Busch Lab

ZMP

syt14a

Ensembl ID:
ENSDARG00000010934
ZFIN ID:
ZDB-GENE-090313-200
Human Orthologue:
SYT14
Human Description:
synaptotagmin XIV [Source:HGNC Symbol;Acc:23143]
Mouse Orthologue:
Syt14
Mouse Description:
synaptotagmin XIV Gene [Source:MGI Symbol;Acc:MGI:2444490]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa10841 Nonsense Available for shipment Available now
sa31941 Essential Splice Site Available for shipment Available now
sa38953 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10841
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
ENSDART00000010831 Nonsense 301 421 4 5
ENSDART00000140164 Nonsense 380 500 5 6
ENSDART00000145938 None None 62 None 2
Genomic Location (Zv9):
Chromosome 13 (position 32073686)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31719634
GRCz11 13 31850084
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTCYTCCCTGATGATCCCCCTCTGCTCTCTCCTGTTGTCAGATGGTT[T/A]GTTCTGTTKTCTAAAGCACTTGATAGGTGGCCAAGTGTACATAATCCGAG
Long Flanking Sequence:
TTTTAAGTTCTCAACTGAGAAATATACCATCAAAAGCCTTGTTGGTTTTGTTTTTATCTTTTTTTTATCTTTCTTAAAAATGTGAACATTAAGTTAGCCTGAACTTAATATAACATTTTATTTTTTGTTGTCTGCACCAAACAAAAAATCAAAATAACTACAAATGTAAATCCACCTGTAATACAGAGAGTTGTGAATGTTTTTTAATCCCCTCAAATAAGTGCTTCATAGACTGTGAAACACAGCCAAATTCAATGTTGACACCTTGTCAGTCAGACTTACACATACTGTATGTATACCCTAGCTTGTAGATAAAAAGCAGAGCATACTTTGTTCTTTATCCTGAAGTGGCGCAGTGTGCTTTATGAACACATTACCTCTGACCTGATGTGATTAACCCTTCAAGCCTTTTGACCTGCTCTTTTTCTCCTGCCATTGTTGACATTCTCTCTCTTCCTCCCTGATGATCCCCCTCTGCTCTCTCCTGTTGTCAGATGGTT[T/A]GTTCTGTTGTCTAAAGCACTTGATAGGTGGCCAAGTGTACATAATCCGAGGTGAGTGTTCTGTGGCTTACCTTTATCAGCATCGGCCGCTGCTCATCCATCTTTCTGTTTTCACGCTTCCTTTCTTCATCGTCGATCCTTGATGTTAGACTGGCGAATGCTTCTACATGGATGGTCTGATCTGTGGAAAATTTGAACGCAAAGAAGTCAAAACAGAAGGAAGATTTAGAAATAGGAAGCACGTTATGCAATGTATTTAGCCGTCATCCATGGAGAAGGTTCAAATGCTGTTATTTTTGGCCACATTATGTTGGATGGTATTGCTAGTATTTTATGTTCTCTGTAGTGATGTTTGCATGAGTCCCATAACCATGTGGTTTAGATTTTTTGTATGCACTTACTAGATCATTTGCTTGGACCATTTTGAGTTTTTGCTGTCATGTGACTAGTTCTCGTCTAAAATGCCAGAGAGATCTTTATAGACTTGGAGCAATGTGAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31941
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010831 Essential Splice Site 317 421 4 5
ENSDART00000140164 Essential Splice Site 396 500 5 6
ENSDART00000145938 None None 62 None 2
Genomic Location (Zv9):
Chromosome 13 (position 32073635)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31719583
GRCz11 13 31850033
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTGTTGTCTAAAGCACTTGATAGGTGGCCAAGTGTACATAATCCGAG[G/A]TGAGTGTTCTGTGGCTTACCTTTATCAGCATCGGCCGCTGCTCATCCATC
Long Flanking Sequence:
TTTTATCTTTTTTTTATCTTTCTTAAAAATGTGAACATTAAGTTAGCCTGAACTTAATATAACATTTTATTTTTTGTTGTCTGCACCAAACAAAAAATCAAAATAACTACAAATGTAAATCCACCTGTAATACAGAGAGTTGTGAATGTTTTTTAATCCCCTCAAATAAGTGCTTCATAGACTGTGAAACACAGCCAAATTCAATGTTGACACCTTGTCAGTCAGACTTACACATACTGTATGTATACCCTAGCTTGTAGATAAAAAGCAGAGCATACTTTGTTCTTTATCCTGAAGTGGCGCAGTGTGCTTTATGAACACATTACCTCTGACCTGATGTGATTAACCCTTCAAGCCTTTTGACCTGCTCTTTTTCTCCTGCCATTGTTGACATTCTCTCTCTTCCTCCCTGATGATCCCCCTCTGCTCTCTCCTGTTGTCAGATGGTTTGTTCTGTTGTCTAAAGCACTTGATAGGTGGCCAAGTGTACATAATCCGAG[G/A]TGAGTGTTCTGTGGCTTACCTTTATCAGCATCGGCCGCTGCTCATCCATCTTTCTGTTTTCACGCTTCCTTTCTTCATCGTCGATCCTTGATGTTAGACTGGCGAATGCTTCTACATGGATGGTCTGATCTGTGGAAAATTTGAACGCAAAGAAGTCAAAACAGAAGGAAGATTTAGAAATAGGAAGCACGTTATGCAATGTATTTAGCCGTCATCCATGGAGAAGGTTCAAATGCTGTTATTTTTGGCCACATTATGTTGGATGGTATTGCTAGTATTTTATGTTCTCTGTAGTGATGTTTGCATGAGTCCCATAACCATGTGGTTTAGATTTTTTGTATGCACTTACTAGATCATTTGCTTGGACCATTTTGAGTTTTTGCTGTCATGTGACTAGTTCTCGTCTAAAATGCCAGAGAGATCTTTATAGACTTGGAGCAATGTGAGTTGTTGTACTGTTTGCTGAAAATTGAGATTAAGAGACCACTTAAAAATTCTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38953
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010831 Nonsense 414 421 5 5
ENSDART00000140164 Nonsense 493 500 6 6
ENSDART00000145938 None None 62 None 2
Genomic Location (Zv9):
Chromosome 13 (position 32067639)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 31713587
GRCz11 13 31844037
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTAACTCACTGGACTGAGATGAAGGAGTCAAAGGGACAGCAGGTGTGT[C/T]GATGGCACAGTCTCCTGGAGTCCTAGAGCATCAGTAAGCCACAGTGATGA
Long Flanking Sequence:
TGTATAACATAATGTCTAAAGTGGACATTCAAAATAAATTGTTACTATATTTTTAAGATATTTTACCAGAAATAAAATCAAAATACCATTTAAGCTCATTACTATCATATGAAAGTCTTATCAATATTTTCATGATCAAATGTTCTTTTGATTGAATTGATGGTAAAAGTATGACAGCTTCTCCAACTGACCTTCTCTTTCCTGCTGTTTCAGATACGTATGTGAAGCTGACTCTGCTCAACTCAATGGGTCAGGAGATGTCCAAGTGTAAGACGTCTGTTTGCCGAGGCCAACCCAATCCCACCTACAAGGAGACTTTTGTTTTCCAGGTAGCTCTGTTTCAGCTCTCCGACGTCACGCTCATCCTGTCCGTCTACAACAAGCGCAGCATGAAACGCAAAGAGATGATTGGCTGGATCTCTCTGGGCCTCAACAGCTCTGGAGAAGAAGAATTAACTCACTGGACTGAGATGAAGGAGTCAAAGGGACAGCAGGTGTGT[C/T]GATGGCACAGTCTCCTGGAGTCCTAGAGCATCAGTAAGCCACAGTGATGATGAGGACGAGGATGAAGATGATGATGATGTGTGTAATGGGATGGGGAGCAGAGAGCAGGTCAGGCCCTCGAATGACCCCCCAAAAGACAGGGCTGGCCCACGCTGCAGTGTATTAAGAAGAACACAAGTAGATCTGGGGATGATGTCCGCTCTTCTTCCCAGTGCATTATGGGAAATGAGCTAGAGAAAATGGTAAGAACAGGGTTAGATGTGACCAGATTAATGGAGGAAACATGTTTGTTTGTTTTTTAAATAGATATTCATTTGTATATTTGTTAACTTGATGTTTCTATTTTTGATCTGCTCGAGATGATTGTTTATAATGGACGTACTGTATGGTGCTTTAGGGTCAAACAGAGGGAAAAAACAAACAAATATCTGTCTTTTTCCTACACCCCATGATGCTTTGCATGATTGGTCATGACAATTGACTAATGAGAAGGTAATACA
Associated Phenotype:
Not determined