Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
A |
G |
2: 69,096,019 (GRCm39) |
I804T |
probably benign |
Het |
Abcb1b |
A |
T |
5: 8,855,441 (GRCm39) |
E25V |
probably damaging |
Het |
Adamts9 |
G |
T |
6: 92,886,774 (GRCm39) |
Y355* |
probably null |
Het |
Akp3 |
A |
G |
1: 87,054,500 (GRCm39) |
M303V |
probably benign |
Het |
Ankrd35 |
A |
T |
3: 96,590,650 (GRCm39) |
E312V |
possibly damaging |
Het |
Arhgap40 |
T |
C |
2: 158,373,294 (GRCm39) |
|
probably null |
Het |
Asxl1 |
T |
C |
2: 153,242,027 (GRCm39) |
L859P |
probably benign |
Het |
Atat1 |
A |
G |
17: 36,220,897 (GRCm39) |
F11L |
probably benign |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Ccdc7a |
A |
T |
8: 129,608,075 (GRCm39) |
H943Q |
unknown |
Het |
Cep135 |
A |
G |
5: 76,764,695 (GRCm39) |
T558A |
probably benign |
Het |
Cfap99 |
A |
G |
5: 34,458,863 (GRCm39) |
E86G |
possibly damaging |
Het |
Cfhr2 |
C |
T |
1: 139,758,801 (GRCm39) |
|
probably null |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Col17a1 |
G |
A |
19: 47,640,622 (GRCm39) |
P992L |
probably damaging |
Het |
Col7a1 |
C |
T |
9: 108,792,331 (GRCm39) |
Q1294* |
probably null |
Het |
Coq8b |
T |
A |
7: 26,939,293 (GRCm39) |
C148S |
probably damaging |
Het |
Csmd2 |
A |
G |
4: 128,171,021 (GRCm39) |
N338S |
|
Het |
Cspg5 |
T |
A |
9: 110,075,959 (GRCm39) |
S232T |
possibly damaging |
Het |
Cyp2c67 |
A |
G |
19: 39,628,341 (GRCm39) |
V201A |
possibly damaging |
Het |
Dlgap3 |
G |
A |
4: 127,089,310 (GRCm39) |
R302H |
possibly damaging |
Het |
Dpy19l2 |
T |
C |
9: 24,539,547 (GRCm39) |
I469V |
probably benign |
Het |
Fam135b |
T |
C |
15: 71,343,412 (GRCm39) |
D401G |
probably damaging |
Het |
Gabbr1 |
G |
T |
17: 37,375,629 (GRCm39) |
G453* |
probably null |
Het |
Gclc |
C |
A |
9: 77,695,498 (GRCm39) |
A440D |
probably damaging |
Het |
Glyat |
T |
C |
19: 12,627,723 (GRCm39) |
I106T |
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,799,071 (GRCm39) |
N474S |
possibly damaging |
Het |
Gm17079 |
T |
C |
14: 51,930,494 (GRCm39) |
H117R |
|
Het |
Ift70a2 |
A |
T |
2: 75,806,613 (GRCm39) |
L633* |
probably null |
Het |
Ildr2 |
A |
G |
1: 166,131,098 (GRCm39) |
D318G |
probably damaging |
Het |
Kcnd2 |
G |
A |
6: 21,216,177 (GRCm39) |
|
probably benign |
Het |
Kif19a |
C |
T |
11: 114,672,034 (GRCm39) |
T207M |
probably damaging |
Het |
Kif3a |
G |
T |
11: 53,477,733 (GRCm39) |
G401* |
probably null |
Het |
Lactbl1 |
T |
A |
4: 136,360,286 (GRCm39) |
L155Q |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,136,023 (GRCm39) |
D1649V |
probably benign |
Het |
Lrrc37 |
C |
T |
11: 103,505,363 (GRCm39) |
A26T |
probably benign |
Het |
Map2k1 |
A |
G |
9: 64,101,105 (GRCm39) |
V191A |
probably benign |
Het |
Mdm4 |
A |
T |
1: 132,931,547 (GRCm39) |
C165S |
probably benign |
Het |
Med27 |
G |
A |
2: 29,399,446 (GRCm39) |
W92* |
probably null |
Het |
Muc20 |
A |
T |
16: 32,614,616 (GRCm39) |
S254T |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,111,247 (GRCm39) |
E1562G |
possibly damaging |
Het |
Nlrp2 |
C |
G |
7: 5,331,571 (GRCm39) |
R275P |
possibly damaging |
Het |
Notch2 |
T |
A |
3: 98,009,703 (GRCm39) |
N543K |
probably damaging |
Het |
Nup214 |
T |
A |
2: 31,924,168 (GRCm39) |
S1566T |
probably benign |
Het |
Nxnl1 |
T |
G |
8: 72,015,437 (GRCm39) |
E157A |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,969,959 (GRCm39) |
L61P |
probably damaging |
Het |
Ogg1 |
A |
T |
6: 113,306,237 (GRCm39) |
I145F |
probably damaging |
Het |
Or10d5j |
T |
C |
9: 39,867,641 (GRCm39) |
T197A |
probably benign |
Het |
Or2b2 |
A |
G |
13: 21,887,440 (GRCm39) |
K90E |
possibly damaging |
Het |
Or2f1 |
G |
A |
6: 42,721,337 (GRCm39) |
R122H |
probably benign |
Het |
Or51h5 |
T |
C |
7: 102,577,149 (GRCm39) |
F105L |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,763,461 (GRCm39) |
D3978G |
unknown |
Het |
Pla2g4e |
T |
G |
2: 120,000,676 (GRCm39) |
D687A |
probably damaging |
Het |
Pla2r1 |
T |
C |
2: 60,288,737 (GRCm39) |
K632E |
probably damaging |
Het |
Plg |
A |
T |
17: 12,610,723 (GRCm39) |
Q212L |
probably damaging |
Het |
Poldip3 |
A |
T |
15: 83,015,698 (GRCm39) |
N306K |
probably damaging |
Het |
Pspn |
A |
G |
17: 57,306,978 (GRCm39) |
L13P |
possibly damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,804,844 (GRCm39) |
E484G |
probably damaging |
Het |
Rbmxl1 |
G |
T |
8: 79,233,286 (GRCm39) |
T19K |
probably damaging |
Het |
Rora |
G |
A |
9: 69,103,365 (GRCm39) |
V31I |
possibly damaging |
Het |
Skint5 |
C |
A |
4: 113,798,036 (GRCm39) |
W182C |
probably damaging |
Het |
Spata31d1c |
A |
T |
13: 65,183,877 (GRCm39) |
Q473L |
probably damaging |
Het |
Tesk2 |
G |
A |
4: 116,659,884 (GRCm39) |
W334* |
probably null |
Het |
Tmem67 |
C |
A |
4: 12,075,484 (GRCm39) |
V277L |
probably benign |
Het |
Trhde |
A |
G |
10: 114,354,082 (GRCm39) |
M537T |
probably damaging |
Het |
Tubb6 |
G |
A |
18: 67,534,981 (GRCm39) |
M293I |
probably benign |
Het |
Ube2ql1 |
A |
T |
13: 69,886,873 (GRCm39) |
L196Q |
probably damaging |
Het |
Ubn1 |
A |
T |
16: 4,873,188 (GRCm39) |
N70I |
probably damaging |
Het |
Ubtf |
A |
T |
11: 102,205,806 (GRCm39) |
S40T |
probably benign |
Het |
Virma |
C |
T |
4: 11,519,249 (GRCm39) |
A782V |
possibly damaging |
Het |
Xpo4 |
A |
G |
14: 57,834,508 (GRCm39) |
S691P |
probably benign |
Het |
Zfat |
A |
C |
15: 68,052,301 (GRCm39) |
F491V |
probably damaging |
Het |
Zfp623 |
T |
G |
15: 75,820,154 (GRCm39) |
V370G |
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 |
IGL02261:Xdh
|
APN |
17 |
74,220,960 (GRCm39) |
missense |
possibly damaging |
0.81 |
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 |
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 |
|