Other mutations in this stock |
Total: 9 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Bltp1 |
A |
T |
3: 37,084,900 (GRCm39) |
|
probably null |
Het |
Col22a1 |
C |
T |
15: 71,718,026 (GRCm39) |
G633E |
unknown |
Het |
Kcnh5 |
G |
A |
12: 75,054,450 (GRCm39) |
P498L |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,374,498 (GRCm39) |
V1879A |
probably benign |
Het |
Rif1 |
T |
C |
2: 52,009,129 (GRCm39) |
S2303P |
probably damaging |
Het |
Sis |
G |
T |
3: 72,850,912 (GRCm39) |
N595K |
probably damaging |
Het |
Tfpi2 |
T |
C |
6: 3,963,414 (GRCm39) |
D220G |
probably benign |
Het |
Ttk |
T |
C |
9: 83,745,501 (GRCm39) |
I616T |
probably damaging |
Het |
Usp49 |
A |
G |
17: 47,991,628 (GRCm39) |
D630G |
probably damaging |
Het |
|
Other mutations in Ttc21b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Ttc21b
|
APN |
2 |
66,073,119 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00467:Ttc21b
|
APN |
2 |
66,018,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00837:Ttc21b
|
APN |
2 |
66,065,915 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01317:Ttc21b
|
APN |
2 |
66,018,700 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01485:Ttc21b
|
APN |
2 |
66,082,234 (GRCm39) |
splice site |
probably benign |
|
IGL01739:Ttc21b
|
APN |
2 |
66,068,200 (GRCm39) |
missense |
probably benign |
|
IGL02282:Ttc21b
|
APN |
2 |
66,022,081 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02431:Ttc21b
|
APN |
2 |
66,082,229 (GRCm39) |
splice site |
probably benign |
|
IGL02478:Ttc21b
|
APN |
2 |
66,018,624 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02487:Ttc21b
|
APN |
2 |
66,065,500 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03327:Ttc21b
|
APN |
2 |
66,068,192 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03346:Ttc21b
|
APN |
2 |
66,068,192 (GRCm39) |
missense |
possibly damaging |
0.92 |
plus-sized
|
UTSW |
2 |
66,073,023 (GRCm39) |
missense |
probably damaging |
1.00 |
puffer
|
UTSW |
2 |
66,057,244 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4696001:Ttc21b
|
UTSW |
2 |
66,061,563 (GRCm39) |
splice site |
probably null |
|
R0049:Ttc21b
|
UTSW |
2 |
66,053,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Ttc21b
|
UTSW |
2 |
66,053,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Ttc21b
|
UTSW |
2 |
66,018,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R0440:Ttc21b
|
UTSW |
2 |
66,066,726 (GRCm39) |
missense |
probably benign |
0.03 |
R0504:Ttc21b
|
UTSW |
2 |
66,053,142 (GRCm39) |
splice site |
probably benign |
|
R0600:Ttc21b
|
UTSW |
2 |
66,069,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R0621:Ttc21b
|
UTSW |
2 |
66,056,355 (GRCm39) |
missense |
probably benign |
0.07 |
R0633:Ttc21b
|
UTSW |
2 |
66,066,577 (GRCm39) |
missense |
probably benign |
|
R0863:Ttc21b
|
UTSW |
2 |
66,073,117 (GRCm39) |
missense |
probably benign |
|
R1617:Ttc21b
|
UTSW |
2 |
66,056,379 (GRCm39) |
missense |
probably benign |
0.22 |
R1837:Ttc21b
|
UTSW |
2 |
66,028,106 (GRCm39) |
missense |
probably benign |
0.01 |
R1844:Ttc21b
|
UTSW |
2 |
66,053,921 (GRCm39) |
nonsense |
probably null |
|
R2120:Ttc21b
|
UTSW |
2 |
66,057,098 (GRCm39) |
missense |
probably benign |
0.12 |
R2205:Ttc21b
|
UTSW |
2 |
66,065,467 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2392:Ttc21b
|
UTSW |
2 |
66,037,794 (GRCm39) |
critical splice donor site |
probably null |
|
R3689:Ttc21b
|
UTSW |
2 |
66,054,488 (GRCm39) |
missense |
probably benign |
0.22 |
R3810:Ttc21b
|
UTSW |
2 |
66,082,577 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3847:Ttc21b
|
UTSW |
2 |
66,073,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R3897:Ttc21b
|
UTSW |
2 |
66,065,413 (GRCm39) |
missense |
probably benign |
0.01 |
R4561:Ttc21b
|
UTSW |
2 |
66,016,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Ttc21b
|
UTSW |
2 |
66,057,257 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5161:Ttc21b
|
UTSW |
2 |
66,059,367 (GRCm39) |
missense |
probably damaging |
0.98 |
R5274:Ttc21b
|
UTSW |
2 |
66,066,627 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5594:Ttc21b
|
UTSW |
2 |
66,066,579 (GRCm39) |
missense |
probably benign |
0.39 |
R6210:Ttc21b
|
UTSW |
2 |
66,066,698 (GRCm39) |
missense |
probably benign |
0.00 |
R6305:Ttc21b
|
UTSW |
2 |
66,018,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R6456:Ttc21b
|
UTSW |
2 |
66,018,675 (GRCm39) |
missense |
probably damaging |
0.97 |
R6482:Ttc21b
|
UTSW |
2 |
66,057,244 (GRCm39) |
missense |
probably benign |
0.12 |
R6645:Ttc21b
|
UTSW |
2 |
66,066,721 (GRCm39) |
missense |
probably benign |
0.01 |
R6800:Ttc21b
|
UTSW |
2 |
66,038,994 (GRCm39) |
splice site |
probably null |
|
R6815:Ttc21b
|
UTSW |
2 |
66,057,134 (GRCm39) |
missense |
probably benign |
0.00 |
R6959:Ttc21b
|
UTSW |
2 |
66,061,656 (GRCm39) |
missense |
probably benign |
0.05 |
R7125:Ttc21b
|
UTSW |
2 |
66,066,670 (GRCm39) |
missense |
probably benign |
0.00 |
R7265:Ttc21b
|
UTSW |
2 |
66,040,517 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7283:Ttc21b
|
UTSW |
2 |
66,039,062 (GRCm39) |
missense |
probably damaging |
0.96 |
R7560:Ttc21b
|
UTSW |
2 |
66,047,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7561:Ttc21b
|
UTSW |
2 |
66,047,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7816:Ttc21b
|
UTSW |
2 |
66,077,705 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8172:Ttc21b
|
UTSW |
2 |
66,082,500 (GRCm39) |
missense |
probably benign |
0.01 |
R8179:Ttc21b
|
UTSW |
2 |
66,031,824 (GRCm39) |
missense |
probably benign |
|
R9047:Ttc21b
|
UTSW |
2 |
66,031,596 (GRCm39) |
missense |
|
|
R9282:Ttc21b
|
UTSW |
2 |
66,056,349 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9336:Ttc21b
|
UTSW |
2 |
66,057,287 (GRCm39) |
missense |
probably benign |
|
R9464:Ttc21b
|
UTSW |
2 |
66,053,866 (GRCm39) |
missense |
probably damaging |
1.00 |
X0013:Ttc21b
|
UTSW |
2 |
66,056,294 (GRCm39) |
nonsense |
probably null |
|
|