ZMP
wdr82
Ensembl ID:
ZFIN ID:
Description:
WD repeat-containing protein 82 [Source:UniProtKB/Swiss-Prot;Acc:Q6NV31]
Human Orthologue:
WDR82
Human Description:
WD repeat domain 82 [Source:HGNC Symbol;Acc:28826]
Mouse Orthologue:
Wdr82
Mouse Description:
WD repeat domain containing 82 Gene [Source:MGI Symbol;Acc:MGI:1924555]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16143 | Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16143
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000007353 | None | None | 313 | None | 9 |
| ENSDART00000007798 | Splice Site | None | 600 | None | 16 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 41424272)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41495872 |
| GRCz11 | 6 | 41493408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGTGTGGACCCCAAACATCAGACTCTACAGGGTCTTGCTTTTCCMTTA[C/T]AGGCTGAAGCCAAACGTGCTTTAAAGCASCTCGCAGAGAGACGCATCAAC
Long Flanking Sequence:
TAAATTAAAAACAATGAAAAGTAAATTTAAAGTAAGTCAAACATAACAAAATTATCGCAAAAGAAAACAAAAATTTTTAAGTAGAATTCTTTTTAAAGCTATGAAACTGATAGTCCTTAATAGTAAACAAAAAGAAAACAGGGCTTTCTGGTAAAACAAAACATATTTCGGTGTCAAGTGAGGACAGTTCTAAACAGGTGTGTTGTGATTCAAATATACAGTCATTACATTCATTCAGCATATTACCACTCTGCTTTTCCATTTACTCTTATCCACCATCTCCACCCACATAAACATACTTTTCCAAACAACACAACTGCCATATAATAAGTCTTCCAGCACTGGATCATAGGAATTGTTTTGGAAAAAGGTTTTGATAGATTGGCTGGAACTGTTGCTGCAATACAAACTTTGTATGTGTGTGTATGTGTCTGCAGGTGAAGGCTGAGATCAGTGTGGACCCCAAACATCAGACTCTACAGGGTCTTGCTTTTCCATTA[C/T]AGGCTGAAGCCAAACGTGCTTTAAAGCAGCTCGCAGAGAGACGCATCAACTACATTCAACTGGTACGACACCTTCATATTACACTGCCCTCCACTAATACTGGCCAATGAGGCAAAAAAAAAAGTTTGTTGTTTAACCTTTTGACTTTCGACTTAAAATACTGACAATTAAAGTTGGGGTGGCATGGTGACTTAGTGGTTAGCACTGTCACCTCACAGCAAGAAGGTCACTGGTTTGAGTCTCGGATGGTCAGTTGTCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCATTCCTCCAGTGCTCTGGTTTCCGCCACAGACCAAAGACATGCAGGTGAATTGAACAAACTAAACTGACCGTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTGAATGAGAGAGTGTTTGGGTGTTTCTAAATAC
Associated Phenotype:
Not determined