ZMP
esyt1a
Ensembl ID:
ZFIN ID:
Human Orthologue:
ESYT1
Human Description:
extended synaptotagmin-like protein 1 [Source:HGNC Symbol;Acc:29534]
Mouse Orthologue:
Esyt1
Mouse Description:
extended synaptotagmin-like protein 1 Gene [Source:MGI Symbol;Acc:MGI:1344426]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24338 | Nonsense | Available for shipment | Available now |
sa24339 | Essential Splice Site | Available for shipment | Available now |
sa43987 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43988 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11243 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24338
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 |
---|---|---|---|---|---|
ENSDART00000032290 | Nonsense | 72 | 1079 | 1 | 31 |
ENSDART00000140463 | Nonsense | 72 | 901 | 1 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 25595721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25381841 |
GRCz11 | 23 | 25308382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTATTTCGGCTTCAGTATCAGTGTAGTTCTGCTCGGGCTCCTGGTTTA[T/A]ATAGGATGGAAACACAGTCGCGATGGGAAAAAAGCGCGACTGCAGAGCGC
Long Flanking Sequence:
TTTTTAAGGTTCTCGGAGTGGTTTTAACAAGACTGCTTGTGGGTTTTTAGGAGGGCTGAAGCCTTTAAACACGCCCCTTCACGCCCTTCACACAAGCAAACTACAAATCTTCAACTTTCCGCTGCAAATGAGTTGACGTCTGTGCTGATTTTGAAAACAGACTGAACGAATTATGCGGCATTTCCCGTTCACACTTAATCGTTCAGGTGGCACTCATTCGTTTTAAACGGTATTGATTAGGTTAATGGTGTCTAGCGCGGAACCGCTGGCAGAAGAAAGGATTTGATGCAGAAATCTCCGATGTCAGTTGATGATGCAGGGCCGAATGCGGGTGCCGCTCCGGAGGCTGCGGACGCGGCCCCGACTACCGATTCCGCTGGAAAACACGCCGTGTCCGTTCTCTGGTCCTTTGGAAAGTGCGTCGGCGCCTTCCTGCCGGTCTACCTGGCTGGTTATTTCGGCTTCAGTATCAGTGTAGTTCTGCTCGGGCTCCTGGTTTA[T/A]ATAGGATGGAAACACAGTCGCGATGGGAAAAAAGCGCGACTGCAGAGCGCGATGTATTTTTTGGAGAACGAACAGGATGTCACAACTACACGAGTGTTCAGAAGTAAACGGGATTTGCCTGCATGGGTAAGGAGTTTTACACCATAATTGGTATCGTTCTGGTTTTTAGCAGCTACAGAAGTGCAGTCCGCAGCGCATCGCATCCTCTCGCACATAGAAAATGATGCAGAATCTTGCGCCTCTTGCTTTTGTTTTTGTCAGCAGCAGCGTGAAAGGTTCTCTGGTGACACTGACAGCTTGATATTAAGTTGTAGTTACTGCATAAAATGTACTAGTTCACCCTCTGCAGTAAAACTTGTTAGTATAACTATATAGGCTAAAATAGTCTACAACCTGTGGACATTTCTTTATTTGCAGTACTCAGTTGTGCGTTTCTTTTAGTCCTTCTTTTAGTGGCGCTTACCATCTGTTACATTATAAACCCGAGTTAACATTATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24339
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 |
---|---|---|---|---|---|
ENSDART00000032290 | Essential Splice Site | 173 | 1079 | 3 | 31 |
ENSDART00000140463 | Essential Splice Site | 173 | 901 | 3 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 25602656)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25388776 |
GRCz11 | 23 | 25315317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTCATCTGCAGACTCTAAGCTTCACTAAAGTTGACTTGGGTGACAGGG[T/C]AAACAAATTCGTTTGTGATCATCATAGAAAGACTTTATTTGCATATGTTG
Long Flanking Sequence:
ATATGATGCCCTAATGTTTGCTTGTGTCAAGGAGCAAATTGTGTCCCATTATATTTTGGTTAACTTTAAATTAAGATTCTGTTAGTACAAATCCTGTACAGCATTTATTAATCTTAGTTAATAACTTTAATCCAACCTTGAGCTTGTTAAAGTAATTTAATGCATTCTGAGCACTAACAATCAGTGACTTTCTTTTAATAAACTAATGTAAACAAAGAGTGCTGTAATACATTTTTTGTTTATTGTTTGTTTATGCCGGTAAATGCACCATGTTACCTATGATCTATTATATGCTTAAAAATATCTTCATTGTTTATTATAATTTCTGCCTATTCTAATTGTCTGTAATTGTCTGGGTTGACAGATATTGCAGCAGGCCTGGCCGTTTGTTGGACAGTATCTGGAAAAGCTGCTGGTGGAAACTATCGCTCCTTCAATCCGAGCTACCAGCGCTCATCTGCAGACTCTAAGCTTCACTAAAGTTGACTTGGGTGACAGGG[T/C]AAACAAATTCGTTTGTGATCATCATAGAAAGACTTTATTTGCATATGTTGCTCATTTACATTGACATCTCAATTTCTGCTTTGTCTGCTCACAAAGGTGTCTGAACCTACTTTTGTTTTGTTTGACCTCTTTAACAGGCTATGAAGGTAGTTGGTGTGAAGGCCTACACTGAGTTCGATAGGCGTCAGGTTATACTGGATCTGTACATCAGGTAGTGTCACTGCTCTCAATTTTTAGCCAGCAGGTTTTTTTTATGCTTGAGTGTGTTGTTTGTTAATGCTTTATATTTAGTATATTTTAATGTAGTATTTTTATTATATAGTTAAACATATTTCTTTAGAAAATGTTATTTATAGTGTGAAAAAAATGCTTTATGCTATTAACCCTTTGATGCACTACATGGGGCTAAAGTGACCCGTCTAAGTTTATTATATCTATATCTATTTTAAAGCTTGTGCATCAAAGAATTGAAATAAACTATAATATCTTATAGTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43987
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032290 | Essential Splice Site | 271 | 1079 | 8 | 31 |
ENSDART00000140463 | Essential Splice Site | 271 | 901 | 8 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 25605787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25391907 |
GRCz11 | 23 | 25318448 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCCTCTGTGTCCCATTTTTTCTGTACGAACCCCTTGCATTCATTTCC[A/T]GTGCCATGTCGGACACTATGATAATGGATGCAATCGCCTCTTTCCTGGTT
Long Flanking Sequence:
TTCTTCATTCGCAGGCCTGTTAGTCCATCGTTTTCTATTTGATATCAATTATCACTTTATAATAGCCTCTTCTTTAACTACAGTGTTGTTTTTACTTCTGTCCTTCACAGAAACTCGACATCAACTGGACTGGCATGACCAATTTATTAGACATACCGGGTTTGAAGTGAGTGCAGTTGTTTTTAGCTTTTTTTTTTTTTTTTTTTGCATCATTCATTTTATTTTTACAGTAGAAATAGACTGCAGTTCAACTACTCATATTAATACAGTAACTCTCTCTTCTCATATGCTTCATTTATTGATAATCAGTAAAGCGCTGGTCTGATTATTCAAAGTCTGCAGAGCTTCCCTCTACTCAAATGAAGCAGGGAAACGCAGTCATTCATATTGATCATAACTTTAACCCATTATAATCACCCATGCTGTCAGATAGTTTAAATGTATTTTGTCTGTGCCTCTGTGTCCCATTTTTTCTGTACGAACCCCTTGCATTCATTTCC[A/T]GTGCCATGTCGGACACTATGATAATGGATGCAATCGCCTCTTTCCTGGTTCTCCCCAATCGTCTCACTGTGCCTTTGGTGGCCAATCTGCACGTAGCACAGCTGCGTTCCCCTCTTCCACGGGTAACACTTCACTGTGCTTTAATGGAGTATTTATCTGTGTTAACCTCTTCATTTTGACTAGATTCATTAGACGTACCAGGGTCAGAAATTAATTTTTTCTATAAGGGGGAATATTAGCCCACTGGAATTAAATGTTATTTTTACCTCTTTGATACTTTGACTTTTAAGTTTGCCTTAGATCAATGACATAGATGTATTTATGCAGCAATAGCATAATGTAAATAGTCTACACACAGGTATATAAATGATACAATTAAAAGTAAGAAATCATTACAGCTGTGCAATTGCAAATACGAGTAAAAGCAGACTCAAATCATTGCAGTCACATTTAACAAAAAAATACTCACAAGGATTCATCAAATTTACATAAACAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43988
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 |
---|---|---|---|---|---|
ENSDART00000032290 | Nonsense | 760 | 1079 | 21 | 31 |
ENSDART00000140463 | Nonsense | 760 | 901 | 21 | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 25626309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25412429 |
GRCz11 | 23 | 25338970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAAGACCGGAAGAATCCATCTGGTGTTAGAATGGGTGCCTAAAATTT[C/A]AGATCCCATCAGACTTGAACAGGTCATATCCTGTTTCTGAAAATGTTTTT
Long Flanking Sequence:
GTCATGTCATATGCCCATGAACATTTCTTGCTTGTTATCAAACTACTTTATAACTGTAACAAGAGGCAATTCCATCATCACTTAATGTTAAAACAACTATCATAATGTTAGTTATCACTATGTTGCTCGTTTTGGATTCTTGAAAGCTATAGAAAGTAAAAATATAAAACAGGAAATATATTGGGGCCATTGCTTTTGTTTACATTGCTTAAAAATGGTGTATATAAAGTAGTAATTTACAGTGATTTAACTGTTTGCAGGGTTAAAGTGAGTCTGAGAGACCTCATCAGTGCTCAGTTTACTGATCAGGTAAGTTCAGCGTTAAAAAAAATGCATACTAGTTTGTTTTTAAACATAATATTTATCATATTTTTTGCATTATATATGGTCGTGAGCTTGTTTACACTTGTTTCTATGTCTTCTTCTGGTGCAGTGGTATACTCTGAATGATGTGAAGACCGGAAGAATCCATCTGGTGTTAGAATGGGTGCCTAAAATTT[C/A]AGATCCCATCAGACTTGAACAGGTCATATCCTGTTTCTGAAAATGTTTTTTTGTTAACCTGAGTTCATTAAATATTAACATTTTGCTGAAGGGTTTTGTGTTTTTTTTTTTCTATTTAGATCCTACAGTACAACTACAGGCAGTCTTACCTGAATAAAATAGTTCCCTCTGCTGCACTGCTGTTTGTTTATATTGAGAGAGCACATGGGCTGCCTGTGGGTTTCTTTTTATTTCCATTCAAATGTATTATGTTTCAGTGACCTTCAATGAATATGATGTATGTTGTCTGCAGTTAAAGAAGAGTGGAAAAGAGCCTAAAGCTGGAGCAGAAGTGTCACTCAAAAATGTATCTTACAGGACCAAAGTAAGACCCTCAAATCATGACACATTTATATTGAGGTTATTAAAATATCAAAAGTTGCAAGGAACAATTTCTACTCCACAAGGTTGTGAATCGCTCCACTTCTCCACAATGGGACGAAGCCCTTCATTTCCTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11243
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 |
---|---|---|---|---|---|
ENSDART00000032290 | Essential Splice Site | 1019 | 1079 | 28 | 31 |
ENSDART00000140463 | None | None | 901 | None | 25 |
Genomic Location (Zv9):
Chromosome 23 (position 25630643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 25416763 |
GRCz11 | 23 | 25343304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAAGACCAGTGTTAAAAAGAAAAGCCTCAAACCAGAGTTCAATGAGAT[G/A]TTAGTAGGAACRTTCATAAATYACTGTCTTTGNNCACAAGAGTGGAAGTT
Long Flanking Sequence:
TGGAAGGGCATCAGCAACATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGTCGACCTCGACTTAATAAAGGGACTAAGCCGAAAAAAAAAGAATGAAATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTGTTATATTACATTATTGTTATATTACATTATATTATTAAACAATGTCTTTTAGAACCAGAAACAAAAATTTTATAAAATGTGACTGTTTTTTTAACTAAACAATTAAGTTTACTTTAGCTGTTCTAAACAAAGGAATAATTTCAAAATTTTAAGTTTGAGAAATCTGACTATAGTCCTCATTTTGATTTCATAAACCTATGTTCCTTCACAGGAACTTGCCGTCCTCCTCTAAGGAACCTCCAGACTCTTACATCTCATTCATTCTTCTTCCGGACAAGAACCGGAACACCAAAAAGAAGACCAGTGTTAAAAAGAAAAGCCTCAAACCAGAGTTCAATGAGAT[G/A]TTAGTAGGAACGTTCATAAATTACTGTCTTTGCACACAAGAGTGGAAGTTACCCATCTTTTGCTCTCTCCTACAGATTTGAGTTTGACATGTCACTTGAAGAAGCAAAGCAGAAACATCTTGAAGTTTCAGTTAAGAACAGCGTTTCCTTCATGAGTCGAGAAAAAGAGCTTCTTGGCAAGGTATTCATACATCAGCAGCATCACAGACACTATTGACCATATTGTTTTGACCATAATTAATCAAATGGGTATTTGAAGAAGTCAATTCTTGTTGATGACATTCCACTATCACCTTTACTCTTTTTGTTTAATTTATAGTGATTAAATGTGACCCTGGACTACAATACCAGTCTTATGTTGTATATTTTTGGCAGTAACCAAAAATGCATTGTATGGGTCTAAATGATTTTTCTTCTATGCCAAAAATCATGATAATATTAGGTAAAGATAATTATCCAGTAATATATTTTGTAAATGTCCTGGTGATGAGTTGTGGCTG
Associated Phenotype:
Not determined