ZMP
zgc:153222
Ensembl ID:
ZFIN ID:
Description:
Synaptosomal-associated protein 47 [Source:UniProtKB/Swiss-Prot;Acc:Q0P4A7]
Human Orthologue:
SNAP47
Human Description:
synaptosomal-associated protein, 47kDa [Source:HGNC Symbol;Acc:30669]
Mouse Orthologue:
Snap47
Mouse Description:
synaptosomal-associated protein, 47 Gene [Source:MGI Symbol;Acc:MGI:1915076]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19659 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19659
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092741 | Essential Splice Site | None | 419 | None | 6 |
ENSDART00000125425 | None | None | 419 | None | 4 |
ENSDART00000137842 | Essential Splice Site | None | 371 | None | 4 |
ENSDART00000144332 | None | None | 34 | None | 2 |
The following transcripts of ENSDARG00000063445 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 3897044)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 3571570 |
GRCz11 | 2 | 3402749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACACCTTGCTGTAGCTGCCACTTTCAATTCTGAAGACATCCTAAAAGG[T/A]ATGAAATATTTCATTTCTGTGGAGGTTATTTCTGTACTTGAGCTGTTTTG
Long Flanking Sequence:
AAAAATACCGTGTGCACACCAGCTCGGTGATATCCTCGTACGGAATAAGTTGTGTGAAAAAATAAATAATGTAAATTAAATACTTGTTAATTCACTATAAAACGAATTTCTGACGTACTTAACTAGACAAATAGTACATACTGTCCCGTCAAATTTAGAGCGGAATCTTTAATCATGGCTGTTGTTGTGTATCGGAGTGTAAACATGAGCGCACCAAACATTCACCCTTTGCTTGGGCTGTTTACATCGCTATAACACAGCAGCGAACTATAATCTGATATTTGCTGATATTTCTTCTGATTTGGCGTTTTAATTAGATGTAGCAGGAAACACTAAAGTAGTGCAGCAAATGTCTCGCATCCGAGAACAATTTGCCTCGCTGCAAACATATCAAATCAACTCAACTTTACAATGTGAAGGGATATTGTTTATCCCAATGCGTACTTTACGTCACACCTTGCTGTAGCTGCCACTTTCAATTCTGAAGACATCCTAAAAGG[T/A]ATGAAATATTTCATTTCTGTGGAGGTTATTTCTGTACTTGAGCTGTTTTGATTATGATTTTAGTCGAAGCCCCTATAATATACGTGTGTGTAATAAATTGAATAGAGATTGTAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATATATATATAGTTAAAAGCTCATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTATGTATGTAGGTTTTTTTTTTACTGGCCTGATTGTAGCCAGTGGCTTTTTACTTTTTTTTACTTGCCTGCCAAAATTTTCACTGGCCCCACCAAAAAAAAAAAAAAAAAAAAAAACAAGTTAATAACTATTTCTTAGCCATTTGTTTCAAATAATGTTTAAAAAAAGTCTGT
Associated Phenotype:
Not determined