Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd9 |
A |
T |
12: 110,943,497 (GRCm39) |
L179H |
probably benign |
Het |
Cacna1h |
C |
A |
17: 25,612,714 (GRCm39) |
A370S |
probably damaging |
Het |
Cc2d2a |
A |
T |
5: 43,876,019 (GRCm39) |
I1053F |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,721,230 (GRCm39) |
V1467A |
probably damaging |
Het |
Cyp4f15 |
T |
A |
17: 32,911,586 (GRCm39) |
L156* |
probably null |
Het |
Dmwd |
T |
A |
7: 18,814,652 (GRCm39) |
L434Q |
probably damaging |
Het |
Dtx4 |
T |
A |
19: 12,450,599 (GRCm39) |
R538* |
probably null |
Het |
Fcgbp |
T |
A |
7: 27,785,695 (GRCm39) |
C377* |
probably null |
Het |
Galntl6 |
G |
T |
8: 58,880,804 (GRCm39) |
H116Q |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,391,148 (GRCm39) |
|
probably null |
Het |
Hydin |
T |
G |
8: 111,053,092 (GRCm39) |
S255A |
probably benign |
Het |
Knstrn |
G |
A |
2: 118,644,723 (GRCm39) |
A48T |
probably damaging |
Het |
Lonrf2 |
T |
C |
1: 38,852,470 (GRCm39) |
D127G |
probably benign |
Het |
Luzp1 |
T |
C |
4: 136,272,609 (GRCm39) |
S12P |
possibly damaging |
Het |
Man2c1 |
A |
T |
9: 57,048,875 (GRCm39) |
H822L |
probably benign |
Het |
Map3k13 |
G |
T |
16: 21,741,028 (GRCm39) |
G785V |
probably benign |
Het |
Mia2 |
A |
G |
12: 59,219,366 (GRCm39) |
H454R |
probably damaging |
Het |
Mib2 |
G |
A |
4: 155,745,629 (GRCm39) |
R61C |
probably damaging |
Het |
Muc15 |
A |
T |
2: 110,561,616 (GRCm39) |
L17F |
probably damaging |
Het |
Myo1c |
C |
T |
11: 75,562,461 (GRCm39) |
P918S |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,114,652 (GRCm39) |
I879V |
probably benign |
Het |
Nomo1 |
T |
A |
7: 45,715,885 (GRCm39) |
S751T |
probably benign |
Het |
Or1j10 |
A |
T |
2: 36,267,117 (GRCm39) |
S110C |
probably benign |
Het |
Or5b24 |
A |
T |
19: 12,912,764 (GRCm39) |
I221L |
possibly damaging |
Het |
Or5g27 |
A |
G |
2: 85,409,793 (GRCm39) |
D70G |
probably damaging |
Het |
Pcdhac2 |
A |
G |
18: 37,278,256 (GRCm39) |
N412S |
probably benign |
Het |
Plk5 |
T |
C |
10: 80,196,035 (GRCm39) |
S235P |
probably benign |
Het |
Ppm1j |
A |
G |
3: 104,692,802 (GRCm39) |
D437G |
probably damaging |
Het |
Rab11fip1 |
T |
C |
8: 27,633,262 (GRCm39) |
E1148G |
probably damaging |
Het |
Rad9b |
T |
C |
5: 122,489,754 (GRCm39) |
N43S |
probably damaging |
Het |
Rc3h2 |
A |
C |
2: 37,304,673 (GRCm39) |
I29S |
possibly damaging |
Het |
Rsf1 |
CG |
CGACGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Homo |
Spdl1 |
T |
A |
11: 34,713,830 (GRCm39) |
|
probably null |
Het |
Spta1 |
A |
T |
1: 174,071,608 (GRCm39) |
|
probably null |
Het |
Stk32c |
A |
T |
7: 138,702,880 (GRCm39) |
V53E |
probably damaging |
Het |
Sugct |
T |
G |
13: 17,497,815 (GRCm39) |
N286T |
possibly damaging |
Het |
Swsap1 |
A |
T |
9: 21,867,971 (GRCm39) |
|
probably null |
Het |
Thbs2 |
T |
A |
17: 14,894,426 (GRCm39) |
D807V |
possibly damaging |
Het |
Tnrc6b |
A |
G |
15: 80,763,974 (GRCm39) |
D492G |
probably damaging |
Het |
Tonsl |
A |
T |
15: 76,514,018 (GRCm39) |
S1184T |
possibly damaging |
Het |
Tpp2 |
T |
A |
1: 44,022,436 (GRCm39) |
Y945N |
probably benign |
Het |
Usp54 |
G |
T |
14: 20,610,937 (GRCm39) |
A1293D |
possibly damaging |
Het |
Vps52 |
A |
T |
17: 34,182,173 (GRCm39) |
K516* |
probably null |
Het |
Zbtb17 |
T |
A |
4: 141,189,110 (GRCm39) |
V10D |
probably damaging |
Het |
Zfp607b |
T |
C |
7: 27,403,464 (GRCm39) |
V640A |
probably benign |
Het |
|
Other mutations in Strc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01102:Strc
|
APN |
2 |
121,195,541 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01152:Strc
|
APN |
2 |
121,201,276 (GRCm39) |
missense |
probably benign |
|
IGL01608:Strc
|
APN |
2 |
121,206,075 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01695:Strc
|
APN |
2 |
121,205,779 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01715:Strc
|
APN |
2 |
121,196,218 (GRCm39) |
splice site |
probably null |
|
IGL01906:Strc
|
APN |
2 |
121,208,115 (GRCm39) |
missense |
probably benign |
|
IGL02135:Strc
|
APN |
2 |
121,195,315 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Strc
|
APN |
2 |
121,199,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Strc
|
APN |
2 |
121,206,272 (GRCm39) |
unclassified |
probably benign |
|
IGL03029:Strc
|
APN |
2 |
121,194,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03176:Strc
|
APN |
2 |
121,202,661 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03272:Strc
|
APN |
2 |
121,202,232 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Strc
|
UTSW |
2 |
121,204,161 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02799:Strc
|
UTSW |
2 |
121,209,717 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Strc
|
UTSW |
2 |
121,205,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Strc
|
UTSW |
2 |
121,198,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Strc
|
UTSW |
2 |
121,210,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R1065:Strc
|
UTSW |
2 |
121,197,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Strc
|
UTSW |
2 |
121,202,558 (GRCm39) |
intron |
probably benign |
|
R1148:Strc
|
UTSW |
2 |
121,202,558 (GRCm39) |
intron |
probably benign |
|
R1203:Strc
|
UTSW |
2 |
121,202,604 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1343:Strc
|
UTSW |
2 |
121,195,596 (GRCm39) |
missense |
probably benign |
0.21 |
R1544:Strc
|
UTSW |
2 |
121,203,219 (GRCm39) |
splice site |
probably null |
|
R1650:Strc
|
UTSW |
2 |
121,211,366 (GRCm39) |
start gained |
probably benign |
|
R1840:Strc
|
UTSW |
2 |
121,209,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Strc
|
UTSW |
2 |
121,201,518 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2035:Strc
|
UTSW |
2 |
121,205,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Strc
|
UTSW |
2 |
121,209,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2158:Strc
|
UTSW |
2 |
121,196,343 (GRCm39) |
missense |
probably benign |
0.10 |
R2219:Strc
|
UTSW |
2 |
121,195,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Strc
|
UTSW |
2 |
121,195,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R4375:Strc
|
UTSW |
2 |
121,211,304 (GRCm39) |
missense |
unknown |
|
R4563:Strc
|
UTSW |
2 |
121,196,286 (GRCm39) |
missense |
probably benign |
0.02 |
R4578:Strc
|
UTSW |
2 |
121,208,484 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4607:Strc
|
UTSW |
2 |
121,203,426 (GRCm39) |
missense |
probably benign |
0.31 |
R4651:Strc
|
UTSW |
2 |
121,204,829 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4652:Strc
|
UTSW |
2 |
121,204,829 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4790:Strc
|
UTSW |
2 |
121,206,075 (GRCm39) |
missense |
probably benign |
0.05 |
R5480:Strc
|
UTSW |
2 |
121,195,300 (GRCm39) |
missense |
probably benign |
0.00 |
R5580:Strc
|
UTSW |
2 |
121,205,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R5679:Strc
|
UTSW |
2 |
121,198,581 (GRCm39) |
missense |
probably benign |
0.03 |
R5703:Strc
|
UTSW |
2 |
121,201,295 (GRCm39) |
missense |
probably benign |
|
R5841:Strc
|
UTSW |
2 |
121,196,358 (GRCm39) |
missense |
probably benign |
0.29 |
R5917:Strc
|
UTSW |
2 |
121,209,790 (GRCm39) |
missense |
probably benign |
|
R5958:Strc
|
UTSW |
2 |
121,207,403 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6320:Strc
|
UTSW |
2 |
121,205,439 (GRCm39) |
missense |
probably benign |
0.16 |
R6619:Strc
|
UTSW |
2 |
121,198,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R6970:Strc
|
UTSW |
2 |
121,208,495 (GRCm39) |
missense |
probably benign |
0.41 |
R7018:Strc
|
UTSW |
2 |
121,199,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Strc
|
UTSW |
2 |
121,201,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Strc
|
UTSW |
2 |
121,199,507 (GRCm39) |
missense |
probably benign |
0.14 |
R7283:Strc
|
UTSW |
2 |
121,209,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R7694:Strc
|
UTSW |
2 |
121,207,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Strc
|
UTSW |
2 |
121,202,229 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7700:Strc
|
UTSW |
2 |
121,202,229 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7756:Strc
|
UTSW |
2 |
121,201,427 (GRCm39) |
missense |
probably benign |
|
R7758:Strc
|
UTSW |
2 |
121,201,427 (GRCm39) |
missense |
probably benign |
|
R7822:Strc
|
UTSW |
2 |
121,208,219 (GRCm39) |
missense |
probably benign |
0.01 |
R7830:Strc
|
UTSW |
2 |
121,205,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R7953:Strc
|
UTSW |
2 |
121,207,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R8137:Strc
|
UTSW |
2 |
121,197,219 (GRCm39) |
missense |
probably damaging |
0.98 |
R8394:Strc
|
UTSW |
2 |
121,209,490 (GRCm39) |
missense |
probably benign |
0.00 |
R8427:Strc
|
UTSW |
2 |
121,208,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Strc
|
UTSW |
2 |
121,208,286 (GRCm39) |
missense |
probably damaging |
0.99 |
R8874:Strc
|
UTSW |
2 |
121,205,353 (GRCm39) |
critical splice donor site |
probably null |
|
R8947:Strc
|
UTSW |
2 |
121,201,470 (GRCm39) |
missense |
probably benign |
0.09 |
R9285:Strc
|
UTSW |
2 |
121,195,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Strc
|
UTSW |
2 |
121,211,336 (GRCm39) |
missense |
unknown |
|
R9386:Strc
|
UTSW |
2 |
121,198,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R9438:Strc
|
UTSW |
2 |
121,198,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Strc
|
UTSW |
2 |
121,207,928 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Strc
|
UTSW |
2 |
121,209,525 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Strc
|
UTSW |
2 |
121,206,002 (GRCm39) |
missense |
probably damaging |
0.98 |
|