Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
G |
A |
2: 69,115,652 (GRCm39) |
R571C |
probably damaging |
Het |
Agr3 |
T |
C |
12: 35,997,590 (GRCm39) |
M100T |
probably benign |
Het |
Ankrd7 |
T |
A |
6: 18,870,007 (GRCm39) |
Y253* |
probably null |
Het |
Atp2c2 |
A |
T |
8: 120,475,801 (GRCm39) |
T565S |
probably benign |
Het |
Ccdc88b |
G |
T |
19: 6,831,151 (GRCm39) |
S597Y |
possibly damaging |
Het |
Celsr2 |
T |
C |
3: 108,320,379 (GRCm39) |
N811S |
probably damaging |
Het |
Cep170 |
A |
T |
1: 176,583,657 (GRCm39) |
D907E |
probably damaging |
Het |
Cip2a |
C |
T |
16: 48,837,736 (GRCm39) |
S812F |
probably benign |
Het |
Clstn1 |
G |
A |
4: 149,719,253 (GRCm39) |
V361M |
probably damaging |
Het |
Cmss1 |
T |
G |
16: 57,131,612 (GRCm39) |
|
probably null |
Het |
Cobl |
T |
C |
11: 12,204,945 (GRCm39) |
T579A |
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Csrp2 |
C |
T |
10: 110,774,601 (GRCm39) |
S172L |
probably benign |
Het |
Fip1l1 |
T |
C |
5: 74,717,770 (GRCm39) |
S235P |
probably damaging |
Het |
Gbgt1 |
T |
A |
2: 28,388,462 (GRCm39) |
|
probably benign |
Het |
Gucy2c |
T |
A |
6: 136,674,997 (GRCm39) |
I1005F |
probably damaging |
Het |
Irak3 |
T |
A |
10: 120,012,225 (GRCm39) |
K88* |
probably null |
Het |
Klc1 |
T |
C |
12: 111,743,467 (GRCm39) |
Y265H |
probably damaging |
Het |
Lamb1 |
G |
A |
12: 31,351,155 (GRCm39) |
V754I |
probably benign |
Het |
Lrguk |
A |
T |
6: 34,020,431 (GRCm39) |
Q58H |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,882,741 (GRCm39) |
D2902G |
probably benign |
Het |
Mtpap |
T |
A |
18: 4,383,244 (GRCm39) |
I207N |
probably damaging |
Het |
Ncdn |
A |
T |
4: 126,643,901 (GRCm39) |
|
probably null |
Het |
Nup160 |
A |
G |
2: 90,547,931 (GRCm39) |
|
probably null |
Het |
Ormdl1 |
A |
G |
1: 53,338,318 (GRCm39) |
|
probably benign |
Het |
Pde5a |
A |
G |
3: 122,596,704 (GRCm39) |
M432V |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,255,088 (GRCm39) |
|
probably benign |
Het |
Plcb2 |
A |
G |
2: 118,545,942 (GRCm39) |
V581A |
probably benign |
Het |
Plpp6 |
T |
A |
19: 28,942,243 (GRCm39) |
N281K |
probably benign |
Het |
Pwp1 |
T |
C |
10: 85,721,760 (GRCm39) |
I422T |
probably benign |
Het |
Rims1 |
T |
C |
1: 22,367,103 (GRCm39) |
N1199S |
probably damaging |
Het |
Sema3c |
T |
C |
5: 17,899,726 (GRCm39) |
L406P |
probably damaging |
Het |
Senp6 |
C |
T |
9: 80,033,525 (GRCm39) |
P84L |
probably damaging |
Het |
Setx |
A |
G |
2: 29,066,941 (GRCm39) |
I2361V |
probably benign |
Het |
Slc25a12 |
C |
T |
2: 71,163,958 (GRCm39) |
V106M |
possibly damaging |
Het |
Slc3a1 |
A |
G |
17: 85,340,274 (GRCm39) |
Y232C |
probably damaging |
Het |
Spata31g1 |
A |
T |
4: 42,973,712 (GRCm39) |
K1015M |
probably damaging |
Het |
Taf1c |
A |
T |
8: 120,325,829 (GRCm39) |
C678S |
probably benign |
Het |
Tcp11l2 |
G |
T |
10: 84,427,004 (GRCm39) |
C156F |
probably damaging |
Het |
Tmem62 |
A |
G |
2: 120,829,594 (GRCm39) |
T316A |
probably benign |
Het |
Ulk4 |
A |
G |
9: 121,102,048 (GRCm39) |
I10T |
probably damaging |
Het |
Vps54 |
T |
C |
11: 21,262,899 (GRCm39) |
I824T |
probably damaging |
Het |
Wdfy3 |
A |
T |
5: 102,037,161 (GRCm39) |
V2042E |
probably damaging |
Het |
Wfdc6b |
A |
T |
2: 164,455,779 (GRCm39) |
E36V |
probably damaging |
Het |
Xpc |
C |
T |
6: 91,468,208 (GRCm39) |
A860T |
probably benign |
Het |
|
Other mutations in Gml2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01649:Gml2
|
APN |
15 |
74,696,070 (GRCm39) |
nonsense |
probably null |
|
R0608:Gml2
|
UTSW |
15 |
74,693,235 (GRCm39) |
critical splice donor site |
probably null |
|
R1087:Gml2
|
UTSW |
15 |
74,695,946 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1130:Gml2
|
UTSW |
15 |
74,693,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R1503:Gml2
|
UTSW |
15 |
74,693,201 (GRCm39) |
nonsense |
probably null |
|
R4408:Gml2
|
UTSW |
15 |
74,696,188 (GRCm39) |
intron |
probably benign |
|
R6802:Gml2
|
UTSW |
15 |
74,696,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R7351:Gml2
|
UTSW |
15 |
74,693,225 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7833:Gml2
|
UTSW |
15 |
74,693,217 (GRCm39) |
nonsense |
probably null |
|
R7910:Gml2
|
UTSW |
15 |
74,692,379 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8513:Gml2
|
UTSW |
15 |
74,696,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R8695:Gml2
|
UTSW |
15 |
74,696,089 (GRCm39) |
missense |
probably benign |
0.05 |
R9377:Gml2
|
UTSW |
15 |
74,695,957 (GRCm39) |
missense |
probably benign |
0.02 |
X0066:Gml2
|
UTSW |
15 |
74,695,899 (GRCm39) |
missense |
probably benign |
0.01 |
|