Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace2 |
A |
G |
X: 162,968,701 (GRCm39) |
T482A |
probably damaging |
Het |
Adh1 |
T |
C |
3: 137,988,546 (GRCm39) |
I173T |
possibly damaging |
Het |
Apoa1 |
T |
C |
9: 46,140,548 (GRCm39) |
S60P |
possibly damaging |
Het |
Blnk |
A |
G |
19: 40,922,929 (GRCm39) |
V396A |
probably benign |
Het |
Borcs8 |
A |
G |
8: 70,619,030 (GRCm39) |
D204G |
probably damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,373,336 (GRCm39) |
|
probably benign |
Het |
Cdkal1 |
T |
G |
13: 29,701,493 (GRCm39) |
I319L |
probably benign |
Het |
Celsr1 |
T |
A |
15: 85,791,922 (GRCm39) |
T2560S |
possibly damaging |
Het |
Chd8 |
A |
G |
14: 52,464,691 (GRCm39) |
|
probably null |
Het |
Cyp4f39 |
T |
C |
17: 32,689,932 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,866,876 (GRCm39) |
N2265S |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,240,187 (GRCm39) |
|
probably benign |
Het |
Epgn |
G |
A |
5: 91,181,816 (GRCm39) |
G133E |
probably damaging |
Het |
Fdx2 |
C |
A |
9: 20,984,766 (GRCm39) |
V13F |
probably benign |
Het |
Gabarapl2 |
A |
G |
8: 112,667,831 (GRCm39) |
Y25C |
probably damaging |
Het |
Gigyf1 |
G |
A |
5: 137,523,826 (GRCm39) |
|
probably null |
Het |
Gm6040 |
G |
A |
8: 21,407,169 (GRCm39) |
|
probably benign |
Het |
Gm8229 |
T |
C |
14: 44,604,054 (GRCm39) |
L81P |
unknown |
Het |
Gstz1 |
A |
G |
12: 87,210,528 (GRCm39) |
E137G |
probably benign |
Het |
Htra1 |
T |
C |
7: 130,538,108 (GRCm39) |
V36A |
probably benign |
Het |
Ifnlr1 |
T |
C |
4: 135,432,578 (GRCm39) |
V338A |
probably benign |
Het |
Igsf8 |
A |
G |
1: 172,140,156 (GRCm39) |
|
probably benign |
Het |
Khdc1a |
T |
A |
1: 21,421,212 (GRCm39) |
F132L |
probably benign |
Het |
Kifc3 |
G |
A |
8: 95,829,108 (GRCm39) |
S561L |
probably damaging |
Het |
Mpi |
T |
C |
9: 57,457,936 (GRCm39) |
T89A |
probably benign |
Het |
Ncor2 |
A |
T |
5: 125,111,467 (GRCm39) |
M1281K |
probably damaging |
Het |
Or4c117 |
T |
C |
2: 88,956,021 (GRCm39) |
N18S |
probably benign |
Het |
Or4k49 |
G |
T |
2: 111,495,333 (GRCm39) |
C254F |
probably damaging |
Het |
Or6c213 |
T |
A |
10: 129,574,181 (GRCm39) |
I202L |
probably benign |
Het |
Or6c66b |
T |
C |
10: 129,377,176 (GRCm39) |
Y257H |
probably damaging |
Het |
Otog |
G |
A |
7: 45,949,571 (GRCm39) |
G2403D |
probably damaging |
Het |
Pdgfb |
C |
A |
15: 79,898,184 (GRCm39) |
A6S |
probably benign |
Het |
Pfkm |
T |
C |
15: 98,021,121 (GRCm39) |
|
probably null |
Het |
Plcb4 |
A |
G |
2: 135,789,041 (GRCm39) |
M274V |
probably benign |
Het |
Ppm1m |
A |
G |
9: 106,074,001 (GRCm39) |
|
probably null |
Het |
Rptn |
A |
G |
3: 93,304,041 (GRCm39) |
D458G |
possibly damaging |
Het |
Sertad3 |
C |
T |
7: 27,175,950 (GRCm39) |
S128F |
probably benign |
Het |
Sgo2b |
A |
T |
8: 64,380,123 (GRCm39) |
L903Q |
probably damaging |
Het |
Slc15a5 |
C |
T |
6: 138,020,598 (GRCm39) |
R245H |
probably benign |
Het |
Slc24a5 |
A |
T |
2: 124,910,218 (GRCm39) |
T40S |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,738,248 (GRCm39) |
N539S |
possibly damaging |
Het |
Tlr11 |
A |
G |
14: 50,600,489 (GRCm39) |
D825G |
probably damaging |
Het |
Top3b |
T |
G |
16: 16,709,334 (GRCm39) |
V674G |
possibly damaging |
Het |
Urb2 |
G |
A |
8: 124,754,976 (GRCm39) |
V228I |
probably benign |
Het |
Usp24 |
C |
T |
4: 106,268,623 (GRCm39) |
A2061V |
possibly damaging |
Het |
Wdr72 |
C |
A |
9: 74,062,212 (GRCm39) |
H453N |
possibly damaging |
Het |
Xkr9 |
T |
C |
1: 13,771,600 (GRCm39) |
M372T |
probably damaging |
Het |
Zc3h12d |
T |
G |
10: 7,743,096 (GRCm39) |
S289A |
probably benign |
Het |
Zfp607b |
A |
T |
7: 27,398,140 (GRCm39) |
M75L |
possibly damaging |
Het |
|
Other mutations in Calhm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01695:Calhm5
|
APN |
10 |
33,968,198 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01966:Calhm5
|
APN |
10 |
33,972,129 (GRCm39) |
missense |
probably benign |
0.00 |
R0781:Calhm5
|
UTSW |
10 |
33,972,013 (GRCm39) |
missense |
probably benign |
0.00 |
R1110:Calhm5
|
UTSW |
10 |
33,972,013 (GRCm39) |
missense |
probably benign |
0.00 |
R5214:Calhm5
|
UTSW |
10 |
33,968,487 (GRCm39) |
missense |
probably damaging |
0.99 |
R5705:Calhm5
|
UTSW |
10 |
33,971,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Calhm5
|
UTSW |
10 |
33,968,198 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6489:Calhm5
|
UTSW |
10 |
33,968,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6863:Calhm5
|
UTSW |
10 |
33,968,451 (GRCm39) |
missense |
probably benign |
0.01 |
R6873:Calhm5
|
UTSW |
10 |
33,968,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R6995:Calhm5
|
UTSW |
10 |
33,972,189 (GRCm39) |
missense |
probably benign |
|
R7169:Calhm5
|
UTSW |
10 |
33,968,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R8263:Calhm5
|
UTSW |
10 |
33,972,192 (GRCm39) |
missense |
probably damaging |
0.98 |
R8327:Calhm5
|
UTSW |
10 |
33,972,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Calhm5
|
UTSW |
10 |
33,968,415 (GRCm39) |
missense |
probably benign |
0.20 |
R9105:Calhm5
|
UTSW |
10 |
33,968,144 (GRCm39) |
missense |
probably benign |
0.00 |
R9438:Calhm5
|
UTSW |
10 |
33,972,049 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Calhm5
|
UTSW |
10 |
33,972,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|