Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
A |
G |
7: 78,740,804 (GRCm39) |
E390G |
probably damaging |
Het |
Ano3 |
A |
G |
2: 110,527,763 (GRCm39) |
S552P |
probably damaging |
Het |
Ccser1 |
A |
G |
6: 61,289,144 (GRCm39) |
S436G |
probably benign |
Het |
Chek2 |
A |
G |
5: 110,996,536 (GRCm39) |
D166G |
probably damaging |
Het |
Cilp |
TGGG |
TGG |
9: 65,187,412 (GRCm39) |
|
probably null |
Het |
Crb1 |
CG |
C |
1: 139,164,824 (GRCm39) |
|
probably null |
Het |
Deup1 |
A |
T |
9: 15,521,910 (GRCm39) |
M85K |
probably damaging |
Het |
Dnaaf10 |
G |
A |
11: 17,179,845 (GRCm39) |
G282E |
probably damaging |
Het |
Exo1 |
A |
G |
1: 175,716,354 (GRCm39) |
Y157C |
probably damaging |
Het |
Ext1 |
T |
A |
15: 52,951,468 (GRCm39) |
I539F |
probably damaging |
Het |
Gcn1 |
T |
C |
5: 115,748,917 (GRCm39) |
V1849A |
possibly damaging |
Het |
Gpr161 |
A |
G |
1: 165,144,877 (GRCm39) |
T389A |
probably benign |
Het |
Hjurp |
TGGG |
TTGCGGG |
1: 88,194,002 (GRCm39) |
|
probably benign |
Het |
Mir205hg |
T |
A |
1: 193,189,768 (GRCm39) |
|
noncoding transcript |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Muc6 |
G |
A |
7: 141,218,313 (GRCm39) |
S2120F |
possibly damaging |
Het |
Ncoa1 |
T |
A |
12: 4,309,342 (GRCm39) |
Y1318F |
probably damaging |
Het |
Or4c120 |
A |
G |
2: 89,001,316 (GRCm39) |
M80T |
probably benign |
Het |
Pml |
T |
C |
9: 58,137,326 (GRCm39) |
H491R |
possibly damaging |
Het |
Rbmxl2 |
T |
G |
7: 106,808,858 (GRCm39) |
S48A |
probably benign |
Het |
Rgs6 |
A |
G |
12: 83,138,620 (GRCm39) |
D318G |
probably damaging |
Het |
Rmc1 |
T |
C |
18: 12,302,286 (GRCm39) |
|
probably benign |
Het |
Sfi1 |
G |
A |
11: 3,136,080 (GRCm39) |
T84I |
possibly damaging |
Het |
Slc2a2 |
A |
G |
3: 28,773,519 (GRCm39) |
M275V |
possibly damaging |
Het |
Sp110 |
GC |
GCC |
1: 85,519,288 (GRCm39) |
|
probably null |
Het |
Specc1 |
T |
C |
11: 62,009,108 (GRCm39) |
V288A |
probably benign |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
Srsf11 |
C |
T |
3: 157,732,377 (GRCm39) |
V118I |
probably damaging |
Het |
St8sia2 |
C |
A |
7: 73,616,567 (GRCm39) |
C136F |
probably damaging |
Het |
Stmn3 |
A |
T |
2: 180,950,993 (GRCm39) |
I21N |
possibly damaging |
Het |
Trak2 |
G |
A |
1: 58,949,222 (GRCm39) |
T526M |
probably benign |
Het |
Ttn |
T |
A |
2: 76,542,311 (GRCm39) |
K25231N |
probably damaging |
Het |
Ugt1a1 |
AT |
A |
1: 88,140,093 (GRCm39) |
|
probably null |
Het |
Vmn1r11 |
A |
T |
6: 57,114,650 (GRCm39) |
I68F |
probably damaging |
Het |
Zfr |
T |
A |
15: 12,140,638 (GRCm39) |
Y228* |
probably null |
Het |
|
Other mutations in 4933416I08Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02528:4933416I08Rik
|
APN |
X |
52,580,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02984:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02988:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL02991:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03014:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03050:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03054:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03055:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03097:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03098:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03134:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
IGL03138:4933416I08Rik
|
UTSW |
X |
52,692,862 (GRCm39) |
unclassified |
noncoding transcript |
|
|