Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp4 |
G |
T |
7: 43,906,210 (GRCm39) |
Y88* |
probably null |
Het |
Aftph |
T |
C |
11: 20,676,994 (GRCm39) |
D205G |
probably damaging |
Het |
Arhgap31 |
T |
C |
16: 38,423,793 (GRCm39) |
I758V |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,591,513 (GRCm39) |
|
probably null |
Het |
Auts2 |
T |
C |
5: 131,469,056 (GRCm39) |
T754A |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,966,216 (GRCm39) |
M4048V |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,024,870 (GRCm39) |
|
probably null |
Het |
Cmpk1 |
C |
T |
4: 114,822,121 (GRCm39) |
A143T |
probably benign |
Het |
Cstf2t |
C |
A |
19: 31,060,536 (GRCm39) |
P24Q |
probably damaging |
Het |
Cwc22 |
A |
G |
2: 77,757,640 (GRCm39) |
S163P |
probably damaging |
Het |
Dnaaf11 |
T |
A |
15: 66,321,326 (GRCm39) |
M272L |
probably benign |
Het |
Faf1 |
T |
A |
4: 109,534,278 (GRCm39) |
|
probably benign |
Het |
Focad |
T |
A |
4: 88,289,043 (GRCm39) |
I1279N |
unknown |
Het |
Gp5 |
T |
C |
16: 30,127,459 (GRCm39) |
D405G |
possibly damaging |
Het |
Guf1 |
C |
A |
5: 69,718,501 (GRCm39) |
N213K |
probably damaging |
Het |
Hacd4 |
T |
C |
4: 88,341,285 (GRCm39) |
T145A |
probably damaging |
Het |
Mast4 |
T |
A |
13: 102,910,781 (GRCm39) |
T621S |
probably damaging |
Het |
Mme |
T |
C |
3: 63,247,534 (GRCm39) |
M273T |
possibly damaging |
Het |
Mos |
A |
G |
4: 3,871,816 (GRCm39) |
|
probably benign |
Het |
Msln |
C |
T |
17: 25,969,004 (GRCm39) |
|
probably null |
Het |
Mtg1 |
A |
T |
7: 139,730,149 (GRCm39) |
Q315L |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,105,354 (GRCm39) |
E1048G |
probably damaging |
Het |
Ndufa9 |
C |
T |
6: 126,821,777 (GRCm39) |
G66D |
probably damaging |
Het |
Nr1i2 |
T |
C |
16: 38,086,333 (GRCm39) |
K44R |
probably benign |
Het |
Nup155 |
T |
A |
15: 8,165,272 (GRCm39) |
M636K |
probably benign |
Het |
Or12d12 |
A |
T |
17: 37,610,673 (GRCm39) |
F213L |
probably benign |
Het |
Or5b96 |
T |
A |
19: 12,867,513 (GRCm39) |
T143S |
probably benign |
Het |
Pde4b |
A |
T |
4: 102,458,832 (GRCm39) |
Q496L |
probably damaging |
Het |
Plekha6 |
T |
C |
1: 133,187,869 (GRCm39) |
V130A |
probably benign |
Het |
Prag1 |
A |
G |
8: 36,569,834 (GRCm39) |
N139S |
probably benign |
Het |
Rbpj-ps3 |
T |
C |
6: 46,507,694 (GRCm39) |
T19A |
probably benign |
Het |
Scai |
A |
G |
2: 38,984,803 (GRCm39) |
|
probably benign |
Het |
Slc12a7 |
A |
G |
13: 73,947,733 (GRCm39) |
T617A |
probably benign |
Het |
Slc15a2 |
T |
C |
16: 36,576,592 (GRCm39) |
M481V |
probably benign |
Het |
Snx5 |
A |
G |
2: 144,112,325 (GRCm39) |
L8P |
probably benign |
Het |
Spg11 |
C |
T |
2: 121,945,152 (GRCm39) |
A123T |
probably damaging |
Het |
Supt6 |
T |
A |
11: 78,113,013 (GRCm39) |
I977F |
probably damaging |
Het |
Tjp3 |
T |
C |
10: 81,114,490 (GRCm39) |
D442G |
probably benign |
Het |
Ttc21b |
A |
T |
2: 66,068,200 (GRCm39) |
N275K |
probably benign |
Het |
Vmn2r50 |
A |
G |
7: 9,771,364 (GRCm39) |
F779S |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,345,482 (GRCm39) |
R2574S |
probably benign |
Het |
Zbp1 |
T |
C |
2: 173,054,038 (GRCm39) |
E161G |
possibly damaging |
Het |
|
Other mutations in Itga11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00933:Itga11
|
APN |
9 |
62,676,587 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01108:Itga11
|
APN |
9 |
62,664,903 (GRCm39) |
missense |
probably benign |
|
IGL01348:Itga11
|
APN |
9 |
62,651,861 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01918:Itga11
|
APN |
9 |
62,680,278 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02237:Itga11
|
APN |
9 |
62,663,057 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02418:Itga11
|
APN |
9 |
62,651,914 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02451:Itga11
|
APN |
9 |
62,642,635 (GRCm39) |
missense |
probably damaging |
1.00 |
sneezy
|
UTSW |
9 |
62,639,391 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4812001:Itga11
|
UTSW |
9 |
62,639,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Itga11
|
UTSW |
9 |
62,683,895 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0013:Itga11
|
UTSW |
9 |
62,683,895 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0032:Itga11
|
UTSW |
9 |
62,681,377 (GRCm39) |
missense |
probably benign |
0.05 |
R0032:Itga11
|
UTSW |
9 |
62,681,377 (GRCm39) |
missense |
probably benign |
0.05 |
R0101:Itga11
|
UTSW |
9 |
62,651,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R0114:Itga11
|
UTSW |
9 |
62,667,584 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0114:Itga11
|
UTSW |
9 |
62,642,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Itga11
|
UTSW |
9 |
62,653,251 (GRCm39) |
missense |
probably benign |
0.22 |
R0310:Itga11
|
UTSW |
9 |
62,667,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R0455:Itga11
|
UTSW |
9 |
62,604,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Itga11
|
UTSW |
9 |
62,659,570 (GRCm39) |
missense |
probably benign |
0.01 |
R0607:Itga11
|
UTSW |
9 |
62,681,653 (GRCm39) |
missense |
probably benign |
0.00 |
R0924:Itga11
|
UTSW |
9 |
62,683,956 (GRCm39) |
missense |
probably benign |
0.14 |
R1085:Itga11
|
UTSW |
9 |
62,585,252 (GRCm39) |
missense |
probably benign |
0.03 |
R1477:Itga11
|
UTSW |
9 |
62,662,493 (GRCm39) |
missense |
probably benign |
|
R1647:Itga11
|
UTSW |
9 |
62,667,652 (GRCm39) |
missense |
probably benign |
0.01 |
R1831:Itga11
|
UTSW |
9 |
62,689,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Itga11
|
UTSW |
9 |
62,585,231 (GRCm39) |
missense |
probably benign |
0.06 |
R1934:Itga11
|
UTSW |
9 |
62,651,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:Itga11
|
UTSW |
9 |
62,670,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R2046:Itga11
|
UTSW |
9 |
62,634,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Itga11
|
UTSW |
9 |
62,639,486 (GRCm39) |
splice site |
probably benign |
|
R2922:Itga11
|
UTSW |
9 |
62,675,912 (GRCm39) |
splice site |
probably benign |
|
R3011:Itga11
|
UTSW |
9 |
62,604,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R3158:Itga11
|
UTSW |
9 |
62,676,560 (GRCm39) |
missense |
probably benign |
0.02 |
R3809:Itga11
|
UTSW |
9 |
62,678,664 (GRCm39) |
missense |
probably benign |
|
R3836:Itga11
|
UTSW |
9 |
62,676,565 (GRCm39) |
missense |
probably benign |
0.00 |
R4051:Itga11
|
UTSW |
9 |
62,662,933 (GRCm39) |
nonsense |
probably null |
|
R4190:Itga11
|
UTSW |
9 |
62,639,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Itga11
|
UTSW |
9 |
62,668,870 (GRCm39) |
missense |
probably damaging |
0.96 |
R4511:Itga11
|
UTSW |
9 |
62,668,870 (GRCm39) |
missense |
probably damaging |
0.96 |
R4678:Itga11
|
UTSW |
9 |
62,642,639 (GRCm39) |
missense |
probably damaging |
0.98 |
R4706:Itga11
|
UTSW |
9 |
62,662,578 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4713:Itga11
|
UTSW |
9 |
62,673,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Itga11
|
UTSW |
9 |
62,684,009 (GRCm39) |
splice site |
probably null |
|
R4909:Itga11
|
UTSW |
9 |
62,662,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Itga11
|
UTSW |
9 |
62,659,530 (GRCm39) |
nonsense |
probably null |
|
R4957:Itga11
|
UTSW |
9 |
62,674,930 (GRCm39) |
missense |
probably benign |
0.00 |
R4962:Itga11
|
UTSW |
9 |
62,668,850 (GRCm39) |
nonsense |
probably null |
|
R5081:Itga11
|
UTSW |
9 |
62,662,478 (GRCm39) |
missense |
probably benign |
0.13 |
R5265:Itga11
|
UTSW |
9 |
62,644,694 (GRCm39) |
missense |
probably benign |
0.05 |
R5308:Itga11
|
UTSW |
9 |
62,663,051 (GRCm39) |
missense |
probably benign |
|
R5398:Itga11
|
UTSW |
9 |
62,653,205 (GRCm39) |
missense |
probably benign |
0.21 |
R5717:Itga11
|
UTSW |
9 |
62,659,531 (GRCm39) |
missense |
probably benign |
0.26 |
R5885:Itga11
|
UTSW |
9 |
62,670,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R5996:Itga11
|
UTSW |
9 |
62,662,955 (GRCm39) |
missense |
probably benign |
0.01 |
R6394:Itga11
|
UTSW |
9 |
62,642,548 (GRCm39) |
splice site |
probably null |
|
R6751:Itga11
|
UTSW |
9 |
62,675,866 (GRCm39) |
missense |
probably benign |
0.02 |
R7041:Itga11
|
UTSW |
9 |
62,659,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R7264:Itga11
|
UTSW |
9 |
62,653,190 (GRCm39) |
missense |
probably benign |
0.02 |
R7509:Itga11
|
UTSW |
9 |
62,689,222 (GRCm39) |
missense |
probably benign |
|
R7601:Itga11
|
UTSW |
9 |
62,604,208 (GRCm39) |
missense |
probably benign |
0.18 |
R7615:Itga11
|
UTSW |
9 |
62,651,300 (GRCm39) |
missense |
probably benign |
0.00 |
R8263:Itga11
|
UTSW |
9 |
62,604,262 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8285:Itga11
|
UTSW |
9 |
62,659,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R8419:Itga11
|
UTSW |
9 |
62,662,460 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8422:Itga11
|
UTSW |
9 |
62,674,960 (GRCm39) |
missense |
probably benign |
0.00 |
R8469:Itga11
|
UTSW |
9 |
62,678,680 (GRCm39) |
missense |
probably benign |
0.00 |
R8475:Itga11
|
UTSW |
9 |
62,651,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Itga11
|
UTSW |
9 |
62,668,823 (GRCm39) |
nonsense |
probably null |
|
R8904:Itga11
|
UTSW |
9 |
62,664,893 (GRCm39) |
missense |
probably benign |
|
R8954:Itga11
|
UTSW |
9 |
62,676,545 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8977:Itga11
|
UTSW |
9 |
62,662,922 (GRCm39) |
missense |
probably damaging |
0.98 |
R9011:Itga11
|
UTSW |
9 |
62,662,909 (GRCm39) |
missense |
probably benign |
0.43 |
R9038:Itga11
|
UTSW |
9 |
62,675,039 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9089:Itga11
|
UTSW |
9 |
62,678,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Itga11
|
UTSW |
9 |
62,659,678 (GRCm39) |
splice site |
probably benign |
|
R9327:Itga11
|
UTSW |
9 |
62,638,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R9487:Itga11
|
UTSW |
9 |
62,670,171 (GRCm39) |
missense |
probably benign |
0.35 |
R9794:Itga11
|
UTSW |
9 |
62,662,868 (GRCm39) |
missense |
probably benign |
0.00 |
|