |
115,898,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Itgb4
|
UTSW |
11 |
115,882,156 (GRCm39) |
missense |
probably benign |
0.07 |
R1713:Itgb4
|
UTSW |
11 |
115,894,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Itgb4
|
UTSW |
11 |
115,879,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Itgb4
|
UTSW |
11 |
115,879,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Itgb4
|
UTSW |
11 |
115,874,590 (GRCm39) |
missense |
probably benign |
0.31 |
R1902:Itgb4
|
UTSW |
11 |
115,871,564 (GRCm39) |
missense |
probably damaging |
0.98 |
R1945:Itgb4
|
UTSW |
11 |
115,884,279 (GRCm39) |
nonsense |
probably null |
|
R2102:Itgb4
|
UTSW |
11 |
115,896,561 (GRCm39) |
missense |
probably benign |
0.23 |
R2184:Itgb4
|
UTSW |
11 |
115,870,450 (GRCm39) |
missense |
probably damaging |
0.96 |
R2334:Itgb4
|
UTSW |
11 |
115,884,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R2401:Itgb4
|
UTSW |
11 |
115,897,389 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3743:Itgb4
|
UTSW |
11 |
115,894,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Itgb4
|
UTSW |
11 |
115,896,752 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4134:Itgb4
|
UTSW |
11 |
115,897,296 (GRCm39) |
missense |
probably benign |
0.03 |
R4280:Itgb4
|
UTSW |
11 |
115,881,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Itgb4
|
UTSW |
11 |
115,879,555 (GRCm39) |
missense |
probably benign |
0.01 |
R4434:Itgb4
|
UTSW |
11 |
115,890,640 (GRCm39) |
missense |
probably benign |
0.10 |
R4505:Itgb4
|
UTSW |
11 |
115,874,087 (GRCm39) |
splice site |
silent |
|
R4585:Itgb4
|
UTSW |
11 |
115,884,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4586:Itgb4
|
UTSW |
11 |
115,884,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4601:Itgb4
|
UTSW |
11 |
115,896,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Itgb4
|
UTSW |
11 |
115,897,431 (GRCm39) |
missense |
probably benign |
0.12 |
R4962:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5029:Itgb4
|
UTSW |
11 |
115,879,417 (GRCm39) |
intron |
probably benign |
|
R5084:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5085:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5124:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5125:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5150:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5175:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5176:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5179:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5207:Itgb4
|
UTSW |
11 |
115,897,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R5263:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5264:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5334:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5337:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5344:Itgb4
|
UTSW |
11 |
115,880,575 (GRCm39) |
missense |
probably null |
0.92 |
R5391:Itgb4
|
UTSW |
11 |
115,875,894 (GRCm39) |
missense |
probably benign |
0.05 |
R5437:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5440:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5654:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5655:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5772:Itgb4
|
UTSW |
11 |
115,879,258 (GRCm39) |
intron |
probably benign |
|
R5812:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5813:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5814:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5863:Itgb4
|
UTSW |
11 |
115,881,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Itgb4
|
UTSW |
11 |
115,881,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5865:Itgb4
|
UTSW |
11 |
115,881,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5951:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5954:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5982:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6043:Itgb4
|
UTSW |
11 |
115,870,212 (GRCm39) |
missense |
probably benign |
0.30 |
R6133:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6134:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6135:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6169:Itgb4
|
UTSW |
11 |
115,885,102 (GRCm39) |
missense |
probably damaging |
0.98 |
R6172:Itgb4
|
UTSW |
11 |
115,891,237 (GRCm39) |
missense |
probably benign |
0.23 |
R6255:Itgb4
|
UTSW |
11 |
115,888,963 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6258:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6259:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6260:Itgb4
|
UTSW |
11 |
115,874,983 (GRCm39) |
missense |
probably benign |
0.00 |
R6612:Itgb4
|
UTSW |
11 |
115,874,897 (GRCm39) |
missense |
probably benign |
0.00 |
R7037:Itgb4
|
UTSW |
11 |
115,896,391 (GRCm39) |
nonsense |
probably null |
|
R7371:Itgb4
|
UTSW |
11 |
115,888,906 (GRCm39) |
missense |
probably benign |
0.29 |
R7605:Itgb4
|
UTSW |
11 |
115,897,302 (GRCm39) |
missense |
probably benign |
0.01 |
R7659:Itgb4
|
UTSW |
11 |
115,870,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7759:Itgb4
|
UTSW |
11 |
115,894,536 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7832:Itgb4
|
UTSW |
11 |
115,891,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Itgb4
|
UTSW |
11 |
115,873,531 (GRCm39) |
missense |
probably benign |
0.18 |
R7923:Itgb4
|
UTSW |
11 |
115,873,525 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8004:Itgb4
|
UTSW |
11 |
115,873,531 (GRCm39) |
missense |
probably benign |
0.00 |
R8143:Itgb4
|
UTSW |
11 |
115,884,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Itgb4
|
UTSW |
11 |
115,882,544 (GRCm39) |
critical splice donor site |
probably null |
|
R8857:Itgb4
|
UTSW |
11 |
115,871,853 (GRCm39) |
missense |
probably benign |
0.04 |
R8863:Itgb4
|
UTSW |
11 |
115,875,898 (GRCm39) |
nonsense |
probably null |
|
R8932:Itgb4
|
UTSW |
11 |
115,879,295 (GRCm39) |
missense |
probably benign |
0.01 |
R9153:Itgb4
|
UTSW |
11 |
115,874,879 (GRCm39) |
missense |
probably benign |
0.00 |
R9207:Itgb4
|
UTSW |
11 |
115,897,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Itgb4
|
UTSW |
11 |
115,898,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Itgb4
|
UTSW |
11 |
115,870,465 (GRCm39) |
missense |
probably benign |
|
R9289:Itgb4
|
UTSW |
11 |
115,885,187 (GRCm39) |
missense |
probably benign |
0.01 |
R9328:Itgb4
|
UTSW |
11 |
115,880,625 (GRCm39) |
missense |
probably benign |
0.00 |
R9435:Itgb4
|
UTSW |
11 |
115,895,855 (GRCm39) |
missense |
probably benign |
0.01 |
R9450:Itgb4
|
UTSW |
11 |
115,874,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Itgb4
|
UTSW |
11 |
115,885,171 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9779:Itgb4
|
UTSW |
11 |
115,882,485 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Itgb4
|
UTSW |
11 |
115,884,278 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Itgb4
|
UTSW |
11 |
115,897,346 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Itgb4
|
UTSW |
11 |
115,888,884 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Itgb4
|
UTSW |
11 |
115,877,637 (GRCm39) |
missense |
probably damaging |
0.99 |
|