Incidental Mutation 'IGL00557:Wdr87-ps'
ID |
332604 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Wdr87-ps
|
Ensembl Gene |
ENSMUSG00000074224 |
Gene Name |
WD repeat domain 87, pseudogene |
Synonyms |
4932431P20Rik |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL00557
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
29223968-29237480 bp(+) (GRCm39) |
Type of Mutation |
exon |
DNA Base Change (assembly) |
A to G
at 29235227 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
|
AlphaFold |
no structure available at present |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000098602
|
SMART Domains |
Protein: ENSMUSP00000096202 Gene: ENSMUSG00000074224
Domain | Start | End | E-Value | Type |
low complexity region
|
233 |
239 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000141713
|
SMART Domains |
Protein: ENSMUSP00000120285 Gene: ENSMUSG00000074224
Domain | Start | End | E-Value | Type |
Blast:WD40
|
94 |
134 |
1e-9 |
BLAST |
WD40
|
139 |
176 |
1.59e1 |
SMART |
WD40
|
228 |
269 |
9.51e1 |
SMART |
WD40
|
272 |
311 |
3.33e-1 |
SMART |
Blast:WD40
|
354 |
393 |
4e-15 |
BLAST |
Blast:WD40
|
445 |
490 |
2e-22 |
BLAST |
Blast:WD40
|
493 |
538 |
8e-15 |
BLAST |
WD40
|
595 |
634 |
1.68e-6 |
SMART |
low complexity region
|
701 |
710 |
N/A |
INTRINSIC |
low complexity region
|
915 |
926 |
N/A |
INTRINSIC |
coiled coil region
|
1135 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1211 |
1230 |
N/A |
INTRINSIC |
low complexity region
|
1239 |
1273 |
N/A |
INTRINSIC |
coiled coil region
|
1347 |
1375 |
N/A |
INTRINSIC |
coiled coil region
|
1399 |
1433 |
N/A |
INTRINSIC |
low complexity region
|
1435 |
1453 |
N/A |
INTRINSIC |
low complexity region
|
1497 |
1519 |
N/A |
INTRINSIC |
coiled coil region
|
1612 |
1707 |
N/A |
INTRINSIC |
coiled coil region
|
1731 |
1989 |
N/A |
INTRINSIC |
coiled coil region
|
2034 |
2072 |
N/A |
INTRINSIC |
coiled coil region
|
2127 |
2154 |
N/A |
INTRINSIC |
coiled coil region
|
2220 |
2302 |
N/A |
INTRINSIC |
coiled coil region
|
2357 |
2561 |
N/A |
INTRINSIC |
low complexity region
|
2993 |
2999 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agpat3 |
A |
T |
10: 78,109,516 (GRCm39) |
|
probably benign |
Het |
Arhgap35 |
T |
C |
7: 16,298,340 (GRCm39) |
T242A |
probably benign |
Het |
Asb15 |
C |
A |
6: 24,558,649 (GRCm39) |
R55S |
probably benign |
Het |
Brca2 |
C |
T |
5: 150,484,003 (GRCm39) |
R2941W |
probably benign |
Het |
Chrng |
T |
C |
1: 87,134,469 (GRCm39) |
V135A |
probably damaging |
Het |
Corin |
G |
T |
5: 72,462,231 (GRCm39) |
H859Q |
probably damaging |
Het |
Cul7 |
A |
G |
17: 46,963,434 (GRCm39) |
E208G |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,172,603 (GRCm39) |
N285S |
possibly damaging |
Het |
Ell2 |
T |
A |
13: 75,904,409 (GRCm39) |
I166N |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,821,657 (GRCm39) |
R5797G |
possibly damaging |
Het |
Galntl6 |
T |
C |
8: 59,364,451 (GRCm39) |
I20V |
possibly damaging |
Het |
Glra2 |
A |
G |
X: 164,072,633 (GRCm39) |
F78L |
possibly damaging |
Het |
Gm12258 |
A |
G |
11: 58,746,896 (GRCm39) |
D51G |
probably benign |
Het |
Gsta2 |
T |
A |
9: 78,238,525 (GRCm39) |
K185* |
probably null |
Het |
Hmgcr |
C |
T |
13: 96,795,786 (GRCm39) |
D294N |
probably benign |
Het |
Iglv2 |
A |
G |
16: 19,079,547 (GRCm39) |
|
probably benign |
Het |
Myo10 |
T |
A |
15: 25,776,466 (GRCm39) |
L63H |
probably damaging |
Het |
P2ry10b |
T |
C |
X: 106,215,243 (GRCm39) |
V201A |
probably benign |
Het |
Psmb2 |
A |
G |
4: 126,571,642 (GRCm39) |
|
probably null |
Het |
Samd4 |
T |
A |
14: 47,290,355 (GRCm39) |
L154H |
probably damaging |
Het |
Sult2a4 |
A |
T |
7: 13,718,870 (GRCm39) |
D124E |
probably damaging |
Het |
Trav9-1 |
A |
T |
14: 53,725,815 (GRCm39) |
Y43F |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,483,681 (GRCm39) |
N506S |
probably damaging |
Het |
Ube3c |
T |
C |
5: 29,824,227 (GRCm39) |
S474P |
probably damaging |
Het |
Zfp942 |
A |
T |
17: 22,148,042 (GRCm39) |
C196S |
probably benign |
Het |
|
Other mutations in Wdr87-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Wdr87-ps
|
APN |
7 |
29,237,047 (GRCm39) |
exon |
noncoding transcript |
|
IGL00505:Wdr87-ps
|
APN |
7 |
29,233,608 (GRCm39) |
exon |
noncoding transcript |
|
IGL00569:Wdr87-ps
|
APN |
7 |
29,233,565 (GRCm39) |
exon |
noncoding transcript |
|
IGL00966:Wdr87-ps
|
APN |
7 |
29,236,888 (GRCm39) |
exon |
noncoding transcript |
|
IGL01668:Wdr87-ps
|
APN |
7 |
29,236,855 (GRCm39) |
exon |
noncoding transcript |
|
K7371:Wdr87-ps
|
UTSW |
7 |
29,230,417 (GRCm39) |
exon |
noncoding transcript |
|
P0037:Wdr87-ps
|
UTSW |
7 |
29,233,039 (GRCm39) |
exon |
noncoding transcript |
|
R0179:Wdr87-ps
|
UTSW |
7 |
29,235,365 (GRCm39) |
exon |
noncoding transcript |
|
R0357:Wdr87-ps
|
UTSW |
7 |
29,235,007 (GRCm39) |
exon |
noncoding transcript |
|
R0358:Wdr87-ps
|
UTSW |
7 |
29,231,636 (GRCm39) |
exon |
noncoding transcript |
|
R0412:Wdr87-ps
|
UTSW |
7 |
29,229,995 (GRCm39) |
exon |
noncoding transcript |
|
R0530:Wdr87-ps
|
UTSW |
7 |
29,229,545 (GRCm39) |
exon |
noncoding transcript |
|
R0600:Wdr87-ps
|
UTSW |
7 |
29,232,690 (GRCm39) |
exon |
noncoding transcript |
|
R0675:Wdr87-ps
|
UTSW |
7 |
29,231,942 (GRCm39) |
exon |
noncoding transcript |
|
R1118:Wdr87-ps
|
UTSW |
7 |
29,233,669 (GRCm39) |
exon |
noncoding transcript |
|
R1395:Wdr87-ps
|
UTSW |
7 |
29,230,812 (GRCm39) |
exon |
noncoding transcript |
|
R1444:Wdr87-ps
|
UTSW |
7 |
29,229,380 (GRCm39) |
exon |
noncoding transcript |
|
R1476:Wdr87-ps
|
UTSW |
7 |
29,234,315 (GRCm39) |
exon |
noncoding transcript |
|
R1534:Wdr87-ps
|
UTSW |
7 |
29,229,854 (GRCm39) |
exon |
noncoding transcript |
|
R1535:Wdr87-ps
|
UTSW |
7 |
29,229,004 (GRCm39) |
exon |
noncoding transcript |
|
R2023:Wdr87-ps
|
UTSW |
7 |
29,230,959 (GRCm39) |
exon |
noncoding transcript |
|
R2127:Wdr87-ps
|
UTSW |
7 |
29,236,565 (GRCm39) |
exon |
noncoding transcript |
|
R2141:Wdr87-ps
|
UTSW |
7 |
29,230,935 (GRCm39) |
exon |
noncoding transcript |
|
R2198:Wdr87-ps
|
UTSW |
7 |
29,226,697 (GRCm39) |
exon |
noncoding transcript |
|
R2201:Wdr87-ps
|
UTSW |
7 |
29,235,950 (GRCm39) |
exon |
noncoding transcript |
|
R2262:Wdr87-ps
|
UTSW |
7 |
29,231,987 (GRCm39) |
exon |
noncoding transcript |
|
R2263:Wdr87-ps
|
UTSW |
7 |
29,231,987 (GRCm39) |
exon |
noncoding transcript |
|
R4874:Wdr87-ps
|
UTSW |
7 |
29,235,608 (GRCm39) |
exon |
noncoding transcript |
|
R5064:Wdr87-ps
|
UTSW |
7 |
29,235,080 (GRCm39) |
exon |
noncoding transcript |
|
R5130:Wdr87-ps
|
UTSW |
7 |
29,228,699 (GRCm39) |
exon |
noncoding transcript |
|
R5366:Wdr87-ps
|
UTSW |
7 |
29,232,964 (GRCm39) |
exon |
noncoding transcript |
|
|
Posted On |
2015-08-05 |