ZMP
WNT8A_DANRE
Ensembl ID:
Description:
Protein Wnt-8a [Source:UniProtKB/Swiss-Prot;Acc:P51028]
Human Orthologue:
WNT8A
Human Description:
wingless-type MMTV integration site family, member 8A [Source:HGNC Symbol;Acc:12788]
Mouse Orthologue:
Wnt8a
Mouse Description:
wingless-related MMTV integration site 8A Gene [Source:MGI Symbol;Acc:MGI:107924]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35723 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35723
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000017635 | Essential Splice Site | None | 359 | None | 7 |
| ENSDART00000132193 | Essential Splice Site | 8 | 387 | None | 7 |
| ENSDART00000144301 | None | None | 264 | 1 | 6 |
| ENSDART00000148044 | None | None | 161 | None | 6 |
| ENSDART00000017635 | Essential Splice Site | None | 359 | None | 7 |
| ENSDART00000132193 | Essential Splice Site | 8 | 387 | None | 7 |
| ENSDART00000144301 | None | None | 264 | 1 | 6 |
| ENSDART00000148044 | None | None | 161 | None | 6 |
The following transcripts of ENSDARG00000052910 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 35622725)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 34152002 |
| GRCz11 | 14 | 34492316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCAAGCAGTCAGTCACTTGTCGTCTGTCTCTTGTGCGTATCCATCTC[A/G]GTGTTTGTGCTTTGCATCTCAAGAAGAAGGGAGGATCGAGCAATCACTGG
Long Flanking Sequence:
GAGATCAAAGCTATTCTGATGCAAAAATGCATGTCCAGTATGCATGTCCAGTGCGGAATCAACAATCTGCCCATTCATGAATACACTACACCATCAACGGCTAAGCCTAATGAATGATTATTAATTAAACAGTCGATGCCTTTTGGACAGTTCAATTCAATCTGTCTCCACAAACGTTAGCGCATTAAATAACTTTTTTATGCAAGTAGGCATTCAAATAATGTTTAATTTTTAAACATTTGTCGAAAATCATACTAAAACATAACATCCCCAGGAAATATATAGTTTAATGAAAATAGACTTACGGGCATAGTGAAAAGTGATAATGCTTTGAAGTGCAATTAAGGCAGAACAATTTCACCGTCGACCTCGAGGTCTTTTCACAGCGAATTGTCAAAGCTTGGGAGATCCCTGTCACTCAAAGTTGGCGACAGGTATAAATGCCTTGCTTATTCAAGCAGTCAGTCACTTGTCGTCTGTCTCTTGTGCGTATCCATCTC[A/G]GTGTTTGTGCTTTGCATCTCAAGAAGAAGGGAGGATCGAGCAATCACTGGTCACTCACGCAGCAATGAACCCTTGCCAGATTTTTGCGTCGTTGGTTATGTCTATATGCTGTCACATACTGTCGTCAACAGCATGGTACAGTCATATTTCATATATTTTTATTTATTACTATTATTTTATTTATGACATTTTTAAATTTGACTTAACCCATGTTGACCTCATGCTTCCTTTTATTCTGTTTTTGCTACACGTAGGTCTGTGAATAACTTCCTGATGACAGGACCAAAGGTAATTACATTTTTTACACCTAAATTCTTGCAGAGCAATTTGTTATTTTATCTTTACATAAAAAATGTCTAAAACGTATACATGTCTAATCAAAGCTCATATTTTACATAAATCAGGCTTATCTCGCATACACCAGCAGTGTACAAGCTGGGGCTCAGAGTGGTATAGAAGAGTGCAAGCATCAGTTCGCATGGGACAGGTGGAACTGCCCG
Associated Phenotype:
Not determined