Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat1 |
A |
G |
8: 112,708,942 (GRCm39) |
C294R |
probably damaging |
Het |
Afap1l1 |
A |
G |
18: 61,870,565 (GRCm39) |
|
probably null |
Het |
Art2a |
C |
T |
7: 101,204,059 (GRCm39) |
V160M |
probably damaging |
Het |
Atp8b3 |
T |
C |
10: 80,366,795 (GRCm39) |
|
probably null |
Het |
Cwc22 |
A |
G |
2: 77,754,883 (GRCm39) |
I231T |
probably damaging |
Het |
Efr3a |
C |
A |
15: 65,726,569 (GRCm39) |
A554E |
probably damaging |
Het |
Fads2b |
T |
C |
2: 85,348,899 (GRCm39) |
Q71R |
probably damaging |
Het |
Fam3b |
T |
C |
16: 97,277,607 (GRCm39) |
T76A |
probably benign |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Gm4454 |
T |
C |
7: 38,268,386 (GRCm39) |
T253A |
probably damaging |
Het |
Gpsm2 |
C |
T |
3: 108,610,361 (GRCm39) |
R33H |
probably damaging |
Het |
Igkv5-39 |
A |
G |
6: 69,877,661 (GRCm39) |
S12P |
probably damaging |
Het |
Itga10 |
G |
A |
3: 96,564,091 (GRCm39) |
|
probably benign |
Het |
Kng1 |
A |
T |
16: 22,898,364 (GRCm39) |
D407V |
probably benign |
Het |
Lrrd1 |
A |
G |
5: 3,901,432 (GRCm39) |
D579G |
probably damaging |
Het |
Plcg1 |
C |
A |
2: 160,603,353 (GRCm39) |
Q1175K |
probably damaging |
Het |
Scml4 |
T |
A |
10: 42,833,746 (GRCm39) |
|
probably benign |
Het |
Slc5a4b |
A |
G |
10: 75,906,449 (GRCm39) |
L390P |
probably damaging |
Het |
Tectb |
A |
G |
19: 55,172,445 (GRCm39) |
Q164R |
probably damaging |
Het |
Trim52 |
C |
T |
14: 106,344,623 (GRCm39) |
Q94* |
probably null |
Het |
Usp17ld |
A |
C |
7: 102,899,870 (GRCm39) |
V354G |
probably benign |
Het |
Usp43 |
T |
C |
11: 67,747,007 (GRCm39) |
H895R |
probably benign |
Het |
Vmn2r24 |
T |
C |
6: 123,781,120 (GRCm39) |
L442P |
probably damaging |
Het |
|
Other mutations in Slc26a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01763:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL01778:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL01779:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL01872:Slc26a4
|
APN |
12 |
31,589,202 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02016:Slc26a4
|
APN |
12 |
31,585,666 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02184:Slc26a4
|
APN |
12 |
31,599,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02267:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL02270:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL02271:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL02347:Slc26a4
|
APN |
12 |
31,578,853 (GRCm39) |
splice site |
probably benign |
|
IGL02543:Slc26a4
|
APN |
12 |
31,578,688 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02803:Slc26a4
|
APN |
12 |
31,572,526 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02885:Slc26a4
|
APN |
12 |
31,575,475 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02974:Slc26a4
|
APN |
12 |
31,579,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03037:Slc26a4
|
APN |
12 |
31,581,686 (GRCm39) |
splice site |
probably benign |
|
cul-de-sac
|
UTSW |
12 |
31,575,567 (GRCm39) |
nonsense |
probably null |
|
discobolus
|
UTSW |
12 |
31,590,532 (GRCm39) |
nonsense |
probably null |
|
R0152:Slc26a4
|
UTSW |
12 |
31,579,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R0677:Slc26a4
|
UTSW |
12 |
31,599,910 (GRCm39) |
critical splice donor site |
probably null |
|
R0961:Slc26a4
|
UTSW |
12 |
31,585,618 (GRCm39) |
missense |
probably benign |
|
R1025:Slc26a4
|
UTSW |
12 |
31,578,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Slc26a4
|
UTSW |
12 |
31,575,567 (GRCm39) |
nonsense |
probably null |
|
R1729:Slc26a4
|
UTSW |
12 |
31,594,493 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2321:Slc26a4
|
UTSW |
12 |
31,590,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R3967:Slc26a4
|
UTSW |
12 |
31,578,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R3970:Slc26a4
|
UTSW |
12 |
31,578,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R4007:Slc26a4
|
UTSW |
12 |
31,590,532 (GRCm39) |
nonsense |
probably null |
|
R4370:Slc26a4
|
UTSW |
12 |
31,579,475 (GRCm39) |
missense |
probably benign |
0.01 |
R4647:Slc26a4
|
UTSW |
12 |
31,590,525 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4648:Slc26a4
|
UTSW |
12 |
31,590,525 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5816:Slc26a4
|
UTSW |
12 |
31,578,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R5932:Slc26a4
|
UTSW |
12 |
31,585,248 (GRCm39) |
critical splice donor site |
probably null |
|
R6675:Slc26a4
|
UTSW |
12 |
31,590,512 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6732:Slc26a4
|
UTSW |
12 |
31,576,599 (GRCm39) |
critical splice donor site |
probably null |
|
R6890:Slc26a4
|
UTSW |
12 |
31,599,950 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7231:Slc26a4
|
UTSW |
12 |
31,597,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7286:Slc26a4
|
UTSW |
12 |
31,579,527 (GRCm39) |
nonsense |
probably null |
|
R7790:Slc26a4
|
UTSW |
12 |
31,594,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7812:Slc26a4
|
UTSW |
12 |
31,594,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R8002:Slc26a4
|
UTSW |
12 |
31,597,969 (GRCm39) |
missense |
probably benign |
0.00 |
R8362:Slc26a4
|
UTSW |
12 |
31,594,506 (GRCm39) |
missense |
probably benign |
0.00 |
R8531:Slc26a4
|
UTSW |
12 |
31,599,911 (GRCm39) |
critical splice donor site |
probably null |
|
R8988:Slc26a4
|
UTSW |
12 |
31,572,523 (GRCm39) |
missense |
probably benign |
0.00 |
R9216:Slc26a4
|
UTSW |
12 |
31,578,659 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9335:Slc26a4
|
UTSW |
12 |
31,575,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R9354:Slc26a4
|
UTSW |
12 |
31,585,255 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9680:Slc26a4
|
UTSW |
12 |
31,585,292 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Slc26a4
|
UTSW |
12 |
31,585,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|