Incidental Mutation 'IGL01668:Wdr87-ps'
| ID |
103374 |
| 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 # |
IGL01668
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
29223968-29237480 bp(+) (GRCm39) |
| Type of Mutation |
exon |
| DNA Base Change (assembly) |
G to A
at 29236855 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: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ap3d1 |
A |
G |
10: 80,554,993 (GRCm39) |
V444A |
possibly damaging |
Het |
| Chd9 |
A |
T |
8: 91,753,404 (GRCm39) |
H1799L |
possibly damaging |
Het |
| Cic |
C |
T |
7: 24,990,629 (GRCm39) |
P1108S |
possibly damaging |
Het |
| Clba1 |
T |
C |
12: 112,773,264 (GRCm39) |
S86P |
probably damaging |
Het |
| Cldn16 |
T |
A |
16: 26,301,296 (GRCm39) |
Y201* |
probably null |
Het |
| Col6a6 |
C |
A |
9: 105,586,470 (GRCm39) |
R1850S |
probably damaging |
Het |
| Cryge |
A |
G |
1: 65,087,857 (GRCm39) |
Y151H |
probably damaging |
Het |
| Dhcr7 |
T |
A |
7: 143,397,048 (GRCm39) |
V180D |
probably damaging |
Het |
| Dmwd |
C |
T |
7: 18,815,080 (GRCm39) |
R577W |
probably damaging |
Het |
| Gm5884 |
A |
G |
6: 128,622,377 (GRCm39) |
|
noncoding transcript |
Het |
| Gm5901 |
C |
T |
7: 105,026,771 (GRCm39) |
R180C |
probably benign |
Het |
| Hook2 |
A |
T |
8: 85,720,207 (GRCm39) |
Y131F |
possibly damaging |
Het |
| Hsf1 |
T |
C |
15: 76,381,162 (GRCm39) |
|
probably null |
Het |
| Ighv1-62-3 |
A |
G |
12: 115,424,613 (GRCm39) |
|
probably benign |
Het |
| Ikbke |
T |
G |
1: 131,184,675 (GRCm39) |
D666A |
probably benign |
Het |
| Il1r1 |
C |
T |
1: 40,352,489 (GRCm39) |
T556I |
probably benign |
Het |
| Larp4 |
T |
C |
15: 99,885,355 (GRCm39) |
S69P |
probably damaging |
Het |
| Lrrc27 |
G |
T |
7: 138,807,827 (GRCm39) |
|
probably benign |
Het |
| Marchf2 |
A |
C |
17: 33,922,070 (GRCm39) |
W97G |
probably damaging |
Het |
| Or4c10b |
C |
A |
2: 89,711,443 (GRCm39) |
P91Q |
probably benign |
Het |
| Or5b21 |
A |
G |
19: 12,839,231 (GRCm39) |
I31V |
probably benign |
Het |
| Or8k28 |
A |
G |
2: 86,285,746 (GRCm39) |
Y290H |
probably damaging |
Het |
| Pah |
T |
A |
10: 87,414,123 (GRCm39) |
I324N |
probably damaging |
Het |
| Pcdhb7 |
A |
G |
18: 37,476,205 (GRCm39) |
E447G |
probably benign |
Het |
| Prex2 |
T |
C |
1: 11,223,869 (GRCm39) |
V731A |
probably benign |
Het |
| Prpsap2 |
A |
G |
11: 61,646,277 (GRCm39) |
V44A |
probably benign |
Het |
| Rp1 |
T |
C |
1: 4,415,941 (GRCm39) |
N1724D |
probably damaging |
Het |
| Sap130 |
A |
G |
18: 31,813,493 (GRCm39) |
N517D |
probably damaging |
Het |
| Slc13a3 |
A |
C |
2: 165,272,212 (GRCm39) |
F277C |
probably damaging |
Het |
| Snx19 |
A |
G |
9: 30,339,119 (GRCm39) |
T86A |
probably benign |
Het |
| Tbc1d32 |
A |
T |
10: 55,999,673 (GRCm39) |
V833D |
probably benign |
Het |
| Washc2 |
A |
G |
6: 116,239,299 (GRCm39) |
D1290G |
probably 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 |
|
|
IGL00505:Wdr87-ps
|
APN |
7 |
29,233,608 (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 |
|
|
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 |
2014-01-21 |
Incidental Mutation