Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aldh7a1 |
A |
T |
18: 56,693,910 (GRCm39) |
|
probably null |
Het |
Atm |
A |
G |
9: 53,415,392 (GRCm39) |
V833A |
probably benign |
Het |
Atp6v1b1 |
A |
T |
6: 83,730,814 (GRCm39) |
I180F |
probably damaging |
Het |
Cwf19l2 |
T |
C |
9: 3,421,286 (GRCm39) |
S188P |
probably benign |
Het |
Gdpd1 |
T |
G |
11: 86,928,707 (GRCm39) |
E240D |
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Htt |
T |
C |
5: 35,056,268 (GRCm39) |
S2681P |
probably damaging |
Het |
Krt18 |
A |
G |
15: 101,939,163 (GRCm39) |
Y249C |
possibly damaging |
Het |
Lrp2 |
G |
T |
2: 69,318,182 (GRCm39) |
P2090T |
probably damaging |
Het |
Lrrc32 |
A |
G |
7: 98,148,090 (GRCm39) |
D290G |
probably benign |
Het |
Man1a |
A |
T |
10: 53,809,619 (GRCm39) |
Y486* |
probably null |
Het |
Mcm9 |
CCTGTCCCTGCTGTCCCTGCTGTCCCTGCTGTCCCTGCTGTCC |
CCTGTCCCTGCTGTCCCTGCTGTCCCTGCTGTCC |
10: 53,413,597 (GRCm39) |
|
probably benign |
Het |
Nin |
A |
T |
12: 70,107,960 (GRCm39) |
C211S |
probably damaging |
Het |
Npat |
A |
C |
9: 53,481,624 (GRCm39) |
I1111L |
probably benign |
Het |
Or5p79 |
A |
G |
7: 108,221,879 (GRCm39) |
I287V |
probably benign |
Het |
Or9i1b |
T |
A |
19: 13,896,535 (GRCm39) |
H50Q |
probably benign |
Het |
Pbx1 |
A |
G |
1: 168,030,935 (GRCm39) |
S228P |
probably damaging |
Het |
Pcsk7 |
G |
T |
9: 45,822,470 (GRCm39) |
R230L |
probably damaging |
Het |
Prom2 |
G |
T |
2: 127,380,183 (GRCm39) |
Q350K |
possibly damaging |
Het |
Racgap1 |
C |
T |
15: 99,522,195 (GRCm39) |
A458T |
possibly damaging |
Het |
Rsf1 |
T |
A |
7: 97,318,985 (GRCm39) |
C912S |
probably damaging |
Het |
Setd2 |
G |
A |
9: 110,377,579 (GRCm39) |
E465K |
possibly damaging |
Het |
Sgk2 |
T |
A |
2: 162,848,758 (GRCm39) |
D269E |
probably benign |
Het |
Spsb1 |
T |
C |
4: 149,991,536 (GRCm39) |
T11A |
probably benign |
Het |
Tln2 |
A |
T |
9: 67,203,095 (GRCm39) |
S509T |
probably benign |
Het |
Trim5 |
A |
T |
7: 103,914,958 (GRCm39) |
D370E |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,715,574 (GRCm39) |
|
probably benign |
Het |
Ubr2 |
C |
A |
17: 47,252,038 (GRCm39) |
G1501C |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,524,343 (GRCm39) |
R112S |
probably benign |
Het |
Vps26b |
T |
C |
9: 26,924,077 (GRCm39) |
Y222C |
probably damaging |
Het |
Wdr64 |
T |
A |
1: 175,603,315 (GRCm39) |
Y198N |
probably benign |
Het |
Xrn1 |
A |
T |
9: 95,880,316 (GRCm39) |
K752I |
possibly damaging |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp386 |
T |
C |
12: 116,023,398 (GRCm39) |
I372T |
probably benign |
Het |
Zfp804a |
T |
C |
2: 82,089,062 (GRCm39) |
Y964H |
possibly 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 |
IGL03110:Itgad
|
APN |
7 |
127,785,157 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|