ZMP
si:dkey-108d22.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate piccolo (Presynaptic cytomatrix protein) (PCLO) [Source:UniProtK
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 19 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1417 | Nonsense | Available for shipment | Available now |
sa17573 | Nonsense | Available for shipment | Available now |
sa33413 | Essential Splice Site | Available for shipment | Available now |
sa20227 | Nonsense | Available for shipment | Available now |
sa11716 | Nonsense | Available for shipment | Available now |
sa20228 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1417
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 1878 | 4152 | 10 | 32 |
ENSDART00000136117 | Nonsense | 1026 | 3096 | 1 | 15 |
ENSDART00000143963 | Nonsense | 1026 | 3298 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10481889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11418516 |
GRCz11 | 4 | 11417365 |
KASP Assay ID:
554-1338.1 (used for ordering genotyping assays)
KASP Sequence:
CTCAGCAGTCACAAACAACTAGAGTACCACTGGCATTCACACGGATAACT[G/T]AATCTATTGAAAGTCAAGAAATTTGTGGTCCAGAGAAAGTAGTTTCTAGC
Long Flanking Sequence:
GAGACAGTGTACCAATAAAACAGCCTCTAGGTCAAGGCTACAAGCCCCATGTTCCCCCTCCTGTACCACCAAAGCCGTCCTCTATCCCTGCAGGCCTAAACTTCAGTCACAAGCAAGGGGAAAGTTTTAAACCTCCCATAGCTCCCAAGCCCATGGCCGGTGCTCAGCCATCCTTAACAGCCCACACTCCCACAAGACCTACAATACTTACTACAAGCAGTGCAGACAACGTCCTTAACTTGAGTCCTTCTGCTGAGAGTAGGACAGGAACCACATCTCCCCTTAAGTCTCCTACATCACCCAGGTTTGGCAAAGTTTTGCGTGACACATATGTTGTTATTACTTTGCCATCTCAGCCCAGTTCACCTACAGAAGGTATCACAACCCAAGCATCAATAAGTCCTAGCCAAGAATCACATCAAAAACTGCCTCCTTCACCACCTCAACCAACTCAGCAGTCACAAACAACTAGAGTACCACTGGCATTCACACGGATAACT[G/T]AATCTATTGAAAGTCAAGAAATTTGTGGTCCAGAGAAAGTAGTTTCTAGCATGAGTCATGTCTATGAGGCTATTTCAGCCTCAACACAGCCTCAAACGGTTATTCCAAATGTTGGTGTTCAGGTAGTTACCACCGAAGTCCAAAGAACCACAGTCTCTGTTGTTCATGAAAGAACACCACCTCCACATCCCATGCCAAGAGCCACTGGCATTTCTGTTGTTCAAGAAACTACTAAACCTGAAGCAGTTCAAATACAGAATGGTCATGCCTATCATCCTGGTGAAGTAGTGGATCTCCGAACCCCAAAAATAGATGCAGTAACATCCATGAAAGGTATAGATCTGTCTTCCTCTGAATCAAGGCGACAGTCTCTTGCTGTTGATAGTGGTGGACGTCAACAAAGTGCTGTGCAGTCATCAGTAGTGAACCTAAGTACTGACACTTCTTCAGTTTCAGTGGTTACCGACAACATAACAATCCTCACGTGCACAGCCACTGTA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa17573
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3358 | 4152 | 13 | 32 |
ENSDART00000136117 | Nonsense | 2514 | 3096 | 3 | 15 |
ENSDART00000143963 | Nonsense | 2514 | 3298 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10487160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11423787 |
GRCz11 | 4 | 11422636 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAAGCAGAAGGTGAAGCCTCTTCTGAGACCTCAGCATTCCAGACTCCCT[C/A]GGGCAGGTCAAAACCTACAAGCCTCCCYATTGTACAAAGTGGGCGTGGAC
Long Flanking Sequence:
GTATAGTATTAGTAGACTGACCTTAGAGAAGCAGGCTGCCAAGCAACTCCCAACATCTATGCTTTACCAGAAACACAAAAACACCAGCAACATTGGCAAGTACTCCTCAATGCAGGATAGCAGGGGTCTAGAAACAGACTATAGTAGTTATCTTGGGTCCAGTAGCTCTTCTCCCAGGTCAAGCAGACTTATGCAGGATGAGATCACCTTTGGGTTACGGAAAAATATTGCCGAACAACAGAAATACCTGGGTTCCACACTTGGGGCCAATTTGGCAGGTTCACTCAATCTGGGTCAAAGCCTGAATCTGAGCCCAGGAATGAGGTCATCTTTAGGAGAAGACTCTTCTTATCCTAGTGGAAGCAGGTCTCGTCCTTCTTCTAGACCCTCATCCGTATATGGGCTTGACTTGTCCATTAAACGAGACCTCTCAAGTTCCTCTCTAAGGCTCAAAGCAGAAGGTGAAGCCTCTTCTGAGACCTCAGCATTCCAGACTCCCT[C/A]GGGCAGGTCAAAACCTACAAGCCTCCCTATTGTACAAAGTGGGCGTGGACGTATTCCTATCGTGGCACAGAATTCAGAGGAAGAGAGCCCACTGAGTCCAGTTGGTCAGCCAATGGGTATGGCACGGGCATCTGCAGGTCCACTCCCACCCATATCTGCAGACTCTCGTGATCAGTTTGGATCATGCATGTCTCTACAAGAATCTCAACAGCAACATCTCAGAGAAGATCCTTCAAGAGGACGTGGCTATGTGCTAATGGATGATCTGCAGGGCACCATGTCTGATAGTGAAGGTAATTTGTTTGTCCACAAACTGTCCTCTTGGAGAGATTCTACATACACAGTCTCAGTTTTTTACTTATCTGTGTTTCATCTTGCAAGTGCTTCTTCTAGTCTATATGAAGGCATTGGTTTTCTGAATACATTTGCTTTCTGTCTTGTCTGAGCTTGCTTATTCTTTGCTTAAAAATGGAAGCAATCACAATGTCACAGTTGTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33413
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Essential Splice Site | 3508 | 4152 | 15 | 32 |
ENSDART00000136117 | Essential Splice Site | 2642 | 3096 | 5 | 15 |
ENSDART00000143963 | Essential Splice Site | 2642 | 3298 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10490468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11427095 |
GRCz11 | 4 | 11425944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTACAAAGATTGTAAAGAAATATTTGTCTGAATGTGCTTATGCATCTTT[A/G]GGGAAAGTTTCACTACCCGTTTCCTCATGCAAGAATAAAACTACTGAGGG
Long Flanking Sequence:
GATTGTATGGGCCAAAGCTGGGCCAGAGAAATTTTGTATAAGATCAAATTGTTTTAGTTTTTTTTTTTTTTTTTTTTGTAAAAAAAAAATAAAGAATTGAGTCCTCAGGGTTTTTTAAGGTTTGCATGTGAGAATAACTGCTCCACTTTGTATAACCATTTCCTTTTCTGTCCCAGATGGCTCTGTATTGTTTGAATATAAGACATACGTACCTTAGCTGTTTCTAGTACCTGATATTACCAGAGGGCCCTTAGGGGTTTGTTTTCACAGACTGGCAAGCAAGACTTTAACGTTTTAATTTCCATCTGTTTTTCTGAAGCGTACCACCTGCGTCGAGAAGAAACCGACTGGTTTGATAAACCGAGAGACGGACGCGCTGAAAACGGACAAGGGATGGAGAGAAGACAGGTATTTGAAATAAAAATCAGCAAAATGCTATTGCAAAAGCATATTACAAAGATTGTAAAGAAATATTTGTCTGAATGTGCTTATGCATCTTT[A/G]GGGAAAGTTTCACTACCCGTTTCCTCATGCAAGAATAAAACTACTGAGGGATCCCAAAGATCGTAGTGTATCAGGTAAGACATGCAACTTGTCAAATACTCTATGCTACTTGGCATTCTGACACGCTCCAACAATGCAGACAGCTGCCCATGGTAAAAGAGGATCTGTTCGCCTACCAGGCAAGCATGGAGAAATGCCCGAGGCTTATGTCTATGCAAACATTAGTTTCGCCATGCTGAGATTGCATTGGCACAGTTTTATTTTAGGCCTACTACTAAACAACACATTATCCCTTCTCCAATTCCCCTTTAGCGTCCTCTTGTGGCGCTTCATTTTGCCAGATCATTGCACACGAAATGTCAACAGACACAAACCCGCTGAGCAAACAGCACATCAGCGGTCTTGCCCCCCTTCTTATGCTTTGGTATGTCACGTAGGTGGGGCTGATTCCCTTCTGTCTGTTGTGTCACTGTTCCTTTAAGCATTAGAACAGGGCAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20227
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3566 | 4152 | 16 | 32 |
ENSDART00000136117 | Nonsense | 2700 | 3096 | 6 | 15 |
ENSDART00000143963 | Nonsense | 2700 | 3298 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10492398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11429025 |
GRCz11 | 4 | 11427874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGACATCGGTGCATATGTGGCCAAAGTATTACCTGGAGGAGCAGCA[G/T]AACAGACGGGGAAGATTGTGGAAGGTAGGCACCTCAATGAAAGGCGGTTA
Long Flanking Sequence:
GGAGCGTTCTGGTGCCAGGCTCAGACTCTATCTTTCTCAATCCTGATAAGGAGAATAACACAAGTTCTTTTCCATGCTCAGAGCCTTCTCCCCAAACAGCACACCTAACACGCATATTCTATTCAGTCAAATATCTGTGTGTGTGTGAACTCGTGAAAATTTATTGGTACAAAAATGTTAAGTACTTAAGCTGGTTAAAACATCAATTGTTGAAATCACTGATGGTTAGAGTAATTGAACCCTTTAATCCAAAATCTTTCAGTTATTGTGTTTGACAATTAAAGGAAATTTACAGATCAAACAAATATAGCAAATTGAACTAAATAATTCCACTTTTCATGCTTGTTCACCCTCTGTGCAGGTATTTGACCTCCTTATTTTAATACAATTTCTCCACAGGAAATGGACTGGGAATTAGAGTGGTTGGAGGGAAAGAGGTCCCGGGAAGCAATGGAGACATCGGTGCATATGTGGCCAAAGTATTACCTGGAGGAGCAGCA[G/T]AACAGACGGGGAAGATTGTGGAAGGTAGGCACCTCAATGAAAGGCGGTTACACTTTAAAAGACATGTTCCTGTGTGGGTTCACTGACTGGGTTAAGCTGAAGCGGTGTATCGATGCTCACTGTCTTTTAAGGCAGAGAGAGAATCGCATGAGTTAACGTTAAAGGGCACAAAGTGACGTGATATTTCAGGGCAGGAGACAGAAAAAAAACAAATGATGTTAATTTGCGTGATTCTTCACCTCCGGGCTTGCAGAATGACTCATTCTTGATGTGAGAGATAAAGATAGAGAAGGAGAAAATGAAGTTGAAGCTTCAGGTTCATGACTGTGTTTCCTCTGCAGTGTATACTGTCGGTGTAGGTGTTGCACAGATCAGTGTTAAATTTATATCGAAACTTTGACTGAGATGTCTCTAGGGTGTTCAGTTCAAAAGAGTTTGAGGTTTTACTGCTTTACCACGGTCTTCTTTACCATGCAGTTATGTAAATGTGCACTTTGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11716
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 |
---|---|---|---|---|---|
ENSDART00000092381 | Nonsense | 3580 | 4152 | 17 | 32 |
ENSDART00000136117 | Nonsense | 2714 | 3096 | 7 | 15 |
ENSDART00000143963 | Nonsense | 2714 | 3298 | 7 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10496209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11432836 |
GRCz11 | 4 | 11431685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTTTATATTTGTATGTGTGTRTTTGCATAGGAATGCAAGTCCTGGAGT[G/A]GAACAACATTTCMTTGAGTGGTAARACGTAMGAGGAGGTGCAAGGGCTGG
Long Flanking Sequence:
TGTGATTATGTATGGGGTTGTCATGGCTACAACAGTCATGTGACTGACGTATATTTTCAAGCTCAGTGTAACAGGCTGGTGTTAAGCTGTGGAGTAATGTGAGCCGGCTGTTTAGTCTCTCACATTAAACAGTAAAATCTTTAAGCGTGTAAATGACCCGAGTACACATTCACCCCCAGGGATCCCAAGCATCCAACGTAACGTAGGAGGTTCGAAACGCCCAAAGAGGGCATACCTGGCCTACCTGAAGACACGCTTTCATCTGTGTAAGTGCGCTAAGAGGTTTTGGTTTGCTGTGACTTGGCGTGAAATCTGTTGCACGTGTTTCCTCTCCTTTCTCACAGGATTTCTTCAGCACAGCTTGTTTAATCGAACTTGATGCTTGATGTTGCAGTGCTTATTACAGTATATTTGATCAAATGTAAATAAAATTCATTGTATAAAGCGGCTGATTTTATATTTGTATGTGTGTGTTTGCATAGGAATGCAAGTCCTGGAGT[G/A]GAACAACATTTCCTTGAGTGGTAAGACGTACGAGGAGGTGCAAGGGCTGGTTGGTCACCAGGTTGGAGAGGCCGAATTATGTATCAGACTGTGAGTGTCAGATTTGCTTAATTAATAGTTATGTGCTACTTTTTATTTCTGTTTTCTATCTAGCTCTGAATGAAACATGATATTTAAAGCCCCAATGTACAAATGCGGATTTACAATTTATTTACCAAATATTCAGACTCAATACTTTGAATATGTTTTAACAAATCTAAATATTAAGAAAATTGCTATTTAAGTTGGGCAAATTAAGTGTTTAGCAAAGCATTTTCCTAATGAATAATTAAGATTTGATACATTTAGGGTACAAAGTATCTGACATATCTTAATGGAACATGATCTGTAAACAATATTCTAATGATTTTTGCCTTAAAAGAAACTATTACCAAAAATAAACCTATGCAACTTGAGACTTTTGTGGTCCAGGGTCACATATTGATTTCCTGCTTGCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20228
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092381 | Essential Splice Site | 3696 | 4152 | 20 | 32 |
ENSDART00000136117 | Essential Splice Site | 2830 | 3096 | 10 | 15 |
ENSDART00000143963 | Essential Splice Site | 2830 | 3298 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 10497178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11433805 |
GRCz11 | 4 | 11432654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAAACAAAAAAACACGTCTTTCCTTACTGCTGATGTTTTTTGTTTCTT[A/T]GAACTCTGAGGGTACAAAAACTCAGTCCCACCCAGTTTCAGGAGAAATCC
Long Flanking Sequence:
CAGGGTCACATATTGATTTCCTGCTTGCTTTACTAAACTCCTCAATTTCTTTTTATCTCCAGTGACATAAATATGCTGTCTGATTCTGATAGCTCCCATCTAGACCTGCATGACCAGGTTAAAGGTGAGAACCTCGAGTCATTGAAAAAGACAATCAAATGAAATTGTCTTAATTAACCACAGTGACTACTAACACCTGACTTCTAAATATACAGGGGACAGACCTCCACGGTCACCAGGTGTGGACCCCAAGCAGCTGGCTGCCGAGCTGCAGAAAGTGTCCCAGCAGCAGGTGCCGTCCTCCTCTGCGTCAGCACTGGATAAACCCTCAGCGTCTGCAGGCTCCAGTGCAGTTCCCAGTCCTGGCCAGCCTGGTTCACCCTCTGTCAGCAAGAAACGCCACAGCAAGGTATGCATATCCCATGTGCACAATTATTTTGGATACAGAAAGTCAAACAAAAAAACACGTCTTTCCTTACTGCTGATGTTTTTTGTTTCTT[A/T]GAACTCTGAGGGTACAAAAACTCAGTCCCACCCAGTTTCAGGAGAAATCCAGGTAGATTTGAGCTCTCATCATCTCAGCTACATCTGTAGCTCATTAAGCAAACCTCCAAGTGGAATTTTAAAACTGTAATTTAGAGACCTGTAAAAGTGGAAATTTCAATATGAAACTATCTACGACTAGAAATTAGCTGCTTATGAATGAACACTCTATGAAATCACTCATATTTAATTTCACACTTAATTCATTGATTAAAAGAGTGTATTTATGTAATAGTCATTTGCCTTTTCAACAGAAGAAAGACATTTTTACTTTCTTCTATGTTGCAGCTTCAAATAAATTATGACAAACAGCTGGGAAATCTCATCGTCCATGTTCTCCAAGCACGGAATCTGGCGCCTCGGGACAATAATGGCTACTCTGATCCATTCGTTAAAGTTTACTTGCTGCCAGGTAGAGGGTAAGTACTTTCTGCAAATCTCAACTTACTGGAATTGAGTCT
Associated Phenotype:
Not determined