Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
C |
T |
16: 20,367,430 (GRCm39) |
T3I |
probably benign |
Het |
Ahi1 |
T |
A |
10: 20,862,976 (GRCm39) |
V717E |
probably damaging |
Het |
Anapc4 |
A |
G |
5: 53,002,672 (GRCm39) |
T238A |
probably damaging |
Het |
Arhgap27 |
A |
T |
11: 103,251,367 (GRCm39) |
C120* |
probably null |
Het |
Bdp1 |
A |
T |
13: 100,178,040 (GRCm39) |
V1943D |
probably damaging |
Het |
Cdc14b |
A |
G |
13: 64,373,461 (GRCm39) |
V141A |
probably damaging |
Het |
Cfap46 |
G |
T |
7: 139,215,062 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
C |
A |
9: 71,633,165 (GRCm39) |
R62L |
possibly damaging |
Het |
Chaf1a |
A |
G |
17: 56,369,573 (GRCm39) |
S522G |
probably benign |
Het |
Cox19 |
A |
G |
5: 139,328,402 (GRCm39) |
F37S |
probably damaging |
Het |
Csmd1 |
G |
A |
8: 16,108,721 (GRCm39) |
S1894L |
probably damaging |
Het |
Cyp4a12a |
A |
T |
4: 115,184,756 (GRCm39) |
R346W |
probably damaging |
Het |
Dip2a |
A |
C |
10: 76,108,396 (GRCm39) |
C1315G |
probably benign |
Het |
Dmxl2 |
A |
C |
9: 54,308,869 (GRCm39) |
W1961G |
probably damaging |
Het |
Dst |
T |
C |
1: 34,240,486 (GRCm39) |
L1945P |
probably damaging |
Het |
Efr3a |
A |
G |
15: 65,691,627 (GRCm39) |
S92G |
probably damaging |
Het |
Ep300 |
C |
T |
15: 81,511,515 (GRCm39) |
T865I |
unknown |
Het |
Ercc6 |
A |
G |
14: 32,248,361 (GRCm39) |
E304G |
probably benign |
Het |
Filip1l |
A |
C |
16: 57,391,300 (GRCm39) |
E629D |
probably damaging |
Het |
Frem1 |
G |
A |
4: 82,938,992 (GRCm39) |
T30I |
possibly damaging |
Het |
Glb1 |
T |
C |
9: 114,246,126 (GRCm39) |
F59S |
probably benign |
Het |
Gli3 |
T |
C |
13: 15,900,144 (GRCm39) |
L1177P |
probably benign |
Het |
Gpatch2l |
A |
G |
12: 86,303,646 (GRCm39) |
T223A |
probably damaging |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,479,565 (GRCm39) |
M4633K |
probably benign |
Het |
Hoxc8 |
T |
A |
15: 102,899,542 (GRCm39) |
Y111N |
probably damaging |
Het |
Ifi207 |
A |
G |
1: 173,556,581 (GRCm39) |
L726P |
probably benign |
Het |
Iqcn |
T |
A |
8: 71,169,453 (GRCm39) |
M1181K |
possibly damaging |
Het |
Iqgap2 |
T |
A |
13: 95,772,163 (GRCm39) |
M1339L |
probably benign |
Het |
Kif21b |
A |
G |
1: 136,087,387 (GRCm39) |
Q901R |
possibly damaging |
Het |
Krtap4-8 |
C |
A |
11: 99,671,234 (GRCm39) |
C79F |
unknown |
Het |
Ldb3 |
T |
C |
14: 34,293,759 (GRCm39) |
N155S |
probably damaging |
Het |
Mad2l1 |
T |
A |
6: 66,516,794 (GRCm39) |
V162E |
probably benign |
Het |
Map7 |
T |
A |
10: 20,109,208 (GRCm39) |
V87E |
unknown |
Het |
Mndal |
A |
T |
1: 173,703,185 (GRCm39) |
D73E |
unknown |
Het |
Msantd1 |
T |
C |
5: 35,075,039 (GRCm39) |
S34P |
probably damaging |
Het |
Myh14 |
T |
C |
7: 44,260,977 (GRCm39) |
Q1838R |
possibly damaging |
Het |
Myh15 |
G |
T |
16: 48,993,369 (GRCm39) |
R1668L |
possibly damaging |
Het |
Ncoa7 |
A |
G |
10: 30,565,796 (GRCm39) |
M666T |
probably damaging |
Het |
Nol6 |
A |
T |
4: 41,116,686 (GRCm39) |
L944Q |
probably benign |
Het |
Or5h27 |
A |
T |
16: 59,006,376 (GRCm39) |
F157I |
unknown |
Het |
Orc1 |
A |
G |
4: 108,445,911 (GRCm39) |
T10A |
probably benign |
Het |
Pcp4l1 |
G |
A |
1: 171,002,034 (GRCm39) |
A42V |
possibly damaging |
Het |
Pglyrp2 |
C |
T |
17: 32,634,893 (GRCm39) |
A490T |
probably benign |
Het |
Pirb |
A |
T |
7: 3,720,187 (GRCm39) |
C395* |
probably null |
Het |
Ppp1r11 |
T |
C |
17: 37,261,900 (GRCm39) |
R12G |
possibly damaging |
Het |
Prlr |
A |
G |
15: 10,346,524 (GRCm39) |
D290G |
probably benign |
Het |
Ptpn21 |
G |
T |
12: 98,646,360 (GRCm39) |
R1033S |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,570,660 (GRCm39) |
L1220P |
possibly damaging |
Het |
Rufy3 |
G |
A |
5: 88,790,811 (GRCm39) |
R504H |
probably damaging |
Het |
Scgb2b21 |
C |
T |
7: 33,219,330 (GRCm39) |
V25I |
probably benign |
Het |
Sh3bgrl2 |
T |
C |
9: 83,430,542 (GRCm39) |
S11P |
possibly damaging |
Het |
Slain2 |
A |
T |
5: 73,132,002 (GRCm39) |
T498S |
probably benign |
Het |
Slc12a4 |
C |
T |
8: 106,682,347 (GRCm39) |
G121S |
probably damaging |
Het |
Slc30a9 |
A |
T |
5: 67,499,462 (GRCm39) |
I307F |
probably damaging |
Het |
Snap91 |
C |
T |
9: 86,655,598 (GRCm39) |
G800R |
unknown |
Het |
Tnc |
G |
T |
4: 63,882,999 (GRCm39) |
|
probably null |
Het |
Trav21-dv12 |
T |
C |
14: 54,113,514 (GRCm39) |
|
probably benign |
Het |
Vac14 |
T |
C |
8: 111,438,252 (GRCm39) |
Y622H |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Wdr35 |
T |
G |
12: 9,037,312 (GRCm39) |
M306R |
probably benign |
Het |
Zan |
A |
T |
5: 137,463,494 (GRCm39) |
S562T |
probably benign |
Het |
|
Other mutations in Txk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02337:Txk
|
APN |
5 |
72,864,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02602:Txk
|
APN |
5 |
72,865,063 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03353:Txk
|
APN |
5 |
72,893,745 (GRCm39) |
missense |
probably benign |
|
BB007:Txk
|
UTSW |
5 |
72,892,536 (GRCm39) |
missense |
probably damaging |
1.00 |
BB017:Txk
|
UTSW |
5 |
72,892,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Txk
|
UTSW |
5 |
72,889,105 (GRCm39) |
critical splice donor site |
probably null |
|
R1509:Txk
|
UTSW |
5 |
72,856,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Txk
|
UTSW |
5 |
72,865,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2913:Txk
|
UTSW |
5 |
72,881,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R2914:Txk
|
UTSW |
5 |
72,881,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R3722:Txk
|
UTSW |
5 |
72,865,078 (GRCm39) |
nonsense |
probably null |
|
R4080:Txk
|
UTSW |
5 |
72,858,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Txk
|
UTSW |
5 |
72,853,964 (GRCm39) |
missense |
probably benign |
0.08 |
R5580:Txk
|
UTSW |
5 |
72,864,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Txk
|
UTSW |
5 |
72,858,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R6310:Txk
|
UTSW |
5 |
72,893,760 (GRCm39) |
missense |
probably benign |
0.01 |
R6382:Txk
|
UTSW |
5 |
72,893,823 (GRCm39) |
intron |
probably benign |
|
R6938:Txk
|
UTSW |
5 |
72,856,492 (GRCm39) |
missense |
probably damaging |
0.99 |
R7225:Txk
|
UTSW |
5 |
72,858,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7337:Txk
|
UTSW |
5 |
72,889,109 (GRCm39) |
nonsense |
probably null |
|
R7436:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Txk
|
UTSW |
5 |
72,893,726 (GRCm39) |
missense |
unknown |
|
R7709:Txk
|
UTSW |
5 |
72,864,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Txk
|
UTSW |
5 |
72,864,900 (GRCm39) |
missense |
probably damaging |
0.96 |
R7930:Txk
|
UTSW |
5 |
72,892,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Txk
|
UTSW |
5 |
72,860,606 (GRCm39) |
splice site |
probably null |
|
R8531:Txk
|
UTSW |
5 |
72,893,720 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8754:Txk
|
UTSW |
5 |
72,889,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8901:Txk
|
UTSW |
5 |
72,858,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Txk
|
UTSW |
5 |
72,891,610 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Txk
|
UTSW |
5 |
72,892,554 (GRCm39) |
missense |
unknown |
|
|