Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bdp1 |
A |
T |
13: 100,191,816 (GRCm39) |
|
probably benign |
Het |
Car8 |
T |
C |
4: 8,183,321 (GRCm39) |
I225V |
probably benign |
Het |
Cc2d2a |
T |
A |
5: 43,892,792 (GRCm39) |
N1390K |
probably damaging |
Het |
Coasy |
T |
C |
11: 100,975,184 (GRCm39) |
V247A |
possibly damaging |
Het |
Dgkq |
A |
G |
5: 108,804,310 (GRCm39) |
V50A |
probably benign |
Het |
Dixdc1 |
A |
T |
9: 50,593,931 (GRCm39) |
|
probably benign |
Het |
Dmxl2 |
G |
A |
9: 54,301,127 (GRCm39) |
A2328V |
probably benign |
Het |
Exoc3l |
C |
A |
8: 106,017,209 (GRCm39) |
V593L |
possibly damaging |
Het |
Eya3 |
T |
C |
4: 132,437,366 (GRCm39) |
S409P |
probably damaging |
Het |
Garin4 |
T |
C |
1: 190,895,713 (GRCm39) |
N310S |
probably benign |
Het |
Gbp4 |
A |
T |
5: 105,284,740 (GRCm39) |
S50T |
probably damaging |
Het |
Gm5885 |
A |
G |
6: 133,507,092 (GRCm39) |
|
noncoding transcript |
Het |
H2ap |
G |
T |
X: 9,713,629 (GRCm39) |
|
probably benign |
Het |
Igkv12-89 |
A |
T |
6: 68,811,970 (GRCm39) |
Y66* |
probably null |
Het |
Kank3 |
T |
C |
17: 34,037,824 (GRCm39) |
V291A |
probably benign |
Het |
Klhl9 |
A |
G |
4: 88,639,407 (GRCm39) |
M278T |
probably damaging |
Het |
Lrrc43 |
G |
A |
5: 123,639,275 (GRCm39) |
D435N |
possibly damaging |
Het |
Ly75 |
A |
T |
2: 60,188,851 (GRCm39) |
S292T |
probably damaging |
Het |
Mchr1 |
G |
A |
15: 81,121,480 (GRCm39) |
V77I |
probably benign |
Het |
Mga |
T |
A |
2: 119,794,535 (GRCm39) |
C2622S |
possibly damaging |
Het |
Neb |
G |
T |
2: 52,186,266 (GRCm39) |
Y935* |
probably null |
Het |
Nt5el |
T |
A |
13: 105,218,808 (GRCm39) |
D47E |
probably damaging |
Het |
Phf20 |
A |
G |
2: 156,136,017 (GRCm39) |
E612G |
possibly damaging |
Het |
Pkhd1 |
A |
G |
1: 20,271,007 (GRCm39) |
L3182P |
probably benign |
Het |
Rnf130 |
T |
C |
11: 49,986,667 (GRCm39) |
V337A |
probably benign |
Het |
Slfn10-ps |
T |
C |
11: 82,923,117 (GRCm39) |
|
noncoding transcript |
Het |
Sorcs1 |
G |
A |
19: 50,322,036 (GRCm39) |
P249L |
probably damaging |
Het |
Spata13 |
C |
T |
14: 60,928,723 (GRCm39) |
R94C |
probably damaging |
Het |
Stk38 |
C |
T |
17: 29,210,390 (GRCm39) |
R63Q |
probably benign |
Het |
Tmem220 |
C |
A |
11: 66,925,014 (GRCm39) |
H174N |
probably benign |
Het |
Tmem68 |
C |
A |
4: 3,560,536 (GRCm39) |
R216L |
probably damaging |
Het |
Trim29 |
G |
A |
9: 43,222,599 (GRCm39) |
V143M |
probably benign |
Het |
Ubqln2 |
T |
C |
X: 152,282,906 (GRCm39) |
L486P |
possibly damaging |
Het |
Usp17le |
G |
A |
7: 104,417,982 (GRCm39) |
Q387* |
probably null |
Het |
Vps33b |
A |
G |
7: 79,937,587 (GRCm39) |
E445G |
probably damaging |
Het |
|
Other mutations in Itgax |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Itgax
|
APN |
7 |
127,734,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00325:Itgax
|
APN |
7 |
127,747,481 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01155:Itgax
|
APN |
7 |
127,744,207 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01461:Itgax
|
APN |
7 |
127,734,190 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01508:Itgax
|
APN |
7 |
127,743,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Itgax
|
APN |
7 |
127,730,378 (GRCm39) |
splice site |
probably null |
|
IGL01864:Itgax
|
APN |
7 |
127,732,935 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02094:Itgax
|
APN |
7 |
127,730,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Itgax
|
APN |
7 |
127,748,295 (GRCm39) |
missense |
probably benign |
|
IGL03406:Itgax
|
APN |
7 |
127,748,370 (GRCm39) |
missense |
possibly damaging |
0.93 |
Adendritic
|
UTSW |
7 |
127,747,744 (GRCm39) |
nonsense |
probably null |
|
PIT4651001:Itgax
|
UTSW |
7 |
127,748,282 (GRCm39) |
missense |
probably benign |
0.11 |
R0366:Itgax
|
UTSW |
7 |
127,748,261 (GRCm39) |
splice site |
probably benign |
|
R0763:Itgax
|
UTSW |
7 |
127,747,112 (GRCm39) |
splice site |
probably benign |
|
R1072:Itgax
|
UTSW |
7 |
127,749,316 (GRCm39) |
missense |
probably damaging |
0.96 |
R1659:Itgax
|
UTSW |
7 |
127,730,063 (GRCm39) |
missense |
probably benign |
0.15 |
R2019:Itgax
|
UTSW |
7 |
127,747,698 (GRCm39) |
missense |
probably benign |
|
R2418:Itgax
|
UTSW |
7 |
127,741,505 (GRCm39) |
missense |
probably damaging |
0.98 |
R3027:Itgax
|
UTSW |
7 |
127,747,744 (GRCm39) |
nonsense |
probably null |
|
R3846:Itgax
|
UTSW |
7 |
127,732,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Itgax
|
UTSW |
7 |
127,735,445 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4021:Itgax
|
UTSW |
7 |
127,732,311 (GRCm39) |
critical splice donor site |
probably null |
|
R4027:Itgax
|
UTSW |
7 |
127,740,438 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4163:Itgax
|
UTSW |
7 |
127,743,872 (GRCm39) |
missense |
probably benign |
0.00 |
R4923:Itgax
|
UTSW |
7 |
127,747,700 (GRCm39) |
missense |
probably benign |
|
R5259:Itgax
|
UTSW |
7 |
127,747,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R5333:Itgax
|
UTSW |
7 |
127,741,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R5347:Itgax
|
UTSW |
7 |
127,740,474 (GRCm39) |
missense |
probably benign |
0.08 |
R5679:Itgax
|
UTSW |
7 |
127,734,162 (GRCm39) |
missense |
probably benign |
0.00 |
R5725:Itgax
|
UTSW |
7 |
127,747,033 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5733:Itgax
|
UTSW |
7 |
127,739,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R5750:Itgax
|
UTSW |
7 |
127,743,878 (GRCm39) |
missense |
probably benign |
0.32 |
R5964:Itgax
|
UTSW |
7 |
127,739,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Itgax
|
UTSW |
7 |
127,730,624 (GRCm39) |
missense |
probably damaging |
0.96 |
R6168:Itgax
|
UTSW |
7 |
127,732,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R6212:Itgax
|
UTSW |
7 |
127,747,025 (GRCm39) |
missense |
probably benign |
0.16 |
R6212:Itgax
|
UTSW |
7 |
127,729,504 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6480:Itgax
|
UTSW |
7 |
127,747,771 (GRCm39) |
missense |
probably benign |
0.12 |
R6484:Itgax
|
UTSW |
7 |
127,732,890 (GRCm39) |
missense |
probably benign |
0.13 |
R6796:Itgax
|
UTSW |
7 |
127,734,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R6844:Itgax
|
UTSW |
7 |
127,747,106 (GRCm39) |
splice site |
probably null |
|
R7287:Itgax
|
UTSW |
7 |
127,747,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Itgax
|
UTSW |
7 |
127,734,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7421:Itgax
|
UTSW |
7 |
127,739,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R7599:Itgax
|
UTSW |
7 |
127,747,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R7710:Itgax
|
UTSW |
7 |
127,735,028 (GRCm39) |
missense |
probably benign |
0.04 |
R7964:Itgax
|
UTSW |
7 |
127,739,590 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8220:Itgax
|
UTSW |
7 |
127,730,090 (GRCm39) |
missense |
probably benign |
0.00 |
R8730:Itgax
|
UTSW |
7 |
127,739,066 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8742:Itgax
|
UTSW |
7 |
127,743,795 (GRCm39) |
missense |
probably benign |
0.28 |
R8812:Itgax
|
UTSW |
7 |
127,732,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Itgax
|
UTSW |
7 |
127,735,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Itgax
|
UTSW |
7 |
127,747,913 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9149:Itgax
|
UTSW |
7 |
127,730,641 (GRCm39) |
missense |
probably benign |
0.01 |
R9310:Itgax
|
UTSW |
7 |
127,741,432 (GRCm39) |
nonsense |
probably null |
|
R9376:Itgax
|
UTSW |
7 |
127,747,935 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9377:Itgax
|
UTSW |
7 |
127,732,849 (GRCm39) |
missense |
probably benign |
0.03 |
R9641:Itgax
|
UTSW |
7 |
127,741,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Itgax
|
UTSW |
7 |
127,734,935 (GRCm39) |
missense |
probably benign |
0.24 |
R9709:Itgax
|
UTSW |
7 |
127,735,500 (GRCm39) |
missense |
probably damaging |
1.00 |
X0061:Itgax
|
UTSW |
7 |
127,728,779 (GRCm39) |
start gained |
probably benign |
|
Z1176:Itgax
|
UTSW |
7 |
127,744,044 (GRCm39) |
missense |
probably benign |
0.24 |
Z1177:Itgax
|
UTSW |
7 |
127,747,234 (GRCm39) |
missense |
probably benign |
0.04 |
|