ZMP
snap25b
Ensembl ID:
ZFIN ID:
Description:
Synaptosomal-associated protein 25-B [Source:UniProtKB/Swiss-Prot;Acc:Q6PC54]
Human Orthologue:
SNAP25
Human Description:
synaptosomal-associated protein, 25kDa [Source:HGNC Symbol;Acc:11132]
Mouse Orthologue:
Snap25
Mouse Description:
synaptosomal-associated protein 25 Gene [Source:MGI Symbol;Acc:MGI:98331]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32130 | Essential Splice Site | Available for shipment | Available now |
sa7432 | Missense | Mutation detected in F1 DNA | Not yet available |
sa36346 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32130
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 |
---|---|---|---|---|---|
ENSDART00000080927 | Essential Splice Site | None | 203 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 12200459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12182981 |
GRCz11 | 17 | 12337047 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCTGCCACACTCTAACCCAAAGCATTTTCCCTCTCTTTTATTTTCTCT[A/G]GCTTTCAAGTAAGAGCTACACTTTCCGTTTGAGTTGAGCAGCTCATCCCT
Long Flanking Sequence:
GTAGGTTTGTATTATCTATTATTTTAATTAATGATGTTATTAGTTAAGATACAGATCTGGGAAAACTATTTTTAACCTAATTTATTAATTAGGGGGGTAAATCCCCCCCAAACCTCCCTGTAATTCGCACCCTGCTTAAACCACATGTTTTTGGACTGTGGGGAAAACTGTAGCACCCAGAGGAAACCCACATGAACACTGCGAAAAATTCATAAACCAATTCTTCATTGTAAAATCTTTATATTTTTTGTGAGTTTTTTTGAGTCCTTAAACTGATGAGTTTCTGTGAATGAACCTGAATATTTCCACAATACTTGCACTCGTCTTCAAAGAACAATACTTTGACAATCATGTGACTTTCTTCTCTGTATGAGTTGCTTTTAAATTCTGTTTGCTCATTGAACTTTTTTAATGCAATGCTGAACCAGATCTGTCTAAAGGACTCACTTTGGTCTGCCACACTCTAACCCAAAGCATTTTCCCTCTCTTTTATTTTCTCT[A/G]GCTTTCAAGTAAGAGCTACACTTTCCGTTTGAGTTGAGCAGCTCATCCCTCCATCCACCATGGCAGACGAGTCCGACATGCGCAACGAGCTGAATGACATGCAGGCCAGAGCCGATCAGCTGGGCGATGAAGTAAGTACACCTTCAACCTCCAGGTCTATAAATAACCCCTAAATACGACAACAAGTGTGTATAAATAGACCCGTCCCAGTGTGAAGGAGAATGAACACACCATGACTTCCAGACACTCGGATTCACATAGGAGTATCATGCATGGAAATAGATGCCAATTACATATATGACATGCGAGTTCATATTTGGATTTCACATATACAGTTAAAGTCCGAACTATGTATATTTGTTCCCCAATTTCTGTTCAACAGAAAGATTTTTTTCACCACATATCTAAACATAATAGTTTTATTAATTAATTTCTAATAACTGATTTATTTTATATTTGCCATGATGACAATACATAACTGGGTATTTAACAAGATGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7432
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 > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080927 | Missense | 60 | 203 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 12180062)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12162584 |
GRCz11 | 17 | 12316650 |
KASP Assay ID:
554-4033.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTCGGGGGCTGTAATTGACTAATGTTTAAATCAGAGCAACTGGAGCGC[A/T]TCGAAGAGGGAATGGATCAGATCAATAAGGACATGAAAGAAGCAGAAAAG
Long Flanking Sequence:
TAGACCAAGTTCTTGGCATGATCTAGCCTAACCACTCATCACATCGTTAAAGTTCTGCGTAGATGTGTTTCTGGACAGCTTAGATGTCATTTGTCATCACCGTTTGTCTGCCAGGATGCAAAGTCTCATTTCATTGCTGTCACCCCTTTGTCCTGACCAGAACAACTCGAGCGTGTTGAAGATGGCATGAACCATATCAACAAAGACATGATGGAAGCTGAGAAAAGTTTAAAAGATGTAGGCAAATGCTGTGGACTAGTATGTCCCTGCGACAAGTAGGTACTGGTGAAGCGTCCAAGGCTCTCACCTGTCTGCTGCTGTCTGACTGTCTCTTGTCACTGTGAATGTTTAAGCCTCTCTCTTTCTTTTTGTCCCTCTCTTTTCCTCCTTGCCTTTCCCTTCTCTTTCTCTCTTTGTCCCCCTTTTCCATACTCTTTATTTCTTTTCTTTTTTTCGGGGGCTGTAATTGACTAATGTTTAAATCAGAGCAACTGGAGCGC[A/T]TCGAAGAGGGAATGGATCAGATCAATAAGGACATGAAAGAAGCAGAAAAGAATTTGACGGATCTAGGAAATCTCTGTGGTCTATGTCCGTGTCCATGTAACAAGTAGGTGATGCCTGTCGCCTGCCTGCCTGCTTGCCTGAACCCGACAAATAGGAAAAAAAAAAAAAGATAAAGCACGTGGCCAGTTTGCACGCTCGCTCTTGCTCGCTCCGTAGCTGCGAATTTCCCCCTTTGCTCTGCCTGGACTACTTCTCTGTGCATGGGGATGCTGGTAGAGCTAAGTCCGTCTGCGGCGCCACTGGTTAACCCATAGTTGTAGCTGTAGGCCCTGCTCTCTGCCGGCTGAATGCGCAAATTTGCTGGGCTCCATGCTTCACTGATCCTTTGGTCAAGGACTGTTGTTCGTAAATGTTAAGTGCCTGCTTGATATGCATGTGCTACTTTTGGAAATGCAAGCATTACACACTTTTTAAATGAACCGCAGATTAAATATTCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36346
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080927 | Essential Splice Site | 94 | 203 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 12179957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12162479 |
GRCz11 | 17 | 12316545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGGATCTAGGAAATCTCTGTGGTCTATGTCCGTGTCCATGTAACAAG[T/C]AGGTGATGCCTGTCGCCTGCCTGCCTGCTTGCCTGAACCCGACAAATAGG
Long Flanking Sequence:
GTCTGCCAGGATGCAAAGTCTCATTTCATTGCTGTCACCCCTTTGTCCTGACCAGAACAACTCGAGCGTGTTGAAGATGGCATGAACCATATCAACAAAGACATGATGGAAGCTGAGAAAAGTTTAAAAGATGTAGGCAAATGCTGTGGACTAGTATGTCCCTGCGACAAGTAGGTACTGGTGAAGCGTCCAAGGCTCTCACCTGTCTGCTGCTGTCTGACTGTCTCTTGTCACTGTGAATGTTTAAGCCTCTCTCTTTCTTTTTGTCCCTCTCTTTTCCTCCTTGCCTTTCCCTTCTCTTTCTCTCTTTGTCCCCCTTTTCCATACTCTTTATTTCTTTTCTTTTTTTCGGGGGCTGTAATTGACTAATGTTTAAATCAGAGCAACTGGAGCGCATCGAAGAGGGAATGGATCAGATCAATAAGGACATGAAAGAAGCAGAAAAGAATTTGACGGATCTAGGAAATCTCTGTGGTCTATGTCCGTGTCCATGTAACAAG[T/C]AGGTGATGCCTGTCGCCTGCCTGCCTGCTTGCCTGAACCCGACAAATAGGAAAAAAAAAAAAAGATAAAGCACGTGGCCAGTTTGCACGCTCGCTCTTGCTCGCTCCGTAGCTGCGAATTTCCCCCTTTGCTCTGCCTGGACTACTTCTCTGTGCATGGGGATGCTGGTAGAGCTAAGTCCGTCTGCGGCGCCACTGGTTAACCCATAGTTGTAGCTGTAGGCCCTGCTCTCTGCCGGCTGAATGCGCAAATTTGCTGGGCTCCATGCTTCACTGATCCTTTGGTCAAGGACTGTTGTTCGTAAATGTTAAGTGCCTGCTTGATATGCATGTGCTACTTTTGGAAATGCAAGCATTACACACTTTTTAAATGAACCGCAGATTAAATATTCACATGTTGTTTACTGGAGGCTGGCAGAGCTGGCTTTTTGTATGGGTTCTCTAAAGGCGAAGCATGTCAATGCATGTGGGTGAGATGGTGGGATAAGTTATCCTGGCGAT
Associated Phenotype:
Not determined