Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alms1 |
C |
A |
6: 85,605,636 (GRCm39) |
Q1960K |
probably benign |
Het |
Arhgef40 |
T |
A |
14: 52,234,865 (GRCm39) |
V1056E |
probably damaging |
Het |
Cdh26 |
T |
A |
2: 178,091,755 (GRCm39) |
F105I |
probably damaging |
Het |
Cep162 |
A |
T |
9: 87,130,432 (GRCm39) |
D59E |
possibly damaging |
Het |
Cngb3 |
A |
T |
4: 19,396,690 (GRCm39) |
T348S |
probably damaging |
Het |
Eci3 |
A |
T |
13: 35,130,963 (GRCm39) |
|
probably null |
Het |
Gapvd1 |
A |
G |
2: 34,615,416 (GRCm39) |
I409T |
probably benign |
Het |
Golga2 |
T |
C |
2: 32,186,735 (GRCm39) |
|
probably null |
Het |
Hoxd3 |
G |
A |
2: 74,577,298 (GRCm39) |
A393T |
probably benign |
Het |
Htr5a |
T |
C |
5: 28,047,658 (GRCm39) |
F71S |
probably damaging |
Het |
Hyou1 |
T |
C |
9: 44,292,707 (GRCm39) |
|
probably null |
Het |
Igsf6 |
C |
A |
7: 120,666,503 (GRCm39) |
|
probably benign |
Het |
Klrb1c |
C |
A |
6: 128,765,515 (GRCm39) |
C25F |
probably benign |
Het |
Lrguk |
C |
A |
6: 34,067,123 (GRCm39) |
T483K |
probably damaging |
Het |
Lrpprc |
A |
T |
17: 85,060,532 (GRCm39) |
|
probably benign |
Het |
Lrrk1 |
A |
T |
7: 65,958,407 (GRCm39) |
|
probably null |
Het |
Megf8 |
G |
A |
7: 25,057,857 (GRCm39) |
G2098D |
probably damaging |
Het |
Nfkbia |
T |
C |
12: 55,537,958 (GRCm39) |
Q165R |
possibly damaging |
Het |
Nipsnap2 |
A |
G |
5: 129,822,354 (GRCm39) |
|
probably benign |
Het |
Phykpl |
C |
T |
11: 51,489,540 (GRCm39) |
T382I |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,240,977 (GRCm39) |
D206G |
possibly damaging |
Het |
Rab26 |
T |
C |
17: 24,752,533 (GRCm39) |
S9G |
probably benign |
Het |
Sema3e |
C |
A |
5: 14,275,670 (GRCm39) |
N258K |
probably benign |
Het |
Slfn10-ps |
T |
A |
11: 82,920,971 (GRCm39) |
|
noncoding transcript |
Het |
Tgm5 |
A |
T |
2: 120,907,277 (GRCm39) |
C149S |
probably damaging |
Het |
Timp4 |
C |
T |
6: 115,226,785 (GRCm39) |
|
probably null |
Het |
Traf7 |
T |
C |
17: 24,731,964 (GRCm39) |
K251E |
probably benign |
Het |
Ugcg |
G |
T |
4: 59,207,763 (GRCm39) |
R34L |
possibly damaging |
Het |
Unc13d |
T |
C |
11: 115,964,444 (GRCm39) |
H300R |
probably damaging |
Het |
Vmn1r20 |
G |
T |
6: 57,408,746 (GRCm39) |
C24F |
probably benign |
Het |
Vmn2r13 |
T |
C |
5: 109,339,883 (GRCm39) |
R31G |
probably damaging |
Het |
Vsig10l |
A |
G |
7: 43,113,002 (GRCm39) |
T87A |
possibly damaging |
Het |
|
Other mutations in Zfp353-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R2040:Zfp353-ps
|
UTSW |
8 |
42,535,333 (GRCm39) |
exon |
noncoding transcript |
|
R2111:Zfp353-ps
|
UTSW |
8 |
42,536,005 (GRCm39) |
exon |
noncoding transcript |
|
R3922:Zfp353-ps
|
UTSW |
8 |
42,536,049 (GRCm39) |
exon |
noncoding transcript |
|
R4679:Zfp353-ps
|
UTSW |
8 |
42,535,251 (GRCm39) |
exon |
noncoding transcript |
|
R5270:Zfp353-ps
|
UTSW |
8 |
42,534,572 (GRCm39) |
exon |
noncoding transcript |
|
R5524:Zfp353-ps
|
UTSW |
8 |
42,535,600 (GRCm39) |
exon |
noncoding transcript |
|
R5772:Zfp353-ps
|
UTSW |
8 |
42,535,647 (GRCm39) |
exon |
noncoding transcript |
|
|