Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambn |
G |
A |
5: 88,604,807 (GRCm39) |
V27M |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,578,015 (GRCm39) |
N222D |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,422,756 (GRCm39) |
T542S |
probably damaging |
Het |
Btbd1 |
A |
T |
7: 81,455,507 (GRCm39) |
I288N |
probably damaging |
Het |
Ctps1 |
C |
T |
4: 120,399,776 (GRCm39) |
V500I |
possibly damaging |
Het |
Cul5 |
A |
C |
9: 53,546,337 (GRCm39) |
V345G |
probably damaging |
Het |
Dchs1 |
A |
G |
7: 105,421,776 (GRCm39) |
Y215H |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 49,973,566 (GRCm39) |
M67K |
possibly damaging |
Het |
Egln2 |
C |
T |
7: 26,859,291 (GRCm39) |
E353K |
possibly damaging |
Het |
Fbxw5 |
G |
T |
2: 25,393,746 (GRCm39) |
A325S |
probably benign |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Gaa |
A |
G |
11: 119,172,091 (GRCm39) |
*207W |
probably null |
Het |
Herc2 |
A |
G |
7: 55,856,492 (GRCm39) |
T3947A |
probably damaging |
Het |
Ifit2 |
T |
A |
19: 34,551,624 (GRCm39) |
I388N |
probably damaging |
Het |
Ikzf4 |
T |
C |
10: 128,472,591 (GRCm39) |
T209A |
possibly damaging |
Het |
Il17re |
A |
T |
6: 113,445,472 (GRCm39) |
|
probably benign |
Het |
Insrr |
T |
A |
3: 87,708,029 (GRCm39) |
L157Q |
probably damaging |
Het |
Kcnq2 |
T |
G |
2: 180,723,483 (GRCm39) |
Y631S |
probably damaging |
Het |
Lrrfip1 |
A |
G |
1: 91,039,890 (GRCm39) |
I198V |
probably benign |
Het |
Mir7684 |
A |
T |
15: 82,273,345 (GRCm39) |
|
probably benign |
Het |
Mphosph9 |
C |
T |
5: 124,398,150 (GRCm39) |
E1049K |
probably damaging |
Het |
Mroh1 |
G |
A |
15: 76,313,360 (GRCm39) |
R611Q |
probably benign |
Het |
Mynn |
A |
T |
3: 30,661,280 (GRCm39) |
I121F |
possibly damaging |
Het |
Ndrg2 |
G |
A |
14: 52,148,566 (GRCm39) |
R32C |
probably damaging |
Het |
Or2ab1 |
T |
C |
11: 58,488,630 (GRCm39) |
I138T |
probably benign |
Het |
Or4p7 |
A |
G |
2: 88,221,725 (GRCm39) |
I45V |
probably benign |
Het |
Ppp1r9b |
A |
G |
11: 94,892,936 (GRCm39) |
E260G |
probably damaging |
Het |
Psd4 |
A |
G |
2: 24,291,756 (GRCm39) |
S652G |
probably damaging |
Het |
Psg25 |
C |
T |
7: 18,255,268 (GRCm39) |
R416H |
probably benign |
Het |
Pygm |
T |
A |
19: 6,438,301 (GRCm39) |
N171K |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,723 (GRCm39) |
D297E |
possibly damaging |
Het |
Selenov |
T |
A |
7: 27,990,004 (GRCm39) |
T167S |
probably benign |
Het |
Serpina10 |
T |
C |
12: 103,583,208 (GRCm39) |
Y358C |
probably damaging |
Het |
Slc27a3 |
T |
C |
3: 90,295,002 (GRCm39) |
R352G |
probably benign |
Het |
Snx33 |
T |
C |
9: 56,833,862 (GRCm39) |
D69G |
probably benign |
Het |
St8sia2 |
G |
T |
7: 73,616,594 (GRCm39) |
P127H |
probably damaging |
Het |
Thbd |
T |
C |
2: 148,248,401 (GRCm39) |
K489R |
probably benign |
Het |
Ttn |
A |
T |
2: 76,767,049 (GRCm39) |
C3039S |
probably damaging |
Het |
Vmn1r167 |
T |
C |
7: 23,204,261 (GRCm39) |
M252V |
probably benign |
Het |
Zfp827 |
G |
A |
8: 79,906,708 (GRCm39) |
V907I |
probably damaging |
Het |
|
Other mutations in Xdh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Xdh
|
APN |
17 |
74,230,101 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL00556:Xdh
|
APN |
17 |
74,191,430 (GRCm39) |
makesense |
probably null |
|
IGL01524:Xdh
|
APN |
17 |
74,230,132 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01604:Xdh
|
APN |
17 |
74,216,332 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01625:Xdh
|
APN |
17 |
74,223,781 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01778:Xdh
|
APN |
17 |
74,207,275 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01804:Xdh
|
APN |
17 |
74,199,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01825:Xdh
|
APN |
17 |
74,198,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01929:Xdh
|
APN |
17 |
74,241,850 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Xdh
|
APN |
17 |
74,220,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02079:Xdh
|
APN |
17 |
74,198,272 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02210:Xdh
|
APN |
17 |
74,250,890 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02365:Xdh
|
APN |
17 |
74,250,885 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02424:Xdh
|
APN |
17 |
74,233,565 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02491:Xdh
|
APN |
17 |
74,193,459 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02525:Xdh
|
APN |
17 |
74,231,990 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02578:Xdh
|
APN |
17 |
74,213,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02793:Xdh
|
APN |
17 |
74,207,576 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Xdh
|
APN |
17 |
74,250,840 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03327:Xdh
|
APN |
17 |
74,223,787 (GRCm39) |
missense |
probably benign |
|
IGL03345:Xdh
|
APN |
17 |
74,213,027 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03353:Xdh
|
APN |
17 |
74,202,781 (GRCm39) |
missense |
possibly damaging |
0.65 |
inky
|
UTSW |
17 |
74,228,346 (GRCm39) |
missense |
probably damaging |
1.00 |
nucleus
|
UTSW |
17 |
74,206,007 (GRCm39) |
nonsense |
probably null |
|
squidgame
|
UTSW |
17 |
74,246,831 (GRCm39) |
missense |
probably benign |
|
R0018:Xdh
|
UTSW |
17 |
74,232,020 (GRCm39) |
missense |
probably benign |
0.00 |
R0018:Xdh
|
UTSW |
17 |
74,232,020 (GRCm39) |
missense |
probably benign |
0.00 |
R0033:Xdh
|
UTSW |
17 |
74,214,627 (GRCm39) |
missense |
probably benign |
0.06 |
R0079:Xdh
|
UTSW |
17 |
74,198,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R0086:Xdh
|
UTSW |
17 |
74,191,433 (GRCm39) |
missense |
probably benign |
|
R0319:Xdh
|
UTSW |
17 |
74,213,096 (GRCm39) |
splice site |
probably benign |
|
R0336:Xdh
|
UTSW |
17 |
74,229,458 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0389:Xdh
|
UTSW |
17 |
74,205,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R0684:Xdh
|
UTSW |
17 |
74,250,886 (GRCm39) |
missense |
probably damaging |
0.97 |
R0930:Xdh
|
UTSW |
17 |
74,230,077 (GRCm39) |
missense |
probably benign |
0.00 |
R1073:Xdh
|
UTSW |
17 |
74,246,831 (GRCm39) |
missense |
probably benign |
|
R1114:Xdh
|
UTSW |
17 |
74,248,144 (GRCm39) |
splice site |
probably benign |
|
R1201:Xdh
|
UTSW |
17 |
74,225,413 (GRCm39) |
missense |
probably benign |
0.05 |
R1230:Xdh
|
UTSW |
17 |
74,198,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R1351:Xdh
|
UTSW |
17 |
74,230,073 (GRCm39) |
missense |
probably benign |
0.02 |
R1470:Xdh
|
UTSW |
17 |
74,198,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Xdh
|
UTSW |
17 |
74,198,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Xdh
|
UTSW |
17 |
74,221,014 (GRCm39) |
nonsense |
probably null |
|
R1548:Xdh
|
UTSW |
17 |
74,220,896 (GRCm39) |
missense |
probably damaging |
0.98 |
R1637:Xdh
|
UTSW |
17 |
74,207,573 (GRCm39) |
missense |
probably benign |
|
R1641:Xdh
|
UTSW |
17 |
74,233,547 (GRCm39) |
missense |
probably benign |
|
R1758:Xdh
|
UTSW |
17 |
74,217,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Xdh
|
UTSW |
17 |
74,214,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Xdh
|
UTSW |
17 |
74,199,746 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2024:Xdh
|
UTSW |
17 |
74,228,300 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2080:Xdh
|
UTSW |
17 |
74,216,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R2157:Xdh
|
UTSW |
17 |
74,229,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2300:Xdh
|
UTSW |
17 |
74,198,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R3783:Xdh
|
UTSW |
17 |
74,200,590 (GRCm39) |
splice site |
probably benign |
|
R3796:Xdh
|
UTSW |
17 |
74,214,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3797:Xdh
|
UTSW |
17 |
74,214,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3798:Xdh
|
UTSW |
17 |
74,214,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3799:Xdh
|
UTSW |
17 |
74,214,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3819:Xdh
|
UTSW |
17 |
74,213,720 (GRCm39) |
missense |
probably benign |
0.35 |
R4085:Xdh
|
UTSW |
17 |
74,223,874 (GRCm39) |
missense |
probably benign |
0.35 |
R4240:Xdh
|
UTSW |
17 |
74,202,790 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4356:Xdh
|
UTSW |
17 |
74,222,685 (GRCm39) |
missense |
probably benign |
0.01 |
R4522:Xdh
|
UTSW |
17 |
74,205,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4523:Xdh
|
UTSW |
17 |
74,205,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4524:Xdh
|
UTSW |
17 |
74,205,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Xdh
|
UTSW |
17 |
74,217,195 (GRCm39) |
missense |
probably benign |
0.19 |
R4617:Xdh
|
UTSW |
17 |
74,225,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R4756:Xdh
|
UTSW |
17 |
74,193,381 (GRCm39) |
missense |
probably benign |
0.24 |
R4761:Xdh
|
UTSW |
17 |
74,217,262 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4815:Xdh
|
UTSW |
17 |
74,213,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Xdh
|
UTSW |
17 |
74,205,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R4896:Xdh
|
UTSW |
17 |
74,217,238 (GRCm39) |
missense |
probably damaging |
0.96 |
R4897:Xdh
|
UTSW |
17 |
74,207,703 (GRCm39) |
missense |
probably benign |
|
R4923:Xdh
|
UTSW |
17 |
74,231,931 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4977:Xdh
|
UTSW |
17 |
74,205,965 (GRCm39) |
missense |
probably benign |
0.05 |
R5030:Xdh
|
UTSW |
17 |
74,198,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R5185:Xdh
|
UTSW |
17 |
74,232,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R5347:Xdh
|
UTSW |
17 |
74,232,027 (GRCm39) |
missense |
probably benign |
|
R5556:Xdh
|
UTSW |
17 |
74,204,759 (GRCm39) |
missense |
probably benign |
0.21 |
R5566:Xdh
|
UTSW |
17 |
74,200,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Xdh
|
UTSW |
17 |
74,250,880 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5635:Xdh
|
UTSW |
17 |
74,220,870 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5662:Xdh
|
UTSW |
17 |
74,248,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5955:Xdh
|
UTSW |
17 |
74,205,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Xdh
|
UTSW |
17 |
74,213,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R6061:Xdh
|
UTSW |
17 |
74,228,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R6412:Xdh
|
UTSW |
17 |
74,242,902 (GRCm39) |
missense |
probably benign |
0.09 |
R6526:Xdh
|
UTSW |
17 |
74,207,546 (GRCm39) |
missense |
probably damaging |
0.97 |
R6558:Xdh
|
UTSW |
17 |
74,200,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6843:Xdh
|
UTSW |
17 |
74,230,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R6932:Xdh
|
UTSW |
17 |
74,229,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R7028:Xdh
|
UTSW |
17 |
74,250,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R7418:Xdh
|
UTSW |
17 |
74,220,960 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7503:Xdh
|
UTSW |
17 |
74,233,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R7653:Xdh
|
UTSW |
17 |
74,204,040 (GRCm39) |
missense |
probably benign |
0.10 |
R7763:Xdh
|
UTSW |
17 |
74,241,829 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7768:Xdh
|
UTSW |
17 |
74,246,831 (GRCm39) |
missense |
probably benign |
|
R7904:Xdh
|
UTSW |
17 |
74,229,467 (GRCm39) |
missense |
probably benign |
0.09 |
R8010:Xdh
|
UTSW |
17 |
74,216,312 (GRCm39) |
nonsense |
probably null |
|
R8067:Xdh
|
UTSW |
17 |
74,207,652 (GRCm39) |
missense |
probably benign |
0.01 |
R8238:Xdh
|
UTSW |
17 |
74,193,412 (GRCm39) |
missense |
probably benign |
|
R8253:Xdh
|
UTSW |
17 |
74,225,377 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8346:Xdh
|
UTSW |
17 |
74,220,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R8350:Xdh
|
UTSW |
17 |
74,241,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R8381:Xdh
|
UTSW |
17 |
74,219,456 (GRCm39) |
missense |
probably benign |
|
R8427:Xdh
|
UTSW |
17 |
74,242,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Xdh
|
UTSW |
17 |
74,206,007 (GRCm39) |
nonsense |
probably null |
|
R8478:Xdh
|
UTSW |
17 |
74,213,053 (GRCm39) |
missense |
probably benign |
0.00 |
R8680:Xdh
|
UTSW |
17 |
74,229,500 (GRCm39) |
missense |
probably benign |
|
R8802:Xdh
|
UTSW |
17 |
74,225,405 (GRCm39) |
missense |
probably benign |
0.00 |
R8984:Xdh
|
UTSW |
17 |
74,228,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8985:Xdh
|
UTSW |
17 |
74,228,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8995:Xdh
|
UTSW |
17 |
74,205,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Xdh
|
UTSW |
17 |
74,217,222 (GRCm39) |
missense |
probably benign |
|
R9149:Xdh
|
UTSW |
17 |
74,222,688 (GRCm39) |
missense |
probably benign |
|
R9181:Xdh
|
UTSW |
17 |
74,232,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Xdh
|
UTSW |
17 |
74,233,541 (GRCm39) |
critical splice donor site |
probably null |
|
R9357:Xdh
|
UTSW |
17 |
74,214,711 (GRCm39) |
missense |
probably damaging |
0.97 |
R9609:Xdh
|
UTSW |
17 |
74,231,990 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9803:Xdh
|
UTSW |
17 |
74,229,455 (GRCm39) |
missense |
probably benign |
|
X0019:Xdh
|
UTSW |
17 |
74,225,449 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Xdh
|
UTSW |
17 |
74,193,423 (GRCm39) |
missense |
probably benign |
|
Z1176:Xdh
|
UTSW |
17 |
74,230,037 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Xdh
|
UTSW |
17 |
74,204,690 (GRCm39) |
missense |
probably damaging |
1.00 |
|