Incidental Mutation 'IGL00505:Wdr87-ps'
| ID |
332520 |
| 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 # |
IGL00505
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
29223968-29237480 bp(+) (GRCm39) |
| Type of Mutation |
exon |
| DNA Base Change (assembly) |
A to C
at 29233608 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: 23 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca15 |
T |
A |
7: 119,968,459 (GRCm39) |
|
probably null |
Het |
| Akap6 |
A |
G |
12: 52,933,885 (GRCm39) |
H459R |
possibly damaging |
Het |
| Anxa5 |
A |
G |
3: 36,511,646 (GRCm39) |
S144P |
possibly damaging |
Het |
| Cacna1h |
T |
G |
17: 25,600,482 (GRCm39) |
T1620P |
probably damaging |
Het |
| Cdc27 |
T |
G |
11: 104,412,258 (GRCm39) |
T444P |
probably benign |
Het |
| Cfap46 |
C |
T |
7: 139,240,605 (GRCm39) |
S56N |
probably damaging |
Het |
| Cntnap5b |
A |
G |
1: 100,306,886 (GRCm39) |
R868G |
possibly damaging |
Het |
| Cyp2j5 |
A |
T |
4: 96,519,012 (GRCm39) |
N421K |
probably damaging |
Het |
| Dhcr7 |
T |
C |
7: 143,400,805 (GRCm39) |
Y323H |
probably damaging |
Het |
| Dnai4 |
G |
T |
4: 102,960,439 (GRCm39) |
S70R |
possibly damaging |
Het |
| Gabrq |
T |
C |
X: 71,881,971 (GRCm39) |
S601P |
probably damaging |
Het |
| Gm3404 |
T |
A |
5: 146,465,095 (GRCm39) |
D278E |
probably damaging |
Het |
| Gpr61 |
A |
G |
3: 108,058,514 (GRCm39) |
M49T |
probably damaging |
Het |
| Map3k20 |
T |
C |
2: 72,219,827 (GRCm39) |
F253S |
probably damaging |
Het |
| Ndst3 |
G |
A |
3: 123,421,599 (GRCm39) |
|
probably benign |
Het |
| Rcor3 |
C |
T |
1: 191,812,271 (GRCm39) |
|
probably benign |
Het |
| Slc15a2 |
C |
A |
16: 36,574,137 (GRCm39) |
C572F |
probably benign |
Het |
| Sp2 |
C |
T |
11: 96,845,387 (GRCm39) |
R578H |
probably damaging |
Het |
| Spaca1 |
A |
G |
4: 34,029,077 (GRCm39) |
I132T |
probably damaging |
Het |
| Spag6 |
C |
A |
2: 18,738,995 (GRCm39) |
N308K |
probably benign |
Het |
| Stac |
C |
T |
9: 111,464,107 (GRCm39) |
R53Q |
probably damaging |
Het |
| Tekt3 |
A |
G |
11: 62,961,064 (GRCm39) |
S78G |
probably benign |
Het |
| Vdac3 |
C |
T |
8: 23,070,393 (GRCm39) |
G172S |
possibly damaging |
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 |
|
|
IGL00557:Wdr87-ps
|
APN |
7 |
29,235,227 (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 |
Incidental Mutation