Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
A |
5: 8,862,656 (GRCm39) |
Y113N |
probably damaging |
Het |
Bcan |
G |
T |
3: 87,901,514 (GRCm39) |
S396Y |
probably damaging |
Het |
Calm3 |
T |
C |
7: 16,651,626 (GRCm39) |
D21G |
probably damaging |
Het |
Cldn23 |
C |
T |
8: 36,293,474 (GRCm39) |
V5M |
possibly damaging |
Het |
D630003M21Rik |
A |
G |
2: 158,047,665 (GRCm39) |
S735P |
probably damaging |
Het |
Dscaml1 |
T |
C |
9: 45,628,730 (GRCm39) |
Y1095H |
probably damaging |
Het |
Esr2 |
T |
C |
12: 76,170,048 (GRCm39) |
T427A |
probably benign |
Het |
Fbxo28 |
T |
C |
1: 182,145,558 (GRCm39) |
I177V |
possibly damaging |
Het |
Fubp1 |
T |
C |
3: 151,926,989 (GRCm39) |
L372P |
possibly damaging |
Het |
Glis1 |
G |
A |
4: 107,491,891 (GRCm39) |
G585E |
probably damaging |
Het |
Gm7258 |
T |
C |
7: 128,197,791 (GRCm39) |
|
noncoding transcript |
Het |
Hecw1 |
C |
T |
13: 14,460,242 (GRCm39) |
R613Q |
probably damaging |
Het |
Kif13b |
T |
C |
14: 65,010,384 (GRCm39) |
S1228P |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,900,512 (GRCm39) |
I738V |
probably damaging |
Het |
Lig1 |
T |
A |
7: 13,044,983 (GRCm39) |
V892D |
probably damaging |
Het |
Lvrn |
T |
A |
18: 47,013,814 (GRCm39) |
Y499N |
probably damaging |
Het |
Ly9 |
C |
A |
1: 171,432,773 (GRCm39) |
W80L |
probably damaging |
Het |
Ngdn |
C |
T |
14: 55,259,656 (GRCm39) |
Q236* |
probably null |
Het |
Nudt7 |
C |
A |
8: 114,878,567 (GRCm39) |
C154* |
probably null |
Het |
Obi1 |
A |
G |
14: 104,716,223 (GRCm39) |
S717P |
probably damaging |
Het |
Or14j10 |
C |
A |
17: 37,934,642 (GRCm39) |
E295* |
probably null |
Het |
Or4f14b |
A |
T |
2: 111,775,447 (GRCm39) |
M118K |
probably damaging |
Het |
Or5b117 |
T |
A |
19: 13,431,741 (GRCm39) |
I47F |
probably damaging |
Het |
Paxbp1 |
A |
G |
16: 90,819,555 (GRCm39) |
|
probably null |
Het |
Pcnt |
G |
T |
10: 76,256,258 (GRCm39) |
Q661K |
probably damaging |
Het |
Plekha1 |
G |
A |
7: 130,487,179 (GRCm39) |
|
probably null |
Het |
Polr1c |
G |
T |
17: 46,558,635 (GRCm39) |
|
probably benign |
Het |
Rac3 |
A |
G |
11: 120,613,421 (GRCm39) |
D58G |
probably null |
Het |
Rgl2 |
C |
T |
17: 34,154,948 (GRCm39) |
R203* |
probably null |
Het |
Ryr1 |
T |
C |
7: 28,767,118 (GRCm39) |
D2948G |
probably damaging |
Het |
Serpina12 |
A |
T |
12: 104,004,179 (GRCm39) |
L151Q |
probably damaging |
Het |
Sf3a1 |
T |
C |
11: 4,127,456 (GRCm39) |
V594A |
possibly damaging |
Het |
Spdl1 |
G |
T |
11: 34,704,187 (GRCm39) |
H549N |
possibly damaging |
Het |
Srp68 |
C |
A |
11: 116,156,300 (GRCm39) |
E147D |
probably damaging |
Het |
Zfp352 |
A |
G |
4: 90,112,453 (GRCm39) |
T198A |
possibly damaging |
Het |
|
Other mutations in Lypd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01066:Lypd5
|
APN |
7 |
24,052,910 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01121:Lypd5
|
APN |
7 |
24,050,976 (GRCm39) |
missense |
probably benign |
|
IGL01689:Lypd5
|
APN |
7 |
24,052,054 (GRCm39) |
splice site |
probably benign |
|
IGL02584:Lypd5
|
APN |
7 |
24,052,993 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02888:Lypd5
|
APN |
7 |
24,052,044 (GRCm39) |
missense |
probably damaging |
0.98 |
R5982:Lypd5
|
UTSW |
7 |
24,052,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R6746:Lypd5
|
UTSW |
7 |
24,052,531 (GRCm39) |
splice site |
probably null |
|
R7951:Lypd5
|
UTSW |
7 |
24,051,060 (GRCm39) |
missense |
probably damaging |
0.96 |
R8704:Lypd5
|
UTSW |
7 |
24,050,982 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8725:Lypd5
|
UTSW |
7 |
24,053,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Lypd5
|
UTSW |
7 |
24,053,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Lypd5
|
UTSW |
7 |
24,051,015 (GRCm39) |
missense |
probably benign |
0.13 |
X0057:Lypd5
|
UTSW |
7 |
24,048,646 (GRCm39) |
utr 5 prime |
probably benign |
|
Z1177:Lypd5
|
UTSW |
7 |
24,052,038 (GRCm39) |
missense |
probably damaging |
1.00 |
|