Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adh5 |
A |
G |
3: 138,156,815 (GRCm39) |
D167G |
probably benign |
Het |
C9orf72 |
A |
T |
4: 35,197,046 (GRCm39) |
W340R |
probably damaging |
Het |
Cand2 |
G |
A |
6: 115,766,471 (GRCm39) |
A359T |
probably benign |
Het |
Cnnm2 |
T |
C |
19: 46,751,434 (GRCm39) |
V408A |
probably benign |
Het |
Eloa |
A |
G |
4: 135,740,290 (GRCm39) |
|
probably benign |
Het |
Ern2 |
T |
C |
7: 121,772,598 (GRCm39) |
|
probably benign |
Het |
Hs6st3 |
A |
G |
14: 120,106,296 (GRCm39) |
|
probably null |
Het |
Hydin |
A |
T |
8: 111,233,108 (GRCm39) |
I1736F |
possibly damaging |
Het |
Ifrd2 |
A |
T |
9: 107,468,290 (GRCm39) |
I253F |
probably benign |
Het |
Kctd7 |
G |
A |
5: 130,181,299 (GRCm39) |
V241I |
possibly damaging |
Het |
Lcp1 |
T |
C |
14: 75,466,740 (GRCm39) |
F616L |
possibly damaging |
Het |
Lyst |
C |
T |
13: 13,835,678 (GRCm39) |
Q1787* |
probably null |
Het |
Mapkbp1 |
A |
T |
2: 119,845,144 (GRCm39) |
T342S |
possibly damaging |
Het |
Mcph1 |
A |
G |
8: 18,719,006 (GRCm39) |
|
probably benign |
Het |
Mctp2 |
T |
C |
7: 71,730,571 (GRCm39) |
H868R |
probably benign |
Het |
Mefv |
T |
C |
16: 3,533,714 (GRCm39) |
T186A |
probably benign |
Het |
Nol9 |
T |
A |
4: 152,142,368 (GRCm39) |
I666N |
probably damaging |
Het |
Or51t4 |
T |
A |
7: 102,597,721 (GRCm39) |
N16K |
probably damaging |
Het |
Or6c205 |
G |
T |
10: 129,086,904 (GRCm39) |
C167F |
possibly damaging |
Het |
Or8b8 |
A |
C |
9: 37,809,531 (GRCm39) |
Y277S |
probably damaging |
Het |
Pum2 |
T |
C |
12: 8,798,955 (GRCm39) |
|
probably null |
Het |
Rpgrip1 |
A |
C |
14: 52,349,685 (GRCm39) |
K24N |
possibly damaging |
Het |
Ryr3 |
T |
A |
2: 112,797,548 (GRCm39) |
T122S |
probably damaging |
Het |
Sfn |
A |
G |
4: 133,328,636 (GRCm39) |
S149P |
probably benign |
Het |
Slc27a2 |
T |
A |
2: 126,409,736 (GRCm39) |
V306D |
probably damaging |
Het |
Slc35a1 |
A |
G |
4: 34,675,584 (GRCm39) |
V81A |
probably benign |
Het |
Trav21-dv12 |
A |
T |
14: 54,113,955 (GRCm39) |
D25V |
probably benign |
Het |
Ttn |
T |
C |
2: 76,598,878 (GRCm39) |
H11018R |
possibly damaging |
Het |
Txn1 |
A |
T |
4: 57,950,883 (GRCm39) |
Y49N |
probably benign |
Het |
Ulk2 |
C |
T |
11: 61,672,886 (GRCm39) |
A903T |
probably damaging |
Het |
Vmn2r77 |
G |
A |
7: 86,444,360 (GRCm39) |
M4I |
unknown |
Het |
Vmn2r85 |
G |
T |
10: 130,254,561 (GRCm39) |
L708I |
probably benign |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Vrk2 |
T |
A |
11: 26,485,638 (GRCm39) |
R117* |
probably null |
Het |
Xpo6 |
A |
T |
7: 125,712,980 (GRCm39) |
|
probably benign |
Het |
Zfp334 |
G |
T |
2: 165,228,869 (GRCm39) |
|
probably benign |
Het |
Zfp958 |
T |
A |
8: 4,678,990 (GRCm39) |
C338* |
probably null |
Het |
|
Other mutations in Zdhhc14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00419:Zdhhc14
|
APN |
17 |
5,802,959 (GRCm39) |
splice site |
probably benign |
|
IGL00909:Zdhhc14
|
APN |
17 |
5,803,067 (GRCm39) |
missense |
probably benign |
|
IGL00964:Zdhhc14
|
APN |
17 |
5,762,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01398:Zdhhc14
|
APN |
17 |
5,762,738 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01483:Zdhhc14
|
APN |
17 |
5,762,733 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02801:Zdhhc14
|
APN |
17 |
5,777,094 (GRCm39) |
splice site |
probably null |
|
R0189:Zdhhc14
|
UTSW |
17 |
5,775,539 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0304:Zdhhc14
|
UTSW |
17 |
5,775,611 (GRCm39) |
splice site |
probably benign |
|
R0648:Zdhhc14
|
UTSW |
17 |
5,543,877 (GRCm39) |
missense |
probably benign |
0.01 |
R1017:Zdhhc14
|
UTSW |
17 |
5,543,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R1595:Zdhhc14
|
UTSW |
17 |
5,543,831 (GRCm39) |
missense |
probably benign |
0.00 |
R2416:Zdhhc14
|
UTSW |
17 |
5,803,283 (GRCm39) |
missense |
probably benign |
|
R3420:Zdhhc14
|
UTSW |
17 |
5,803,366 (GRCm39) |
makesense |
probably null |
|
R3421:Zdhhc14
|
UTSW |
17 |
5,803,366 (GRCm39) |
makesense |
probably null |
|
R4063:Zdhhc14
|
UTSW |
17 |
5,802,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Zdhhc14
|
UTSW |
17 |
5,777,131 (GRCm39) |
missense |
probably benign |
0.01 |
R5359:Zdhhc14
|
UTSW |
17 |
5,543,821 (GRCm39) |
missense |
probably benign |
|
R6236:Zdhhc14
|
UTSW |
17 |
5,543,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7029:Zdhhc14
|
UTSW |
17 |
5,698,186 (GRCm39) |
missense |
probably damaging |
0.97 |
R7350:Zdhhc14
|
UTSW |
17 |
5,777,151 (GRCm39) |
missense |
probably benign |
0.44 |
R7873:Zdhhc14
|
UTSW |
17 |
5,762,729 (GRCm39) |
missense |
probably benign |
0.37 |
R8247:Zdhhc14
|
UTSW |
17 |
5,736,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Zdhhc14
|
UTSW |
17 |
5,762,689 (GRCm39) |
missense |
probably damaging |
0.98 |
R8865:Zdhhc14
|
UTSW |
17 |
5,775,570 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8969:Zdhhc14
|
UTSW |
17 |
5,775,555 (GRCm39) |
missense |
probably benign |
0.12 |
R9133:Zdhhc14
|
UTSW |
17 |
5,803,283 (GRCm39) |
missense |
probably benign |
|
R9291:Zdhhc14
|
UTSW |
17 |
5,698,237 (GRCm39) |
missense |
probably benign |
0.02 |
R9433:Zdhhc14
|
UTSW |
17 |
5,781,779 (GRCm39) |
missense |
probably benign |
0.03 |
|