ZMP
si:dkey-266j7.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens PCLO, piccolo (Presynaptic cytomatrix protein) (PCLO) [Source:Uni
Human Orthologue:
BSN
Human Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Mouse Orthologue:
Bsn
Mouse Description:
bassoon Gene [Source:MGI Symbol;Acc:MGI:1277955]
Alleles
There are 18 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18586 | Essential Splice Site | Available for shipment | Available now |
sa11698 | Essential Splice Site | Available for shipment | Available now |
sa15776 | Nonsense | Available for shipment | Available now |
sa10741 | Nonsense | Available for shipment | Available now |
sa13696 | Nonsense | Available for shipment | Available now |
sa11836 | Nonsense | Available for shipment | Available now |
sa23238 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18586
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048657 | Essential Splice Site | 213 | 4478 | 4 | 55 |
ENSDART00000136955 | None | None | 1644 | None | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9087038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9664014 |
GRCz11 | 18 | 9633204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTTAGAAGCTGAATTGAATAAAGAGCCACCAAAAAGCTGCCCCTTAT[G/A]TAAAGAGAYCCTCAAGAAAAYCCCACAAAACTATARCTCTTGCACTTCTT
Long Flanking Sequence:
TTCAGCAGATTTGAAACCACCTACATCAGAAGCCCAAAAGCAGAAAAGTGAAGTCTTACCTGCCAAGTCTGATCAACCACATAAACCCGAACCATCTAAACAAGAAACAGATTTCTTCAGCTTCGGGTTTGGTGGCTCTCAGTCAAGATCACAATCTCCTCAGCCCACTGTGTCTGCTGTCTCTGATAAAGTTTTTGGCTTTGGCTCCTCCTTCCTAAACTCAGCATCAAACTTAATCTCCTCTGCTGAACCATCTAAAACTCCGCCAACATCTCGAAAGGGTTCTACAATTTCTCAGACTTCAAGCAAGACCATACCAACACCTCCCACTTCTCGAAAAGGATCAGTAGCTCCACCAGAGTCAAAACTAAATCCACCTCCAGTGCAGTCTAAGCCAACGTCTACACCAACGCAAGAACAGAAAGGGCCACCAGATGTTCAACCATCCAAACCTTTAGAAGCTGAATTGAATAAAGAGCCACCAAAAAGCTGCCCCTTAT[G/A]TAAAGAGACCCTCAAGAAAACCCCACAAAACTATAGCTCTTGCACTTCTTGCAAGAGCATTGTTTGTAATCTCTGTGGATTTAATCCCAATCCTCATCAAACTGATGTAAGTATATGTGTTTTACATTTTGATGTTGCATTAGCACAGTTCATAAATTAATCATAGTTGAATGATTATAGATTTGATGGTCACATGATACAAATACAATCAAGATATGACTCTATTTGAGGATCTTTTGTATTATCTACAGGTGAAGGAGTGGCTGTGTTTGACTTGTCAGATGCATAAAACTTCAGGACCTCCTCTTCCTCAACCAGAGCCACAATCTAATATAGCACTTGCACCAGCATCTCCACTGAAGGAAAAAACTCAGGTTTCACCTTCTCCTGAGAAAAAGCCAAGTGTTACAGCTGACCAGGACAAGAAGCCTCTTGCAGAGACTAAAGAACTAAAAACACCAAATACTCAAAAATCTAAAGGTGATGTTCCTTCTTCCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11698
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 |
---|---|---|---|---|---|
ENSDART00000048657 | Essential Splice Site | 1831 | 4478 | 24 | 55 |
ENSDART00000136955 | None | None | 1644 | None | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9124532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9701509 |
GRCz11 | 18 | 9670699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTAGAGATGTTCAGCCACCAGCCAGTGTTTCAATTCAAATTCCCATTC[A/G]GAGACTAGTGGAAACCAGATCAGATATTGCACCAYCAKTACWTCAAGCCR
Long Flanking Sequence:
ATCAGCAATTACAGACAAACCAACTGTTGCACCCATGACTGCTGAAAAAGTTGACCATGTGAAAATGTCAACTACACCAGCTCTTACACCTATTGTTCAATCTCAAGAAAAACCTTTAATAGAGACTTCAATTGTTGTTCAAATGCCAGATCATATTTCCTCTTCATTGAAGCACCCAGTTGTAGAACAAACTCCAGTTTCAGCACCTACTCTGCCATCTACTACATTAAAGAATCAAGTACCTACAGCTATCGCCATTGTTGCTACTATGCCAGACACACTCCTATGCCAGGTCACGTCTACATCTCAGTCAGTGGAACAAGCATCAACTTCTGTTCCAACAATGGTACCATCCTCAGTTCCAGCTAGCATCGTCTCTACAGACCCAACAAGCTCAGCTGTTGTACAAGTGGCCACACCACCATCTGCTCATACCACGTTACCTGCTTTGATTAGAGATGTTCAGCCACCAGCCAGTGTTTCAATTCAAATTCCCATTC[A/G]GAGACTAGTGGAAACCAGATCAGATATTGCACCACCATTACATCAAGCCACTCCTATTTCACCCCCAGTGAGTCACATGGAGTGTATTGCTGCAAAGACAGTCTCTGTTGTTTCTCCTACTATTACTACAACTGTTGCTTTTGAAAATTCACTTTCCCATCCCGTTAAATCAATGCTGGCTGATTCTCAGCCAACAATGACACAAATACCGCAGAAAATAATTCCAGATAATGCAATTCCTCCAATTGAACAGAAACCACAAAGCCAGATTAGTTTCAGATTGCCAAATCTAGAAAAAACTGTTAACGATGAGAAAGTCCAACCTGTTATTGTTAGTGTTTCTCCCATTACTTATGCAGCCACAGTATCGAGTTTTGTTTCTCCTTGTGTGGCATCTGCAAAACCTTACATTTCTCAGGAAAGAACGGATAAACCAGTAATTTCATTTCCACCACCTCCCCTTGCTACACCCCCAGAATTACCATATAGCACAGTACCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15776
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 |
---|---|---|---|---|---|
ENSDART00000048657 | Nonsense | 2352 | 4478 | 27 | 55 |
ENSDART00000136955 | Nonsense | 269 | 1644 | 1 | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9127339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9704316 |
GRCz11 | 18 | 9673506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAATGTTGTGGAAGATGACGGTACACCAGTTGATCTKACATCTGGTAGA[C/T]RAACAGTTTGCTGYGATGTTATTTACWGRCTTCCGTTCACAGGGAGCTGC
Long Flanking Sequence:
AAATTGTGAATCTTAGTGCTGAAATAATCCCCAGTCCAACTCTGTCTGTTGTAAATGATAGCATAACAATAGTCACTTGCACAGCTACAATTGCCTACAATAACAATAGCACAGTTGACAAGCCTCTGGACCTTGGAAATGCTACTTCAGTGCCTCTTTCACTTACCACATACAATCCATTTGAGCCTCTTGCACAGATTGTATATAGACCAGTAAATTCTCAACCTAAGCCTCCAGCTAGTGCAGAGATTCCTGTTAACCTATCAAACAGATCTGCCACAATCAGCGCCCCTCCTCTAATGCCTCTTACTGTAGCCCCAGTGAGCTTCACAAATGGCACTGTTGGTATACCAATGCATACAGAGCCATCAGTGGTTGGACCTGTAGATCTCACCACATCTAAGCCATTGAATACCATGGTTGCTTTGTCCTCATCTTCTGGAGTGGTCACAAATGTTGTGGAAGATGACGGTACACCAGTTGATCTTACATCTGGTAGA[C/T]GAACAGTTTGCTGTGATGTTATTTACAGGCTTCCGTTCACAGGGAGCTGCAGAACACAGCCTCCTGTGACAACACAACCAGACACTCAAATTGGCTATGAAATTGATGATGCCGAAATGCCTGTCATTGAAAATCTCAGTACCATGAAGACATCGATATCGGACAGTAATTTCAAAGAGACTGGGCTCCTTAGTTATGAAAGGAAGAATGGATTCACCTATCAGAATGGGGCACCTGAGGGAGCCATGGATTTGACATCAGCTAAAATGTCAATGGGTGTGTATGACAGTGTACATATACGTGTATGTTTTATATTATTTTATTTTTATGCTAATGTTTATTGATTTTGTCTGAGTGTTTTCTGTGATTTACTTTTTGAATGTGTTGATTTTCATTCTTGTCTTTTTCTGTTTCTTTGTTTTTTGAACAGATGCATGCATTTGCCTCCGTGTTGTGCCTCAATGTTTTGGCTTTGCATCCTGCTAATCTGATGACACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10741
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 |
---|---|---|---|---|---|
ENSDART00000048657 | Nonsense | 2754 | 4478 | 28 | 55 |
ENSDART00000136955 | Nonsense | 671 | 1644 | 2 | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9128886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9705863 |
GRCz11 | 18 | 9675053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACAATTCAATGTCWYCTGCGGTTTCCACCCATGACTCCACATTAGTT[C/T]AAAACTGGCAATCAACAACAGYACAGCACAGTTCAAACWTTCCTGWAACA
Long Flanking Sequence:
CCCCAAATTTCCCTGATTTAGATGACAGCAAGAGCCAGCAGTACAAGGCAGAACATGAATTTTTACAATTAGAGAAGCTAAAGCAGCTGTGTCTAGCTGAAGAGCTTGAATGGGAGAGACAAGAGATACAGCGTTATCGTGAACAAGAGCAATTCATTGTGCAGAAGGAGCTGGAGGAACTACAGAACATGAAGCAGCAGCTTCTAATGCAGCAAGAAGAAGAAAGAAAAGCCCAACTGATCCTTCAACAAGAAACCTTTGCACAGCAGCAACATCAGTTAGAGCAGATCCATCGATTACAGAAGCAACTACAGCAACAGTTGGAAGAACAAAAGATATACCCATATGGGTTCGGCCCAATTGAGGGGATGTCCCCACCTATGGGCTCAAACATTATACTTGACTCAAAATATTCTGGGGGAGATAATGGACAGTATTGGCCAGTAAAGGATGACAATTCAATGTCTTCTGCGGTTTCCACCCATGACTCCACATTAGTT[C/T]AAAACTGGCAATCAACAACAGTACAGCACAGTTCAAACATTCCTGTAACAGTGAGTGCACAGACAAAGGAGCAAATGCAGTTGTCCACAAACATGTCTGATTCAGCAAAGCAAGAGCAAAATCTAGGGTTAAGTGGTAAGAAACTGATCGAGAGTGGTGTTCAAACGGATGATGAAGACGAAGTTGAGAAGATTCCATCTGGCAGAAAGAGAAGAAGTAGGAGAAGTGTAGATAGCTGTGTTCAAACTGATGATGAGGATCAGGATGAGTGGGATGTTCCTGTTCGGAGTAGGCGCAGGTCTCGTTCCAGTAGATATGCTGATGGAGAGAAGGGTAAAAGCTCTAAGGTGTCAAGTATTGCGATTCAGACTGTAGCAGAGATTTCAGTTCAGACAGAGCATTCGGGAACCATTAGAAGATCTCCTGTTAGGGCTCAAGTGGACACAAAGGTAGATTTACAGAGAGAGGGCCAAACAGAAAGTGATTCAGATATTACATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13696
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 |
---|---|---|---|---|---|
ENSDART00000048657 | Nonsense | 4027 | 4478 | 40 | 55 |
ENSDART00000136955 | None | None | 1644 | None | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9147477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9724454 |
GRCz11 | 18 | 9693644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGCTCCGAGAGAAAACAAYGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTARGTGTGTGTGTGTRTNNGTGTA
Long Flanking Sequence:
CCTTCTTGCTGTGAGGCGATAGTGCAAACCACTTAGGCACAGTGCCGTCTATATAATAATAATATAAATTAGAATTAGATTAATTACATTTAATTCAAAATTCCTAAAAATTAAACATTAAAAATCAATTTTCTTGCCTGTTAGTGTTATATAAAATTGATTTAAATATGTCACCATATAGAATTACTACAAATCTACAAAGGCCTTTGAAATATGACATTTGAGACACATTACATTTAGATTATGATGTATCAGCACTAGTGACTCACTTCAGCATTGACTGCCTTATTGGATTTAAATGGCAGCATCTTGGTGCTTATTCTACAGTGAAATCAAATTTGAGTGGATTGCTGGTATTATGCATCTCATAATAAATCTGTCCCTCAGCTTCAAATCAACTACGACAGGAATATGGGCAATCTGATTGTTCACGTGCTACAAGCAAGAAACCTCGCTCCGAGAGAAAACAACGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTAGGTGTGTGTGTGTGTGTGTAAGTTTGGGTGTGTGTGCGTTATAGTGTTAAAGTAAGTGAGTGTAAGTGTGCTGAATGAAATATTTAGAGAGACAAATGTTTGTTTTATGTTTGTTCTTGTCTACATATATAAGTGTTTATGTAATTGTGTTTGATTTACTGTCAGATTTTTTTAGTTATTTTCAGTGATTTCTTTCCCCCGGTTTTATTTAATTTTATATTTTCCGTTGTCGCTTTTCTCCTGGCCTTCCAGAAATCATCTTTTCCCTTTAGTATTAAGATTCTGGGTGTACTCATGAGTATGGTAAAACATCGCTGAAGGCAAAAAAAAAAATATATATATATATATTAGTTATAAATTAGTTGAATGAATGTATATTAAGCATAAAACATAAAAGTAATCGTTACCTGATGAACAAGTGTTTGACGAAATATATAGGCACAGTGTTAAAGAATAGCCATGTCAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11836
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 |
---|---|---|---|---|---|
ENSDART00000048657 | Nonsense | 4027 | 4478 | 40 | 55 |
ENSDART00000136955 | None | None | 1644 | None | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9147477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9724454 |
GRCz11 | 18 | 9693644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCGCTCCGAGAGAAAACAAYGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTARGTGTGTGTGTGTRTNNGTGTA
Long Flanking Sequence:
CCTTCTTGCTGTGAGGCGATAGTGCAAACCACTTAGGCACAGTGCCGTCTATATAATAATAATATAAATTAGAATTAGATTAATTACATTTAATTCAAAATTCCTAAAAATTAAACATTAAAAATCAATTTTCTTGCCTGTTAGTGTTATATAAAATTGATTTAAATATGTCACCATATAGAATTACTACAAATCTACAAAGGCCTTTGAAATATGACATTTGAGACACATTACATTTAGATTATGATGTATCAGCACTAGTGACTCACTTCAGCATTGACTGCCTTATTGGATTTAAATGGCAGCATCTTGGTGCTTATTCTACAGTGAAATCAAATTTGAGTGGATTGCTGGTATTATGCATCTCATAATAAATCTGTCCCTCAGCTTCAAATCAACTACGACAGGAATATGGGCAATCTGATTGTTCACGTGCTACAAGCAAGAAACCTCGCTCCGAGAGAAAACAACGGATACACAGACCCTTTCGTCAAAGTCTA[T/A]CTCTTACCAGGCAGAGGGTGAGTATCTGTAGGTGTGTGTGTGTGTGTGTAAGTTTGGGTGTGTGTGCGTTATAGTGTTAAAGTAAGTGAGTGTAAGTGTGCTGAATGAAATATTTAGAGAGACAAATGTTTGTTTTATGTTTGTTCTTGTCTACATATATAAGTGTTTATGTAATTGTGTTTGATTTACTGTCAGATTTTTTTAGTTATTTTCAGTGATTTCTTTCCCCCGGTTTTATTTAATTTTATATTTTCCGTTGTCGCTTTTCTCCTGGCCTTCCAGAAATCATCTTTTCCCTTTAGTATTAAGATTCTGGGTGTACTCATGAGTATGGTAAAACATCGCTGAAGGCAAAAAAAAAAATATATATATATATATTAGTTATAAATTAGTTGAATGAATGTATATTAAGCATAAAACATAAAAGTAATCGTTACCTGATGAACAAGTGTTTGACGAAATATATAGGCACAGTGTTAAAGAATAGCCATGTCAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23238
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 |
---|---|---|---|---|---|
ENSDART00000048657 | Nonsense | 4219 | 4478 | 47 | 55 |
ENSDART00000136955 | None | None | 1644 | None | 3 |
ENSDART00000142816 | None | None | 231 | None | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 9158768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9735745 |
GRCz11 | 18 | 9704935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGCCGGAAACGCCATCGCTGCAGCGGAAGCTGCCGTCCATCAATCC[C/T]GACTCCAGCCAAGTAACCCTTACTACTTCACATGAGCTCACAGCCTCTCT
Long Flanking Sequence:
TACAGTCTTCTGTGTCATTTTTATACAATGATTTGATGCTAGGGAAATGTGTATTATTATTATTATTATTATTATTATTATTACTGAAAACTGTTGAGCAGCTTAATATTTTGGTGAAATGCGAAATAAATGATCTCTTTGATAATCAGAAAGTTACAATTTTTCAATCAACTTTCTATTATCTTTTTTTAAATTTTACTGTCACATTTGATCAATTGTATCTATGCAAGTTTAAATCTTATAGACCCCCAACTAAGATCTAAGAGATACTGAAGATCAGTGGTGTATTAATCCAGAGCACATACTGTATGTTTACAGATACACAGGTCCCTACAATAGAAAAGTCCCACAGTAGTCCCGGCAGCTCCAAATCCTCCTCTGAGGGTCACTTGCGCTCACATGGCCCATCACGAAGCCAAAGCAAAGGCAGCGTCACCCAAGCACACTTGGAGGAGGCCGGAAACGCCATCGCTGCAGCGGAAGCTGCCGTCCATCAATCC[C/T]GACTCCAGCCAAGTAACCCTTACTACTTCACATGAGCTCACAGCCTCTCTGTTTTTCTGTCTTTCTTTCTGTCTGTCCTCTTGTTCTCGCACTCTTCCGCTATTTCTTTACCATTCCCTCTCACCCTCACATTTCTGACACTTTCTTTTTTTCAGTAAGTTTAGTTCTTCTTTTCATCGTTTAATGTTAATATTGTAAAACCTACACCTAAAATCACTAATTATAAACATAATAGCGCATAATATAAGAAATCGTATTGTTCAGTGGTGTCCAAACTTGGTCCTGGGGGGCCGTTGTCCTGCAAAGTTTAGTTCCAACCCTAATCAGACACACCTAGGCTGGCTAATCTCTTACTAGGCTTTCTAGAAAAATCTGTGCAAGTATGTTGAGGCAAGTTGGAGCTAAAATCTGCAAGACACCAGCCTTCCAGGACCGAGTTTGGGCACCCTTGGTATAATTGAAGTGCCCCTGTTATGCTTTTTTGAGTTTTGTCCTTTATG
Associated Phenotype:
Not determined