Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700093K21Rik |
A |
T |
11: 23,467,357 (GRCm39) |
M92K |
probably benign |
Het |
4931406C07Rik |
T |
C |
9: 15,212,660 (GRCm39) |
|
probably null |
Het |
A430005L14Rik |
G |
A |
4: 154,045,357 (GRCm39) |
V129M |
probably damaging |
Het |
Actg2 |
T |
C |
6: 83,499,801 (GRCm39) |
T150A |
possibly damaging |
Het |
Actn1 |
A |
T |
12: 80,306,806 (GRCm39) |
D20E |
probably benign |
Het |
Alcam |
C |
T |
16: 52,091,136 (GRCm39) |
E461K |
probably damaging |
Het |
Anapc1 |
G |
A |
2: 128,518,128 (GRCm39) |
P242L |
probably benign |
Het |
Ankrd49 |
A |
T |
9: 14,692,674 (GRCm39) |
D163E |
probably benign |
Het |
Atp8b5 |
G |
A |
4: 43,372,903 (GRCm39) |
R1149Q |
possibly damaging |
Het |
Cacnb3 |
G |
T |
15: 98,540,455 (GRCm39) |
V328F |
probably damaging |
Het |
Camk4 |
T |
C |
18: 33,309,275 (GRCm39) |
I226T |
probably damaging |
Het |
Ccdc148 |
T |
C |
2: 58,892,176 (GRCm39) |
D172G |
probably damaging |
Het |
Cdh12 |
A |
G |
15: 21,520,491 (GRCm39) |
I319V |
probably damaging |
Het |
Cenpc1 |
T |
C |
5: 86,209,857 (GRCm39) |
|
probably benign |
Het |
Cfap69 |
A |
C |
5: 5,632,457 (GRCm39) |
N15K |
probably damaging |
Het |
Ckap2l |
A |
C |
2: 129,127,087 (GRCm39) |
S364A |
possibly damaging |
Het |
Clic6 |
G |
A |
16: 92,324,972 (GRCm39) |
G36R |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,749,583 (GRCm39) |
Y417C |
probably benign |
Het |
Cstf3 |
T |
A |
2: 104,494,623 (GRCm39) |
|
probably benign |
Het |
Cyp4f39 |
G |
A |
17: 32,711,304 (GRCm39) |
A484T |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,527,963 (GRCm39) |
N3829D |
probably damaging |
Het |
Dntt |
C |
A |
19: 41,017,923 (GRCm39) |
P16T |
probably benign |
Het |
Dym |
T |
A |
18: 75,258,583 (GRCm39) |
I447N |
probably damaging |
Het |
Elmo1 |
T |
C |
13: 20,773,841 (GRCm39) |
V617A |
probably benign |
Het |
Elovl7 |
G |
A |
13: 108,419,160 (GRCm39) |
G264D |
probably damaging |
Het |
Epha7 |
T |
A |
4: 28,947,571 (GRCm39) |
Y610* |
probably null |
Het |
Fn1 |
T |
C |
1: 71,636,814 (GRCm39) |
I178V |
probably benign |
Het |
Fndc9 |
T |
C |
11: 46,129,152 (GRCm39) |
Y224H |
probably benign |
Het |
Gad1 |
T |
C |
2: 70,404,521 (GRCm39) |
V137A |
probably damaging |
Het |
Gapvd1 |
A |
G |
2: 34,590,773 (GRCm39) |
|
probably null |
Het |
Gbp11 |
C |
T |
5: 105,475,277 (GRCm39) |
C357Y |
probably damaging |
Het |
Gcc1 |
G |
A |
6: 28,419,163 (GRCm39) |
A390V |
probably benign |
Het |
Gm6811 |
A |
G |
17: 21,314,185 (GRCm39) |
|
noncoding transcript |
Het |
Htt |
A |
T |
5: 34,985,918 (GRCm39) |
D1063V |
probably damaging |
Het |
Igfn1 |
C |
T |
1: 135,898,839 (GRCm39) |
A576T |
probably damaging |
Het |
Il12rb2 |
T |
C |
6: 67,280,485 (GRCm39) |
Y240C |
probably damaging |
Het |
Kcnip2 |
A |
C |
19: 45,782,979 (GRCm39) |
D134E |
probably damaging |
Het |
Kif2b |
C |
A |
11: 91,466,798 (GRCm39) |
R495I |
probably damaging |
Het |
Lef1 |
T |
C |
3: 130,993,938 (GRCm39) |
|
probably benign |
Het |
Lias |
C |
T |
5: 65,548,981 (GRCm39) |
R4C |
probably damaging |
Het |
Lpcat2 |
T |
C |
8: 93,591,560 (GRCm39) |
V68A |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,505,768 (GRCm39) |
S2067T |
probably benign |
Het |
Lrrc8e |
A |
T |
8: 4,284,190 (GRCm39) |
K138N |
probably damaging |
Het |
Map4k5 |
G |
A |
12: 69,852,082 (GRCm39) |
H767Y |
probably benign |
Het |
Mga |
C |
A |
2: 119,791,333 (GRCm39) |
T2406K |
possibly damaging |
Het |
Mtx1 |
A |
T |
3: 89,116,648 (GRCm39) |
S418T |
probably benign |
Het |
Myh7 |
C |
T |
14: 55,224,973 (GRCm39) |
M531I |
probably benign |
Het |
Myorg |
C |
T |
4: 41,497,947 (GRCm39) |
R561H |
probably benign |
Het |
Ncaph2 |
T |
A |
15: 89,255,427 (GRCm39) |
M555K |
probably damaging |
Het |
Nckap1 |
C |
T |
2: 80,348,286 (GRCm39) |
S889N |
probably benign |
Het |
Ncoa6 |
T |
C |
2: 155,244,584 (GRCm39) |
|
probably benign |
Het |
Nrp2 |
A |
G |
1: 62,822,479 (GRCm39) |
S691G |
probably benign |
Het |
Odad2 |
T |
C |
18: 7,222,554 (GRCm39) |
T572A |
probably benign |
Het |
Odf2l |
A |
T |
3: 144,845,543 (GRCm39) |
|
probably null |
Het |
Or5aq6 |
T |
A |
2: 86,923,081 (GRCm39) |
H220L |
probably benign |
Het |
Pcdh20 |
A |
G |
14: 88,705,410 (GRCm39) |
V630A |
probably damaging |
Het |
Pebp4 |
T |
C |
14: 70,285,923 (GRCm39) |
|
probably null |
Het |
Ppfia3 |
T |
A |
7: 45,006,090 (GRCm39) |
M301L |
probably benign |
Het |
Ppp1r21 |
C |
A |
17: 88,858,097 (GRCm39) |
Q203K |
probably benign |
Het |
Prr23a1 |
T |
C |
9: 98,725,406 (GRCm39) |
V256A |
probably benign |
Het |
Rbfox1 |
A |
G |
16: 7,110,091 (GRCm39) |
R150G |
possibly damaging |
Het |
Rnps1-ps |
A |
T |
6: 7,982,943 (GRCm39) |
|
noncoding transcript |
Het |
Robo3 |
T |
C |
9: 37,329,005 (GRCm39) |
R1238G |
possibly damaging |
Het |
Rp9 |
T |
G |
9: 22,365,097 (GRCm39) |
Q35P |
probably damaging |
Het |
Rsrc1 |
C |
A |
3: 67,262,808 (GRCm39) |
A254E |
probably damaging |
Het |
Shtn1 |
T |
A |
19: 58,998,222 (GRCm39) |
K390N |
probably damaging |
Het |
Sidt2 |
C |
T |
9: 45,864,517 (GRCm39) |
V71I |
probably benign |
Het |
Sirt7 |
A |
G |
11: 120,515,365 (GRCm39) |
V97A |
possibly damaging |
Het |
Slc14a2 |
A |
G |
18: 78,206,419 (GRCm39) |
S466P |
probably benign |
Het |
Slc2a10 |
T |
A |
2: 165,357,361 (GRCm39) |
D340E |
probably benign |
Het |
Slc36a2 |
A |
C |
11: 55,075,735 (GRCm39) |
N17K |
probably benign |
Het |
Slc4a10 |
A |
C |
2: 62,155,071 (GRCm39) |
N1086T |
probably benign |
Het |
Sptb |
T |
C |
12: 76,676,423 (GRCm39) |
D177G |
probably damaging |
Het |
Srpk2 |
A |
T |
5: 23,730,748 (GRCm39) |
|
probably null |
Het |
Sucla2 |
T |
G |
14: 73,830,121 (GRCm39) |
V386G |
probably damaging |
Het |
Susd1 |
G |
T |
4: 59,424,089 (GRCm39) |
N45K |
possibly damaging |
Het |
Tbxas1 |
T |
C |
6: 38,994,822 (GRCm39) |
|
probably benign |
Het |
Topors |
C |
T |
4: 40,261,776 (GRCm39) |
E503K |
probably damaging |
Het |
Trpv5 |
T |
C |
6: 41,634,731 (GRCm39) |
R533G |
probably benign |
Het |
Tshr |
A |
G |
12: 91,504,115 (GRCm39) |
H351R |
possibly damaging |
Het |
Ube2f |
G |
A |
1: 91,203,037 (GRCm39) |
V94M |
probably damaging |
Het |
Ugdh |
A |
G |
5: 65,580,521 (GRCm39) |
S216P |
probably damaging |
Het |
Unc45b |
T |
A |
11: 82,802,531 (GRCm39) |
|
probably null |
Het |
Vmn1r226 |
A |
G |
17: 20,908,335 (GRCm39) |
E189G |
probably damaging |
Het |
Xrcc6 |
T |
G |
15: 81,913,900 (GRCm39) |
D75E |
probably benign |
Het |
Ypel1 |
A |
G |
16: 16,921,474 (GRCm39) |
L70P |
probably damaging |
Het |
Zcwpw1 |
A |
T |
5: 137,795,022 (GRCm39) |
R73W |
probably damaging |
Het |
Zfp219 |
T |
C |
14: 52,246,512 (GRCm39) |
E160G |
probably damaging |
Het |
Zfp804b |
G |
T |
5: 7,229,533 (GRCm39) |
|
probably benign |
Het |
Zscan22 |
C |
A |
7: 12,640,730 (GRCm39) |
P325T |
probably damaging |
Het |
|
Other mutations in Itga3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00926:Itga3
|
APN |
11 |
94,956,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02020:Itga3
|
APN |
11 |
94,948,216 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02413:Itga3
|
APN |
11 |
94,959,597 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02562:Itga3
|
APN |
11 |
94,959,619 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4508001:Itga3
|
UTSW |
11 |
94,946,719 (GRCm39) |
missense |
probably benign |
0.20 |
R0485:Itga3
|
UTSW |
11 |
94,952,796 (GRCm39) |
missense |
probably benign |
0.05 |
R1548:Itga3
|
UTSW |
11 |
94,937,745 (GRCm39) |
critical splice donor site |
probably null |
|
R2062:Itga3
|
UTSW |
11 |
94,944,902 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2088:Itga3
|
UTSW |
11 |
94,943,320 (GRCm39) |
missense |
probably benign |
0.10 |
R2679:Itga3
|
UTSW |
11 |
94,959,136 (GRCm39) |
splice site |
probably benign |
|
R3697:Itga3
|
UTSW |
11 |
94,953,551 (GRCm39) |
missense |
probably benign |
0.00 |
R3839:Itga3
|
UTSW |
11 |
94,948,095 (GRCm39) |
critical splice donor site |
probably null |
|
R4210:Itga3
|
UTSW |
11 |
94,953,449 (GRCm39) |
missense |
probably benign |
0.00 |
R4533:Itga3
|
UTSW |
11 |
94,948,119 (GRCm39) |
missense |
probably benign |
0.15 |
R4849:Itga3
|
UTSW |
11 |
94,967,097 (GRCm39) |
missense |
probably benign |
|
R4863:Itga3
|
UTSW |
11 |
94,952,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4889:Itga3
|
UTSW |
11 |
94,959,127 (GRCm39) |
missense |
probably benign |
0.13 |
R5218:Itga3
|
UTSW |
11 |
94,953,574 (GRCm39) |
missense |
probably benign |
0.01 |
R6046:Itga3
|
UTSW |
11 |
94,953,541 (GRCm39) |
missense |
probably benign |
0.28 |
R6087:Itga3
|
UTSW |
11 |
94,943,269 (GRCm39) |
critical splice donor site |
probably null |
|
R6210:Itga3
|
UTSW |
11 |
94,959,717 (GRCm39) |
intron |
probably benign |
|
R6341:Itga3
|
UTSW |
11 |
94,946,677 (GRCm39) |
splice site |
probably null |
|
R6666:Itga3
|
UTSW |
11 |
94,956,652 (GRCm39) |
missense |
probably benign |
0.00 |
R6998:Itga3
|
UTSW |
11 |
94,942,288 (GRCm39) |
missense |
probably benign |
0.00 |
R7106:Itga3
|
UTSW |
11 |
94,946,699 (GRCm39) |
missense |
probably benign |
0.00 |
R7164:Itga3
|
UTSW |
11 |
94,943,305 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7267:Itga3
|
UTSW |
11 |
94,967,188 (GRCm39) |
intron |
probably benign |
|
R7421:Itga3
|
UTSW |
11 |
94,959,681 (GRCm39) |
missense |
probably benign |
0.20 |
R7514:Itga3
|
UTSW |
11 |
94,956,722 (GRCm39) |
nonsense |
probably null |
|
R7533:Itga3
|
UTSW |
11 |
94,937,344 (GRCm39) |
missense |
probably benign |
0.45 |
R7736:Itga3
|
UTSW |
11 |
94,967,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8145:Itga3
|
UTSW |
11 |
94,943,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R8303:Itga3
|
UTSW |
11 |
94,953,466 (GRCm39) |
missense |
probably benign |
0.42 |
R8459:Itga3
|
UTSW |
11 |
94,959,633 (GRCm39) |
missense |
probably benign |
|
R8464:Itga3
|
UTSW |
11 |
94,953,566 (GRCm39) |
missense |
probably benign |
0.28 |
R8951:Itga3
|
UTSW |
11 |
94,944,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R8984:Itga3
|
UTSW |
11 |
94,953,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Itga3
|
UTSW |
11 |
94,956,625 (GRCm39) |
missense |
probably benign |
0.09 |
R9695:Itga3
|
UTSW |
11 |
94,946,520 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Itga3
|
UTSW |
11 |
94,947,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|