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) question?
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

DomainStartEndE-ValueType
low complexity region 233 239 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141713
SMART Domains Protein: ENSMUSP00000120285
Gene: ENSMUSG00000074224

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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