Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
T |
C |
7: 119,373,072 (GRCm39) |
S192P |
probably damaging |
Het |
Amy1 |
T |
A |
3: 113,355,339 (GRCm39) |
Y348F |
probably damaging |
Het |
Brpf3 |
C |
A |
17: 29,040,258 (GRCm39) |
P893H |
probably benign |
Het |
Cage1 |
T |
C |
13: 38,200,395 (GRCm39) |
T702A |
possibly damaging |
Het |
Cdk11b |
A |
G |
4: 155,734,060 (GRCm39) |
|
probably benign |
Het |
Cdk5rap3 |
T |
C |
11: 96,802,729 (GRCm39) |
Y207C |
probably damaging |
Het |
Cenpc1 |
T |
C |
5: 86,183,394 (GRCm39) |
K465R |
probably damaging |
Het |
Cldn14 |
A |
C |
16: 93,716,486 (GRCm39) |
L120R |
possibly damaging |
Het |
Cyp2c69 |
A |
T |
19: 39,831,507 (GRCm39) |
C435* |
probably null |
Het |
Dmxl2 |
T |
A |
9: 54,323,046 (GRCm39) |
E1446V |
probably damaging |
Het |
Dnah17 |
T |
A |
11: 118,017,116 (GRCm39) |
D208V |
probably damaging |
Het |
Eif4g3 |
G |
T |
4: 137,915,394 (GRCm39) |
G1430V |
possibly damaging |
Het |
Eif5 |
T |
A |
12: 111,509,227 (GRCm39) |
D284E |
probably benign |
Het |
Fam47e |
T |
C |
5: 92,710,376 (GRCm39) |
L125P |
probably damaging |
Het |
Far1 |
A |
G |
7: 113,167,344 (GRCm39) |
I476M |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,819,242 (GRCm39) |
I4992L |
probably benign |
Het |
Gli3 |
T |
A |
13: 15,899,698 (GRCm39) |
N1028K |
possibly damaging |
Het |
Gucy1a1 |
T |
C |
3: 82,004,941 (GRCm39) |
K615E |
probably damaging |
Het |
Gykl1 |
G |
T |
18: 52,828,280 (GRCm39) |
S496I |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,573,170 (GRCm39) |
|
probably null |
Het |
Kif24 |
A |
T |
4: 41,423,498 (GRCm39) |
V251E |
probably damaging |
Het |
Nupr1 |
T |
C |
7: 126,224,518 (GRCm39) |
Y30C |
probably damaging |
Het |
Or5b119 |
T |
A |
19: 13,457,119 (GRCm39) |
M148L |
probably benign |
Het |
Or5g29 |
A |
G |
2: 85,421,342 (GRCm39) |
I153V |
probably benign |
Het |
Or5w14 |
A |
T |
2: 87,541,815 (GRCm39) |
L145* |
probably null |
Het |
Or8g26 |
T |
A |
9: 39,095,594 (GRCm39) |
I40N |
probably damaging |
Het |
P2ry1 |
T |
A |
3: 60,911,215 (GRCm39) |
I118N |
possibly damaging |
Het |
Pcdh1 |
C |
T |
18: 38,332,263 (GRCm39) |
V247M |
probably benign |
Het |
Pdia5 |
A |
G |
16: 35,250,293 (GRCm39) |
V222A |
possibly damaging |
Het |
Plce1 |
G |
A |
19: 38,713,495 (GRCm39) |
|
probably null |
Het |
Ppm1m |
T |
C |
9: 106,074,427 (GRCm39) |
R239G |
probably damaging |
Het |
Pramel30 |
C |
T |
4: 144,056,837 (GRCm39) |
P7S |
probably damaging |
Het |
Prkcz |
A |
T |
4: 155,352,652 (GRCm39) |
F492I |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,346,912 (GRCm39) |
I269T |
possibly damaging |
Het |
Scoc |
T |
C |
8: 84,184,965 (GRCm39) |
S2G |
unknown |
Het |
Spesp1 |
A |
T |
9: 62,179,921 (GRCm39) |
M329K |
probably benign |
Het |
Ston2 |
T |
C |
12: 91,615,104 (GRCm39) |
K435E |
probably damaging |
Het |
Synj2 |
A |
T |
17: 6,026,149 (GRCm39) |
L69F |
probably damaging |
Het |
Tigd5 |
T |
C |
15: 75,781,842 (GRCm39) |
I68T |
probably damaging |
Het |
Tmcc2 |
A |
T |
1: 132,286,720 (GRCm39) |
M577K |
probably damaging |
Het |
Tmem131l |
A |
T |
3: 83,849,798 (GRCm39) |
I263N |
possibly damaging |
Het |
Trip13 |
T |
C |
13: 74,061,439 (GRCm39) |
E408G |
probably benign |
Het |
Txnl4b |
T |
C |
8: 110,295,735 (GRCm39) |
|
probably null |
Het |
Ube2o |
T |
C |
11: 116,430,369 (GRCm39) |
E1123G |
probably damaging |
Het |
Vmn1r123 |
A |
G |
7: 20,896,774 (GRCm39) |
H222R |
possibly damaging |
Het |
Vmn2r73 |
G |
T |
7: 85,522,140 (GRCm39) |
H66Q |
probably benign |
Het |
Zc3h13 |
T |
A |
14: 75,567,863 (GRCm39) |
V1052D |
probably benign |
Het |
|
Other mutations in Itga2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00809:Itga2
|
APN |
13 |
115,014,161 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01481:Itga2
|
APN |
13 |
114,996,168 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01666:Itga2
|
APN |
13 |
114,973,627 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01730:Itga2
|
APN |
13 |
114,990,947 (GRCm39) |
splice site |
probably benign |
|
IGL01965:Itga2
|
APN |
13 |
114,984,600 (GRCm39) |
splice site |
probably benign |
|
IGL01987:Itga2
|
APN |
13 |
114,984,482 (GRCm39) |
nonsense |
probably null |
|
IGL02334:Itga2
|
APN |
13 |
115,001,845 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02381:Itga2
|
APN |
13 |
114,993,258 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02562:Itga2
|
APN |
13 |
114,973,106 (GRCm39) |
unclassified |
probably benign |
|
IGL03191:Itga2
|
APN |
13 |
114,973,020 (GRCm39) |
unclassified |
probably benign |
|
IGL03209:Itga2
|
APN |
13 |
115,017,168 (GRCm39) |
missense |
probably damaging |
1.00 |
P0007:Itga2
|
UTSW |
13 |
115,002,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Itga2
|
UTSW |
13 |
115,007,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0023:Itga2
|
UTSW |
13 |
115,007,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0025:Itga2
|
UTSW |
13 |
115,007,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0029:Itga2
|
UTSW |
13 |
115,007,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0062:Itga2
|
UTSW |
13 |
115,007,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0062:Itga2
|
UTSW |
13 |
115,007,032 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0149:Itga2
|
UTSW |
13 |
114,973,115 (GRCm39) |
unclassified |
probably benign |
|
R0152:Itga2
|
UTSW |
13 |
115,002,850 (GRCm39) |
missense |
probably benign |
0.06 |
R0496:Itga2
|
UTSW |
13 |
114,990,435 (GRCm39) |
missense |
probably benign |
0.00 |
R0502:Itga2
|
UTSW |
13 |
114,982,392 (GRCm39) |
missense |
probably benign |
0.15 |
R0599:Itga2
|
UTSW |
13 |
114,993,186 (GRCm39) |
splice site |
probably benign |
|
R0688:Itga2
|
UTSW |
13 |
114,976,090 (GRCm39) |
missense |
probably benign |
0.00 |
R0704:Itga2
|
UTSW |
13 |
114,998,911 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0760:Itga2
|
UTSW |
13 |
114,996,168 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0811:Itga2
|
UTSW |
13 |
115,007,150 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0812:Itga2
|
UTSW |
13 |
115,007,150 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0836:Itga2
|
UTSW |
13 |
114,993,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R1196:Itga2
|
UTSW |
13 |
115,002,691 (GRCm39) |
critical splice donor site |
probably null |
|
R1546:Itga2
|
UTSW |
13 |
114,985,956 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1639:Itga2
|
UTSW |
13 |
114,993,832 (GRCm39) |
missense |
probably benign |
0.00 |
R1834:Itga2
|
UTSW |
13 |
114,993,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:Itga2
|
UTSW |
13 |
114,993,262 (GRCm39) |
missense |
probably damaging |
0.98 |
R2180:Itga2
|
UTSW |
13 |
114,985,917 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2190:Itga2
|
UTSW |
13 |
115,007,141 (GRCm39) |
missense |
probably benign |
0.05 |
R2518:Itga2
|
UTSW |
13 |
115,017,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R3885:Itga2
|
UTSW |
13 |
115,005,835 (GRCm39) |
missense |
probably benign |
0.35 |
R3962:Itga2
|
UTSW |
13 |
114,976,054 (GRCm39) |
missense |
probably damaging |
0.99 |
R4094:Itga2
|
UTSW |
13 |
115,007,161 (GRCm39) |
missense |
probably benign |
0.01 |
R4193:Itga2
|
UTSW |
13 |
115,023,185 (GRCm39) |
nonsense |
probably null |
|
R4290:Itga2
|
UTSW |
13 |
115,002,709 (GRCm39) |
missense |
probably damaging |
0.98 |
R4459:Itga2
|
UTSW |
13 |
114,980,019 (GRCm39) |
missense |
probably damaging |
0.97 |
R4460:Itga2
|
UTSW |
13 |
114,980,019 (GRCm39) |
missense |
probably damaging |
0.97 |
R4628:Itga2
|
UTSW |
13 |
115,014,229 (GRCm39) |
missense |
probably benign |
0.03 |
R4655:Itga2
|
UTSW |
13 |
115,009,805 (GRCm39) |
missense |
probably benign |
0.00 |
R4716:Itga2
|
UTSW |
13 |
114,993,909 (GRCm39) |
missense |
probably damaging |
0.98 |
R4896:Itga2
|
UTSW |
13 |
114,990,302 (GRCm39) |
nonsense |
probably null |
|
R5093:Itga2
|
UTSW |
13 |
114,992,717 (GRCm39) |
missense |
probably benign |
0.00 |
R5488:Itga2
|
UTSW |
13 |
114,979,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Itga2
|
UTSW |
13 |
114,979,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Itga2
|
UTSW |
13 |
115,021,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R5767:Itga2
|
UTSW |
13 |
114,976,106 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5790:Itga2
|
UTSW |
13 |
115,004,742 (GRCm39) |
missense |
probably benign |
0.02 |
R5923:Itga2
|
UTSW |
13 |
115,021,055 (GRCm39) |
missense |
probably benign |
0.02 |
R6163:Itga2
|
UTSW |
13 |
115,002,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R6227:Itga2
|
UTSW |
13 |
114,976,097 (GRCm39) |
missense |
probably benign |
0.30 |
R6283:Itga2
|
UTSW |
13 |
115,005,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Itga2
|
UTSW |
13 |
114,980,009 (GRCm39) |
missense |
probably benign |
|
R6510:Itga2
|
UTSW |
13 |
115,009,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R6742:Itga2
|
UTSW |
13 |
114,973,061 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6869:Itga2
|
UTSW |
13 |
115,012,073 (GRCm39) |
splice site |
probably null |
|
R7073:Itga2
|
UTSW |
13 |
114,996,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7111:Itga2
|
UTSW |
13 |
115,037,066 (GRCm39) |
missense |
unknown |
|
R7236:Itga2
|
UTSW |
13 |
115,014,227 (GRCm39) |
missense |
probably benign |
|
R7269:Itga2
|
UTSW |
13 |
115,023,225 (GRCm39) |
nonsense |
probably null |
|
R7296:Itga2
|
UTSW |
13 |
114,993,930 (GRCm39) |
splice site |
probably null |
|
R7350:Itga2
|
UTSW |
13 |
114,973,738 (GRCm39) |
missense |
probably damaging |
0.98 |
R7375:Itga2
|
UTSW |
13 |
115,005,753 (GRCm39) |
missense |
probably benign |
0.06 |
R7501:Itga2
|
UTSW |
13 |
115,012,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7687:Itga2
|
UTSW |
13 |
115,002,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7766:Itga2
|
UTSW |
13 |
114,990,427 (GRCm39) |
missense |
probably benign |
|
R7810:Itga2
|
UTSW |
13 |
115,002,715 (GRCm39) |
missense |
probably benign |
0.15 |
R8038:Itga2
|
UTSW |
13 |
114,990,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R8948:Itga2
|
UTSW |
13 |
115,009,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R9132:Itga2
|
UTSW |
13 |
115,014,298 (GRCm39) |
nonsense |
probably null |
|
R9153:Itga2
|
UTSW |
13 |
115,001,941 (GRCm39) |
missense |
probably benign |
0.00 |
R9159:Itga2
|
UTSW |
13 |
115,014,298 (GRCm39) |
nonsense |
probably null |
|
R9651:Itga2
|
UTSW |
13 |
115,020,991 (GRCm39) |
missense |
probably benign |
0.00 |
R9652:Itga2
|
UTSW |
13 |
115,020,991 (GRCm39) |
missense |
probably benign |
0.00 |
R9653:Itga2
|
UTSW |
13 |
115,020,991 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Itga2
|
UTSW |
13 |
114,993,868 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1177:Itga2
|
UTSW |
13 |
114,990,237 (GRCm39) |
critical splice donor site |
probably null |
|
|