ZMP
stx8
Ensembl ID:
ZFIN ID:
Description:
syntaxin-8 [Source:RefSeq peptide;Acc:NP_956669]
Human Orthologue:
STX8
Human Description:
syntaxin 8 [Source:HGNC Symbol;Acc:11443]
Mouse Orthologue:
Stx8
Mouse Description:
syntaxin 8 Gene [Source:MGI Symbol;Acc:MGI:1890156]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13970 | Nonsense | Available for shipment | Available now |
| sa44633 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13970
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060547 | Nonsense | 180 | 235 | 6 | 8 |
| ENSDART00000146442 | None | None | 54 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 18207481)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23246801 |
| GRCz11 | 6 | 19718122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAGTAGACAAAAACAGATGGGTCAAGAAATCGGCAATGAGCTWGATGAA[C/T]AAAACGGTGAGTGAAAAGTGCAGTAGCCTATATATGACAGGTCTGGCTGA
Long Flanking Sequence:
ACTTGTGGTGGATGAGAAGATTCCCCCCAAAAATGTGTAAAGCGCTTTGAGTGTCCAGAAAAGTGCTATGTAAATGTCAGGGATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATAAATAACAGGGTTTTAAAACGTGTTAAGCATGTTCTTTATTAAATTAATTTTTTGTTAAAAATAATATAACCAACTGCTAAAATTGATTTATGTTTCTGCAGTGTAAATATAAGCATTATAAATGGGATTTGCACGTAGTACTATACACAATGTTGTCATTATTATATGTGTGCATCAGTTGTGTCACTTCTCTGTCATTCATAATTCTTTGCCCTTTTGTTTTTGTGTGGTTTACATATTTTGTCTGAATATACCTCTGTCCTCTTTTGTGTCTTGCTCTTTAGCCCAGGATGCTGGCCTGGATGCTCTGGCGTCAGTCTTAAGTAGACAAAAACAGATGGGTCAAGAAATCGGCAATGAGCTAGATGAA[C/T]AAAACGGTGAGTGAAAAGTGCAGTAGCCTATATATGACAGGTCTGGCTGAACATCCACATGTTTTTCTATGAATAACGTCTAATTTGTGGTCAGGTTGGTTTTACTTTGTCACGCTGCTCTATCGCTAAACTACATATGATGTCATTGGCTTTAAAATGAGCATTTTTTTCCAGTGGAAAATGTGGAATGGTACATGGAAACTCTCACCTGGTCTATCACATTTTTAAACTTCTTCCCAATGCAATGTTTCAAACTTATTTTATAAACATAAGACATCGCACAGAGACATCACATCATTGTAGTGAATCTATTTGAGTTGGAATGTGAGAACATGGAGGAATCACATAGTATGTACATGGAGTAGACTGAGCACAGGTCAGTCATCTGTGACCTCATCTGAAGGTCACAGGTGCTTTTAACTTTTCCCACACGGCCTTTCCAACCTTTTAATGCTGGAGTGGTGAAAACAGATAGACTTATATACAGATATATATAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44633
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060547 | Essential Splice Site | 216 | 235 | None | 8 |
| ENSDART00000146442 | Essential Splice Site | 35 | 54 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 18123658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 23330624 |
| GRCz11 | 6 | 19801945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAGTGTCCTTTATTCATTAAGATGTTTTGTGTGTGTGTTTGATTTC[A/G]GGCATGATGGTGGTGATTGTTCTTCTTCTAATCGCCATCATTGTTGTGGC
Long Flanking Sequence:
TGCTGTTCTTGCACTATTGCACAATACAATTGATTGGGACAGAATAATAATAATTATGCCTATTATTTGTAGTATTTTCATAGTGATTTAAACTACCTCTTCAATATGCACATCAAGAAACAAAAAGCTAGTTTTTACTGCATATAGTTTGTGGAAGAATGACTGAGTGTGTTTATCGCTCGCTCGACCGTACACACACCCACAGATATATTTCAGCAGTTGTGTGGCTCGATAAACATGCTGATTTGCATCATCACTGATGACAGGTAATGCTTGAAATATAAACGTCATGTCTGTTATCTTAAGATACATCACTTATGTCAGGTTTCCACTTTTTTCTTGTGCTTGAAAGTTAAAACAGCCCTGCTATGAATTGTCAGTCACTGAAATGGCCCCCCACCAATTTGAGTCCCCTGGTTTAGAAGAAAGTGTCTGGTGCATATGGAAAGGAAAAGAGTGTCCTTTATTCATTAAGATGTTTTGTGTGTGTGTTTGATTTC[A/G]GGCATGATGGTGGTGATTGTTCTTCTTCTAATCGCCATCATTGTTGTGGCCTGTTGGCAGTAATGAAGAAGATGAAGATGCCACAGATATGAACTATAGAGACTTTCTGTCTGTATATAGTGGTGAGTGATGGATTCACGCAGTATCCGAACAGACTGGACATGTAATCACATCTCTGCACACAGCTCTCTTTTTTCTCGTACAGTAATGGAACACATAACTGGGTTAAAGCCAAGAAATGGACCACTATGAAGAACTGAATTCTTAGCTCCACAGATAACGATCAAAGTAGGATTCGGAATGGAAAGAAAAATAGAAAAGAGCTTTGAAAGGTTTTGAATATTATTATGAATAAAACCATGAGCCCAAGATGCTCCAAGGGGGGAAACTATTTAAATTCTTTGTTTGGCAGTGAAGAAAATGATCCGTATCCATCGTGTAAACAGGGACTGAGTCACAAAGCAATACCGAGTTTTGAGCTCTACTGTTGGGGTAAATAG
Associated Phenotype:
Not determined