Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap23 |
T |
C |
11: 97,343,230 (GRCm39) |
V504A |
probably benign |
Het |
Atr |
T |
G |
9: 95,744,945 (GRCm39) |
N87K |
probably benign |
Het |
Auts2 |
A |
T |
5: 132,287,887 (GRCm39) |
L32* |
probably null |
Het |
Bptf |
A |
G |
11: 106,938,066 (GRCm39) |
V2675A |
possibly damaging |
Het |
Brdt |
C |
T |
5: 107,525,881 (GRCm39) |
|
probably null |
Het |
Ccdc162 |
T |
C |
10: 41,445,841 (GRCm39) |
K444E |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,501,280 (GRCm39) |
D96G |
probably damaging |
Het |
Cpq |
C |
A |
15: 33,594,265 (GRCm39) |
Y425* |
probably null |
Het |
Eri1 |
A |
G |
8: 35,943,632 (GRCm39) |
Y221H |
probably damaging |
Het |
Fbln2 |
A |
G |
6: 91,246,955 (GRCm39) |
E1065G |
probably damaging |
Het |
Focad |
T |
C |
4: 88,249,264 (GRCm39) |
V837A |
unknown |
Het |
Ica1 |
G |
A |
6: 8,658,265 (GRCm39) |
T284I |
probably benign |
Het |
Isg15 |
C |
T |
4: 156,285,158 (GRCm39) |
|
probably null |
Het |
Ltbp4 |
T |
C |
7: 27,019,101 (GRCm39) |
T1073A |
possibly damaging |
Het |
Mmp16 |
A |
T |
4: 18,054,491 (GRCm39) |
R332S |
probably benign |
Het |
Myg1 |
G |
C |
15: 102,246,171 (GRCm39) |
G349R |
probably damaging |
Het |
Or2a25 |
T |
C |
6: 42,888,946 (GRCm39) |
L163S |
probably damaging |
Het |
Or2ag19 |
T |
C |
7: 106,444,598 (GRCm39) |
V260A |
possibly damaging |
Het |
Or5b21 |
T |
C |
19: 12,839,970 (GRCm39) |
V277A |
probably damaging |
Het |
Or7g12 |
A |
G |
9: 18,899,299 (GRCm39) |
N5S |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,378,695 (GRCm39) |
H78R |
possibly damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,897,197 (GRCm39) |
N121D |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,271,389 (GRCm39) |
T3055A |
possibly damaging |
Het |
Ppp5c |
C |
T |
7: 16,749,350 (GRCm39) |
V160M |
probably damaging |
Het |
Ptpn23 |
G |
A |
9: 110,215,347 (GRCm39) |
R1438* |
probably null |
Het |
Ptpro |
G |
A |
6: 137,420,583 (GRCm39) |
W183* |
probably null |
Het |
Pygm |
T |
C |
19: 6,443,815 (GRCm39) |
M592T |
probably damaging |
Het |
Qdpr |
A |
G |
5: 45,602,072 (GRCm39) |
V68A |
probably damaging |
Het |
Rfc5 |
A |
C |
5: 117,523,523 (GRCm39) |
S92A |
probably damaging |
Het |
Ripor3 |
T |
C |
2: 167,831,715 (GRCm39) |
Q362R |
probably benign |
Het |
Ror1 |
G |
A |
4: 100,298,352 (GRCm39) |
C575Y |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,149,242 (GRCm39) |
|
probably null |
Het |
Ugp2 |
A |
T |
11: 21,279,025 (GRCm39) |
V387D |
probably damaging |
Het |
Umodl1 |
T |
C |
17: 31,211,062 (GRCm39) |
S747P |
possibly damaging |
Het |
Vtcn1 |
A |
T |
3: 100,732,893 (GRCm39) |
I7F |
possibly damaging |
Het |
Zfp507 |
C |
T |
7: 35,494,827 (GRCm39) |
R72H |
probably benign |
Het |
|
Other mutations in Skint9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02399:Skint9
|
APN |
4 |
112,246,447 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02417:Skint9
|
APN |
4 |
112,271,335 (GRCm39) |
splice site |
probably benign |
|
IGL03111:Skint9
|
APN |
4 |
112,248,921 (GRCm39) |
missense |
probably benign |
0.01 |
land_lubber
|
UTSW |
4 |
112,248,174 (GRCm39) |
nonsense |
probably null |
|
R0390:Skint9
|
UTSW |
4 |
112,246,376 (GRCm39) |
missense |
probably benign |
0.21 |
R0400:Skint9
|
UTSW |
4 |
112,271,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Skint9
|
UTSW |
4 |
112,246,398 (GRCm39) |
missense |
probably benign |
0.02 |
R1757:Skint9
|
UTSW |
4 |
112,271,159 (GRCm39) |
missense |
probably benign |
0.03 |
R3195:Skint9
|
UTSW |
4 |
112,248,148 (GRCm39) |
missense |
probably benign |
0.37 |
R3196:Skint9
|
UTSW |
4 |
112,248,148 (GRCm39) |
missense |
probably benign |
0.37 |
R4329:Skint9
|
UTSW |
4 |
112,249,062 (GRCm39) |
missense |
probably damaging |
0.98 |
R4855:Skint9
|
UTSW |
4 |
112,248,208 (GRCm39) |
missense |
probably benign |
|
R4986:Skint9
|
UTSW |
4 |
112,248,910 (GRCm39) |
missense |
probably benign |
0.00 |
R5093:Skint9
|
UTSW |
4 |
112,246,447 (GRCm39) |
missense |
probably benign |
0.01 |
R5844:Skint9
|
UTSW |
4 |
112,271,080 (GRCm39) |
missense |
probably benign |
0.01 |
R5897:Skint9
|
UTSW |
4 |
112,271,113 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7123:Skint9
|
UTSW |
4 |
112,248,174 (GRCm39) |
nonsense |
probably null |
|
R7406:Skint9
|
UTSW |
4 |
112,246,428 (GRCm39) |
missense |
probably benign |
0.00 |
R7591:Skint9
|
UTSW |
4 |
112,248,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R9364:Skint9
|
UTSW |
4 |
112,248,915 (GRCm39) |
missense |
probably benign |
0.09 |
R9481:Skint9
|
UTSW |
4 |
112,248,915 (GRCm39) |
missense |
probably benign |
0.09 |
R9548:Skint9
|
UTSW |
4 |
112,276,346 (GRCm39) |
missense |
probably benign |
0.02 |
R9554:Skint9
|
UTSW |
4 |
112,248,915 (GRCm39) |
missense |
probably benign |
0.09 |
|