Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
G |
5: 114,333,295 (GRCm39) |
E473G |
probably damaging |
Het |
Acp7 |
T |
C |
7: 28,310,464 (GRCm39) |
M458V |
probably benign |
Het |
Acrbp |
G |
T |
6: 125,039,436 (GRCm39) |
C485F |
probably damaging |
Het |
Actn2 |
T |
C |
13: 12,324,493 (GRCm39) |
I117V |
probably benign |
Het |
Ahr |
T |
C |
12: 35,554,970 (GRCm39) |
E383G |
probably damaging |
Het |
Cacna2d4 |
A |
T |
6: 119,213,698 (GRCm39) |
H39L |
probably benign |
Het |
Cdh11 |
G |
T |
8: 103,400,502 (GRCm39) |
N155K |
probably damaging |
Het |
Cldnd1 |
T |
A |
16: 58,549,959 (GRCm39) |
N47K |
possibly damaging |
Het |
Ddb1 |
C |
T |
19: 10,590,309 (GRCm39) |
R279W |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,331,135 (GRCm39) |
D104E |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 30,988,674 (GRCm39) |
S3386T |
probably benign |
Het |
Galnt18 |
T |
A |
7: 111,147,920 (GRCm39) |
E352V |
probably benign |
Het |
Gm5407 |
T |
A |
16: 49,117,757 (GRCm39) |
|
noncoding transcript |
Het |
Gucy1b2 |
T |
C |
14: 62,671,283 (GRCm39) |
|
probably benign |
Het |
Guf1 |
C |
A |
5: 69,715,820 (GRCm39) |
L87I |
probably damaging |
Het |
Hikeshi |
A |
G |
7: 89,585,034 (GRCm39) |
S57P |
probably damaging |
Het |
Igkv17-121 |
T |
A |
6: 68,013,851 (GRCm39) |
V17D |
probably damaging |
Het |
Lama1 |
T |
A |
17: 68,105,981 (GRCm39) |
L2072Q |
probably benign |
Het |
Lrrc31 |
T |
C |
3: 30,733,415 (GRCm39) |
E433G |
probably benign |
Het |
Mrc1 |
T |
A |
2: 14,298,289 (GRCm39) |
L715* |
probably null |
Het |
Nbeal2 |
T |
G |
9: 110,460,501 (GRCm39) |
K1778Q |
probably damaging |
Het |
Or4c35 |
A |
T |
2: 89,808,493 (GRCm39) |
I124F |
probably damaging |
Het |
Or51a39 |
C |
A |
7: 102,363,090 (GRCm39) |
G177C |
probably damaging |
Het |
Or5m3 |
T |
A |
2: 85,838,942 (GRCm39) |
V274E |
probably damaging |
Het |
Ppp1r3a |
T |
A |
6: 14,722,064 (GRCm39) |
|
probably benign |
Het |
Prss37 |
T |
C |
6: 40,495,984 (GRCm39) |
Y6C |
probably benign |
Het |
Rapgef6 |
A |
G |
11: 54,586,915 (GRCm39) |
Q1602R |
probably damaging |
Het |
Rbm15b |
T |
C |
9: 106,763,173 (GRCm39) |
T332A |
probably damaging |
Het |
S100a7l2 |
C |
T |
3: 90,995,626 (GRCm39) |
R92H |
unknown |
Het |
Snrnp70 |
C |
A |
7: 45,026,283 (GRCm39) |
|
probably benign |
Het |
Spidr |
T |
C |
16: 15,707,618 (GRCm39) |
E893G |
probably damaging |
Het |
Stxbp2 |
T |
C |
8: 3,683,342 (GRCm39) |
I74T |
probably damaging |
Het |
Tgm2 |
G |
A |
2: 157,973,410 (GRCm39) |
Q234* |
probably null |
Het |
Thbd |
T |
C |
2: 148,248,716 (GRCm39) |
D384G |
probably benign |
Het |
Zan |
T |
C |
5: 137,418,278 (GRCm39) |
N2940S |
unknown |
Het |
Zmat3 |
T |
A |
3: 32,399,701 (GRCm39) |
N100I |
probably damaging |
Het |
|
Other mutations in Itgad |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00777:Itgad
|
APN |
7 |
127,803,022 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02036:Itgad
|
APN |
7 |
127,788,993 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02589:Itgad
|
APN |
7 |
127,780,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02648:Itgad
|
APN |
7 |
127,782,546 (GRCm39) |
intron |
probably benign |
|
IGL02735:Itgad
|
APN |
7 |
127,792,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03088:Itgad
|
APN |
7 |
127,802,204 (GRCm39) |
missense |
probably benign |
0.01 |
BB007:Itgad
|
UTSW |
7 |
127,782,280 (GRCm39) |
missense |
probably benign |
0.01 |
BB017:Itgad
|
UTSW |
7 |
127,782,280 (GRCm39) |
missense |
probably benign |
0.01 |
R0060:Itgad
|
UTSW |
7 |
127,802,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Itgad
|
UTSW |
7 |
127,802,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Itgad
|
UTSW |
7 |
127,788,403 (GRCm39) |
missense |
probably benign |
0.02 |
R0211:Itgad
|
UTSW |
7 |
127,803,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Itgad
|
UTSW |
7 |
127,803,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:Itgad
|
UTSW |
7 |
127,789,150 (GRCm39) |
splice site |
probably benign |
|
R0326:Itgad
|
UTSW |
7 |
127,797,550 (GRCm39) |
missense |
probably benign |
0.00 |
R0646:Itgad
|
UTSW |
7 |
127,773,176 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0947:Itgad
|
UTSW |
7 |
127,774,865 (GRCm39) |
missense |
probably benign |
0.08 |
R1439:Itgad
|
UTSW |
7 |
127,782,178 (GRCm39) |
missense |
probably benign |
0.44 |
R1454:Itgad
|
UTSW |
7 |
127,791,309 (GRCm39) |
missense |
probably benign |
0.02 |
R1503:Itgad
|
UTSW |
7 |
127,797,293 (GRCm39) |
missense |
probably benign |
0.00 |
R1531:Itgad
|
UTSW |
7 |
127,777,542 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Itgad
|
UTSW |
7 |
127,802,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R1602:Itgad
|
UTSW |
7 |
127,790,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Itgad
|
UTSW |
7 |
127,804,279 (GRCm39) |
missense |
probably benign |
|
R2278:Itgad
|
UTSW |
7 |
127,804,342 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2851:Itgad
|
UTSW |
7 |
127,803,732 (GRCm39) |
missense |
probably benign |
0.01 |
R3029:Itgad
|
UTSW |
7 |
127,777,543 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3080:Itgad
|
UTSW |
7 |
127,784,959 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3150:Itgad
|
UTSW |
7 |
127,790,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3176:Itgad
|
UTSW |
7 |
127,790,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3177:Itgad
|
UTSW |
7 |
127,790,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3276:Itgad
|
UTSW |
7 |
127,790,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3277:Itgad
|
UTSW |
7 |
127,790,153 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3833:Itgad
|
UTSW |
7 |
127,785,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4541:Itgad
|
UTSW |
7 |
127,797,287 (GRCm39) |
missense |
probably benign |
0.13 |
R4649:Itgad
|
UTSW |
7 |
127,788,703 (GRCm39) |
missense |
probably benign |
0.01 |
R4753:Itgad
|
UTSW |
7 |
127,822,875 (GRCm39) |
makesense |
probably null |
|
R4852:Itgad
|
UTSW |
7 |
127,797,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R4931:Itgad
|
UTSW |
7 |
127,803,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Itgad
|
UTSW |
7 |
127,789,015 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5116:Itgad
|
UTSW |
7 |
127,803,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Itgad
|
UTSW |
7 |
127,797,395 (GRCm39) |
critical splice donor site |
probably null |
|
R5233:Itgad
|
UTSW |
7 |
127,792,600 (GRCm39) |
splice site |
probably null |
|
R5334:Itgad
|
UTSW |
7 |
127,788,458 (GRCm39) |
missense |
probably damaging |
0.99 |
R5731:Itgad
|
UTSW |
7 |
127,797,726 (GRCm39) |
missense |
probably benign |
0.19 |
R5760:Itgad
|
UTSW |
7 |
127,802,537 (GRCm39) |
missense |
probably benign |
0.02 |
R5896:Itgad
|
UTSW |
7 |
127,773,188 (GRCm39) |
missense |
probably benign |
0.34 |
R5955:Itgad
|
UTSW |
7 |
127,788,653 (GRCm39) |
missense |
probably benign |
0.00 |
R6247:Itgad
|
UTSW |
7 |
127,784,959 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6659:Itgad
|
UTSW |
7 |
127,785,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R7027:Itgad
|
UTSW |
7 |
127,782,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R7104:Itgad
|
UTSW |
7 |
127,797,550 (GRCm39) |
missense |
probably benign |
0.00 |
R7120:Itgad
|
UTSW |
7 |
127,773,146 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R7272:Itgad
|
UTSW |
7 |
127,804,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7303:Itgad
|
UTSW |
7 |
127,789,351 (GRCm39) |
missense |
probably benign |
|
R7324:Itgad
|
UTSW |
7 |
127,788,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R7565:Itgad
|
UTSW |
7 |
127,782,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R7566:Itgad
|
UTSW |
7 |
127,791,279 (GRCm39) |
missense |
probably benign |
0.40 |
R7930:Itgad
|
UTSW |
7 |
127,782,280 (GRCm39) |
missense |
probably benign |
0.01 |
R8550:Itgad
|
UTSW |
7 |
127,803,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R8816:Itgad
|
UTSW |
7 |
127,797,542 (GRCm39) |
nonsense |
probably null |
|
R8849:Itgad
|
UTSW |
7 |
127,789,157 (GRCm39) |
splice site |
probably benign |
|
R8952:Itgad
|
UTSW |
7 |
127,789,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R9345:Itgad
|
UTSW |
7 |
127,788,479 (GRCm39) |
missense |
probably benign |
0.02 |
R9354:Itgad
|
UTSW |
7 |
127,785,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Itgad
|
UTSW |
7 |
127,777,552 (GRCm39) |
missense |
probably benign |
0.09 |
R9614:Itgad
|
UTSW |
7 |
127,803,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R9623:Itgad
|
UTSW |
7 |
127,803,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9773:Itgad
|
UTSW |
7 |
127,789,222 (GRCm39) |
missense |
probably damaging |
0.97 |
RF019:Itgad
|
UTSW |
7 |
127,791,380 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Itgad
|
UTSW |
7 |
127,789,259 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Itgad
|
UTSW |
7 |
127,788,673 (GRCm39) |
missense |
probably damaging |
1.00 |
|