Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5031439G07Rik |
T |
C |
15: 84,833,459 (GRCm39) |
K442E |
probably damaging |
Het |
Adamts1 |
G |
A |
16: 85,594,940 (GRCm39) |
R340* |
probably null |
Het |
Afg3l2 |
T |
C |
18: 67,556,047 (GRCm39) |
N428S |
possibly damaging |
Het |
Aqp12 |
G |
A |
1: 92,934,332 (GRCm39) |
D70N |
probably damaging |
Het |
Astn1 |
T |
A |
1: 158,338,679 (GRCm39) |
C475* |
probably null |
Het |
Atp2b1 |
G |
A |
10: 98,852,893 (GRCm39) |
|
probably null |
Het |
Cbln2 |
T |
C |
18: 86,734,877 (GRCm39) |
S217P |
possibly damaging |
Het |
Ces2h |
T |
C |
8: 105,741,182 (GRCm39) |
L58P |
probably damaging |
Het |
Cfap43 |
C |
T |
19: 47,736,433 (GRCm39) |
G1353R |
possibly damaging |
Het |
Crcp |
A |
G |
5: 130,088,672 (GRCm39) |
M91V |
probably benign |
Het |
Cubn |
A |
G |
2: 13,367,139 (GRCm39) |
V1577A |
possibly damaging |
Het |
Dthd1 |
A |
G |
5: 63,000,271 (GRCm39) |
H531R |
probably benign |
Het |
Fam120a |
G |
T |
13: 49,039,219 (GRCm39) |
A979E |
possibly damaging |
Het |
Fam3d |
A |
G |
14: 8,364,863 (GRCm38) |
I16T |
probably damaging |
Het |
Fat2 |
C |
T |
11: 55,147,051 (GRCm39) |
G3982S |
probably damaging |
Het |
Fbxo44 |
C |
G |
4: 148,240,726 (GRCm39) |
R220S |
probably damaging |
Het |
Fcnb |
T |
A |
2: 27,966,791 (GRCm39) |
K247N |
probably damaging |
Het |
Gtf2a1l |
A |
G |
17: 88,976,152 (GRCm39) |
N5S |
|
Het |
Htr3a |
T |
A |
9: 48,812,752 (GRCm39) |
D229V |
possibly damaging |
Het |
Ipo11 |
A |
C |
13: 107,037,324 (GRCm39) |
L173* |
probably null |
Het |
Jam3 |
C |
A |
9: 27,010,253 (GRCm39) |
G244W |
probably damaging |
Het |
Mrpl52 |
C |
T |
14: 54,664,541 (GRCm39) |
R12* |
probably null |
Het |
Myo15a |
A |
G |
11: 60,368,011 (GRCm39) |
Y257C |
possibly damaging |
Het |
Myocd |
G |
A |
11: 65,086,018 (GRCm39) |
P215L |
possibly damaging |
Het |
Ndst1 |
T |
C |
18: 60,840,954 (GRCm39) |
T243A |
probably benign |
Het |
Obox5 |
A |
T |
7: 15,492,800 (GRCm39) |
T252S |
probably benign |
Het |
Or5m13b |
A |
G |
2: 85,753,731 (GRCm39) |
T40A |
probably benign |
Het |
Or6c75 |
T |
C |
10: 129,337,301 (GRCm39) |
F183L |
probably damaging |
Het |
Or7g34 |
A |
C |
9: 19,477,843 (GRCm39) |
V276G |
probably damaging |
Het |
Osbpl1a |
T |
C |
18: 12,890,747 (GRCm39) |
S377G |
possibly damaging |
Het |
Pfkl |
A |
G |
10: 77,841,273 (GRCm39) |
|
probably null |
Het |
Prdm16 |
A |
T |
4: 154,613,366 (GRCm39) |
N20K |
probably damaging |
Het |
Prkd1 |
A |
G |
12: 50,431,976 (GRCm39) |
I589T |
probably damaging |
Het |
Scnn1b |
G |
A |
7: 121,516,938 (GRCm39) |
G525S |
probably damaging |
Het |
Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,718,329 (GRCm39) |
|
probably benign |
Het |
Wap |
T |
C |
11: 6,586,725 (GRCm39) |
T125A |
probably benign |
Het |
Wdr86 |
C |
T |
5: 24,923,005 (GRCm39) |
R229Q |
probably benign |
Het |
|
Other mutations in Lypd11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00840:Lypd11
|
APN |
7 |
24,422,931 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02953:Lypd11
|
APN |
7 |
24,422,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Lypd11
|
APN |
7 |
24,422,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R0144:Lypd11
|
UTSW |
7 |
24,423,015 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0485:Lypd11
|
UTSW |
7 |
24,422,170 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0652:Lypd11
|
UTSW |
7 |
24,423,622 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0963:Lypd11
|
UTSW |
7 |
24,423,047 (GRCm39) |
missense |
probably benign |
0.00 |
R5290:Lypd11
|
UTSW |
7 |
24,422,836 (GRCm39) |
missense |
probably benign |
0.04 |
R6134:Lypd11
|
UTSW |
7 |
24,425,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7128:Lypd11
|
UTSW |
7 |
24,425,424 (GRCm39) |
critical splice donor site |
probably null |
|
R7191:Lypd11
|
UTSW |
7 |
24,422,759 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9061:Lypd11
|
UTSW |
7 |
24,422,173 (GRCm39) |
missense |
possibly damaging |
0.96 |
X0062:Lypd11
|
UTSW |
7 |
24,422,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|