Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
T |
C |
10: 87,066,173 (GRCm39) |
S119P |
possibly damaging |
Het |
Agtpbp1 |
T |
A |
13: 59,661,966 (GRCm39) |
I282F |
probably damaging |
Het |
Armh1 |
A |
T |
4: 117,071,425 (GRCm39) |
M355K |
possibly damaging |
Het |
Cep128 |
A |
T |
12: 90,986,096 (GRCm39) |
D1013E |
probably benign |
Het |
Clock |
A |
T |
5: 76,393,267 (GRCm39) |
|
probably null |
Het |
Cspg4b |
T |
G |
13: 113,483,075 (GRCm39) |
V1559G |
|
Het |
D630003M21Rik |
G |
A |
2: 158,058,698 (GRCm39) |
Q401* |
probably null |
Het |
Dnah17 |
C |
A |
11: 117,915,997 (GRCm39) |
V4302L |
probably benign |
Het |
Drc3 |
A |
G |
11: 60,261,386 (GRCm39) |
Y179C |
probably benign |
Het |
Erbb3 |
T |
C |
10: 128,410,318 (GRCm39) |
T647A |
probably benign |
Het |
Esrp2 |
T |
C |
8: 106,860,908 (GRCm39) |
T205A |
probably benign |
Het |
Fbxw7 |
T |
C |
3: 84,874,872 (GRCm39) |
|
probably null |
Het |
Fmn1 |
C |
T |
2: 113,356,159 (GRCm39) |
P965S |
unknown |
Het |
Fndc7 |
C |
T |
3: 108,777,979 (GRCm39) |
V412M |
possibly damaging |
Het |
G2e3 |
C |
A |
12: 51,415,839 (GRCm39) |
A525E |
probably damaging |
Het |
Gcfc2 |
C |
T |
6: 81,918,371 (GRCm39) |
R354C |
probably damaging |
Het |
Ggt1 |
T |
A |
10: 75,421,508 (GRCm39) |
N510K |
probably damaging |
Het |
Gnas |
C |
T |
2: 174,140,820 (GRCm39) |
T389I |
unknown |
Het |
Hapln3 |
C |
T |
7: 78,767,121 (GRCm39) |
R306H |
probably benign |
Het |
Hydin |
T |
C |
8: 111,320,444 (GRCm39) |
L4496P |
possibly damaging |
Het |
Iqgap2 |
T |
A |
13: 95,867,952 (GRCm39) |
I219L |
probably benign |
Het |
Kcnj2 |
T |
C |
11: 110,963,309 (GRCm39) |
S234P |
probably benign |
Het |
Lipf |
T |
A |
19: 33,950,465 (GRCm39) |
S286T |
probably damaging |
Het |
Lrrc32 |
G |
T |
7: 98,148,545 (GRCm39) |
G442W |
probably damaging |
Het |
Megf10 |
GGCAGCAACAGCACCAGCAGCAACAGCACCAGCAGCA |
GGCAGCAACAGCACCAGCAGCA |
18: 57,427,071 (GRCm39) |
|
probably benign |
Het |
Mtmr4 |
T |
C |
11: 87,488,550 (GRCm39) |
V68A |
probably damaging |
Het |
Mug2 |
T |
C |
6: 122,055,754 (GRCm39) |
S1146P |
possibly damaging |
Het |
Naa35 |
T |
C |
13: 59,745,919 (GRCm39) |
I75T |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,316,432 (GRCm39) |
M496V |
probably benign |
Het |
Nthl1 |
A |
T |
17: 24,857,631 (GRCm39) |
I277F |
possibly damaging |
Het |
Or10a3 |
A |
C |
7: 108,479,889 (GRCm39) |
I308S |
probably damaging |
Het |
Or4p8 |
T |
C |
2: 88,728,122 (GRCm39) |
|
probably benign |
Het |
Osr1 |
A |
T |
12: 9,629,253 (GRCm39) |
Y42F |
probably damaging |
Het |
Rad54l2 |
G |
A |
9: 106,594,422 (GRCm39) |
R369W |
probably damaging |
Het |
Ryr3 |
T |
A |
2: 112,465,691 (GRCm39) |
T4828S |
probably benign |
Het |
Slc25a54 |
T |
A |
3: 109,010,133 (GRCm39) |
C211S |
probably damaging |
Het |
Ube4b |
C |
T |
4: 149,483,238 (GRCm39) |
R10Q |
possibly damaging |
Het |
Usp9y |
G |
A |
Y: 1,304,411 (GRCm39) |
Q2440* |
probably null |
Het |
Yars1 |
G |
T |
4: 129,104,291 (GRCm39) |
V312L |
probably benign |
Het |
Zfp26 |
G |
A |
9: 20,352,630 (GRCm39) |
T145I |
probably benign |
Het |
Zic5 |
T |
C |
14: 122,701,525 (GRCm39) |
N402S |
unknown |
Het |
|
Other mutations in Nepn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01122:Nepn
|
APN |
10 |
52,267,911 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01731:Nepn
|
APN |
10 |
52,276,660 (GRCm39) |
missense |
probably benign |
0.00 |
R0099:Nepn
|
UTSW |
10 |
52,277,181 (GRCm39) |
missense |
probably damaging |
0.96 |
R0123:Nepn
|
UTSW |
10 |
52,276,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R0134:Nepn
|
UTSW |
10 |
52,276,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R0225:Nepn
|
UTSW |
10 |
52,276,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R0613:Nepn
|
UTSW |
10 |
52,277,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Nepn
|
UTSW |
10 |
52,276,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R2969:Nepn
|
UTSW |
10 |
52,276,983 (GRCm39) |
nonsense |
probably null |
|
R3731:Nepn
|
UTSW |
10 |
52,280,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Nepn
|
UTSW |
10 |
52,276,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R3958:Nepn
|
UTSW |
10 |
52,276,804 (GRCm39) |
missense |
probably benign |
|
R4423:Nepn
|
UTSW |
10 |
52,267,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5002:Nepn
|
UTSW |
10 |
52,267,850 (GRCm39) |
missense |
probably benign |
|
R5294:Nepn
|
UTSW |
10 |
52,276,896 (GRCm39) |
missense |
probably benign |
0.02 |
R5580:Nepn
|
UTSW |
10 |
52,280,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R5607:Nepn
|
UTSW |
10 |
52,277,233 (GRCm39) |
missense |
probably benign |
0.10 |
R5986:Nepn
|
UTSW |
10 |
52,280,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Nepn
|
UTSW |
10 |
52,267,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7256:Nepn
|
UTSW |
10 |
52,277,089 (GRCm39) |
missense |
probably benign |
0.01 |
R8213:Nepn
|
UTSW |
10 |
52,267,855 (GRCm39) |
missense |
probably benign |
0.00 |
R8432:Nepn
|
UTSW |
10 |
52,267,880 (GRCm39) |
missense |
probably benign |
0.15 |
R8463:Nepn
|
UTSW |
10 |
52,276,896 (GRCm39) |
missense |
probably benign |
0.23 |
R9315:Nepn
|
UTSW |
10 |
52,267,869 (GRCm39) |
missense |
probably benign |
0.02 |
R9684:Nepn
|
UTSW |
10 |
52,276,801 (GRCm39) |
missense |
probably benign |
0.34 |
|