ZMP
esyt3
Ensembl ID:
ZFIN ID:
Description:
extended synaptotagmin-3 [Source:RefSeq peptide;Acc:NP_001116705]
Human Orthologue:
ESYT3
Human Description:
extended synaptotagmin-like protein 3 [Source:HGNC Symbol;Acc:24295]
Mouse Orthologue:
Esyt3
Mouse Description:
extended synaptotagmin-like protein 3 Gene [Source:MGI Symbol;Acc:MGI:1098699]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31712 | Nonsense | Available for shipment | Available now |
sa18472 | Nonsense | Available for shipment | Available now |
sa34636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41414 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17355 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31712
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 |
---|---|---|---|---|---|
ENSDART00000027443 | Nonsense | 202 | 861 | 5 | 23 |
The following transcripts of ENSDARG00000006422 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24833855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23989641 |
GRCz11 | 9 | 23800510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCAACTGTAGTTACGAGGCTGATGTGGACATTGATGCTGATGTAAAC[C/T]GAGCCATTAAAGTAGGAATCAAAGGGCTTCAGGTTAGTGAAGGAAAGTAC
Long Flanking Sequence:
TTTGCAAATGTTAGTGTCAACTTAGAGTAAAAACAAATCCGCCATTAGCATTAGCACATGCAGCAACTACTGGCACTGCACTTCCACTTCTTCTTTCAAATGGGGTTTCCCAGTCAAAGACAAAGGGGAATAGTTATTTTGTAAATTTAACAAGGTTATGTTATGTTGTCTACGAGTACAAAAAATGTTTGTCTGAGATTACTCAGAAAAACTGAGTAAATAAAAAAGGCACAATGTCTTGTGTTTTGAACAAACCCTAATGAATTCTAAACTACATTTATTCATGTAAAGCTACGAACTTACATTTTTTTGTTGATTTCACTAATTAAACCTGATAATATTTACAAACGCTCAGAATCATTTTTATCAGTGTACTAACTCCTTTATGACTGCTGTAATGTGTGGTCTTGTAACCATCTAAATCTGATATGTTTTACGACTCTGCTCTTTTCATCAACTGTAGTTACGAGGCTGATGTGGACATTGATGCTGATGTAAAC[C/T]GAGCCATTAAAGTAGGAATCAAAGGGCTTCAGGTTAGTGAAGGAAAGTACTGAATTTTTGAAGTGATACTTCCATGTATCATGCATTTCAGTGATTCAAACTGAAACTCTTAGCAGTATTTTTTCTGTCTTTAGCCATCACATGATCCTTCAGAAGTCATTCTAACATGCTGCTTTAATGCTCAAGAAGCATTTCTCATTATGACCAATGTTGAAAACCTGTAGATCCTTCAGCCAGTGTTACAAATATTAGATAGTGATTTGATTGTTTATCTGCCTAAATTGATTAGCATCATTTAAAAGATTTGTACGCTGGCCAAGAGAGCTCAACATGCCGCAGAGCGAATAACAAAATCACCAGCAAATTAAAAAAATGTCTTCATTCGTTTGACAGCACACGTGTTGCAAATCCTCACAATGCAAACACAAATAAAAGAAATGTGTTGCAAATCCTAACAACACATGCGCATTTTGATATAAAAAAACAAAACAAAAGTTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18472
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 |
---|---|---|---|---|---|
ENSDART00000027443 | Nonsense | 241 | 861 | 6 | 23 |
The following transcripts of ENSDARG00000006422 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24832210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23987996 |
GRCz11 | 9 | 23798865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATTGGCCAGGCACCCCTTGTAGGTGGAGTCAYTATGTTTTTCATTCGT[C/T]GACCTGTGAGTATGGACAATGCTTAAAATTGGTTTGTTTWAAGTATATAT
Long Flanking Sequence:
AATCAGGGGTCGCCACAACAGAATGAACCGCAAACTTATCCAGCATATGTTTACACAATGGATGCCCTTTCAGCTACAACCAAGTACTGGGTAACATCCATACACTCTTGCATTCACACTCATACACTACCATCAATTTAGTTTATTCAATTCACTTATAGCGCATGTCTTTAGACCCAATTAAACCGGTGCACCTGGAGGAAACCCATGCGAACATAGGGAGAACATGCTCACCCCACACATAAACACCAACTGACCCAGTCGGGACCAGCGACCTTCTTGCTGTGATGCGATGATCGAGTCATCATGTCATTCTCCCCTCATTAATTACCTCATTCAATGTACAAGAAAATGAAAATGAAAGCTATGTATGTTTTATCATTATCATTAATATTATTGATGTTGTTGTCGTTTAGCTTCAGGGGATGCTGCGTGTAATTCTAGAACCTCTGATTGGCCAGGCACCCCTTGTAGGTGGAGTCACTATGTTTTTCATTCGT[C/T]GACCTGTGAGTATGGACAATGCTTAAAATTGGTTTGTTTAAAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACAGTTGAAGTCAAAATTGTTAGCCCCCTTTTGATTTTTTTTTTCTTTTTTAAAAATTTTCCCAAATGATGTTTGACAGAGCTAGGAAATTTTCACAGTATGTCTGATAATGTTTTTTTCTTCTAGAAAAAGTCTTAAGCAGTTTTGAATTTTTTTTAAACAATTTTTGGGACAAAATTATTAGCCCCTTTAAGCTAATTTTTTTTCGATTGTGTACAGAACAAACCATCGTTATAGAACTTGCCTAATTACTATAACCTGTCTAGTTCACCTTATTAACCTAGTTAAGCCTTTAAATGTCACTATCAGATGTATAGAAGTGTCTTGAAAAATATCAAGTAAAATATTATTTACTGTCATCATTGCAAAGATAAAATAAATCAGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34636
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027443 | Nonsense | 289 | 861 | 8 | 23 |
The following transcripts of ENSDARG00000006422 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24828476)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23984262 |
GRCz11 | 9 | 23795131 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCTCTCTCATGGTTCTGCCCAATCGCATGTGCTTCCCTTTAATTGAT[C/T]AAGTCAAGGTTGAACAAATGAGGTTTCCTCTTCCTCGAGTAAGACTGAGC
Long Flanking Sequence:
GGATGAGTTGGAAAAGATATAGCAACTTAATTCAGTATAGTTTGGAGGTTTGGTGTTAGTTTGGTGTTTGTAGTATGAACAGTCTAGGAGGAGATGCATTCTTAAGAAGAAGATGGAAGAATAGTAATAAGTTTATGTAGTGTAACAGTATGTTGGCTTCTCAAACCATCATAAATATTTCATTTTTAGTACAAATGTAGTTATTTATTTCAGCAAGCTCTTATCTCATACATTTCTAAAATAATCCAAGAATGAACTAACATAATCTGCCATCCATGTTTCCTATGAAACTCTTGCACTTACAGACCTCTAGTTGATAAATCCAACATATCTAATCCCTTTTTCTCAATAAATAGGACAAACGTGATACTCTGTGTTCATCATCACCATCAAATCTGAATGTCTGTTTCCTCTGTAGTCATTTGTCAGAATCAGCCATTGTGGACGTCATCGCCTCTCTCATGGTTCTGCCCAATCGCATGTGCTTCCCTTTAATTGAT[C/T]AAGTCAAGGTTGAACAAATGAGGTTTCCTCTTCCTCGAGTAAGACTGAGCATGATTGGTTGTTTTTGTCAAAATATATGTTTGTTTTTAAACTGGAGAATAAGTTAGACTATGTGAACATCTTCAGGGTGTTGTACGCGTCCATGTTCTGGAAGCCCGCGATCTTGTAGCAAAGGACTCACACATGATGGGACTAGTAAAGGGCAAGTCAGATCCATATACTGTGCTGAGAGTTGGAAACAAGCATTTCAAAACAAAGACCATCAAAGAAACTCTGAATCCACGCTGGAATGAAGTTTATGAGGTGATTATGAGTTGCCGTTCTGGTTTATATGCAGGACTTTTTAGTTGGGAAATGACAAAATTTGAAGAGATCTCATTAATATATCTTTAAACAGTTTGTCATTCATGAAGCCCCGGGGCAGGAGTTGGAGGTGGAACTCTACGATGAAGACAAAGACGCTGATGACTTTTTGGGCAGGTAATGTCGATCATGCTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41414
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027443 | Nonsense | 664 | 861 | 18 | 23 |
The following transcripts of ENSDARG00000006422 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24821897)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23977683 |
GRCz11 | 9 | 23788552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCAAGTTCCATTTTCAGTTGTGCCCTTAAATGATCTTCAAGCAGAGTA[T/A]CCTCCCTACAGACGAAGCACTTTTGTGGGCTCAGAGGGGCTGCAATCGAC
Long Flanking Sequence:
TTTCAGGCAATTTGCGGCACTTAAAAAAACAAAACTGTGAACTAAGTAAAAAATTAATTATGTTTAAACGCATGAAAATAGACAGTAGTTGTATGTGTTGCTTCAAAAGATGCTTGCTTAGGTAAAACCCTTTTCTTATTTAGATCTTTTGCAGAATAATTCTGTATGTTAGCTGAATAATGCTATGTTTGTTCTGAAATGTAATCTATGGTTAACAAAACTTCATATCTTTCCTCCTACTAGATTCTTACATTAGAGAAACAACAACCAAAGGTTGTCACTTCAGCACCTCAGGATAAAAATACATCAACCCCAAATCGTCCTGAGCCACGTACTCCAAATCCAACTTCAAATCCAGTTCCAAATCCAGCTCCACCTCCGGCTGCAGCTCAGCTAGTACAGAGCAACCCAAAAGAAAAAGGGCCCATTTCATCAGTCCCGCTCTCTAAAACCCAAGTTCCATTTTCAGTTGTGCCCTTAAATGATCTTCAAGCAGAGTA[T/A]CCTCCCTACAGACGAAGCACTTTTGTGGGCTCAGAGGGGCTGCAATCGACCCCTTCCACCCCCGGTCCAATGCGACGCTATGATTCCCACAGCCTTTTGTCTGAGAACTCGATTGCTTCTTCACGCGTTGATCTCACAGACAGTTACCCTTACCCAGAGTAGGTACAATATTCTATGCTGTATATGTTTATTGTTTTTTTTTTTTTTTCAATCTAGCATTTTATACAACTCCAATTATTTCAAAGCACATGGTTGGGAAAATGAAAATAACAGTACTGCCAATATTAGCTTCAGCTATTAAATAATGTAATTTCAGTAAAATAGCTCTAAAGAGACATTATTCAGGCACAGTTATTACAGTGATGATTTGGTTTTCTTCATTAACAGTGTGAATGTCGCAAAGTATGTGAAGTGAACTCATTTCTTTAGCAGCTTTTTATAAGGCAACAATGCTATTATTCAGCATAGATAGTTTAAAAATAATACAGTTTACCACATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17355
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 |
---|---|---|---|---|---|
ENSDART00000027443 | Nonsense | 689 | 861 | 18 | 23 |
The following transcripts of ENSDARG00000006422 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 24821824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 23977610 |
GRCz11 | 9 | 23788479 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGGGCTCAGAGGGGCTGCAATCGACCCCTTCCACCCCCGGTCCAATG[C/T]GACGCTATGATTCCCACAGCCTTTTGTCWGAGAACTCGATTGCTTCTTCA
Long Flanking Sequence:
GAAAATAGACAGTAGTTGTATGTGTTGCTTCAAAAGATGCTTGCTTAGGTAAAACCCTTTTCTTATTTAGATCTTTTGCAGAATAATTCTGTATGTTAGCTGAATAATGCTATGTTTGTTCTGAAATGTAATCTATGGTTAACAAAACTTCATATCTTTCCTCCTACTAGATTCTTACATTAGAGAAACAACAACCAAAGGTTGTCACTTCAGCACCTCAGGATAAAAATACATCAACCCCAAATCGTCCTGAGCCACGTACTCCAAATCCAACTTCAAATCCAGTTCCAAATCCAGCTCCACCTCCGGCTGCAGCTCAGCTAGTACAGAGCAACCCAAAAGAAAAAGGGCCCATTTCATCAGTCCCGCTCTCTAAAACCCAAGTTCCATTTTCAGTTGTGCCCTTAAATGATCTTCAAGCAGAGTATCCTCCCTACAGACGAAGCACTTTTGTGGGCTCAGAGGGGCTGCAATCGACCCCTTCCACCCCCGGTCCAATG[C/T]GACGCTATGATTCCCACAGCCTTTTGTCTGAGAACTCGATTGCTTCTTCACGCGTTGATCTCACAGACAGTTACCCTTACCCAGAGTAGGTACAATATTCTATGCTGTATATGTTTATTGTTTTTTTTTTTTTTTCAATCTAGCATTTTATACAACTCCAATTATTTCAAAGCACATGGTTGGGAAAATGAAAATAACAGTACTGCCAATATTAGCTTCAGCTATTAAATAATGTAATTTCAGTAAAATAGCTCTAAAGAGACATTATTCAGGCACAGTTATTACAGTGATGATTTGGTTTTCTTCATTAACAGTGTGAATGTCGCAAAGTATGTGAAGTGAACTCATTTCTTTAGCAGCTTTTTATAAGGCAACAATGCTATTATTCAGCATAGATAGTTTAAAAATAATACAGTTTACCACATAGTCCAGCACGGATGATAGGGTTTGTCTTTTGACTTGCAGTCACTCTCTGACATCTGCACTTTAGAATATTTATT
Associated Phenotype:
Not determined