Busch Lab

ZMP

stxbp5b

Ensembl ID:
ENSDARG00000029234
ZFIN ID:
ZDB-GENE-090821-5
Human Orthologue:
STXBP5
Human Description:
syntaxin binding protein 5 (tomosyn) [Source:HGNC Symbol;Acc:19665]
Mouse Orthologue:
Stxbp5
Mouse Description:
syntaxin binding protein 5 (tomosyn) Gene [Source:MGI Symbol;Acc:MGI:1926058]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa39146 Nonsense Mutation detected in F1 DNA Not yet available
sa42867 Nonsense Mutation detected in F1 DNA Not yet available
sa36311 Nonsense Mutation detected in F1 DNA Not yet available
sa22995 Nonsense Available for shipment Available now
sa12880 Nonsense Available for shipment Available now
sa39145 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39146
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098731 Nonsense 220 1158 6 28
Genomic Location (Zv9):
Chromosome 17 (position 7138846)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7143112
GRCz11 17 7300342
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGACTCACCCTGGACCAGTAGTTCACATCAGCGATAACCCCATGGAT[G/T]AAGGAAAAGTAAGTTTGAACTACAGTTAAGATTATATGTTTCCCTACAAA
Long Flanking Sequence:
ACATTAGCAGGAGGATGAAGGTGAAACCAGGGTGGACATTTCAGCAAGACAATGATCCAAAACACAACCAAGGAAACTCCCAGATGCTTTCAGAGAAAGAAAATCAAGCTGCAGAATTGCCTAGCCAATCACCTTACTTGAATTGAATAGAAAATACAAACTAAAGATCAGATTTGATAGACGAGACCCACAGAACCATCAAGATAACACTGTTGAAGTCGGGAAAAAAACTCTTACCTGAGCAATGCACAGGCACGTGCACAGGTAGGGCCCAGCATGTCCCTTTTTTCTCTTGGAGAAAAAATGCCCCTCAAATGAATGAAAGTGGCCCTTCACTAATCGATCGCCCGGTTTGAATCTTGATGCATGAGCTTTTAATACCTCCTATGAATATTTAAAGTATTTTCTTCAGAAATAAGCAGTCAAGTCTCTTTTTTTTAAACAGTTCATCAAAGACTCACCCTGGACCAGTAGTTCACATCAGCGATAACCCCATGGAT[G/T]AAGGAAAAGTAAGTTTGAACTACAGTTAAGATTATATGTTTCCCTACAAATCACTTTCTGAATGCTCCGCTTTCAGTCTGCACCATTCAAGAGCAGTTGCTCTCTTTTTGCAGCTTTTAATTGGTTTTGAATGTGGGATAGTTGTGCTGTGGGACTTGAAATCGAAGAAGGCAGACTACCGCTACAACTATGATGAGGTGAGACATTGTTATTGCATATAATAGTTGTCCCCGATTTTGTGATCTAGATCTTTTTTTTTAAAGCAGACCTATTTAGTTTTGTTTTAGTAATGTCTTCAATAGGGATGGGATAAACTCATCAAATAAAAGTGTTCAGATGTGGCCACAGTAAGTACGTTTACATGAGCACCAATAATTAGATTTTAAAACGATTAAGACGTTACTCTGATTAAGAGTTGACCATGTAAACATTGATTTTTGATGAATTGAATCTGATTAAAGTCATAATCGAAGCTGAAATGGAATCAAGACACGTTGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42867
Status:
Mutation detected in F1 DNA
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
ENSDART00000098731 Nonsense 471 1158 14 28
Genomic Location (Zv9):
Chromosome 17 (position 7120505)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7124771
GRCz11 17 7282001
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATATTACTCTCTTTTTGTTTTCTTCCTGAAACAGGCATGCTGATGGAT[C/A]GATCAAGTTTTGGGATGCCTCAGCTTGTGAGTTTCTTTCTAAAACAATAT
Long Flanking Sequence:
AGCAGGAGAAAATAATATCTATTTTTTGCGAGAGTGGGACTGAAAAATTGCTCTGGCGCAGGTCTTTACTCTCAAGTCGAAAACAACAAACTCAGCACTGTAAGGTCGATCAGTTCTCTCTCAAAACTGTGACCGCTCTCTAAATACCATCTCTTCATCCAAATCACTGCACAGACACAGGTGTTAGGAATGTTTTTGATTGACCTACTTTTCCTCTCGTGACTGCCATTAAGTATAAAAATTACAAAAAAACAAGGCATGTCTTCAAAAGCTACCTCAGTGTTGTATTACCGAGGTCATACTTATGTCACTATAAAACTGTCTGTCCTTGTAAACCTCCAAAATCAGTACACACACTAGCTCTTTGCTGCCGAAGTCTATTCATGTTTGATAATTGTATTAGAAAGTAAAAGCATTTATTGTTGTTGAAAGCTTTTAAATGTGAAGTCTTCATATTACTCTCTTTTTGTTTTCTTCCTGAAACAGGCATGCTGATGGAT[C/A]GATCAAGTTTTGGGATGCCTCAGCTTGTGAGTTTCTTTCTAAAACAATATACACTGAAATTTTATGTCCCAAGCTTATAGAACCACAATGTTTGGAGTTGGAAAAACACAATAGATGCTTGTGGATTCTGCAAATTCATTACTTAAACAGAAGATTTCCAAAGATTTGGAAGCACTCAGAGCTACATTAAAGGATTAGTTTGCTCCAAAAAATAATATTTCTGTTACTAATTACCTTCATGTAGTTTCAATCCTGAGATATCTTCAGAACACAAATTAAAGAGATAGTTCACCCATATCTTAAAATTAAATCACCATTACCTTTAAACCTTTAGGAGTTTCTTTCTTCTGTTGAACAAAAAACTGTTAACGTTGACTTCCATAATAGGAAAAACAAATACTATGGAAGTCAATGGTAGCAAGTTTTCAGCTTTCTTCAGAGTATCTTGCTTTGTGTTCAGTAGAATAAAGAAAGTCAAATGGGTTGGGAACAAATAAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36311
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098731 Nonsense 583 1158 16 28
Genomic Location (Zv9):
Chromosome 17 (position 7114408)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7118674
GRCz11 17 7275904
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAATCTCCAGAGGGTGGAGGAGACCAGGCGTCGGCTGTTTCCACCCCA[G/T]GAACTGCACCCAGCCCTCAGACCAGCCTGCCTCAGTCTCACCCCTCCACA
Long Flanking Sequence:
TGAATTCTATCTATTTCTATTTTATACATTTTTTAAAGTAACTTTTTTAGTGTAATACGAATTAGTTTTTTTATCATGTAATATTTTAATGTATATCCATTTGGCCACGAAATAGCCATAAGTTGCTGATGTGGCAATAAATATGTAATAAATAAATAAATAAATAGCCTATAATGAGAACTTTTTTGTTGGAAATACTAAATTATTACAGCTTGCATCGATAATTCAGTTCATACAGTTGTTTTTGGTCCAGATACATGATAAAAATATAAAATAAACATTAGTTTTAATAATGATTATCTATATAAAGCCGGCCTGATTTTCAAAACTAAGTTTTAACGATATATTGTGTAGCCCTACTACAAATACACTTGTTGAAATGTGTGTTAATGCCGGTTCACATATGTGCGTAGCTGTTGGAGGTGCGTATGCAGTGTGAGCTGAATGAAGTGGAATCTCCAGAGGGTGGAGGAGACCAGGCGTCGGCTGTTTCCACCCCA[G/T]GAACTGCACCCAGCCCTCAGACCAGCCTGCCTCAGTCTCACCCCTCCACAAGCAGCAACAACTCCTGCGACGGCCTTCGGGATAACGTGCCCTGCCTCAAGTACGACCTGCTTTCATTTACTTTGTGAAGTTTATTTATAAACTTAATTTCGAGAGGAGCACCTGCTTATGATTGATAGCACCTGGTCCACATTAGCTAACACTGATTTACCAATCAGACGACTCCTTATCCACTATAAATAACCAGAGTATCTTACTTCAGCCATCTTCGTCTTGAAGAATCCTCCCTTCCACCCTTACTCCTCCCATTTCCTTGTCAGGGCAGCACGGAGGCCTAGTGGTTAGCACCACGGCCGCACAGCAAGAATGTCACCGGCTCGGACACGTCCTGGCCACACATTTCTGTGCGGAGTTTGCATGTTCTCCTAGTGTTTGCGTGGGTTTTCACCGGGCTCTCCGGTTTCCTCCCACAGATCAAAAACATGTAATATAAGTAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22995
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098731 Nonsense 743 1158 20 28
Genomic Location (Zv9):
Chromosome 17 (position 7101366)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7105632
GRCz11 17 7262862
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGCTGTAGGCTCCGGTTCACCGTGCAATTCTGATGAAGACAGCAAA[C/T]AAAAGTTCATTGAGAGGGGTACAGTACATACAGCATACAAAAAATACCAA
Long Flanking Sequence:
ATGAGGGTGAGTTAATGTTGGCAATATATTTGTATGGATTTTGCATTTTAAAATGTCATTTTAATTTATAAATAAATATATTACATTTTTGCATAATTTCCTACAAAGGCCACTGTGTGCATGGTTTGGAAATACTGGTAGTTCCGCCAATCCAATGCTAATCCTCTGCCAGTTTCTTTTGGCGATGCATAAATTACACACTGTATTTTAAAGACAGACATATTGACAAACACTGCAATGCCAGAGCATTGGACGTGAAGCTCTGTTATAGTTGAAAAAGCCTCCAGCACAGCAAAAAATTAAAACAATTCTGCAAGCGTCATCAGAATTCTAGTCAGGTGTGCTGACCAAGGAAATTTCATTTACAAGGAATTTGACTTTGATATGCAGATAGTTGCCAAACGTTACGTAAGACCCCATTGGCTGTGTCACATTATTATGCAGACTGTGTTGTTGCTGTAGGCTCCGGTTCACCGTGCAATTCTGATGAAGACAGCAAA[C/T]AAAAGTTCATTGAGAGGGGTACAGTACATACAGCATACAAAAAATACCAAAAAAATTCAAAATTGTCCTTGCAAAGTCTTTATTTTCTTTTTTAACACATTTTCCAGTGAAGACCAAAAGCAAGCGGATATCCAAGACTGTTGCCAATGACTTTGGTACTGTATTATGTTCATATTATGGATATCTGGGTCTCTCAGTCTCTGTACTAATGGGCTCCTGTGGACTAACCAAATGAACTAACCAAACCATTTCAACTGGGTTTGCTGCTTAAATACAAACTAGAGCTGACCTTTGTGTGTCTGTTGCTTGGTGGTCAAGCCTGCCAGTATAAACTGGGCTAGTGAGAACTTTTACGTTTTAATTGTAAGCCATTTTTACTGTTGCAGAAGCTGTCACCTTGTGAATGATTCATGAGTGCATGTTACTCTAAGGGTGTTTTCACATTTAGTTTGAATGTCTGGTTTGCTCTGTCACTGCTCTGATGCCCTTCCAGACACAAC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa19160
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098731 Essential Splice Site 860 1158 23 28
Genomic Location (Zv9):
Chromosome 17 (position 7091799)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7096065
GRCz11 17 7253295
KASP Assay ID:
2261-0587.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACACCAGAGCAGAGGATGCAACAGCCTGTGGGCGTTTCTTTCTGTGG[T/G]GAGACTTGATTTGCATTTGTAATGTATGTAAAACTGCATGGAGGTTCTTA
Long Flanking Sequence:
GACTATAGCCACACAGCGGTGTTTAAACCCCTTACAAAAGGTAATTTTGCGTAATAGGTCCCTTTTAAAATCTTAATGCACATACAATTAATTTAATAAGAATACACCATCAGTATATTAACTGAATGCTGTGCTTATTTTAATCTTTTAGTATATTTTTTTCAGGGCTCCTGAAGTGCTCCAAGCTTTATTTTGCTTTAGAAACACTTGCTAATTCTTTTTTTTTTTGTCTTTTTGTCCCTCACTGTATTCTCTGTAGATGCCAGAGACAACTCATTCAGCCGCTCGCGCAGCTCCAGTGTGACCAGCATTGACAGAGAGTCACGGGAGGTCATTTCCTCCTTTTACTTTTGCGACTCTCTGTCCAAGAAGAGCGAGACGCTGGCAGTACCCAGTCTGTGGGTGGGCACCTCACTGGGCAGCATGTTGGCCATCGCCCTCACCGTTCCCTCCACACCAGAGCAGAGGATGCAACAGCCTGTGGGCGTTTCTTTCTGTGG[T/G]GAGACTTGATTTGCATTTGTAATGTATGTAAAACTGCATGGAGGTTCTTAAAGGGACAGTTCACCCAAAACTGAAAATTACCTCATCGTATATGTATATATAGGTAATATATATATATATATATATATATATATATATATATATATATATATATANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNACATACATATATATATATATATATATATATATATATATATATATATATATATACATATCGCATATATATATATATATATATATATATATATACACATGACTAAAGTCTTGTCGTCGATGTCAGTTGTAAGAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTGGTAAAGTAGCAGATGAGTCATCTGTTGAACTGCATCCCAATTATCACAAATATTGCAGAAGACCTACTGGAACCCGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12880
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098731 Nonsense 1004 1158 25 28
Genomic Location (Zv9):
Chromosome 17 (position 7082849)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7087115
GRCz11 17 7244345
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGTGAACTACCTTCCTCTGACGGACATGAGGATAGCCAGAAYCTTCTG[T/A]TTCTCAAACCAAGGCCAAGCCCTRTACCTCACATCGCCCACTGAGATCCA
Long Flanking Sequence:
ATTTTCAATTCAATTCAATTCAGCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTCACATAAATTGTCATAGTAACTGGATTAGGGTAGATCAGTTTTTAGTGTTTAAGTTCAGTTCAGTTTAGCTCAGTTCAGTGTGGTTTGAAATCGTTACTTAGCACTTATCCAAAATGTGCATAAATATAGGTGGATGGAAACGTAGCTAGTGTCATCTTTGCATTTAAAATGCAATAACTGAGCGAATGACACTTGAGAGTGATAAACCTGCATAAGGTCTCATTCACATACATGACATAACCATATCATGATTATAAAGGTTTAATGACAGTCTTATGATCGCCCCTTCAAGTAAAGTGTTACAATTATTTTATTTTATTTTTTTACACTGTTCTGAACATGTCTGTTTTCAGTTTGCCCAGCCTGCGGCCATTGCTGGATGTGAACTACCTTCCTCTGACGGACATGAGGATAGCCAGAACCTTCTG[T/A]TTCTCAAACCAAGGCCAAGCCCTGTACCTCACATCGCCCACTGAGATCCAAAGAATCACCTATAGCCAGGAAACCTGTGAAAACCTGCAGGTCAGACATGGCCTTCATGCTCTACTCTGTGTGCACGATGTATCCCATTAAAAATCCATTCATTTGAAACATAGATGGAGATTTACCTTTTGAATACTTTCAGTGGTTAAATTGCTAATTGAAATTATTTTGCTCAACAATTGATGATTGTGACAAATTCAGTTTGCATCTAATTCTTTCACTTCCTGTCACTTGAACCTAAAATAATCATAAATGATAAGTTAGAAAAAGGTTTAAGCAAGTTACAAGAGTGTTCATAGTGAGCTGTTTACGTTTAGCTTGTGACGAAAAACCCAACTTGCATGATTCAACCAAACACTCAAGAGCTCTTTCTTGTGAACATTTAGGTGTATGGGTTTTAAAACCAGCCTAGAGCACAATCTACTGTTTAAAACTAGCCTAGAGGGCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39145
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098731 Essential Splice Site 1146 1158 28 28
Genomic Location (Zv9):
Chromosome 17 (position 7071347)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7075613
GRCz11 17 7232843
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGCCAATTTATTGTTGTTTTCATGAACAATTCCTGTTTGTCTTCTCCA[G/A]ATGATGCTGAAATACAAGGACAAGAAATGGTACCAGCTCTGAGGGCCTGT
Long Flanking Sequence:
ATCCCTCTGGCCACTGTGCAGGATTTGTGTCTGTCATTCCCAAGAAGAATTGATGCTGAATGGGCCGCAAAAGGAGGCCCTACACCATACTAATGATTTATTGTGGTCTAAAACTAGGCGTTTAGGTTTCATTGTCTAACCCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACACCTGCCTGTAATTATCACGTGGTGTTCAGGTCCTAATTAATTGGTTCAGGTGTGTTTGATATGGGTAGCAACTGAAATCTGCAGGAAGGTGGCTCTCCAGGAACAGGATTGGCCACCCCTGGTCTAACCTCTGTATGTATGCGCAATCCAATTTAAAATACAGAAGCAATTCTCAGCTTTCGAGTTCACTAGGTTTTAAAATGCAGCCATATACTTTAGGCCACGCAAAATATTTGTGTTGGCCAATTTATTGTTGTTTTCATGAACAATTCCTGTTTGTCTTCTCCA[G/A]ATGATGCTGAAATACAAGGACAAGAAATGGTACCAGCTCTGAGGGCCTGTAGGGAGTCAGCAGAAGACAGCAGATCCATCATCTCTCCTCGGTTTCTTCCTTCTCTTCTCTTCTCTTTCCCTCTCTGTGATGTCTTGAGACTCGGCACAACGTCCCGCGGCATTACCTCCAGCAGAGGAGACAGGAGGCGAAGGATCCAGACAAGCCAAACGCATCGGGACGGGATTACCAGGCACTAAAGTTTCCTCTTCTGAAAACAAAAAGCCGCGGTTCTTGTCTTGTAGAGGTGGCTTTTCACCGGTGCTGCCCCGTTGTTTACCGTCATCCGCCCCACGCTGTCATTTTCACTGCCATTCGATCTGCGAAGGAAACTACACAGAGAAAGACAACGAATGAAATAGAGACTAACGTGTGCAGCATTGCCAAGCTTAATGCTTCTGATAATCTGTCACTAGTGCAAGAAAACATTGCATGTCTAGTGATTTCATGTAGGAAATTAG
Associated Phenotype:
Not determined