Busch Lab

ZMP

esyt1b

Ensembl ID:
ENSDARG00000014239
ZFIN ID:
ZDB-GENE-040724-209
Description:
Novel protein similar to mouse and human membrane bound C2 domain containing protein (MBC2) [Source:
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 10 alleles of this gene:

Allele Name Consequence Status Availability
sa13012 Nonsense Available for shipment Available now
sa10630 Nonsense Available for shipment Available now
sa20822 Nonsense Available for shipment Available now
sa40794 Nonsense Mutation detected in F1 DNA Not yet available
sa30880 Nonsense Mutation detected in F1 DNA Not yet available
sa26837 Nonsense Mutation detected in F1 DNA Not yet available
sa1525 Essential Splice Site F2 line generated Not yet available

Mutation Details

Allele Name:
sa13012
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014819 Nonsense 317 1032 9 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 352 1076 9 31
Genomic Location (Zv9):
Chromosome 6 (position 52235795)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52284977
GRCz11 6 52284976
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGATGGCCGGCATGTCTGACCCGTACGCCATTGTCCGAGTCGGACCA[C/T]AAACCTTSAAATCCCATCACCTGGACAACACKCTCAGTCCCAAATGGGGT
Long Flanking Sequence:
AGCAGTTTAGGTCAGTGGATGTTTTCATCCCGAACATAACAAAAGGGTAGTACATTTGCCCAGAGTGTCTTGTTGAGTTTTTATACATCAAAGCAGTTTCTCAAAATATGTGTCAAAATAAAATGTGTCAACAAAAATCATTCACAAAAAAAGTTGTGGCCAAATTAAGACTCAAAATCACCCAAGAGTGGATGAAAACATCCTCAACAGCACATAAGGGTTAAAGCAACACAACTTTTGCATTGTTAGAGCCGTGCTTAGTTTTTGTTCTACATTTAAAGTGCAAGAAGAAATAGTCCTCTTATTTTAAAAGCAGAAGTAAACTAAGAGCATCTAAAGCATCACTTTACCAGTTAACATTAGATCTCTTCCCTTTTCTTGTTCAGGGAGTTGTGCGTATTCACCTGCTGGAGGCTGATAATCTAGCTGCGAAGGATAATTATGTAAAGGGTGTGATGGCCGGCATGTCTGACCCGTACGCCATTGTCCGAGTCGGACCA[C/T]AAACCTTCAAATCCCATCACCTGGACAACACGCTCAGTCCCAAATGGGGTGAAGTGTATGAGGTGGGTGTTAAAATAATAATAAGACTTAAATTCAAGTGCCCCATCAGGCTATTTTAGACGTTCTCCTACAATGTTTACATCCATGCCAAGTCAAACAACATCAGCTCCTTTATTTTCTGAAATGGTTCAATGATCTGCTCTCTCTTAAGCATTTTTAATGCTTTATTACAAAATGTGCATAAAAATCGGTGAATGGAAACATAATTACTGACCAACAGCTTAAGAGAACATCTGAAAAGCATGATATGGGCACTTTAGGACTTATATTTGTGTTGATATATCAACATGTCTGTCTTTTGGTTCAAACCATTTCCGCCACATACTGTCTCTGTCTAGCCATGCAGTGTGTGTGTGTGTGTGTGTGTGGTGTGTTTTCAGTGTTTCATGCATGCATGTGTGTCTGTCAGGTTGTCGTTCATGAGGTGCCTGGTCAGGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10630
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014819 Nonsense 746 1032 23 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 705 1076 20 31
Genomic Location (Zv9):
Chromosome 6 (position 52263496)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52312678
GRCz11 6 52312677
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCAGTGCCGTCTGCAGCTCTCCTGTTTKTGTATGTGGAGCAAGCATAT[G/T]AGCTTCCTGTGAGTATTAACACTAATGTTAGCTCTTTAAWTAGCTCATTT
Long Flanking Sequence:
TTTTCATAAATCTGTCATAAACATGTCTATTAAAATTGTGTCATGCACAACAAACAATGTCAACTTAGCAAATGTCACTTAATGCCAGTTGTTATAAGCATGTATAAATTCACATTCATGTGTCTTGTCATGATTATAAAGGTTTAAAGGCAGTCTTTTGAACACCTCTTCAAGTAAAGTGATACCATATAAGGATAAATTAAGCGCAGAGATTCTCATGCATGGCTGTGTTTGTGTGTCAGTGGTTTTCTCTGAGCGATGTAAAGCGTGGTCGTGTTCACCTCGCTCTGGAGTGGCTTCCCACTGTAACTAAACCAGAGAAACTACAGCAGGTGAGAGAGCCGTCTGTCTTCCTAAACTAACCTCTGTCTGAATATACGTTGATGAAACTAACTGGTTGACTTGTTCAACAGGTGCTGCATTTCCAGTCAAAGAGCTCATTTCTGAATAAGGCAGTGCCGTCTGCAGCTCTCCTGTTTGTGTATGTGGAGCAAGCATAT[G/T]AGCTTCCTGTGAGTATTAACACTAATGTTAGCTCTTTAAATAGCTCATTTATTCTACTAGGCTGCAATGAGATTATATAGAGAGCTAATGAAGACTGAGAACCTCAGGCGAGAGACCTCAGTTTCAAATACTGCAGAAAAGGCTTATTTTAGTCCAATTATCTAGAAATTCTTAAATCAAGCAGCATTTTCTAGATGACTAAAAAATTTGTCTTGCTTTCAGAAATAGTGTGGCAAGATTAAGTGAGTTTTTCCTTAAAACAAGCAAAATAATCTGCCTAAATTATAAGCAGAATACTGTTATTTCAAAGTCAAAACAAGGTTATTTTCTTTCATTTATCAAATATGAAAGTAGACATTTACAAATTATTTTTATTTGACCAAAATGTACCCAAAAGAGCCTATATTTAACAACTCATCATAATAACACATTTTTTTCAACACCAAGTTATAATATTTGAATAACTTCTAAAGGAGCATGTGGCATTAAAAAGGGATAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20822
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014819 None None 1032 None 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 840 1076 24 31
Genomic Location (Zv9):
Chromosome 6 (position 52269026)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52318208
GRCz11 6 52318207
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGAAGGATGGTCTGATGGGTGGGATGGTGAAGGGGAAAAGTGACCCGTA[T/A]GTTAAGATCCACATCGGTGACACAACATTTAAGAGTCACGTAATCAAGGA
Long Flanking Sequence:
ATTGGCAAAACAGAAAATATCAGACGTCAATGTATTCTAAAATGTAATGTAAATTGTTTATTTACTATATATATATATATATATATATATATATATATATATATATATATATATTATATTATAACTATTATTATTATTGAATAATTATTACATTTGCATTTTCACATGAGCACTCTTGCTTAAATGTTATTATTTAAATATGCCATGTCTAATTAATAAAATAATATAAACAAAAAACTATAGTAGTGTCCAGACTTTTTACACCGTAATACATGCATAAAATATATATTGGGAAAATGGCTCTAAATGAAGTATGGAAGCACTTAATACAATCATTGCAATATTATTAAAAACAATATATAATGGCCCTCTTTCCAGCATAGCAGTGAGGTGTTGTGATGTTTTCAGGGTGTTCTGCGGCTCATCCTGCTGGAGGCTCAAGATCTGGTGGCGAAGGATGGTCTGATGGGTGGGATGGTGAAGGGGAAAAGTGACCCGTA[T/A]GTTAAGATCCACATCGGTGACACAACATTTAAGAGTCACGTAATCAAGGAGAACCTCAACCCCACCTGGAATGAGATGTATGAGGTGCGCTCAGGACTGCAGGTTTATGGAGGTTGATGTTAAAAATGGTTTGAAATGGAATATCATGTAATCAATGTGTTTTCCAGCTGGTTCTGACCTCCAGCTCCTCTTCTGAAGTGCTCGTAGAGGTTTTCGACAAGGATATGGACAAAGATGACTTTTTAGGGAGGTATGTAGATATGTGGTTATGGTTGGTTGTTTAAAATTAATTGGGTTAACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATAATAACAGTATATTACAATTTAATATATAACAATAAAACCATGAGCGTTTTTTTTTAATAAATTTATTTATTTGTTCATAGATACAAGGTTAATTAAAATTAACAAAATATTAAATTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40794
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014819 Nonsense 823 1032 26 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 1049 1076 31 31
ENSDART00000014819 Nonsense 823 1032 26 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 1049 1076 31 31
Genomic Location (Zv9):
Chromosome 6 (position 52272815)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52321997
GRCz11 6 52321996
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAGCAGCCGCTGGGCTCTCTGGTTCTGCCAATCAGAGAGCTGCTTTCT[A/T]AAACAGACCTGCTGATGGACCAATGGCTGAGTCTGGATGGAGCAGCTGCT
Long Flanking Sequence:
GTTGCTGTTAAGTATATATTTGAGAAATCATGTGGAACCAATTAGTTCAGGAGCCAAACTAGTCTTATCACTTGATATACTGTTGAAATGTGAATTATTATACGCCCTTTGATATTTGTTTTCTTTTTTTTCCAAATGATGTTTAACAGAGCAAGAAAATTTTCACAGTATTTTTGATAATATTTTATCTTCTAGAGAAAGTCTTATCTGCTTTATTTCAACTAGAATAAAAGCAGTTTTTAATTTTTTTAAAAACATTTTAAGATCAAAATTATTAGCCCTATTAAGCTATATATTCTTTGATAGTCTACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCTTAACCTGCCTAGTAAACCTTCTAAATGTCAGTAATAATCATTGACGGTGTATTTTGATGTATTTTTCTCTCTTTTCTCCATCACAGCTTTCCAGTGCATTCGAGCAGCCGCTGGGCTCTCTGGTTCTGCCAATCAGAGAGCTGCTTTCT[A/T]AAACAGACCTGCTGATGGACCAATGGCTGAGTCTGGATGGAGCAGCTGCTGACAGTCAGATTCTTCTCAGAGCTCAACTCAAGGTCAGACTGAGCTTTTTCTGATCGCTTTCTCCAACCTGTCCTTTCAGTTTATATAAACTTCACTTCTTTCAGTCTGTTACATTCATTTCTGCAGGTAATGTCATGTTGTGTCTAGAGGTGTATCCATCAAATGGTCAGAAATTGCAGATCCAAAGCATTTTCTTAATTTATTCTCTATTTTTTTGTTCTCCGATTCTGACTGGCATACAAACTGTGTTACGACTATTTTAAAGTACAAAATATGTAAACTGAGCATAAACCAAAGCTGTACGCATTTCTGTTTGGGCATGTTTAGGCGATCTCTCAAAGTTTTATGTTTTAAAAATGAGCTTTTTCTAGTCAGCATCTCTGGTATTGGCAGCCTAATACAATGCGGAGGGCTGTTGTGTAGGACTGAATGGTTTTATACTGTGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30880
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014819 Nonsense 823 1032 26 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 1049 1076 31 31
ENSDART00000014819 Nonsense 823 1032 26 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 1049 1076 31 31
Genomic Location (Zv9):
Chromosome 6 (position 52272815)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52321997
GRCz11 6 52321996
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAGCAGCCGCTGGGCTCTCTGGTTCTGCCAATCAGAGAGCTGCTTTCT[A/T]AAACAGACCTGCTGATGGACCAATGGCTGAGTCTGGATGGAGCAGCTGCT
Long Flanking Sequence:
GTTGCTGTTAAGTATATATTTGAGAAATCATGTGGAACCAATTAGTTCAGGAGCCAAACTAGTCTTATCACTTGATATACTGTTGAAATGTGAATTATTATACGCCCTTTGATATTTGTTTTCTTTTTTTTCCAAATGATGTTTAACAGAGCAAGAAAATTTTCACAGTATTTTTGATAATATTTTATCTTCTAGAGAAAGTCTTATCTGCTTTATTTCAACTAGAATAAAAGCAGTTTTTAATTTTTTTAAAAACATTTTAAGATCAAAATTATTAGCCCTATTAAGCTATATATTCTTTGATAGTCTACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCTTAACCTGCCTAGTAAACCTTCTAAATGTCAGTAATAATCATTGACGGTGTATTTTGATGTATTTTTCTCTCTTTTCTCCATCACAGCTTTCCAGTGCATTCGAGCAGCCGCTGGGCTCTCTGGTTCTGCCAATCAGAGAGCTGCTTTCT[A/T]AAACAGACCTGCTGATGGACCAATGGCTGAGTCTGGATGGAGCAGCTGCTGACAGTCAGATTCTTCTCAGAGCTCAACTCAAGGTCAGACTGAGCTTTTTCTGATCGCTTTCTCCAACCTGTCCTTTCAGTTTATATAAACTTCACTTCTTTCAGTCTGTTACATTCATTTCTGCAGGTAATGTCATGTTGTGTCTAGAGGTGTATCCATCAAATGGTCAGAAATTGCAGATCCAAAGCATTTTCTTAATTTATTCTCTATTTTTTTGTTCTCCGATTCTGACTGGCATACAAACTGTGTTACGACTATTTTAAAGTACAAAATATGTAAACTGAGCATAAACCAAAGCTGTACGCATTTCTGTTTGGGCATGTTTAGGCGATCTCTCAAAGTTTTATGTTTTAAAAATGAGCTTTTTCTAGTCAGCATCTCTGGTATTGGCAGCCTAATACAATGCGGAGGGCTGTTGTGTAGGACTGAATGGTTTTATACTGTGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26837
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
ENSDART00000014819 Nonsense 842 1032 26 35
ENSDART00000140223 None None 314 None 10
ENSDART00000144174 Nonsense 1068 1076 31 31
Genomic Location (Zv9):
Chromosome 6 (position 52272872)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52322054
GRCz11 6 52322053
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCTGATGGACCAATGGCTGAGTCTGGATGGAGCAGCTGCTGACAGT[C/T]AGATTCTTCTCAGAGCTCAACTCAAGGTCAGACTGAGCTTTTTCTGATCG
Long Flanking Sequence:
ACTAGTCTTATCACTTGATATACTGTTGAAATGTGAATTATTATACGCCCTTTGATATTTGTTTTCTTTTTTTTCCAAATGATGTTTAACAGAGCAAGAAAATTTTCACAGTATTTTTGATAATATTTTATCTTCTAGAGAAAGTCTTATCTGCTTTATTTCAACTAGAATAAAAGCAGTTTTTAATTTTTTTAAAAACATTTTAAGATCAAAATTATTAGCCCTATTAAGCTATATATTCTTTGATAGTCTACAGAACAAACCATCGTTATACAATAACTTGCCTAATTACCTTAACCTGCCTAGTAAACCTTCTAAATGTCAGTAATAATCATTGACGGTGTATTTTGATGTATTTTTCTCTCTTTTCTCCATCACAGCTTTCCAGTGCATTCGAGCAGCCGCTGGGCTCTCTGGTTCTGCCAATCAGAGAGCTGCTTTCTAAAACAGACCTGCTGATGGACCAATGGCTGAGTCTGGATGGAGCAGCTGCTGACAGT[C/T]AGATTCTTCTCAGAGCTCAACTCAAGGTCAGACTGAGCTTTTTCTGATCGCTTTCTCCAACCTGTCCTTTCAGTTTATATAAACTTCACTTCTTTCAGTCTGTTACATTCATTTCTGCAGGTAATGTCATGTTGTGTCTAGAGGTGTATCCATCAAATGGTCAGAAATTGCAGATCCAAAGCATTTTCTTAATTTATTCTCTATTTTTTTGTTCTCCGATTCTGACTGGCATACAAACTGTGTTACGACTATTTTAAAGTACAAAATATGTAAACTGAGCATAAACCAAAGCTGTACGCATTTCTGTTTGGGCATGTTTAGGCGATCTCTCAAAGTTTTATGTTTTAAAAATGAGCTTTTTCTAGTCAGCATCTCTGGTATTGGCAGCCTAATACAATGCGGAGGGCTGTTGTGTAGGACTGAATGGTTTTATACTGTGAAAACAACCAACGGGATGTGCTTTATCCCACTTATTACATGCCTTATATGACAAATTAGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1525
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014819 Essential Splice Site 934 1032 32 35
ENSDART00000140223 Essential Splice Site 217 314 7 10
ENSDART00000144174 None None 1076 None 31
Genomic Location (Zv9):
Chromosome 6 (position 52284657)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 52333839
GRCz11 6 52333838
KASP Assay ID:
554-1449.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCCATGTCCTTCCAGAAGAAGCTGACGCTGCTCGTCCACAACTGCAGG[T/A]CTGAGCTACACTCATGACGAGTTNNTGAGTTATCTCTGTNNGTGTGAAGTTT
Long Flanking Sequence:
ATTCACTTGTTACGTTTAGTAACAACTCGACCTCGTCGTCTGTCCACGAAAATACCTCTCTTGCTTTCTTTGCCATCGCGTTTAATGTTCAACCGGCGTTTGTTAACTAACAATAACAAAATGCCGAGCGTGACGCATGCTTTCTGTTTATACTAGAACGTGCGTGCCCAGTGTGTGCGAATGGTCACGTGATATACATTTTTGGTGGCGTAGTTTGGACGGAAATATGTTCAGAGACGCTAGGTGAAACACTAGTGTGGACACGGAACTTTTTTGATCTGAAACGCCGTTTTAAAACTAAAATGCACTAGTGTAAACGGGGCCTTCAACAATTAACTGAGATTTTGTCTTTTATCCAGATCTTGGATTCCAAAATGGCGGCTTTAGTGGCGATGGGTTCAGGTCCGGTTTTGAGTAACAAGCAAACGGCCACAACAGGACAAATCCAGCTCTCCATGTCCTTCCAGAAGAAGCTGACGCTGCTCGTCCACAACTGCAGG[T/A]CTGAGCTACACTCATGACGAGTTTATGAGTTATCTCTGTGTGTGAAGTTTGAGGTGATTCCAGGACGCTGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGGGGTCTGGTCACATCATCTAAGGACAGCTTAGACACTTACGTCTCCATCATTCTGCTGCCAGATAAAAGCAAGGCCACCAAGAGAAAGACCAGTGTGAAGAAGAAAACCCTCAATCCAGAGTTCAATGAAAAGTATGTGTGGGTGGGTGAATGTGTAGAAGTGTGTGCGCGTGTATATGTAGGGGTAGGGAAATTATTCAGACCCTCTTAATTGTTTTGCTCTTTGTTATTGCAGCCGTTTGCTAAAATCAATTATTTTACCTCATCGTTGGAGAATGACAACAGTTTGGTGCGATTTAGAGGAAATGGGGTGGAGAGTGACG
Associated Phenotype:
Not determined