Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
C |
A |
8: 41,279,357 (GRCm39) |
R583S |
probably benign |
Het |
Bcl9l |
C |
T |
9: 44,416,560 (GRCm39) |
T211I |
possibly damaging |
Het |
C6 |
A |
G |
15: 4,827,802 (GRCm39) |
I724V |
probably benign |
Het |
Cacna2d4 |
T |
A |
6: 119,247,710 (GRCm39) |
|
probably null |
Het |
Casp4 |
A |
G |
9: 5,322,844 (GRCm39) |
E40G |
possibly damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Dnah7a |
A |
C |
1: 53,483,631 (GRCm39) |
M3382R |
possibly damaging |
Het |
Dst |
T |
C |
1: 34,235,033 (GRCm39) |
L3526P |
probably damaging |
Het |
Eya4 |
A |
G |
10: 23,035,008 (GRCm39) |
S116P |
probably benign |
Het |
Gabra4 |
T |
A |
5: 71,729,510 (GRCm39) |
E423D |
probably benign |
Het |
Ighv1-67 |
T |
G |
12: 115,567,643 (GRCm39) |
T90P |
probably damaging |
Het |
Kcnh8 |
A |
G |
17: 53,266,471 (GRCm39) |
T828A |
probably benign |
Het |
Nr5a2 |
A |
G |
1: 136,868,145 (GRCm39) |
|
probably null |
Het |
Nup214 |
C |
T |
2: 31,921,287 (GRCm39) |
P1237S |
probably benign |
Het |
Phactr3 |
A |
G |
2: 177,920,792 (GRCm39) |
D215G |
probably damaging |
Het |
Phf2 |
G |
T |
13: 48,959,315 (GRCm39) |
P897Q |
unknown |
Het |
Pla2r1 |
T |
C |
2: 60,285,545 (GRCm39) |
R690G |
probably damaging |
Het |
Ppargc1b |
A |
G |
18: 61,445,314 (GRCm39) |
S181P |
possibly damaging |
Het |
Sele |
A |
T |
1: 163,877,699 (GRCm39) |
I165F |
probably damaging |
Het |
Srcap |
T |
C |
7: 127,141,625 (GRCm39) |
S1626P |
probably benign |
Het |
Tenm2 |
A |
G |
11: 35,959,285 (GRCm39) |
I1088T |
probably benign |
Het |
Tnrc18 |
T |
C |
5: 142,775,927 (GRCm39) |
S69G |
probably damaging |
Het |
Trmt5 |
C |
A |
12: 73,328,232 (GRCm39) |
E324* |
probably null |
Het |
Zfp277 |
A |
G |
12: 40,378,687 (GRCm39) |
V390A |
possibly damaging |
Het |
|
Other mutations in Ttll3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01338:Ttll3
|
APN |
6 |
113,371,690 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01677:Ttll3
|
APN |
6 |
113,389,945 (GRCm39) |
missense |
probably benign |
|
IGL01697:Ttll3
|
APN |
6 |
113,376,690 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01944:Ttll3
|
APN |
6 |
113,391,076 (GRCm39) |
missense |
probably benign |
|
IGL03068:Ttll3
|
APN |
6 |
113,386,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Ttll3
|
UTSW |
6 |
113,375,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R0472:Ttll3
|
UTSW |
6 |
113,386,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R0625:Ttll3
|
UTSW |
6 |
113,385,864 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1868:Ttll3
|
UTSW |
6 |
113,369,725 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2026:Ttll3
|
UTSW |
6 |
113,375,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Ttll3
|
UTSW |
6 |
113,386,003 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2128:Ttll3
|
UTSW |
6 |
113,389,895 (GRCm39) |
missense |
probably benign |
0.31 |
R2896:Ttll3
|
UTSW |
6 |
113,369,683 (GRCm39) |
missense |
probably benign |
0.15 |
R2903:Ttll3
|
UTSW |
6 |
113,384,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R2906:Ttll3
|
UTSW |
6 |
113,369,471 (GRCm39) |
unclassified |
probably benign |
|
R4659:Ttll3
|
UTSW |
6 |
113,391,102 (GRCm39) |
missense |
probably benign |
|
R4746:Ttll3
|
UTSW |
6 |
113,384,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Ttll3
|
UTSW |
6 |
113,389,901 (GRCm39) |
missense |
probably benign |
0.00 |
R5358:Ttll3
|
UTSW |
6 |
113,378,292 (GRCm39) |
missense |
probably benign |
0.26 |
R5372:Ttll3
|
UTSW |
6 |
113,378,382 (GRCm39) |
nonsense |
probably null |
|
R5525:Ttll3
|
UTSW |
6 |
113,389,939 (GRCm39) |
missense |
probably benign |
|
R5548:Ttll3
|
UTSW |
6 |
113,370,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5694:Ttll3
|
UTSW |
6 |
113,376,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R5993:Ttll3
|
UTSW |
6 |
113,374,992 (GRCm39) |
nonsense |
probably null |
|
R6119:Ttll3
|
UTSW |
6 |
113,371,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6268:Ttll3
|
UTSW |
6 |
113,369,524 (GRCm39) |
missense |
probably benign |
0.00 |
R6719:Ttll3
|
UTSW |
6 |
113,375,993 (GRCm39) |
intron |
probably benign |
|
R6852:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
R6852:Ttll3
|
UTSW |
6 |
113,376,116 (GRCm39) |
frame shift |
probably null |
|
R6852:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R6853:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R6854:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7170:Ttll3
|
UTSW |
6 |
113,390,839 (GRCm39) |
missense |
probably benign |
0.41 |
R7239:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7302:Ttll3
|
UTSW |
6 |
113,386,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R7330:Ttll3
|
UTSW |
6 |
113,376,125 (GRCm39) |
frame shift |
probably null |
|
R7330:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7586:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7587:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7701:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7702:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7776:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
R7793:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
R7797:Ttll3
|
UTSW |
6 |
113,371,738 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7824:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7825:Ttll3
|
UTSW |
6 |
113,376,120 (GRCm39) |
frame shift |
probably null |
|
R7825:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7826:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7827:Ttll3
|
UTSW |
6 |
113,376,123 (GRCm39) |
frame shift |
probably null |
|
R7827:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7831:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7832:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R7833:Ttll3
|
UTSW |
6 |
113,386,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R7966:Ttll3
|
UTSW |
6 |
113,376,118 (GRCm39) |
frame shift |
probably null |
|
R8344:Ttll3
|
UTSW |
6 |
113,371,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R8418:Ttll3
|
UTSW |
6 |
113,371,734 (GRCm39) |
missense |
probably benign |
0.04 |
R8768:Ttll3
|
UTSW |
6 |
113,385,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9017:Ttll3
|
UTSW |
6 |
113,389,850 (GRCm39) |
missense |
probably benign |
0.00 |
R9036:Ttll3
|
UTSW |
6 |
113,376,657 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9090:Ttll3
|
UTSW |
6 |
113,369,596 (GRCm39) |
missense |
probably benign |
|
R9271:Ttll3
|
UTSW |
6 |
113,369,596 (GRCm39) |
missense |
probably benign |
|
R9329:Ttll3
|
UTSW |
6 |
113,369,635 (GRCm39) |
missense |
probably benign |
|
R9532:Ttll3
|
UTSW |
6 |
113,385,970 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9535:Ttll3
|
UTSW |
6 |
113,389,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R9725:Ttll3
|
UTSW |
6 |
113,386,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|