Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ckap2l |
A |
T |
2: 129,127,299 (GRCm39) |
M293K |
probably benign |
Het |
Col4a4 |
C |
T |
1: 82,471,312 (GRCm39) |
G681E |
unknown |
Het |
Dnai7 |
A |
G |
6: 145,127,502 (GRCm39) |
V469A |
probably benign |
Het |
Efcab7 |
G |
A |
4: 99,735,372 (GRCm39) |
R132H |
probably benign |
Het |
Elovl4 |
T |
C |
9: 83,662,817 (GRCm39) |
T239A |
probably benign |
Het |
Fank1 |
A |
G |
7: 133,481,621 (GRCm39) |
D240G |
probably damaging |
Het |
Fbln5 |
T |
A |
12: 101,723,703 (GRCm39) |
M346L |
possibly damaging |
Het |
Fbxl21 |
T |
C |
13: 56,680,136 (GRCm39) |
F174L |
probably benign |
Het |
Gns |
A |
G |
10: 121,216,090 (GRCm39) |
D279G |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,555,265 (GRCm39) |
V2502A |
probably benign |
Het |
Large2 |
A |
G |
2: 92,205,088 (GRCm39) |
|
probably benign |
Het |
Lrrc8b |
A |
T |
5: 105,628,118 (GRCm39) |
I155F |
probably damaging |
Het |
Morc2b |
T |
C |
17: 33,357,353 (GRCm39) |
I140V |
probably benign |
Het |
Mrgprb5 |
G |
A |
7: 47,817,796 (GRCm39) |
S313L |
probably benign |
Het |
Nectin4 |
A |
T |
1: 171,211,273 (GRCm39) |
T266S |
probably benign |
Het |
Nsd1 |
C |
T |
13: 55,395,159 (GRCm39) |
A1023V |
possibly damaging |
Het |
Or51a39 |
T |
C |
7: 102,363,558 (GRCm39) |
T21A |
probably benign |
Het |
Paqr8 |
A |
G |
1: 21,005,332 (GRCm39) |
H162R |
possibly damaging |
Het |
Pclo |
G |
A |
5: 14,726,937 (GRCm39) |
|
probably benign |
Het |
Phactr4 |
T |
C |
4: 132,098,293 (GRCm39) |
D325G |
probably damaging |
Het |
Plcg2 |
A |
T |
8: 118,361,532 (GRCm39) |
E1255V |
possibly damaging |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Polr3b |
A |
T |
10: 84,503,280 (GRCm39) |
Q399L |
probably benign |
Het |
Ppp1r35 |
G |
A |
5: 137,778,286 (GRCm39) |
|
probably benign |
Het |
Psd3 |
A |
T |
8: 68,166,377 (GRCm39) |
D919E |
probably benign |
Het |
Ptgs2 |
A |
G |
1: 149,978,481 (GRCm39) |
T198A |
possibly damaging |
Het |
Ptpn14 |
T |
C |
1: 189,564,997 (GRCm39) |
|
probably null |
Het |
Ptprk |
A |
G |
10: 28,461,582 (GRCm39) |
Y39C |
probably damaging |
Het |
R3hdm4 |
A |
G |
10: 79,749,175 (GRCm39) |
Y75H |
probably benign |
Het |
Rsph4a |
A |
G |
10: 33,785,379 (GRCm39) |
Y430C |
probably damaging |
Het |
Samd12 |
C |
T |
15: 53,723,669 (GRCm39) |
C8Y |
probably damaging |
Het |
Sema3e |
A |
C |
5: 14,276,662 (GRCm39) |
L314F |
probably damaging |
Het |
Sis |
A |
G |
3: 72,857,089 (GRCm39) |
F401L |
probably damaging |
Het |
Smoc1 |
T |
A |
12: 81,151,474 (GRCm39) |
S64T |
probably damaging |
Het |
Socs5 |
T |
A |
17: 87,441,769 (GRCm39) |
H236Q |
probably damaging |
Het |
Spaca1 |
C |
A |
4: 34,049,863 (GRCm39) |
R45L |
possibly damaging |
Het |
Spag6 |
A |
G |
2: 18,750,324 (GRCm39) |
K457E |
probably benign |
Het |
Stat2 |
T |
A |
10: 128,116,934 (GRCm39) |
|
probably null |
Het |
Tcp11l2 |
A |
G |
10: 84,449,524 (GRCm39) |
I496M |
probably damaging |
Het |
Ttll4 |
A |
G |
1: 74,725,535 (GRCm39) |
I648V |
possibly damaging |
Het |
Vmn2r67 |
T |
C |
7: 84,801,453 (GRCm39) |
Y161C |
probably damaging |
Het |
Wnt5b |
A |
T |
6: 119,410,813 (GRCm39) |
V171E |
probably damaging |
Het |
Zfp236 |
T |
C |
18: 82,648,219 (GRCm39) |
K933E |
probably damaging |
Het |
Zfp236 |
T |
C |
18: 82,676,198 (GRCm39) |
E373G |
probably damaging |
Het |
Zfp617 |
A |
G |
8: 72,686,885 (GRCm39) |
Y405C |
probably damaging |
Het |
Zranb1 |
CTGATGATGATG |
CTGATGATGATGATG |
7: 132,584,556 (GRCm39) |
|
probably benign |
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 |
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 |
R7804:Itgb4
|
UTSW |
11 |
115,894,510 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|