Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap2a2 |
T |
A |
7: 141,209,186 (GRCm39) |
S793T |
probably benign |
Het |
Btnl6 |
T |
C |
17: 34,727,153 (GRCm39) |
D459G |
probably damaging |
Het |
Cacna1g |
C |
A |
11: 94,347,977 (GRCm39) |
D704Y |
probably damaging |
Het |
Cry2 |
A |
G |
2: 92,244,060 (GRCm39) |
I371T |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,882,632 (GRCm39) |
F384I |
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,187,301 (GRCm39) |
|
probably null |
Het |
Hecw1 |
G |
T |
13: 14,552,382 (GRCm39) |
D72E |
probably damaging |
Het |
Htt |
T |
A |
5: 35,064,924 (GRCm39) |
W3046R |
probably damaging |
Het |
Hydin |
A |
T |
8: 110,993,995 (GRCm39) |
N10Y |
unknown |
Het |
Ighv8-8 |
T |
A |
12: 115,257,760 (GRCm39) |
T94S |
probably benign |
Het |
Igkv4-58 |
A |
G |
6: 69,477,538 (GRCm39) |
S20P |
probably damaging |
Het |
Il4i1 |
T |
C |
7: 44,486,919 (GRCm39) |
|
probably benign |
Het |
Kif13a |
A |
T |
13: 46,918,099 (GRCm39) |
S403T |
probably benign |
Het |
Klhl40 |
T |
C |
9: 121,612,446 (GRCm39) |
L616P |
probably damaging |
Het |
Krt7 |
T |
C |
15: 101,325,491 (GRCm39) |
L440P |
possibly damaging |
Het |
Lpin1 |
A |
G |
12: 16,594,678 (GRCm39) |
L755P |
probably damaging |
Het |
Magee2 |
C |
A |
X: 103,899,134 (GRCm39) |
E506* |
probably null |
Het |
Mast3 |
G |
A |
8: 71,234,207 (GRCm39) |
R143* |
probably null |
Het |
Med12 |
T |
A |
X: 100,321,695 (GRCm39) |
H459Q |
probably benign |
Het |
Mmp3 |
T |
C |
9: 7,450,149 (GRCm39) |
S294P |
probably benign |
Het |
Muc6 |
T |
C |
7: 141,234,349 (GRCm39) |
Y714C |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,074,349 (GRCm39) |
L662S |
probably damaging |
Het |
Notch4 |
G |
T |
17: 34,791,542 (GRCm39) |
C567F |
probably damaging |
Het |
Nprl3 |
A |
G |
11: 32,200,256 (GRCm39) |
I20T |
probably damaging |
Het |
Or10ag2 |
A |
T |
2: 87,248,587 (GRCm39) |
D65V |
possibly damaging |
Het |
Pcdhb19 |
A |
G |
18: 37,631,665 (GRCm39) |
T487A |
possibly damaging |
Het |
Phlpp2 |
A |
G |
8: 110,667,467 (GRCm39) |
E1332G |
probably benign |
Het |
Pick1 |
T |
C |
15: 79,125,481 (GRCm39) |
S113P |
probably damaging |
Het |
Ptpru |
T |
C |
4: 131,507,178 (GRCm39) |
E1023G |
probably damaging |
Het |
Rspry1 |
A |
C |
8: 95,376,962 (GRCm39) |
I382L |
probably benign |
Het |
Sf3b3 |
A |
C |
8: 111,566,586 (GRCm39) |
V248G |
probably damaging |
Het |
Smg5 |
T |
A |
3: 88,253,759 (GRCm39) |
Y126* |
probably null |
Het |
Spin1 |
T |
C |
13: 51,281,973 (GRCm39) |
V22A |
probably benign |
Het |
Stab1 |
C |
T |
14: 30,872,220 (GRCm39) |
R1189Q |
possibly damaging |
Het |
Sytl5 |
A |
G |
X: 9,829,939 (GRCm39) |
D538G |
probably damaging |
Het |
Taar7e |
T |
A |
10: 23,913,813 (GRCm39) |
M101K |
probably damaging |
Het |
Taf4 |
A |
G |
2: 179,576,847 (GRCm39) |
V578A |
probably damaging |
Het |
Tmem266 |
G |
T |
9: 55,344,517 (GRCm39) |
C383F |
probably benign |
Het |
Trim34a |
T |
C |
7: 103,910,140 (GRCm39) |
|
probably null |
Het |
Vmn2r104 |
T |
C |
17: 20,249,866 (GRCm39) |
T802A |
probably damaging |
Het |
Vmn2r32 |
A |
C |
7: 7,467,029 (GRCm39) |
I833S |
probably damaging |
Het |
Vmn2r85 |
T |
C |
10: 130,262,328 (GRCm39) |
D137G |
probably benign |
Het |
Vps13c |
C |
T |
9: 67,853,308 (GRCm39) |
S2467L |
probably benign |
Het |
|
Other mutations in Cby2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01304:Cby2
|
APN |
14 |
75,830,085 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01556:Cby2
|
APN |
14 |
75,821,551 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Cby2
|
APN |
14 |
75,820,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R0071:Cby2
|
UTSW |
14 |
75,821,621 (GRCm39) |
missense |
probably benign |
0.00 |
R1645:Cby2
|
UTSW |
14 |
75,821,089 (GRCm39) |
missense |
probably benign |
0.12 |
R1738:Cby2
|
UTSW |
14 |
75,830,497 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R1844:Cby2
|
UTSW |
14 |
75,820,850 (GRCm39) |
missense |
probably benign |
0.12 |
R4773:Cby2
|
UTSW |
14 |
75,820,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Cby2
|
UTSW |
14 |
75,830,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R5201:Cby2
|
UTSW |
14 |
75,821,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Cby2
|
UTSW |
14 |
75,820,666 (GRCm39) |
missense |
probably benign |
0.00 |
R5880:Cby2
|
UTSW |
14 |
75,821,243 (GRCm39) |
missense |
probably benign |
0.02 |
R6915:Cby2
|
UTSW |
14 |
75,830,098 (GRCm39) |
missense |
probably benign |
0.37 |
R7399:Cby2
|
UTSW |
14 |
75,830,077 (GRCm39) |
missense |
probably benign |
0.00 |
R8054:Cby2
|
UTSW |
14 |
75,821,339 (GRCm39) |
missense |
probably benign |
0.00 |
R8062:Cby2
|
UTSW |
14 |
75,830,046 (GRCm39) |
missense |
probably benign |
0.13 |
R8172:Cby2
|
UTSW |
14 |
75,829,241 (GRCm39) |
splice site |
probably null |
|
R8998:Cby2
|
UTSW |
14 |
75,820,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Cby2
|
UTSW |
14 |
75,820,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R9550:Cby2
|
UTSW |
14 |
75,820,603 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Cby2
|
UTSW |
14 |
75,820,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|