Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
C |
A |
11: 100,370,081 (GRCm39) |
V994F |
probably damaging |
Het |
Arfgap3 |
T |
C |
15: 83,214,741 (GRCm39) |
T182A |
probably benign |
Het |
Bcl2l14 |
T |
C |
6: 134,409,102 (GRCm39) |
|
probably benign |
Het |
Cabin1 |
T |
C |
10: 75,553,511 (GRCm39) |
M1183V |
possibly damaging |
Het |
Ccr7 |
A |
T |
11: 99,036,103 (GRCm39) |
I273K |
possibly damaging |
Het |
Cd40 |
A |
G |
2: 164,912,681 (GRCm39) |
M211V |
possibly damaging |
Het |
Coro2b |
T |
G |
9: 62,338,609 (GRCm39) |
E208A |
probably damaging |
Het |
Dennd5a |
A |
C |
7: 109,517,968 (GRCm39) |
M556R |
probably damaging |
Het |
Efcab2 |
A |
T |
1: 178,265,062 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
T |
C |
1: 63,787,114 (GRCm39) |
|
probably benign |
Het |
Fbxw8 |
A |
C |
5: 118,215,636 (GRCm39) |
|
probably benign |
Het |
Fhip1a |
T |
C |
3: 85,629,802 (GRCm39) |
E263G |
probably benign |
Het |
Frem1 |
T |
C |
4: 82,939,007 (GRCm39) |
D25G |
probably benign |
Het |
Ift52 |
A |
G |
2: 162,871,702 (GRCm39) |
K178R |
probably benign |
Het |
Kit |
T |
C |
5: 75,810,192 (GRCm39) |
|
probably benign |
Het |
Map1a |
T |
C |
2: 121,137,859 (GRCm39) |
|
probably null |
Het |
Mxra7 |
G |
T |
11: 116,701,696 (GRCm39) |
|
probably benign |
Het |
Myt1 |
C |
A |
2: 181,453,024 (GRCm39) |
S7* |
probably null |
Het |
Nphs1 |
C |
T |
7: 30,180,803 (GRCm39) |
|
probably benign |
Het |
Or10h28 |
C |
T |
17: 33,487,940 (GRCm39) |
R81* |
probably null |
Het |
Or1l8 |
C |
A |
2: 36,817,514 (GRCm39) |
G204V |
possibly damaging |
Het |
Osgin2 |
A |
T |
4: 15,998,085 (GRCm39) |
D512E |
possibly damaging |
Het |
Pde4b |
T |
A |
4: 102,399,352 (GRCm39) |
|
probably benign |
Het |
Rasef |
G |
T |
4: 73,666,841 (GRCm39) |
T146K |
possibly damaging |
Het |
Ren1 |
T |
A |
1: 133,284,256 (GRCm39) |
V207D |
probably damaging |
Het |
S100a8 |
A |
G |
3: 90,577,180 (GRCm39) |
D59G |
probably damaging |
Het |
Sdcbp |
G |
A |
4: 6,377,143 (GRCm39) |
|
probably null |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Slamf7 |
A |
T |
1: 171,466,751 (GRCm39) |
D151E |
probably benign |
Het |
Slco1b2 |
A |
G |
6: 141,628,980 (GRCm39) |
M561V |
probably benign |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Stard9 |
T |
C |
2: 120,523,331 (GRCm39) |
I662T |
probably benign |
Het |
Vwf |
T |
A |
6: 125,632,028 (GRCm39) |
V20D |
unknown |
Het |
Znhit6 |
G |
T |
3: 145,300,440 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gtf3c3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Gtf3c3
|
APN |
1 |
54,455,114 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00435:Gtf3c3
|
APN |
1 |
54,466,694 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01128:Gtf3c3
|
APN |
1 |
54,468,035 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0243:Gtf3c3
|
UTSW |
1 |
54,442,695 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0271:Gtf3c3
|
UTSW |
1 |
54,467,971 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0571:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R0965:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R0968:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1069:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1111:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1112:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1113:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1114:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1117:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1119:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1228:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1230:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1231:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1313:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1313:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1382:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1397:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1414:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1497:Gtf3c3
|
UTSW |
1 |
54,477,098 (GRCm39) |
missense |
probably benign |
|
R1556:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Gtf3c3
|
UTSW |
1 |
54,444,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Gtf3c3
|
UTSW |
1 |
54,438,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Gtf3c3
|
UTSW |
1 |
54,473,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1767:Gtf3c3
|
UTSW |
1 |
54,456,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1799:Gtf3c3
|
UTSW |
1 |
54,459,583 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1861:Gtf3c3
|
UTSW |
1 |
54,477,997 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1940:Gtf3c3
|
UTSW |
1 |
54,468,117 (GRCm39) |
splice site |
probably benign |
|
R3804:Gtf3c3
|
UTSW |
1 |
54,463,166 (GRCm39) |
critical splice donor site |
probably null |
|
R4496:Gtf3c3
|
UTSW |
1 |
54,463,291 (GRCm39) |
missense |
probably benign |
0.03 |
R4621:Gtf3c3
|
UTSW |
1 |
54,458,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R5131:Gtf3c3
|
UTSW |
1 |
54,458,657 (GRCm39) |
splice site |
probably null |
|
R5320:Gtf3c3
|
UTSW |
1 |
54,445,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5605:Gtf3c3
|
UTSW |
1 |
54,455,085 (GRCm39) |
missense |
probably benign |
0.06 |
R5854:Gtf3c3
|
UTSW |
1 |
54,458,596 (GRCm39) |
missense |
probably benign |
0.01 |
R6050:Gtf3c3
|
UTSW |
1 |
54,445,229 (GRCm39) |
missense |
probably benign |
0.00 |
R6441:Gtf3c3
|
UTSW |
1 |
54,445,197 (GRCm39) |
missense |
probably benign |
0.03 |
R6892:Gtf3c3
|
UTSW |
1 |
54,455,100 (GRCm39) |
missense |
probably benign |
0.00 |
R7114:Gtf3c3
|
UTSW |
1 |
54,462,666 (GRCm39) |
missense |
probably benign |
|
R7299:Gtf3c3
|
UTSW |
1 |
54,456,867 (GRCm39) |
missense |
probably benign |
0.01 |
R7441:Gtf3c3
|
UTSW |
1 |
54,459,607 (GRCm39) |
missense |
probably benign |
0.00 |
R7586:Gtf3c3
|
UTSW |
1 |
54,442,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R7615:Gtf3c3
|
UTSW |
1 |
54,462,731 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7634:Gtf3c3
|
UTSW |
1 |
54,458,800 (GRCm39) |
splice site |
probably null |
|
R7739:Gtf3c3
|
UTSW |
1 |
54,444,198 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8349:Gtf3c3
|
UTSW |
1 |
54,468,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8449:Gtf3c3
|
UTSW |
1 |
54,468,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Gtf3c3
|
UTSW |
1 |
54,468,031 (GRCm39) |
missense |
probably benign |
|
R8955:Gtf3c3
|
UTSW |
1 |
54,462,722 (GRCm39) |
missense |
probably benign |
0.00 |
R9290:Gtf3c3
|
UTSW |
1 |
54,477,997 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9353:Gtf3c3
|
UTSW |
1 |
54,445,211 (GRCm39) |
missense |
possibly damaging |
0.70 |
|