Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Als2 |
A |
G |
1: 59,254,631 (GRCm39) |
M242T |
probably damaging |
Het |
Atad1 |
C |
T |
19: 32,684,348 (GRCm39) |
V17I |
probably benign |
Het |
Bag4 |
A |
G |
8: 26,258,136 (GRCm39) |
V397A |
probably damaging |
Het |
Brd7 |
A |
G |
8: 89,070,218 (GRCm39) |
V396A |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cdhr4 |
T |
A |
9: 107,870,466 (GRCm39) |
I123N |
possibly damaging |
Het |
Cep68 |
A |
G |
11: 20,189,186 (GRCm39) |
F609L |
probably benign |
Het |
Clec3b |
C |
A |
9: 122,980,178 (GRCm39) |
P24T |
possibly damaging |
Het |
Ctsg |
T |
A |
14: 56,339,869 (GRCm39) |
T9S |
probably benign |
Het |
Dalrd3 |
A |
T |
9: 108,448,725 (GRCm39) |
|
probably benign |
Het |
Dock6 |
A |
T |
9: 21,753,222 (GRCm39) |
V286E |
possibly damaging |
Het |
Dpep2 |
G |
A |
8: 106,711,723 (GRCm39) |
A568V |
probably benign |
Het |
Dph5 |
A |
C |
3: 115,720,390 (GRCm39) |
Q192P |
possibly damaging |
Het |
Eppin |
T |
A |
2: 164,433,698 (GRCm39) |
R37* |
probably null |
Het |
Esyt1 |
A |
G |
10: 128,348,293 (GRCm39) |
L865P |
possibly damaging |
Het |
Exoc6b |
A |
G |
6: 84,981,990 (GRCm39) |
L102P |
probably damaging |
Het |
Foxo6 |
A |
G |
4: 120,125,232 (GRCm39) |
I521T |
possibly damaging |
Het |
Guca1a |
A |
T |
17: 47,705,578 (GRCm39) |
|
probably benign |
Het |
Hpx |
A |
G |
7: 105,241,430 (GRCm39) |
F327S |
probably damaging |
Het |
Hspa12b |
A |
G |
2: 130,980,515 (GRCm39) |
M145V |
probably null |
Het |
Hspa4 |
A |
T |
11: 53,161,809 (GRCm39) |
S448T |
probably benign |
Het |
Kbtbd6 |
T |
C |
14: 79,690,759 (GRCm39) |
Y422H |
probably benign |
Het |
Lama4 |
A |
T |
10: 38,937,441 (GRCm39) |
D677V |
probably benign |
Het |
Ldb1 |
C |
T |
19: 46,024,195 (GRCm39) |
E111K |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,281,029 (GRCm39) |
S3823P |
probably damaging |
Het |
Man1a2 |
G |
A |
3: 100,499,189 (GRCm39) |
T415I |
probably benign |
Het |
Map3k2 |
T |
C |
18: 32,333,099 (GRCm39) |
|
probably benign |
Het |
Morn5 |
T |
A |
2: 35,945,038 (GRCm39) |
Y87* |
probably null |
Het |
Mpp3 |
T |
C |
11: 101,900,501 (GRCm39) |
D326G |
probably benign |
Het |
Mrgprx1 |
T |
C |
7: 47,671,336 (GRCm39) |
H137R |
probably benign |
Het |
Nav2 |
C |
A |
7: 49,102,260 (GRCm39) |
P292T |
probably damaging |
Het |
Nlrp2 |
C |
A |
7: 5,338,566 (GRCm39) |
|
probably null |
Het |
Noxo1 |
G |
A |
17: 24,918,030 (GRCm39) |
S112N |
probably damaging |
Het |
Nudt9 |
G |
T |
5: 104,212,885 (GRCm39) |
K319N |
probably benign |
Het |
Or8b38 |
A |
T |
9: 37,973,233 (GRCm39) |
I206L |
probably benign |
Het |
Osbpl7 |
C |
A |
11: 96,958,528 (GRCm39) |
Q728K |
probably damaging |
Het |
Pcsk1 |
A |
T |
13: 75,280,282 (GRCm39) |
E702D |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,205,933 (GRCm39) |
D1492G |
probably damaging |
Het |
Plekhg1 |
A |
G |
10: 3,908,103 (GRCm39) |
K1007E |
possibly damaging |
Het |
Ppp6r3 |
G |
A |
19: 3,514,693 (GRCm39) |
P141S |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,473,977 (GRCm39) |
T354A |
probably damaging |
Het |
Ptk2 |
C |
A |
15: 73,192,675 (GRCm39) |
W181L |
probably benign |
Het |
Rif1 |
T |
A |
2: 51,995,527 (GRCm39) |
H915Q |
probably benign |
Het |
Selenbp2 |
G |
T |
3: 94,611,371 (GRCm39) |
V361L |
probably benign |
Het |
Slamf7 |
A |
G |
1: 171,468,625 (GRCm39) |
L89P |
probably damaging |
Het |
Slc6a21 |
G |
A |
7: 44,937,505 (GRCm39) |
V599M |
probably damaging |
Het |
Sltm |
G |
T |
9: 70,494,467 (GRCm39) |
S921I |
probably damaging |
Het |
Smc4 |
C |
A |
3: 68,913,544 (GRCm39) |
A44E |
probably damaging |
Het |
Tdrd5 |
A |
T |
1: 156,087,513 (GRCm39) |
|
probably benign |
Het |
Tead2 |
T |
A |
7: 44,866,845 (GRCm39) |
I68N |
probably damaging |
Het |
Tnks1bp1 |
T |
A |
2: 84,902,143 (GRCm39) |
S1680T |
probably damaging |
Het |
Topbp1 |
T |
C |
9: 103,197,438 (GRCm39) |
V386A |
possibly damaging |
Het |
Tpx2 |
C |
A |
2: 152,724,207 (GRCm39) |
P328T |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,576,332 (GRCm39) |
I24854F |
probably damaging |
Het |
Zbtb11 |
G |
A |
16: 55,794,552 (GRCm39) |
R43H |
possibly damaging |
Het |
Zfp609 |
A |
G |
9: 65,610,611 (GRCm39) |
L784S |
possibly damaging |
Het |
Zfp703 |
T |
C |
8: 27,470,036 (GRCm39) |
S567P |
probably damaging |
Het |
Zfp750 |
A |
G |
11: 121,404,455 (GRCm39) |
I140T |
probably benign |
Het |
|
Other mutations in Alg8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01395:Alg8
|
APN |
7 |
97,027,383 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02349:Alg8
|
APN |
7 |
97,029,101 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0238:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0238:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0239:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0239:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1109:Alg8
|
UTSW |
7 |
97,032,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1429:Alg8
|
UTSW |
7 |
97,039,499 (GRCm39) |
missense |
probably benign |
0.18 |
R3838:Alg8
|
UTSW |
7 |
97,037,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5343:Alg8
|
UTSW |
7 |
97,036,126 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5622:Alg8
|
UTSW |
7 |
97,036,006 (GRCm39) |
splice site |
probably benign |
|
R5910:Alg8
|
UTSW |
7 |
97,039,493 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5963:Alg8
|
UTSW |
7 |
97,029,037 (GRCm39) |
missense |
probably benign |
0.00 |
R6484:Alg8
|
UTSW |
7 |
97,032,135 (GRCm39) |
missense |
probably benign |
|
R6735:Alg8
|
UTSW |
7 |
97,032,189 (GRCm39) |
missense |
probably benign |
0.05 |
R7896:Alg8
|
UTSW |
7 |
97,040,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7957:Alg8
|
UTSW |
7 |
97,040,131 (GRCm39) |
missense |
probably benign |
0.04 |
R7958:Alg8
|
UTSW |
7 |
97,036,128 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9226:Alg8
|
UTSW |
7 |
97,027,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Alg8
|
UTSW |
7 |
97,027,486 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9802:Alg8
|
UTSW |
7 |
97,027,486 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Alg8
|
UTSW |
7 |
97,032,968 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Alg8
|
UTSW |
7 |
97,020,869 (GRCm39) |
missense |
probably benign |
|
|