Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5430401F13Rik |
CAGAAAGGAAAAGGTGGCCAG |
CAGAAAGGAAAAGGTGGCCAGCAAAAACAGAAAGGAAAAGGTGGCCAG |
6: 131,529,846 (GRCm39) |
|
probably benign |
Het |
5430401F13Rik |
AGAAAGGAAAAGGTGGCCAG |
AGAAAGGAAAAGGTGGCCAGCAAAAACAGAAAGGAAAAGGTGGCCAG |
6: 131,529,847 (GRCm39) |
|
probably benign |
Het |
Apc |
A |
AATAAAGCCC |
18: 34,415,062 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
TGGCTGTGGCTG |
TGGCTGTGGCTGCGGCTGTGGCTG |
19: 47,129,695 (GRCm39) |
|
probably benign |
Het |
Casz1 |
CACA |
C |
4: 149,036,761 (GRCm39) |
|
probably benign |
Het |
Dock4 |
GTGCCGGTGCCCGT |
G |
12: 40,894,398 (GRCm39) |
|
probably null |
Het |
F11r |
CCCCCCCCC |
CCCCCCCCCCC |
1: 171,288,758 (GRCm39) |
|
probably benign |
Het |
Fam171b |
C |
CAGCAGA |
2: 83,643,240 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
GCGTGTGCTGGT |
GCGTGTGCTGGTACGTGTGCTGGT |
5: 110,526,005 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
GTGCTGGTG |
GTGCTGGTGCGTCTGCTGGTG |
5: 110,526,009 (GRCm39) |
|
probably benign |
Het |
Iqcf4 |
TCCTTTT |
TCCTTTTCCTTTTCCTTGTCCTTTTCCTTTTCCTTTGCCTTTT |
9: 106,447,816 (GRCm39) |
|
probably benign |
Het |
Iqgap1 |
AGGCCACCACTGCTCACAGGTGCTGTACCT |
A |
7: 80,373,499 (GRCm39) |
|
probably null |
Het |
Kmt2c |
GCT |
GCTCCT |
5: 25,520,762 (GRCm39) |
|
probably benign |
Het |
Lrtm1 |
TAGCCTCAGTGGCC |
T |
14: 28,743,400 (GRCm39) |
|
probably null |
Het |
Med12l |
AACA |
AACAACA |
3: 59,183,379 (GRCm39) |
|
probably benign |
Het |
Med12l |
AGC |
AGCCGC |
3: 59,183,394 (GRCm39) |
|
probably benign |
Het |
Rassf6 |
C |
CTGCCTCACTCATGGTCCTGTAGAGCAATGGGGATTA |
5: 90,756,801 (GRCm39) |
|
probably null |
Het |
Sh3pxd2b |
TGTGCC |
TGTGCCCGTGCC |
11: 32,373,051 (GRCm39) |
|
probably benign |
Het |
Sorcs2 |
ATACATACATACCT |
AT |
5: 36,311,155 (GRCm39) |
|
probably null |
Het |
Spmap2l |
CCAG |
CCAGCGATCCTCCCCAGTCCCGCAAGGTCAG |
5: 77,164,273 (GRCm39) |
|
probably benign |
Het |
Sry |
TGCTGCTGCTGCTGCTG |
T |
Y: 2,662,595 (GRCm39) |
|
probably null |
Het |
Stard8 |
GAG |
GAGTAG |
X: 98,110,130 (GRCm39) |
|
probably null |
Het |
Tcof1 |
GATCCCCTTGGC |
GATCCCCTTGGCTGCTGAGATGGGCACTTTCCCAGATATCCCCTTGGC |
18: 60,966,645 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
GCTGCTGCTGCT |
GCTGCTGCTGCTGCTTCTGCTGCTGCT |
15: 72,673,169 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
CTGCTGCT |
CTGCTGCTGCTGCTGTTGCTGCT |
15: 72,673,173 (GRCm39) |
|
probably benign |
Het |
Vmn1r74 |
CAGAGCCACCAAGTACCT |
C |
7: 11,581,067 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Abca2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Abca2
|
APN |
2 |
25,335,975 (GRCm39) |
splice site |
probably null |
|
IGL01102:Abca2
|
APN |
2 |
25,323,968 (GRCm39) |
splice site |
probably benign |
|
IGL01322:Abca2
|
APN |
2 |
25,336,794 (GRCm39) |
splice site |
probably null |
|
IGL01402:Abca2
|
APN |
2 |
25,332,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Abca2
|
APN |
2 |
25,327,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Abca2
|
APN |
2 |
25,336,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Abca2
|
APN |
2 |
25,334,406 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01661:Abca2
|
APN |
2 |
25,333,007 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01804:Abca2
|
APN |
2 |
25,336,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Abca2
|
APN |
2 |
25,334,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Abca2
|
APN |
2 |
25,333,107 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02158:Abca2
|
APN |
2 |
25,337,891 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02173:Abca2
|
APN |
2 |
25,331,909 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02419:Abca2
|
APN |
2 |
25,336,849 (GRCm39) |
missense |
probably benign |
|
IGL02532:Abca2
|
APN |
2 |
25,325,148 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02572:Abca2
|
APN |
2 |
25,323,329 (GRCm39) |
missense |
possibly damaging |
0.95 |
Abseiling
|
UTSW |
2 |
25,337,015 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0126:Abca2
|
UTSW |
2 |
25,333,742 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0140:Abca2
|
UTSW |
2 |
25,328,097 (GRCm39) |
critical splice donor site |
probably null |
|
R0372:Abca2
|
UTSW |
2 |
25,327,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Abca2
|
UTSW |
2 |
25,332,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R0505:Abca2
|
UTSW |
2 |
25,324,906 (GRCm39) |
missense |
probably benign |
0.22 |
R0570:Abca2
|
UTSW |
2 |
25,337,417 (GRCm39) |
splice site |
probably null |
|
R1037:Abca2
|
UTSW |
2 |
25,328,240 (GRCm39) |
splice site |
probably benign |
|
R1283:Abca2
|
UTSW |
2 |
25,336,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Abca2
|
UTSW |
2 |
25,330,542 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1464:Abca2
|
UTSW |
2 |
25,337,846 (GRCm39) |
splice site |
probably benign |
|
R1468:Abca2
|
UTSW |
2 |
25,331,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R1468:Abca2
|
UTSW |
2 |
25,331,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R1480:Abca2
|
UTSW |
2 |
25,323,409 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1545:Abca2
|
UTSW |
2 |
25,332,370 (GRCm39) |
missense |
probably benign |
0.17 |
R1562:Abca2
|
UTSW |
2 |
25,336,331 (GRCm39) |
missense |
probably benign |
0.43 |
R1569:Abca2
|
UTSW |
2 |
25,329,197 (GRCm39) |
missense |
probably benign |
0.45 |
R1586:Abca2
|
UTSW |
2 |
25,337,228 (GRCm39) |
missense |
probably damaging |
0.98 |
R1635:Abca2
|
UTSW |
2 |
25,334,868 (GRCm39) |
missense |
probably benign |
0.03 |
R1699:Abca2
|
UTSW |
2 |
25,337,363 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1754:Abca2
|
UTSW |
2 |
25,324,345 (GRCm39) |
missense |
probably benign |
0.01 |
R1760:Abca2
|
UTSW |
2 |
25,333,055 (GRCm39) |
missense |
probably benign |
0.00 |
R2040:Abca2
|
UTSW |
2 |
25,333,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Abca2
|
UTSW |
2 |
25,327,517 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2111:Abca2
|
UTSW |
2 |
25,327,517 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2248:Abca2
|
UTSW |
2 |
25,323,476 (GRCm39) |
splice site |
probably benign |
|
R2323:Abca2
|
UTSW |
2 |
25,335,187 (GRCm39) |
missense |
probably benign |
0.00 |
R2418:Abca2
|
UTSW |
2 |
25,328,001 (GRCm39) |
missense |
probably benign |
0.22 |
R2419:Abca2
|
UTSW |
2 |
25,328,001 (GRCm39) |
missense |
probably benign |
0.22 |
R3816:Abca2
|
UTSW |
2 |
25,336,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Abca2
|
UTSW |
2 |
25,331,590 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4431:Abca2
|
UTSW |
2 |
25,332,864 (GRCm39) |
missense |
probably benign |
|
R4468:Abca2
|
UTSW |
2 |
25,334,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Abca2
|
UTSW |
2 |
25,333,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R4839:Abca2
|
UTSW |
2 |
25,330,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R4933:Abca2
|
UTSW |
2 |
25,334,839 (GRCm39) |
missense |
probably benign |
0.25 |
R4970:Abca2
|
UTSW |
2 |
25,328,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Abca2
|
UTSW |
2 |
25,332,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R5112:Abca2
|
UTSW |
2 |
25,328,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R5327:Abca2
|
UTSW |
2 |
25,335,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R5378:Abca2
|
UTSW |
2 |
25,336,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Abca2
|
UTSW |
2 |
25,326,510 (GRCm39) |
critical splice donor site |
probably null |
|
R5725:Abca2
|
UTSW |
2 |
25,329,412 (GRCm39) |
missense |
probably damaging |
0.98 |
R5825:Abca2
|
UTSW |
2 |
25,326,748 (GRCm39) |
missense |
probably benign |
0.36 |
R5837:Abca2
|
UTSW |
2 |
25,323,371 (GRCm39) |
missense |
probably benign |
0.34 |
R5840:Abca2
|
UTSW |
2 |
25,323,371 (GRCm39) |
missense |
probably benign |
0.34 |
R5851:Abca2
|
UTSW |
2 |
25,332,322 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6262:Abca2
|
UTSW |
2 |
25,334,922 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6344:Abca2
|
UTSW |
2 |
25,327,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R6547:Abca2
|
UTSW |
2 |
25,323,350 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6640:Abca2
|
UTSW |
2 |
25,337,015 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6980:Abca2
|
UTSW |
2 |
25,330,878 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6981:Abca2
|
UTSW |
2 |
25,334,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R7070:Abca2
|
UTSW |
2 |
25,333,007 (GRCm39) |
missense |
probably benign |
0.06 |
R7080:Abca2
|
UTSW |
2 |
25,336,116 (GRCm39) |
missense |
probably benign |
0.37 |
R7187:Abca2
|
UTSW |
2 |
25,327,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Abca2
|
UTSW |
2 |
25,332,088 (GRCm39) |
missense |
probably benign |
0.00 |
R7297:Abca2
|
UTSW |
2 |
25,332,088 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:Abca2
|
UTSW |
2 |
25,327,915 (GRCm39) |
missense |
probably benign |
0.02 |
R7561:Abca2
|
UTSW |
2 |
25,336,707 (GRCm39) |
missense |
probably damaging |
0.98 |
R7766:Abca2
|
UTSW |
2 |
25,331,540 (GRCm39) |
missense |
probably benign |
0.04 |
R8084:Abca2
|
UTSW |
2 |
25,323,979 (GRCm39) |
missense |
probably benign |
0.32 |
R8150:Abca2
|
UTSW |
2 |
25,337,393 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:Abca2
|
UTSW |
2 |
25,336,508 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8753:Abca2
|
UTSW |
2 |
25,332,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R8970:Abca2
|
UTSW |
2 |
25,335,728 (GRCm39) |
missense |
probably benign |
0.12 |
R9057:Abca2
|
UTSW |
2 |
25,331,584 (GRCm39) |
missense |
probably benign |
0.05 |
R9378:Abca2
|
UTSW |
2 |
25,329,094 (GRCm39) |
missense |
probably benign |
0.02 |
R9502:Abca2
|
UTSW |
2 |
25,326,895 (GRCm39) |
nonsense |
probably null |
|
R9688:Abca2
|
UTSW |
2 |
25,324,459 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9770:Abca2
|
UTSW |
2 |
25,328,979 (GRCm39) |
critical splice donor site |
probably null |
|
RF064:Abca2
|
UTSW |
2 |
25,337,409 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Abca2
|
UTSW |
2 |
25,334,122 (GRCm39) |
missense |
probably benign |
0.39 |
|