Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
A |
T |
6: 23,078,875 (GRCm39) |
Y712* |
probably null |
Het |
Adcy5 |
A |
G |
16: 35,118,970 (GRCm39) |
D1107G |
probably damaging |
Het |
Ankhd1 |
C |
A |
18: 36,727,876 (GRCm39) |
T504K |
probably damaging |
Het |
Asb18 |
C |
T |
1: 89,880,533 (GRCm39) |
C160Y |
possibly damaging |
Het |
Capn13 |
A |
G |
17: 73,629,050 (GRCm39) |
S586P |
probably damaging |
Het |
Cdhr2 |
A |
T |
13: 54,882,550 (GRCm39) |
T1199S |
probably benign |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Cnot8 |
A |
G |
11: 58,002,228 (GRCm39) |
E87G |
probably benign |
Het |
Crnkl1 |
C |
A |
2: 145,762,591 (GRCm39) |
E525* |
probably null |
Het |
Eif2d |
T |
C |
1: 131,092,854 (GRCm39) |
|
probably benign |
Het |
Flywch1 |
A |
G |
17: 23,979,388 (GRCm39) |
S416P |
probably damaging |
Het |
Glcci1 |
T |
C |
6: 8,582,757 (GRCm39) |
S373P |
probably damaging |
Het |
Gli3 |
A |
G |
13: 15,899,327 (GRCm39) |
R905G |
probably damaging |
Het |
Hcn4 |
T |
C |
9: 58,766,450 (GRCm39) |
V706A |
unknown |
Het |
Ift74 |
T |
C |
4: 94,513,018 (GRCm39) |
|
probably null |
Het |
Ighv8-6 |
A |
T |
12: 115,129,700 (GRCm39) |
S19T |
probably damaging |
Het |
Knl1 |
T |
A |
2: 118,919,312 (GRCm39) |
N1821K |
probably benign |
Het |
Msx1 |
G |
A |
5: 37,981,344 (GRCm39) |
P112S |
possibly damaging |
Het |
Nes |
A |
G |
3: 87,882,968 (GRCm39) |
D409G |
probably benign |
Het |
Nsmf |
A |
T |
2: 24,945,968 (GRCm39) |
I152F |
possibly damaging |
Het |
Nt5c1a |
T |
A |
4: 123,109,867 (GRCm39) |
I322N |
probably damaging |
Het |
Or7g27 |
T |
C |
9: 19,250,497 (GRCm39) |
V247A |
possibly damaging |
Het |
Pnpla8 |
A |
G |
12: 44,330,248 (GRCm39) |
T49A |
probably benign |
Het |
Ptx3 |
A |
G |
3: 66,132,196 (GRCm39) |
Y239C |
probably damaging |
Het |
Rarg |
G |
T |
15: 102,150,374 (GRCm39) |
|
probably null |
Het |
Slc33a1 |
G |
A |
3: 63,850,806 (GRCm39) |
T506I |
probably benign |
Het |
Spem2 |
T |
G |
11: 69,708,521 (GRCm39) |
H148P |
probably benign |
Het |
Vmn2r14 |
G |
A |
5: 109,368,054 (GRCm39) |
H313Y |
probably damaging |
Het |
|
Other mutations in Trim24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00225:Trim24
|
APN |
6 |
37,880,583 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01307:Trim24
|
APN |
6 |
37,942,570 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01790:Trim24
|
APN |
6 |
37,922,548 (GRCm39) |
missense |
probably benign |
|
IGL02525:Trim24
|
APN |
6 |
37,922,653 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02557:Trim24
|
APN |
6 |
37,942,434 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02671:Trim24
|
APN |
6 |
37,937,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02795:Trim24
|
APN |
6 |
37,896,324 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02889:Trim24
|
APN |
6 |
37,934,696 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02930:Trim24
|
APN |
6 |
37,928,380 (GRCm39) |
splice site |
probably benign |
|
IGL03076:Trim24
|
APN |
6 |
37,942,567 (GRCm39) |
missense |
probably damaging |
0.98 |
accomodating
|
UTSW |
6 |
37,896,332 (GRCm39) |
missense |
probably damaging |
1.00 |
apprehensive
|
UTSW |
6 |
37,934,435 (GRCm39) |
splice site |
probably benign |
|
Flexible
|
UTSW |
6 |
37,880,588 (GRCm39) |
critical splice donor site |
probably benign |
|
Lithe
|
UTSW |
6 |
37,935,504 (GRCm39) |
missense |
probably damaging |
1.00 |
Nervous
|
UTSW |
6 |
37,934,664 (GRCm39) |
missense |
probably damaging |
1.00 |
perturbed
|
UTSW |
6 |
37,896,427 (GRCm39) |
critical splice donor site |
probably null |
|
pliant
|
UTSW |
6 |
37,896,426 (GRCm39) |
critical splice donor site |
probably null |
|
qualmish
|
UTSW |
6 |
37,880,587 (GRCm39) |
critical splice donor site |
probably null |
|
Queasy
|
UTSW |
6 |
37,885,240 (GRCm39) |
missense |
probably damaging |
0.99 |
squeamish
|
UTSW |
6 |
37,892,137 (GRCm39) |
nonsense |
probably null |
|
uneasy
|
UTSW |
6 |
37,933,412 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4651001:Trim24
|
UTSW |
6 |
37,877,667 (GRCm39) |
critical splice donor site |
probably null |
|
R0037:Trim24
|
UTSW |
6 |
37,934,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R0037:Trim24
|
UTSW |
6 |
37,934,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R0183:Trim24
|
UTSW |
6 |
37,920,415 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0471:Trim24
|
UTSW |
6 |
37,892,130 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0485:Trim24
|
UTSW |
6 |
37,934,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Trim24
|
UTSW |
6 |
37,848,169 (GRCm39) |
missense |
probably benign |
|
R0609:Trim24
|
UTSW |
6 |
37,934,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Trim24
|
UTSW |
6 |
37,935,494 (GRCm39) |
splice site |
probably null |
|
R0734:Trim24
|
UTSW |
6 |
37,896,400 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0855:Trim24
|
UTSW |
6 |
37,892,137 (GRCm39) |
nonsense |
probably null |
|
R1131:Trim24
|
UTSW |
6 |
37,934,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R1141:Trim24
|
UTSW |
6 |
37,892,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Trim24
|
UTSW |
6 |
37,933,412 (GRCm39) |
critical splice donor site |
probably null |
|
R1460:Trim24
|
UTSW |
6 |
37,941,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Trim24
|
UTSW |
6 |
37,892,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R1868:Trim24
|
UTSW |
6 |
37,928,447 (GRCm39) |
missense |
probably damaging |
0.99 |
R1888:Trim24
|
UTSW |
6 |
37,934,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R1888:Trim24
|
UTSW |
6 |
37,934,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R1894:Trim24
|
UTSW |
6 |
37,934,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R1913:Trim24
|
UTSW |
6 |
37,934,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R2254:Trim24
|
UTSW |
6 |
37,935,612 (GRCm39) |
missense |
probably benign |
|
R2511:Trim24
|
UTSW |
6 |
37,880,587 (GRCm39) |
critical splice donor site |
probably null |
|
R2849:Trim24
|
UTSW |
6 |
37,933,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R3878:Trim24
|
UTSW |
6 |
37,941,708 (GRCm39) |
missense |
probably benign |
0.14 |
R4084:Trim24
|
UTSW |
6 |
37,892,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Trim24
|
UTSW |
6 |
37,941,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R4292:Trim24
|
UTSW |
6 |
37,877,627 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4633:Trim24
|
UTSW |
6 |
37,933,371 (GRCm39) |
missense |
probably damaging |
0.98 |
R4651:Trim24
|
UTSW |
6 |
37,934,774 (GRCm39) |
critical splice donor site |
probably null |
|
R4652:Trim24
|
UTSW |
6 |
37,934,774 (GRCm39) |
critical splice donor site |
probably null |
|
R4686:Trim24
|
UTSW |
6 |
37,885,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R5000:Trim24
|
UTSW |
6 |
37,935,547 (GRCm39) |
missense |
probably benign |
0.01 |
R5213:Trim24
|
UTSW |
6 |
37,934,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R5258:Trim24
|
UTSW |
6 |
37,896,335 (GRCm39) |
missense |
probably benign |
0.37 |
R5292:Trim24
|
UTSW |
6 |
37,880,539 (GRCm39) |
missense |
probably benign |
0.23 |
R5395:Trim24
|
UTSW |
6 |
37,934,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5547:Trim24
|
UTSW |
6 |
37,942,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Trim24
|
UTSW |
6 |
37,942,536 (GRCm39) |
missense |
probably benign |
0.19 |
R5670:Trim24
|
UTSW |
6 |
37,942,536 (GRCm39) |
missense |
probably benign |
0.19 |
R5849:Trim24
|
UTSW |
6 |
37,934,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5927:Trim24
|
UTSW |
6 |
37,935,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5932:Trim24
|
UTSW |
6 |
37,934,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R6286:Trim24
|
UTSW |
6 |
37,896,426 (GRCm39) |
critical splice donor site |
probably null |
|
R6374:Trim24
|
UTSW |
6 |
37,930,484 (GRCm39) |
missense |
probably benign |
0.12 |
R6449:Trim24
|
UTSW |
6 |
37,880,587 (GRCm39) |
critical splice donor site |
probably null |
|
R6723:Trim24
|
UTSW |
6 |
37,928,403 (GRCm39) |
missense |
probably benign |
0.00 |
R6731:Trim24
|
UTSW |
6 |
37,920,420 (GRCm39) |
missense |
probably damaging |
0.99 |
R6975:Trim24
|
UTSW |
6 |
37,896,427 (GRCm39) |
critical splice donor site |
probably null |
|
R7000:Trim24
|
UTSW |
6 |
37,935,613 (GRCm39) |
missense |
probably benign |
0.24 |
R7067:Trim24
|
UTSW |
6 |
37,934,775 (GRCm39) |
splice site |
probably null |
|
R7126:Trim24
|
UTSW |
6 |
37,896,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Trim24
|
UTSW |
6 |
37,942,456 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7486:Trim24
|
UTSW |
6 |
37,934,774 (GRCm39) |
critical splice donor site |
probably null |
|
R7779:Trim24
|
UTSW |
6 |
37,896,333 (GRCm39) |
missense |
probably damaging |
0.99 |
R7779:Trim24
|
UTSW |
6 |
37,896,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Trim24
|
UTSW |
6 |
37,934,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R8096:Trim24
|
UTSW |
6 |
37,935,592 (GRCm39) |
missense |
probably benign |
0.03 |
R8184:Trim24
|
UTSW |
6 |
37,848,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R8323:Trim24
|
UTSW |
6 |
37,892,233 (GRCm39) |
critical splice donor site |
probably null |
|
R8476:Trim24
|
UTSW |
6 |
37,922,578 (GRCm39) |
nonsense |
probably null |
|
R8705:Trim24
|
UTSW |
6 |
37,880,588 (GRCm39) |
critical splice donor site |
probably benign |
|
R8770:Trim24
|
UTSW |
6 |
37,934,435 (GRCm39) |
splice site |
probably benign |
|
R9021:Trim24
|
UTSW |
6 |
37,933,949 (GRCm39) |
missense |
probably damaging |
0.99 |
R9166:Trim24
|
UTSW |
6 |
37,934,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R9212:Trim24
|
UTSW |
6 |
37,896,335 (GRCm39) |
missense |
probably benign |
0.37 |
R9350:Trim24
|
UTSW |
6 |
37,892,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9678:Trim24
|
UTSW |
6 |
37,942,449 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Trim24
|
UTSW |
6 |
37,930,471 (GRCm39) |
missense |
possibly damaging |
0.90 |
|