Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
7530416G11Rik |
T |
C |
15: 85,378,370 (GRCm39) |
D91G |
unknown |
Het |
Adam10 |
T |
C |
9: 70,647,425 (GRCm39) |
Y42H |
probably damaging |
Het |
Baiap3 |
A |
T |
17: 25,469,235 (GRCm39) |
C183S |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
Bmp1 |
C |
T |
14: 70,715,406 (GRCm39) |
V910M |
probably benign |
Het |
Brdt |
G |
A |
5: 107,507,802 (GRCm39) |
A677T |
probably benign |
Het |
Cadps2 |
A |
T |
6: 23,587,578 (GRCm39) |
M304K |
probably damaging |
Het |
Car9 |
A |
T |
4: 43,507,267 (GRCm39) |
D71V |
possibly damaging |
Het |
Chml |
A |
T |
1: 175,514,723 (GRCm39) |
Y399* |
probably null |
Het |
Cilk1 |
T |
A |
9: 78,075,071 (GRCm39) |
|
probably benign |
Het |
Clasp1 |
A |
G |
1: 118,430,765 (GRCm39) |
|
probably benign |
Het |
Cntnap5b |
G |
A |
1: 99,700,572 (GRCm39) |
|
probably null |
Het |
Cpvl |
A |
T |
6: 53,951,605 (GRCm39) |
|
probably null |
Het |
Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly damaging |
Het |
Cxcl16 |
T |
C |
11: 70,346,255 (GRCm39) |
Y226C |
probably damaging |
Het |
Dio3 |
G |
T |
12: 110,246,444 (GRCm39) |
R260L |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,353,796 (GRCm39) |
L724P |
probably damaging |
Het |
Dnah7a |
A |
C |
1: 53,495,816 (GRCm39) |
F3214V |
possibly damaging |
Het |
Dpy19l4 |
A |
T |
4: 11,295,999 (GRCm39) |
Y223* |
probably null |
Het |
Ets2 |
A |
T |
16: 95,512,818 (GRCm39) |
K101N |
probably benign |
Het |
Fbn2 |
A |
T |
18: 58,323,341 (GRCm39) |
Y200* |
probably null |
Het |
Fem1c |
A |
T |
18: 46,639,015 (GRCm39) |
I329N |
probably damaging |
Het |
Fhip1b |
A |
G |
7: 105,037,431 (GRCm39) |
I384T |
probably damaging |
Het |
Gm8919 |
T |
C |
3: 11,724,530 (GRCm39) |
|
noncoding transcript |
Het |
H2-Q5 |
A |
T |
17: 35,616,056 (GRCm39) |
H206L |
probably benign |
Het |
Hexa |
T |
C |
9: 59,464,602 (GRCm39) |
F164S |
probably benign |
Het |
Hk1 |
G |
T |
10: 62,194,194 (GRCm39) |
|
probably benign |
Het |
Itih4 |
G |
A |
14: 30,623,626 (GRCm39) |
G915R |
probably damaging |
Het |
Kcnq5 |
A |
T |
1: 21,475,292 (GRCm39) |
|
probably null |
Het |
Krtap10-4 |
A |
T |
10: 77,662,630 (GRCm39) |
|
probably benign |
Het |
Maml3 |
G |
T |
3: 51,763,013 (GRCm39) |
H650Q |
probably damaging |
Het |
Mief1 |
C |
A |
15: 80,132,454 (GRCm39) |
P112Q |
probably benign |
Het |
Morc3 |
A |
G |
16: 93,661,856 (GRCm39) |
E472G |
probably benign |
Het |
Nap1l1 |
T |
A |
10: 111,328,741 (GRCm39) |
Y223* |
probably null |
Het |
Nfix |
A |
T |
8: 85,453,119 (GRCm39) |
W312R |
probably damaging |
Het |
Nfkbie |
A |
T |
17: 45,869,510 (GRCm39) |
N155I |
probably damaging |
Het |
Nlgn2 |
A |
T |
11: 69,724,912 (GRCm39) |
M118K |
probably damaging |
Het |
Nlrp5 |
A |
T |
7: 23,117,173 (GRCm39) |
Y299F |
probably benign |
Het |
Nnt |
T |
C |
13: 119,494,072 (GRCm39) |
I556V |
possibly damaging |
Het |
Oasl2 |
A |
T |
5: 115,037,857 (GRCm39) |
I85F |
possibly damaging |
Het |
Ogg1 |
A |
C |
6: 113,305,393 (GRCm39) |
T69P |
probably damaging |
Het |
Olfml2a |
G |
T |
2: 38,847,733 (GRCm39) |
V431L |
probably damaging |
Het |
Or4d5 |
T |
C |
9: 40,012,102 (GRCm39) |
H228R |
possibly damaging |
Het |
Or5p79 |
A |
T |
7: 108,221,711 (GRCm39) |
M231L |
probably benign |
Het |
Palb2 |
G |
T |
7: 121,723,946 (GRCm39) |
A601E |
probably benign |
Het |
Pcdhb20 |
G |
A |
18: 37,638,849 (GRCm39) |
M458I |
probably benign |
Het |
Pde11a |
T |
C |
2: 76,121,585 (GRCm39) |
D332G |
possibly damaging |
Het |
Pkd1l1 |
C |
T |
11: 8,908,964 (GRCm39) |
E347K |
unknown |
Het |
Pou2af1 |
G |
A |
9: 51,149,525 (GRCm39) |
V206I |
possibly damaging |
Het |
Prr16 |
A |
G |
18: 51,251,139 (GRCm39) |
D46G |
possibly damaging |
Het |
Pus1 |
A |
G |
5: 110,928,184 (GRCm39) |
M1T |
probably null |
Het |
Pygm |
T |
A |
19: 6,441,439 (GRCm39) |
V566D |
possibly damaging |
Het |
Rb1 |
T |
A |
14: 73,499,954 (GRCm39) |
|
probably benign |
Het |
Rhoj |
A |
T |
12: 75,446,980 (GRCm39) |
K200* |
probably null |
Het |
Rnf213 |
A |
G |
11: 119,328,521 (GRCm39) |
I1985V |
possibly damaging |
Het |
Septin11 |
G |
T |
5: 93,310,113 (GRCm39) |
M305I |
possibly damaging |
Het |
Setdb2 |
T |
C |
14: 59,653,153 (GRCm39) |
Y383C |
probably damaging |
Het |
Sfpq |
G |
C |
4: 126,915,404 (GRCm39) |
Q65H |
unknown |
Het |
Skic8 |
A |
G |
9: 54,635,463 (GRCm39) |
V46A |
probably benign |
Het |
Stard3nl |
G |
T |
13: 19,554,434 (GRCm39) |
A180E |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,801,066 (GRCm39) |
N1094S |
probably benign |
Het |
Trf |
C |
T |
9: 103,089,184 (GRCm39) |
A554T |
possibly damaging |
Het |
Trmt13 |
T |
C |
3: 116,388,476 (GRCm39) |
|
probably benign |
Het |
Tubb3 |
A |
G |
8: 124,147,658 (GRCm39) |
D197G |
probably damaging |
Het |
Ube2e3 |
A |
G |
2: 78,749,056 (GRCm39) |
H135R |
probably damaging |
Het |
Ugt1a10 |
A |
T |
1: 87,983,204 (GRCm39) |
M1L |
possibly damaging |
Het |
Vmn1r233 |
A |
T |
17: 21,214,677 (GRCm39) |
I91N |
possibly damaging |
Het |
Vmn2r88 |
A |
T |
14: 51,655,531 (GRCm39) |
D580V |
probably damaging |
Het |
Vps33b |
A |
G |
7: 79,940,866 (GRCm39) |
Y593C |
probably benign |
Het |
Wdr19 |
A |
G |
5: 65,385,885 (GRCm39) |
T622A |
possibly damaging |
Het |
Wdr3 |
C |
T |
3: 100,047,516 (GRCm39) |
R853Q |
probably damaging |
Het |
Xirp1 |
T |
C |
9: 119,845,572 (GRCm39) |
T1104A |
probably benign |
Het |
Yipf1 |
G |
A |
4: 107,201,880 (GRCm39) |
|
probably null |
Het |
Zbtb17 |
A |
G |
4: 141,193,809 (GRCm39) |
D651G |
probably damaging |
Het |
Zbtb42 |
C |
T |
12: 112,646,976 (GRCm39) |
R384W |
probably damaging |
Het |
Zbtb43 |
A |
T |
2: 33,344,055 (GRCm39) |
M390K |
probably benign |
Het |
Zfp462 |
C |
T |
4: 55,011,889 (GRCm39) |
T1285M |
probably damaging |
Het |
|
Other mutations in Dpysl4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Dpysl4
|
APN |
7 |
138,676,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01836:Dpysl4
|
APN |
7 |
138,676,089 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02447:Dpysl4
|
APN |
7 |
138,678,516 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02515:Dpysl4
|
APN |
7 |
138,676,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03169:Dpysl4
|
APN |
7 |
138,679,826 (GRCm39) |
splice site |
probably null |
|
PIT4382001:Dpysl4
|
UTSW |
7 |
138,669,494 (GRCm39) |
nonsense |
probably null |
|
R0012:Dpysl4
|
UTSW |
7 |
138,677,799 (GRCm39) |
missense |
probably benign |
0.32 |
R0012:Dpysl4
|
UTSW |
7 |
138,677,799 (GRCm39) |
missense |
probably benign |
0.32 |
R1624:Dpysl4
|
UTSW |
7 |
138,669,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Dpysl4
|
UTSW |
7 |
138,670,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Dpysl4
|
UTSW |
7 |
138,670,215 (GRCm39) |
missense |
probably benign |
|
R1885:Dpysl4
|
UTSW |
7 |
138,676,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1995:Dpysl4
|
UTSW |
7 |
138,676,686 (GRCm39) |
missense |
probably benign |
|
R2698:Dpysl4
|
UTSW |
7 |
138,676,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R3032:Dpysl4
|
UTSW |
7 |
138,676,152 (GRCm39) |
missense |
probably benign |
0.01 |
R3762:Dpysl4
|
UTSW |
7 |
138,676,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R3851:Dpysl4
|
UTSW |
7 |
138,680,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R3852:Dpysl4
|
UTSW |
7 |
138,680,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Dpysl4
|
UTSW |
7 |
138,670,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Dpysl4
|
UTSW |
7 |
138,671,906 (GRCm39) |
missense |
probably benign |
|
R5608:Dpysl4
|
UTSW |
7 |
138,678,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R5762:Dpysl4
|
UTSW |
7 |
138,671,853 (GRCm39) |
missense |
probably benign |
|
R5887:Dpysl4
|
UTSW |
7 |
138,676,192 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6022:Dpysl4
|
UTSW |
7 |
138,666,000 (GRCm39) |
unclassified |
probably benign |
|
R6060:Dpysl4
|
UTSW |
7 |
138,669,324 (GRCm39) |
start codon destroyed |
probably null |
|
R6180:Dpysl4
|
UTSW |
7 |
138,670,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Dpysl4
|
UTSW |
7 |
138,679,734 (GRCm39) |
missense |
probably benign |
|
R6809:Dpysl4
|
UTSW |
7 |
138,673,576 (GRCm39) |
missense |
probably benign |
0.19 |
R6949:Dpysl4
|
UTSW |
7 |
138,671,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7647:Dpysl4
|
UTSW |
7 |
138,679,689 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7695:Dpysl4
|
UTSW |
7 |
138,666,039 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R7751:Dpysl4
|
UTSW |
7 |
138,669,456 (GRCm39) |
missense |
probably benign |
|
R8129:Dpysl4
|
UTSW |
7 |
138,666,076 (GRCm39) |
missense |
probably benign |
0.04 |
R9538:Dpysl4
|
UTSW |
7 |
138,670,230 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1189:Dpysl4
|
UTSW |
7 |
138,669,324 (GRCm39) |
start codon destroyed |
probably null |
|
Z1192:Dpysl4
|
UTSW |
7 |
138,669,324 (GRCm39) |
start codon destroyed |
probably null |
|
|