Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm1 |
A |
C |
4: 144,255,567 (GRCm39) |
D329A |
probably damaging |
Het |
Abcc12 |
T |
A |
8: 87,264,962 (GRCm39) |
H661L |
probably damaging |
Het |
Acsbg2 |
C |
G |
17: 57,154,710 (GRCm39) |
A481P |
probably damaging |
Het |
Aknad1 |
T |
A |
3: 108,688,501 (GRCm39) |
C610S |
probably benign |
Het |
Anapc1 |
T |
A |
2: 128,520,138 (GRCm39) |
K226N |
probably damaging |
Het |
Aqp11 |
A |
T |
7: 97,375,896 (GRCm39) |
I251N |
possibly damaging |
Het |
Arid1a |
G |
T |
4: 133,418,487 (GRCm39) |
T1032K |
unknown |
Het |
Atg16l1 |
T |
C |
1: 87,717,187 (GRCm39) |
V538A |
probably benign |
Het |
Atp7b |
A |
T |
8: 22,501,089 (GRCm39) |
L938Q |
probably damaging |
Het |
Bbs1 |
C |
T |
19: 4,956,042 (GRCm39) |
A44T |
probably damaging |
Het |
Btbd9 |
A |
T |
17: 30,749,188 (GRCm39) |
V42E |
probably damaging |
Het |
Carmil3 |
C |
G |
14: 55,730,333 (GRCm39) |
S15R |
probably damaging |
Het |
Cfap44 |
T |
A |
16: 44,241,583 (GRCm39) |
F651L |
probably benign |
Het |
Clcn3 |
A |
T |
8: 61,386,104 (GRCm39) |
|
probably benign |
Het |
Copb1 |
A |
T |
7: 113,849,329 (GRCm39) |
D91E |
probably benign |
Het |
Ctr9 |
G |
A |
7: 110,643,154 (GRCm39) |
A509T |
possibly damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Emc1 |
A |
G |
4: 139,098,320 (GRCm39) |
D767G |
probably damaging |
Het |
Fads1 |
G |
A |
19: 10,164,261 (GRCm39) |
|
probably benign |
Het |
Fcgbpl1 |
A |
G |
7: 27,852,837 (GRCm39) |
K1375E |
probably benign |
Het |
Frrs1 |
T |
C |
3: 116,690,437 (GRCm39) |
F27L |
probably damaging |
Het |
Lrig3 |
A |
C |
10: 125,846,088 (GRCm39) |
D839A |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,382,107 (GRCm39) |
|
probably benign |
Het |
Myo6 |
T |
C |
9: 80,190,816 (GRCm39) |
V789A |
possibly damaging |
Het |
Nasp |
A |
G |
4: 116,462,968 (GRCm39) |
|
probably benign |
Het |
Nsmaf |
A |
G |
4: 6,408,680 (GRCm39) |
Y700H |
probably damaging |
Het |
Plekhs1 |
T |
G |
19: 56,466,948 (GRCm39) |
S260A |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
R3hdm1 |
T |
C |
1: 128,138,929 (GRCm39) |
|
probably benign |
Het |
Rtcb |
A |
T |
10: 85,785,315 (GRCm39) |
|
probably benign |
Het |
Suco |
A |
T |
1: 161,673,154 (GRCm39) |
|
probably null |
Het |
Synrg |
G |
T |
11: 83,899,479 (GRCm39) |
D562Y |
probably damaging |
Het |
Tfip11 |
T |
C |
5: 112,479,875 (GRCm39) |
S265P |
possibly damaging |
Het |
Ucp3 |
G |
T |
7: 100,134,250 (GRCm39) |
V288L |
probably benign |
Het |
Xylt1 |
G |
T |
7: 117,233,928 (GRCm39) |
G485V |
probably damaging |
Het |
Yars1 |
A |
G |
4: 129,090,981 (GRCm39) |
T130A |
probably benign |
Het |
Zfp652 |
A |
T |
11: 95,644,295 (GRCm39) |
R205* |
probably null |
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 |
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 |
R6278:Itga2
|
UTSW |
13 |
114,982,424 (GRCm39) |
missense |
probably benign |
0.05 |
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 |
|
|