Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox3 |
A |
G |
5: 35,747,083 (GRCm39) |
T167A |
probably benign |
Het |
Aox1 |
T |
G |
1: 58,134,316 (GRCm39) |
D1096E |
probably damaging |
Het |
Arid4a |
A |
T |
12: 71,122,721 (GRCm39) |
D1034V |
probably damaging |
Het |
Ccdc168 |
G |
A |
1: 44,097,178 (GRCm39) |
P1307S |
possibly damaging |
Het |
Chaf1b |
T |
A |
16: 93,684,022 (GRCm39) |
L91Q |
probably damaging |
Het |
Copb2 |
G |
T |
9: 98,463,320 (GRCm39) |
D512Y |
probably damaging |
Het |
Daam1 |
A |
G |
12: 71,988,981 (GRCm39) |
E127G |
unknown |
Het |
Dhx16 |
A |
G |
17: 36,194,154 (GRCm39) |
I422V |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,098,771 (GRCm39) |
V2043I |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
A |
G |
9: 7,147,717 (GRCm39) |
V971A |
probably benign |
Het |
Elapor1 |
A |
G |
3: 108,375,149 (GRCm39) |
S573P |
probably benign |
Het |
Elmo1 |
A |
G |
13: 20,633,682 (GRCm39) |
H448R |
probably benign |
Het |
Fndc1 |
A |
T |
17: 7,988,567 (GRCm39) |
V1165D |
unknown |
Het |
Hapln1 |
G |
A |
13: 89,749,571 (GRCm39) |
G39S |
possibly damaging |
Het |
Igkv6-13 |
C |
A |
6: 70,434,765 (GRCm39) |
V27L |
probably benign |
Het |
Krt28 |
A |
T |
11: 99,255,936 (GRCm39) |
I441N |
possibly damaging |
Het |
Lgr5 |
A |
T |
10: 115,298,669 (GRCm39) |
D286E |
probably damaging |
Het |
Mapkap1 |
A |
G |
2: 34,513,442 (GRCm39) |
Y448C |
probably damaging |
Het |
Or2f1 |
T |
C |
6: 42,721,489 (GRCm39) |
Y173H |
possibly damaging |
Het |
Or5t9 |
T |
A |
2: 86,659,876 (GRCm39) |
V260E |
probably damaging |
Het |
Ppt1 |
A |
C |
4: 122,738,242 (GRCm39) |
N89T |
probably damaging |
Het |
Prss3b |
T |
G |
6: 41,009,345 (GRCm39) |
D163A |
possibly damaging |
Het |
Ptgs1 |
G |
T |
2: 36,127,267 (GRCm39) |
R51L |
probably damaging |
Het |
Slc47a2 |
A |
G |
11: 61,204,520 (GRCm39) |
F277S |
possibly damaging |
Het |
Smcr8 |
A |
G |
11: 60,668,897 (GRCm39) |
E15G |
probably benign |
Het |
Tbce |
A |
G |
13: 14,173,004 (GRCm39) |
S476P |
possibly damaging |
Het |
Tmem131l |
A |
T |
3: 83,805,517 (GRCm39) |
|
probably benign |
Het |
Unc5c |
T |
C |
3: 141,495,534 (GRCm39) |
Y468H |
probably damaging |
Het |
Ush1c |
A |
T |
7: 45,878,664 (GRCm39) |
L117H |
probably damaging |
Het |
Wdfy4 |
A |
G |
14: 32,822,860 (GRCm39) |
|
probably null |
Het |
Zfat |
C |
A |
15: 68,051,959 (GRCm39) |
A605S |
probably benign |
Het |
Zfp853 |
T |
A |
5: 143,275,416 (GRCm39) |
Q68L |
unknown |
Het |
Zfyve16 |
G |
A |
13: 92,644,764 (GRCm39) |
T1146I |
probably damaging |
Het |
|
Other mutations in Zfa-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00960:Zfa-ps
|
APN |
10 |
52,420,043 (GRCm39) |
exon |
noncoding transcript |
|
R0057:Zfa-ps
|
UTSW |
10 |
52,421,202 (GRCm39) |
exon |
noncoding transcript |
|
R0057:Zfa-ps
|
UTSW |
10 |
52,421,202 (GRCm39) |
exon |
noncoding transcript |
|
R1159:Zfa-ps
|
UTSW |
10 |
52,419,654 (GRCm39) |
exon |
noncoding transcript |
|
R2145:Zfa-ps
|
UTSW |
10 |
52,419,373 (GRCm39) |
exon |
noncoding transcript |
|
R2290:Zfa-ps
|
UTSW |
10 |
52,421,112 (GRCm39) |
exon |
noncoding transcript |
|
R2509:Zfa-ps
|
UTSW |
10 |
52,420,339 (GRCm39) |
exon |
noncoding transcript |
|
R3738:Zfa-ps
|
UTSW |
10 |
52,420,636 (GRCm39) |
exon |
noncoding transcript |
|
R4035:Zfa-ps
|
UTSW |
10 |
52,420,636 (GRCm39) |
exon |
noncoding transcript |
|
R4290:Zfa-ps
|
UTSW |
10 |
52,419,807 (GRCm39) |
exon |
noncoding transcript |
|
R4545:Zfa-ps
|
UTSW |
10 |
52,421,032 (GRCm39) |
exon |
noncoding transcript |
|
R5135:Zfa-ps
|
UTSW |
10 |
52,419,118 (GRCm39) |
exon |
noncoding transcript |
|
R5270:Zfa-ps
|
UTSW |
10 |
52,419,552 (GRCm39) |
exon |
noncoding transcript |
|
|