Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,772,977 (GRCm39) |
K1232E |
possibly damaging |
Het |
Angel1 |
A |
G |
12: 86,767,057 (GRCm39) |
Y440H |
probably damaging |
Het |
Bclaf1 |
A |
G |
10: 20,199,524 (GRCm39) |
Q20R |
probably damaging |
Het |
Bivm |
A |
T |
1: 44,177,793 (GRCm39) |
R364S |
probably damaging |
Het |
Brwd1 |
G |
A |
16: 95,818,804 (GRCm39) |
P1343S |
probably damaging |
Het |
Cckar |
A |
G |
5: 53,863,839 (GRCm39) |
S41P |
probably benign |
Het |
Cep68 |
A |
T |
11: 20,190,079 (GRCm39) |
V311D |
probably damaging |
Het |
Cip2a |
T |
A |
16: 48,833,612 (GRCm39) |
F571Y |
probably benign |
Het |
Fhdc1 |
C |
A |
3: 84,352,133 (GRCm39) |
V1031F |
probably benign |
Het |
Gcn1 |
G |
A |
5: 115,714,207 (GRCm39) |
A116T |
possibly damaging |
Het |
Gucy1a1 |
A |
T |
3: 82,002,066 (GRCm39) |
F671Y |
possibly damaging |
Het |
Hddc2 |
A |
T |
10: 31,190,583 (GRCm39) |
M48L |
possibly damaging |
Het |
Kif18a |
A |
T |
2: 109,128,471 (GRCm39) |
I376L |
probably damaging |
Het |
Lbr |
C |
T |
1: 181,648,267 (GRCm39) |
C398Y |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,085,723 (GRCm39) |
K1855R |
possibly damaging |
Het |
Or2v2 |
T |
A |
11: 49,004,254 (GRCm39) |
I100L |
probably benign |
Het |
Or5b98 |
G |
A |
19: 12,931,520 (GRCm39) |
C189Y |
possibly damaging |
Het |
Or8d2b |
A |
G |
9: 38,788,609 (GRCm39) |
I46V |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,455,734 (GRCm39) |
S705T |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,097,834 (GRCm39) |
Y26C |
probably benign |
Het |
Pgm2l1 |
A |
G |
7: 99,899,508 (GRCm39) |
T41A |
probably damaging |
Het |
Prss58 |
T |
C |
6: 40,874,244 (GRCm39) |
D144G |
probably damaging |
Het |
Rrp12 |
T |
C |
19: 41,861,344 (GRCm39) |
|
probably null |
Het |
Sash1 |
A |
G |
10: 8,606,006 (GRCm39) |
S795P |
possibly damaging |
Het |
Sec16a |
A |
G |
2: 26,312,167 (GRCm39) |
Y1998H |
probably benign |
Het |
Slc22a21 |
T |
C |
11: 53,860,329 (GRCm39) |
D34G |
probably damaging |
Het |
Slco4c1 |
C |
G |
1: 96,772,381 (GRCm39) |
|
probably null |
Het |
Srsf6 |
T |
C |
2: 162,776,636 (GRCm39) |
|
probably benign |
Het |
Tgfb2 |
T |
C |
1: 186,364,735 (GRCm39) |
H253R |
probably damaging |
Het |
Top3b |
A |
T |
16: 16,701,383 (GRCm39) |
I232F |
probably damaging |
Het |
Tsc22d1 |
T |
A |
14: 76,656,320 (GRCm39) |
M851K |
probably benign |
Het |
Ttn |
A |
G |
2: 76,762,855 (GRCm39) |
V3268A |
possibly damaging |
Het |
Unc79 |
A |
T |
12: 103,149,703 (GRCm39) |
Q2599L |
probably damaging |
Het |
Vmn1r192 |
T |
A |
13: 22,371,465 (GRCm39) |
I252F |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,636,996 (GRCm39) |
T693A |
probably benign |
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 |
IGL02877:Trim24
|
APN |
6 |
37,942,581 (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 |
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 |
|