Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot4 |
A |
T |
12: 84,090,178 (GRCm39) |
I292F |
probably benign |
Het |
Adamdec1 |
A |
G |
14: 68,807,551 (GRCm39) |
S370P |
probably damaging |
Het |
Ankar |
T |
C |
1: 72,698,324 (GRCm39) |
K692R |
probably benign |
Het |
Ano6 |
T |
C |
15: 95,818,261 (GRCm39) |
|
probably null |
Het |
Asns |
G |
A |
6: 7,675,443 (GRCm39) |
Q520* |
probably null |
Het |
Bbs12 |
C |
T |
3: 37,373,639 (GRCm39) |
T144I |
probably damaging |
Het |
C8g |
C |
T |
2: 25,388,955 (GRCm39) |
G186D |
probably damaging |
Het |
Clptm1l |
T |
C |
13: 73,754,403 (GRCm39) |
F109S |
probably damaging |
Het |
Coa8 |
G |
A |
12: 111,717,652 (GRCm39) |
V171I |
probably benign |
Het |
Col4a1 |
G |
A |
8: 11,252,973 (GRCm39) |
|
probably benign |
Het |
Cpn2 |
T |
C |
16: 30,078,501 (GRCm39) |
D400G |
probably damaging |
Het |
Dgke |
G |
C |
11: 88,941,288 (GRCm39) |
Y298* |
probably null |
Het |
Dnah5 |
G |
A |
15: 28,297,159 (GRCm39) |
R1451Q |
possibly damaging |
Het |
Dock8 |
A |
G |
19: 25,038,584 (GRCm39) |
D90G |
probably damaging |
Het |
Dok7 |
A |
C |
5: 35,223,890 (GRCm39) |
D143A |
probably damaging |
Het |
Elk3 |
G |
A |
10: 93,120,653 (GRCm39) |
A62V |
probably damaging |
Het |
Epha2 |
T |
A |
4: 141,035,738 (GRCm39) |
M58K |
probably damaging |
Het |
Erp27 |
G |
T |
6: 136,885,098 (GRCm39) |
D233E |
probably benign |
Het |
Gm5174 |
T |
A |
10: 86,493,045 (GRCm39) |
|
noncoding transcript |
Het |
Gxylt2 |
A |
G |
6: 100,760,107 (GRCm39) |
D214G |
probably damaging |
Het |
Hrob |
G |
A |
11: 102,145,972 (GRCm39) |
E83K |
probably benign |
Het |
Ifi35 |
A |
T |
11: 101,349,069 (GRCm39) |
I238F |
probably damaging |
Het |
Ighmbp2 |
T |
C |
19: 3,311,467 (GRCm39) |
T983A |
probably benign |
Het |
Lrp1 |
C |
A |
10: 127,403,374 (GRCm39) |
K2066N |
possibly damaging |
Het |
Mansc1 |
T |
G |
6: 134,587,816 (GRCm39) |
|
probably null |
Het |
Mapre3 |
T |
C |
5: 31,020,582 (GRCm39) |
F101S |
probably damaging |
Het |
Mettl8 |
T |
C |
2: 70,812,357 (GRCm39) |
T58A |
probably benign |
Het |
Mical1 |
G |
T |
10: 41,362,064 (GRCm39) |
R857L |
possibly damaging |
Het |
Nacad |
T |
C |
11: 6,550,581 (GRCm39) |
D870G |
probably benign |
Het |
Nectin1 |
A |
G |
9: 43,702,607 (GRCm39) |
D118G |
probably damaging |
Het |
Nlrp2 |
A |
T |
7: 5,325,380 (GRCm39) |
L26Q |
probably damaging |
Het |
Or10a3m |
A |
G |
7: 108,312,671 (GRCm39) |
D25G |
probably benign |
Het |
Pamr1 |
T |
C |
2: 102,464,693 (GRCm39) |
S281P |
possibly damaging |
Het |
Pcdhgc5 |
T |
A |
18: 37,954,814 (GRCm39) |
V696E |
probably damaging |
Het |
Pde4d |
G |
T |
13: 110,074,582 (GRCm39) |
A396S |
probably benign |
Het |
Pecam1 |
G |
T |
11: 106,575,076 (GRCm39) |
C510* |
probably null |
Het |
Pga5 |
C |
T |
19: 10,652,513 (GRCm39) |
G76S |
probably damaging |
Het |
Phldb3 |
A |
T |
7: 24,323,571 (GRCm39) |
H435L |
possibly damaging |
Het |
Piezo1 |
T |
C |
8: 123,213,112 (GRCm39) |
R1884G |
possibly damaging |
Het |
Ripk4 |
T |
C |
16: 97,564,782 (GRCm39) |
H43R |
probably damaging |
Het |
Rtn3 |
A |
G |
19: 7,412,476 (GRCm39) |
V785A |
probably damaging |
Het |
Safb2 |
A |
G |
17: 56,873,491 (GRCm39) |
|
probably benign |
Het |
Sephs1 |
T |
C |
2: 4,910,393 (GRCm39) |
F288L |
probably damaging |
Het |
Sez6l |
A |
G |
5: 112,586,266 (GRCm39) |
|
probably null |
Het |
Siglece |
A |
G |
7: 43,308,741 (GRCm39) |
L204P |
probably damaging |
Het |
Sis |
T |
C |
3: 72,857,151 (GRCm39) |
D380G |
probably damaging |
Het |
Slamf9 |
G |
T |
1: 172,304,033 (GRCm39) |
R126L |
probably benign |
Het |
Sorl1 |
A |
G |
9: 42,003,669 (GRCm39) |
L209P |
probably damaging |
Het |
Sptbn1 |
A |
C |
11: 30,095,925 (GRCm39) |
I310S |
probably damaging |
Het |
Tex52 |
A |
G |
6: 128,356,645 (GRCm39) |
T113A |
probably benign |
Het |
Trav6-3 |
T |
A |
14: 53,667,628 (GRCm39) |
Y33* |
probably null |
Het |
Vmn2r102 |
A |
G |
17: 19,914,943 (GRCm39) |
E836G |
possibly damaging |
Het |
Wdsub1 |
C |
T |
2: 59,708,819 (GRCm39) |
C18Y |
probably damaging |
Het |
Zfp341 |
C |
A |
2: 154,485,474 (GRCm39) |
H637N |
possibly damaging |
Het |
Zfp445 |
C |
T |
9: 122,682,552 (GRCm39) |
S463N |
probably benign |
Het |
Zfp612 |
G |
A |
8: 110,816,358 (GRCm39) |
D522N |
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 |
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 |
|