Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
T |
6: 121,645,074 (GRCm39) |
Q975L |
probably damaging |
Het |
Acad10 |
T |
C |
5: 121,783,522 (GRCm39) |
Y301C |
probably damaging |
Het |
Akr7a5 |
T |
A |
4: 139,041,492 (GRCm39) |
S134T |
probably damaging |
Het |
Aldh4a1 |
C |
T |
4: 139,375,472 (GRCm39) |
T527I |
probably damaging |
Het |
Atf2 |
A |
G |
2: 73,676,676 (GRCm39) |
V146A |
probably damaging |
Het |
C2cd6 |
A |
T |
1: 59,036,640 (GRCm39) |
|
probably benign |
Het |
Caml |
T |
C |
13: 55,776,390 (GRCm39) |
S210P |
probably damaging |
Het |
Casp1 |
A |
C |
9: 5,303,105 (GRCm39) |
R186S |
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cdhr1 |
T |
A |
14: 36,807,557 (GRCm39) |
Q361L |
possibly damaging |
Het |
Chrna3 |
T |
A |
9: 54,923,290 (GRCm39) |
T173S |
probably benign |
Het |
Commd6 |
A |
G |
14: 101,874,463 (GRCm39) |
V47A |
probably damaging |
Het |
Dmrtc2 |
T |
C |
7: 24,572,138 (GRCm39) |
|
probably benign |
Het |
Dock3 |
T |
C |
9: 106,863,215 (GRCm39) |
D721G |
probably damaging |
Het |
Dpp10 |
T |
C |
1: 123,339,532 (GRCm39) |
S332G |
probably benign |
Het |
Dst |
A |
G |
1: 34,227,909 (GRCm39) |
E1834G |
probably damaging |
Het |
Espl1 |
T |
A |
15: 102,222,460 (GRCm39) |
L1034Q |
probably damaging |
Het |
Gtf2ird2 |
C |
T |
5: 134,220,088 (GRCm39) |
T22M |
probably damaging |
Het |
Hyal2 |
T |
C |
9: 107,449,411 (GRCm39) |
L389P |
probably damaging |
Het |
Lipa |
T |
C |
19: 34,471,435 (GRCm39) |
D380G |
probably damaging |
Het |
Marchf5 |
T |
G |
19: 37,194,674 (GRCm39) |
W111G |
probably damaging |
Het |
Or8h7 |
T |
C |
2: 86,721,499 (GRCm39) |
T7A |
possibly damaging |
Het |
Pfkfb2 |
A |
T |
1: 130,627,774 (GRCm39) |
I391N |
probably damaging |
Het |
Sec31a |
T |
C |
5: 100,533,114 (GRCm39) |
S544G |
probably benign |
Het |
Spaca3 |
G |
A |
11: 80,754,911 (GRCm39) |
|
probably null |
Het |
Syne3 |
T |
C |
12: 104,920,565 (GRCm39) |
S544G |
probably benign |
Het |
Tctn3 |
T |
C |
19: 40,585,967 (GRCm39) |
E526G |
probably benign |
Het |
Tll1 |
A |
T |
8: 64,523,314 (GRCm39) |
I466K |
probably benign |
Het |
Ttbk1 |
A |
G |
17: 46,781,556 (GRCm39) |
V399A |
possibly damaging |
Het |
Vmn1r47 |
T |
C |
6: 89,999,435 (GRCm39) |
L189P |
probably damaging |
Het |
Vmn2r100 |
T |
A |
17: 19,751,547 (GRCm39) |
L530* |
probably null |
Het |
Yipf3 |
T |
C |
17: 46,561,384 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Slc26a9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Slc26a9
|
APN |
1 |
131,685,266 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01131:Slc26a9
|
APN |
1 |
131,683,280 (GRCm39) |
splice site |
probably null |
|
IGL01544:Slc26a9
|
APN |
1 |
131,687,233 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01845:Slc26a9
|
APN |
1 |
131,685,256 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02125:Slc26a9
|
APN |
1 |
131,687,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Slc26a9
|
APN |
1 |
131,691,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02267:Slc26a9
|
APN |
1 |
131,680,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03137:Slc26a9
|
APN |
1 |
131,691,615 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03324:Slc26a9
|
APN |
1 |
131,691,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0588:Slc26a9
|
UTSW |
1 |
131,681,749 (GRCm39) |
splice site |
probably benign |
|
R0611:Slc26a9
|
UTSW |
1 |
131,690,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R0639:Slc26a9
|
UTSW |
1 |
131,691,542 (GRCm39) |
missense |
probably damaging |
0.97 |
R0654:Slc26a9
|
UTSW |
1 |
131,692,768 (GRCm39) |
missense |
probably benign |
0.00 |
R0926:Slc26a9
|
UTSW |
1 |
131,680,954 (GRCm39) |
missense |
probably benign |
0.40 |
R1109:Slc26a9
|
UTSW |
1 |
131,686,536 (GRCm39) |
missense |
probably benign |
0.05 |
R1521:Slc26a9
|
UTSW |
1 |
131,678,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Slc26a9
|
UTSW |
1 |
131,693,750 (GRCm39) |
missense |
probably benign |
|
R1728:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1729:Slc26a9
|
UTSW |
1 |
131,693,750 (GRCm39) |
missense |
probably benign |
|
R1729:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1730:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1739:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1762:Slc26a9
|
UTSW |
1 |
131,693,750 (GRCm39) |
missense |
probably benign |
|
R1762:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1783:Slc26a9
|
UTSW |
1 |
131,693,750 (GRCm39) |
missense |
probably benign |
|
R1783:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1784:Slc26a9
|
UTSW |
1 |
131,693,750 (GRCm39) |
missense |
probably benign |
|
R1784:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1785:Slc26a9
|
UTSW |
1 |
131,693,750 (GRCm39) |
missense |
probably benign |
|
R1785:Slc26a9
|
UTSW |
1 |
131,691,608 (GRCm39) |
missense |
probably benign |
0.05 |
R1992:Slc26a9
|
UTSW |
1 |
131,690,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Slc26a9
|
UTSW |
1 |
131,691,001 (GRCm39) |
splice site |
probably benign |
|
R3008:Slc26a9
|
UTSW |
1 |
131,693,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R3409:Slc26a9
|
UTSW |
1 |
131,691,682 (GRCm39) |
missense |
probably benign |
|
R3879:Slc26a9
|
UTSW |
1 |
131,696,969 (GRCm39) |
missense |
probably benign |
0.39 |
R4064:Slc26a9
|
UTSW |
1 |
131,690,925 (GRCm39) |
missense |
probably benign |
0.01 |
R4088:Slc26a9
|
UTSW |
1 |
131,695,587 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4657:Slc26a9
|
UTSW |
1 |
131,680,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R5005:Slc26a9
|
UTSW |
1 |
131,693,625 (GRCm39) |
missense |
probably damaging |
0.99 |
R6255:Slc26a9
|
UTSW |
1 |
131,691,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6418:Slc26a9
|
UTSW |
1 |
131,686,228 (GRCm39) |
missense |
probably benign |
0.06 |
R6442:Slc26a9
|
UTSW |
1 |
131,686,555 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6674:Slc26a9
|
UTSW |
1 |
131,692,756 (GRCm39) |
missense |
probably benign |
0.01 |
R6719:Slc26a9
|
UTSW |
1 |
131,689,523 (GRCm39) |
missense |
probably benign |
0.13 |
R7202:Slc26a9
|
UTSW |
1 |
131,690,526 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7214:Slc26a9
|
UTSW |
1 |
131,687,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R7238:Slc26a9
|
UTSW |
1 |
131,686,556 (GRCm39) |
nonsense |
probably null |
|
R7389:Slc26a9
|
UTSW |
1 |
131,696,986 (GRCm39) |
makesense |
probably null |
|
R7439:Slc26a9
|
UTSW |
1 |
131,690,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Slc26a9
|
UTSW |
1 |
131,690,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7470:Slc26a9
|
UTSW |
1 |
131,691,781 (GRCm39) |
missense |
probably benign |
0.33 |
R7515:Slc26a9
|
UTSW |
1 |
131,681,711 (GRCm39) |
missense |
probably damaging |
0.99 |
R7652:Slc26a9
|
UTSW |
1 |
131,691,634 (GRCm39) |
missense |
probably benign |
0.06 |
R7655:Slc26a9
|
UTSW |
1 |
131,690,982 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7656:Slc26a9
|
UTSW |
1 |
131,690,982 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8278:Slc26a9
|
UTSW |
1 |
131,689,514 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8790:Slc26a9
|
UTSW |
1 |
131,683,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R9064:Slc26a9
|
UTSW |
1 |
131,680,703 (GRCm39) |
missense |
probably benign |
|
R9639:Slc26a9
|
UTSW |
1 |
131,678,409 (GRCm39) |
missense |
probably damaging |
0.98 |
R9670:Slc26a9
|
UTSW |
1 |
131,681,688 (GRCm39) |
missense |
probably benign |
0.00 |
R9681:Slc26a9
|
UTSW |
1 |
131,681,691 (GRCm39) |
missense |
probably benign |
0.01 |
R9775:Slc26a9
|
UTSW |
1 |
131,690,970 (GRCm39) |
missense |
possibly damaging |
0.67 |
|