Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad11 |
T |
G |
9: 104,001,299 (GRCm39) |
V615G |
probably damaging |
Het |
Apaf1 |
T |
G |
10: 90,897,567 (GRCm39) |
E305D |
possibly damaging |
Het |
Apol10b |
A |
G |
15: 77,469,419 (GRCm39) |
S253P |
probably damaging |
Het |
Bbs9 |
T |
A |
9: 22,479,015 (GRCm39) |
C153S |
probably damaging |
Het |
Bicra |
C |
T |
7: 15,723,247 (GRCm39) |
G90D |
probably damaging |
Het |
Clca4a |
A |
C |
3: 144,667,735 (GRCm39) |
L412R |
probably damaging |
Het |
Cul3 |
A |
T |
1: 80,249,281 (GRCm39) |
D597E |
possibly damaging |
Het |
Cxcr5 |
A |
G |
9: 44,424,964 (GRCm39) |
|
probably null |
Het |
Dnah10 |
T |
C |
5: 124,824,782 (GRCm39) |
I646T |
possibly damaging |
Het |
Focad |
T |
A |
4: 88,192,450 (GRCm39) |
V593D |
unknown |
Het |
Fsip2 |
T |
A |
2: 82,812,683 (GRCm39) |
S3001T |
probably benign |
Het |
Ganab |
T |
A |
19: 8,888,477 (GRCm39) |
Y511N |
probably damaging |
Het |
Gdf9 |
T |
A |
11: 53,327,467 (GRCm39) |
L141Q |
probably damaging |
Het |
Gpr180 |
A |
G |
14: 118,385,596 (GRCm39) |
D136G |
probably benign |
Het |
Hsd3b9 |
T |
C |
3: 98,363,710 (GRCm39) |
E45G |
probably benign |
Het |
Ly75 |
C |
T |
2: 60,146,565 (GRCm39) |
A1238T |
probably benign |
Het |
Macc1 |
T |
C |
12: 119,410,738 (GRCm39) |
V502A |
probably damaging |
Het |
Mroh4 |
T |
C |
15: 74,478,527 (GRCm39) |
K923E |
probably damaging |
Het |
Msh3 |
G |
A |
13: 92,487,939 (GRCm39) |
P93S |
possibly damaging |
Het |
Myo18a |
A |
G |
11: 77,714,966 (GRCm39) |
D474G |
probably damaging |
Het |
Npat |
T |
A |
9: 53,481,522 (GRCm39) |
Y1077N |
probably benign |
Het |
Or4c109 |
A |
T |
2: 88,817,939 (GRCm39) |
S202R |
probably damaging |
Het |
Or6c69 |
T |
G |
10: 129,747,752 (GRCm39) |
T132P |
probably damaging |
Het |
Or6k14 |
A |
C |
1: 173,927,630 (GRCm39) |
H202P |
probably damaging |
Het |
Or8u8 |
A |
T |
2: 86,011,949 (GRCm39) |
|
probably null |
Het |
Paqr5 |
T |
G |
9: 61,880,076 (GRCm39) |
T59P |
probably benign |
Het |
Phyhipl |
C |
T |
10: 70,395,085 (GRCm39) |
G329R |
probably damaging |
Het |
Pomgnt1 |
T |
C |
4: 116,013,086 (GRCm39) |
Y430H |
probably damaging |
Het |
Pramel21 |
T |
C |
4: 143,343,927 (GRCm39) |
F409S |
probably benign |
Het |
Prkd3 |
A |
T |
17: 79,264,662 (GRCm39) |
M651K |
probably damaging |
Het |
Puf60 |
A |
T |
15: 75,942,623 (GRCm39) |
M440K |
probably damaging |
Het |
Recql4 |
A |
G |
15: 76,594,009 (GRCm39) |
|
probably null |
Het |
Sgk1 |
A |
C |
10: 21,874,059 (GRCm39) |
M320L |
probably benign |
Het |
Slc27a4 |
T |
C |
2: 29,702,627 (GRCm39) |
F509S |
probably damaging |
Het |
Sorbs1 |
T |
C |
19: 40,351,706 (GRCm39) |
T235A |
probably damaging |
Het |
Srrm3 |
A |
G |
5: 135,898,130 (GRCm39) |
|
probably benign |
Het |
Tex15 |
C |
T |
8: 34,063,528 (GRCm39) |
T986I |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Zswim4 |
T |
C |
8: 84,955,517 (GRCm39) |
M301V |
possibly damaging |
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 |
|
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 |
|
|