ZMP
zgc:158677
Ensembl ID:
ZFIN IDs:
Description:
synaptic vesicle protein 2B homolog [Source:RefSeq peptide;Acc:NP_001076464]
Human Orthologue:
SV2B
Human Description:
synaptic vesicle glycoprotein 2B [Source:HGNC Symbol;Acc:16874]
Mouse Orthologue:
Sv2b
Mouse Description:
synaptic vesicle glycoprotein 2 b Gene [Source:MGI Symbol;Acc:MGI:1927338]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34020 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20877 | Nonsense | Available for shipment | Available now |
| sa977 | Essential Splice Site | Available for shipment | Available now |
| sa16646 | Nonsense | Available for shipment | Available now |
| sa25355 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34020
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080106 | Nonsense | 151 | 689 | 2 | 13 |
| ENSDART00000124676 | Nonsense | 151 | 689 | 1 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 16043436)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15026315 |
| GRCz11 | 7 | 15274602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCGCTCTGCCCAGTGCTGAGAAAGACATGTGCCTGTCCAATGCAGAC[A/T]AGGGCATGCTGGGTAAGTAAAATAGCCTGGAGATACATTCGGTGACTGAG
Long Flanking Sequence:
TTTAGCATTTTTCTGGTCTACAAAATAAGAATAACACGTTTCAAGCCAAAATGGATGACCCTTACCAAAACAATATAAACCAGCAGGGAGAAGCATATCCAACATATGGGGAGGGAGGAGAATACACTTACCCCTATCAAACAGACTATCCACGCCAGGAAGAGGATGATGCTGCTAGTGATGCCACCGAAGGCCATGATGAGGATGATCAGATGTACGAGGGAGAGTACCAGGGTGTCCCACATCCAGATGAGATCAAGGAAGCGCGGAGAGCAGCCCGAAGGGAGGCCCGGATGAAGGCCAGAATGGCAGCAGAGGTGGAGGAGGAAACATTGCCAGATCAGTATGAAAGCATCATGGAGGACTGCGGTCACGGACGCTTTCAGTGGACCCTCTTCACCGTGCTGGGTTTGGCCCTGATGGCTGACGGTGTGGAGTGTTTCGTAGTGAGTTTCGCTCTGCCCAGTGCTGAGAAAGACATGTGCCTGTCCAATGCAGAC[A/T]AGGGCATGCTGGGTAAGTAAAATAGCCTGGAGATACATTCGGTGACTGAGAGATCTTAACTACAATTTAAGAAAGCACTCCATCGGTTTGATAGCATACGTGTTGCAAATATGGATCAGTTCGGATGTTTTTAAAGCGCATTTTATGTTTATTAATATTTAACAAAAACCAAGTGTGTGTAATCATTTTTATTTTTATTTATTTTCTGTGCATTAGAGACAGTTTGGCCTCGAAACATTCAAGTGTATCTGGCAAAACTGACTAACATTTTCTCATTGTGACCACCAAATTCTCACAACGCAAACAAATGAAGTAAACATGCTGCATTTTCTCACAACACAAACACATTAAGAATATGCTCTAATTTCCTCACAACACATGCAAATAGCACTGAACACAATGGAAATGTTTCAAGGTGACCCAAAAAGGTGACAAACCTGGATTATGTTATGGTTATTGTGGTTGATAATATACAAAAGACAGGCAAGACATGCAATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20877
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080106 | Nonsense | 242 | 689 | 4 | 13 |
| ENSDART00000124676 | Nonsense | 242 | 689 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 16057448)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15040327 |
| GRCz11 | 7 | 15288614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTACGCTGAGTTTCTACAGATGGACAAGAGAGGAGAACATCTCAGCTG[G/A]CTGTGCTTGTTCTGGATGCTGGGAGGACTGTACGCTTCCTTCACTGCATG
Long Flanking Sequence:
TGTGCCAATGGGGTAAGCAAATTAATCTTGTTTTTTCTTTTGATGTAAGATTATTTTGCTTACCCCATTGGCAAATTATTTTGCTTGTTTTACAGAAAAACTCACTTAATATTGGCATATTATTTCTCAAAACAAGACAATTTGTTTTGCTTGTCTAGAAAATGCTTCTTGATATAAGACATTTTAGATATTTAGACTAGAAATAAGACAAAAAATCTAAGCAAGAAAAGCATTTTTTGCAGTGTATGGAAGTCAATGGCTGCTTTTTTTTTTTACCATTTCTCCCTTGTGTTTTTAACAGAAGAAAAAAAACTTAAACAGCTTTAAAAGAAGTTGAGGATGAGTAAATGATGACAGAATTTTTCAGGTTTGGGGCGAACTATCCCCTTGATTAAAAAAAATTGTGATGTGTCCTGCAGGATTGGCGGGTCAATTCCAGTCGTCTACACATATTACGCTGAGTTTCTACAGATGGACAAGAGAGGAGAACATCTCAGCTG[G/A]CTGTGCTTGTTCTGGATGCTGGGAGGACTGTACGCTTCCTTCACTGCATGGGGAATCATCCCACATTATGGTACCTTACTGTTATTCCTTAAAATGTTTCTAAATAAATAATTATATAATAATAAATATACCGTTGTAAGTCAGAATTATTAGCCCCTCTGTGATTTTATTTCTTTTTGTAAATATTTCCTAAATGATGTTTAACAGAGCAAGGACTTTTTCACAGTATGTCTGATAATATTTTTTCTCATGGATAAGTCTTACTTGTTTTATTTCAACTAGAATAAAAGCAGATAAAAAATTTTGGAAACCATTTTAAGGTCAATATTATTAGCTGCCCTTAAGCAATATTTTTTTTCCGAGGGTCTACAGAACAAACCATCATTATACAATAACTTGCCTAATTACCCTATCCTGCCTAGTTAACCTAATTAACCTAGTTAAACCACTTTAAGCTGAATACTAGTGTCTTGAAAAATATCTAGTAAAATATTATGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa977
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080106 | Essential Splice Site | 310 | 689 | 5 | 13 |
| ENSDART00000124676 | Essential Splice Site | 310 | 689 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 16060160)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15043039 |
| GRCz11 | 7 | 15291326 |
KASP Assay ID:
554-0882.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCGCAGGGCTGGTGTTCATGCCAGAGAGTCCTCGTTTCCTTCTAGAGG[T/C]AAAATAGTTCTAWGATRGTTTACTAGTAACACACTCACACACNNNNNNNN
Long Flanking Sequence:
CTAGCAATGTGCACTAGCAAAAGCAAAAACATTGTAAATTTTGATTTTACACAAATTAAAGAAACAAATAAATTATTATTTGCCATAGAGATAAAAGGAAATGCATGTATTATATCATCCGTCCATTCATTCATTCATTTTCCTTTGGCTTAGTCTCTGATTTCCACAGCAGAATGGACCTCCCACTACTCCAGTATACTGTTTAAACAGTGGATACCCTTCCAGCCACATCCTAGTACTCGGAAATATTACTATTATGTCAAAATCTTTAATTGAAAGTTTGAATTGTTGCCTGGAGAGCTATCTGAATATGTTGAAGCTGTGTTTCGTGTAAATTCTGAGTGTTTGGCTTGTGTTTTGTTCAGGCTGGGGGTTCAGTATGGGCACCGAGTTCCAGTTCCACAGTTGGAGGGTGTTTGTTCTGGTTTGTTTCCTTCCCTCTGTGGCTGCTCTCGCAGGGCTGGTGTTCATGCCAGAGAGTCCTCGTTTCCTTCTAGAGG[T/C]AAAATAGTTCTATGATAGTTTACTAGTAACACACTCACACACACATAGAAACACACTTCTATTGTTTTACTATTTTATATATAATTATTTATTCAGAAGAAAAATACTGTTTACTGTGAAAGTTCTGTTCTAAATGTAAGAATGAAAACTTAACAGTATATACTTTGATACTGTAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATATATATATATATATATATATAGATAGATAGATATATATAATATGAATATTAATATATGAATATAAATATGTAAAAATCAATTTTTTCAAATTAACAATCATACTAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTTTTGTATATAAAAATATTTAAATACACAAATACATGCATATATTTGAGAAAAATGTTTATTTATATTTAGATATAAAATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16646
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080106 | Nonsense | 482 | 689 | 10 | 13 |
| ENSDART00000124676 | Nonsense | 482 | 689 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 16067782)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15050661 |
| GRCz11 | 7 | 15298948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACATCGAAATAAGAAATGTGAAGTTCGAGGATTCGCTCTTTGAGAATTG[T/A]TATTTTGARGACATCAAATCAACAGAGACCTTCTTCGAGAACTGCACCCT
Long Flanking Sequence:
GAGGCTCTACAGGTAACTCACAGCCTAGCCAATCCTCCATTATTTTTAAAATTTTACACCAGAATGGATAAACTAGACAACATTCCTAGATCATGTGTAAATATGTACCCTCTTCTTCTTCTTGAAGCACAATGTTTATGAAAGGTGGGGGGGAGAAGCGCAATGTTGATGAAAAGTGTGGGGGGAGGGGAGGGCAGGCCAGAATCATTGTGGCAGGCCAGATAGACCGTCAGGCCACCAGGAAATGTCCCGGTTCTGCCTCTAATGAAAATCATCAATATTAATAAAAAACAAATGACAATAAAACACAACACAAATAAATGGTTGTTTTCTTGAAATAACACACACGTAAGTTTGCTACAAGGATTTTCAGATCCTTAGTTAGATTCTTCAGTTCATTTCAAATAAAGTAGTTTTAAATAAGCATTTCTGTGTATTTGCAGGTTTATCAACATCGAAATAAGAAATGTGAAGTTCGAGGATTCGCTCTTTGAGAATTG[T/A]TATTTTGAGGACATCAAATCAACAGAGACCTTCTTCGAGAACTGCACCCTGAAAAACACAGTCTTCTACAATACCGGTAATCAACTCAAACAAAACTAGATTAGTGTTTTTTTAATGTTTTCAAATCTGTCTTTTGACCCATATATTGACCTTCATCCCAGTTGATATTTGATGCTTTTTCATCATTAAGGATTGTTTTACGACGCTCTTGTCATGTTTCTTTCAGACCTGTGGGAAGATTCCAAGTTCATTAACTGTAACCTGGAAAACACAACGTTTTTGCACCCCAAAAAAGGCTGCCATCTCAATTTCCAGGAGGAAAATGACATCCTGATCTATCTAGACAGCTTCCTGGGCAGTTTGTCTGTAATACCAGGCAACATCTTAGCAGGTCTATTAATGGATAAAATAGGACGACTTAAAATTATAGGTGAGTGAAGAAAGCTAATATAAATGGCCCATTCACATGGGGTGTCAGCGTCAGCATTGCCGAACTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25355
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000080106 | Nonsense | 505 | 689 | 10 | 13 |
| ENSDART00000124676 | Nonsense | 505 | 689 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 16067851)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15050730 |
| GRCz11 | 7 | 15299017 |
KASP Assay ID:
554-7497.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACAGAGACCTTCTTCGAGAACTGCACCCTGAAAAACACAGTCTTCTA[C/A]AATACCGGTAATCAACTCAAACAAAACTAGATTAGTGTTTTTTTAATGTT
Long Flanking Sequence:
AAACTAGACAACATTCCTAGATCATGTGTAAATATGTACCCTCTTCTTCTTCTTGAAGCACAATGTTTATGAAAGGTGGGGGGGAGAAGCGCAATGTTGATGAAAAGTGTGGGGGGAGGGGAGGGCAGGCCAGAATCATTGTGGCAGGCCAGATAGACCGTCAGGCCACCAGGAAATGTCCCGGTTCTGCCTCTAATGAAAATCATCAATATTAATAAAAAACAAATGACAATAAAACACAACACAAATAAATGGTTGTTTTCTTGAAATAACACACACGTAAGTTTGCTACAAGGATTTTCAGATCCTTAGTTAGATTCTTCAGTTCATTTCAAATAAAGTAGTTTTAAATAAGCATTTCTGTGTATTTGCAGGTTTATCAACATCGAAATAAGAAATGTGAAGTTCGAGGATTCGCTCTTTGAGAATTGTTATTTTGAGGACATCAAATCAACAGAGACCTTCTTCGAGAACTGCACCCTGAAAAACACAGTCTTCTA[C/A]AATACCGGTAATCAACTCAAACAAAACTAGATTAGTGTTTTTTTAATGTTTTCAAATCTGTCTTTTGACCCATATATTGACCTTCATCCCAGTTGATATTTGATGCTTTTTCATCATTAAGGATTGTTTTACGACGCTCTTGTCATGTTTCTTTCAGACCTGTGGGAAGATTCCAAGTTCATTAACTGTAACCTGGAAAACACAACGTTTTTGCACCCCAAAAAAGGCTGCCATCTCAATTTCCAGGAGGAAAATGACATCCTGATCTATCTAGACAGCTTCCTGGGCAGTTTGTCTGTAATACCAGGCAACATCTTAGCAGGTCTATTAATGGATAAAATAGGACGACTTAAAATTATAGGTGAGTGAAGAAAGCTAATATAAATGGCCCATTCACATGGGGTGTCAGCGTCAGCATTGCCGAACTGAATTGTGGGTCTATCGGCATCACTTCAGTAGTGTTGCTCGCTGCAGAAGTTGGGAATTTTTCAACTTTTTAA
Associated Phenotype:
Not determined