Busch Lab

ZMP

sypl2a

Ensembl ID:
ENSDARG00000055307
ZFIN ID:
ZDB-GENE-040426-1434
Description:
synaptophysin-like 2a [Source:RefSeq peptide;Acc:NP_956961]
Human Orthologue:
SYPL2
Human Description:
synaptophysin-like 2 [Source:HGNC Symbol;Acc:27638]
Mouse Orthologue:
Sypl2
Mouse Description:
synaptophysin-like 2 Gene [Source:MGI Symbol;Acc:MGI:1328311]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41888 Nonsense Mutation detected in F1 DNA Not yet available
sa41889 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41888
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077649 Nonsense 67 235 3 7
ENSDART00000145427 Nonsense 67 235 3 6
Genomic Location (Zv9):
Chromosome 11 (position 37206248)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36103476
GRCz11 11 36365459
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAAATGTCCAGACAAAGATGATGTTGATGTTACTGCTAATTTTGGATA[T/A]CCATTCAGGTATAAACAACCACATTTCAATCCTATTTCTATACATTTTTA
Long Flanking Sequence:
TGTTATTATTATTATTATTATTGTTGTTATGTTTGTATTCATTATTAACTAATTTTAAAATGAAGACCCTATTTTAAAGGTGGACAACATATAAATTAGATATCTAAAAACATATGTACACAGTCAATCAGTACAAATGTTTTTGTCAGGATTTACTGAAGAAACGCAGTGAAATACTAGTGATGAAATAGCTGGGAAACAGATGTCATTGCATATGCGTATCAAGTTTTATTTTCAGAGACAAAATATGTGGGAGGAGAGATTTAAACTAATTATGCAATGTTAATGGTGCAATCCTAAAGTCATTTTGCTACTCTGAAAAGAACATTTTCAAATACACAGATGTCTTATAAAGGTTTTTTGTGTGCGTGTGTGTGTTTTTATTTTTAGGTTTTTACCATTTGTGCCTTTGCAACCACTGGTGGTTATGTTGGATCCACTGTTTTCACTCTTAAATGTCCAGACAAAGATGATGTTGATGTTACTGCTAATTTTGGATA[T/A]CCATTCAGGTATAAACAACCACATTTCAATCCTATTTCTATACATTTTTACTATTAAAATGTTGTCTGGTTGAAAGTCATGCAATTAAGGAAGACTTGTTCACGCCAACAGTGAAAACCTTAAACAATTAGGGCTAGGCGATAAGGCAAAAATGCTATCTTGATAATTATTTTCCAATGTTAACGGTATACATTTCGATATAAGTTGTTATGCTTCCAGATTTAAAAGAGTATCCCAATGATGACTGAAGCCACAAATATAACATATTTTTGGCCGATAAATTTCCGGTAGCCGAAAATTTACATCTTGGTAGTCGAAAATTTTATATCAACACAATCCCATTTGTAAGAGTAACAAATAATAACTTGACTTTGAGTTGATCAATTGGAAAAGTGGCAGAAGGTAGATCTTTAGATCTGTTGAACTGCATCCCAATTATCACAAATACTGCAGAAGACCTATTGTAACTCAATCAGACCACAGATTTTCTCAGATATCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41889
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077649 Nonsense 210 235 6 7
ENSDART00000145427 Nonsense 210 235 6 6
Genomic Location (Zv9):
Chromosome 11 (position 37213029)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36110257
GRCz11 11 36372240
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTAGCTTTTTGGATTCCTGAACCTGATTCTGTGGGCAGGGAACTGCTG[G/A]TTCATCTACAAGGAGACTCCGTTTCACAAGCCGGCAAACCCACCAGTAAA
Long Flanking Sequence:
TACTGTCCACCGGAGGTCGCATTTCAGTCACGGATACATACTTTGAGAGCCTTTCTGAATGAATGAAATATGCGGTTTTCTATCAAGCAGTGGCAGTGGGCGGTTTTGTAAACCAAAACAAAGACAGCCATTCCGGCACGTAACAAACATTTTTAGAGCAGAATATCTGACTTTAGCATTGTTTTTAAGATAAACAAGAATGTTCACTTGGCATGTTTCTTGAACGAGTCAAAAACTTACAAACAGCTCCTTTAATAATAACAGGGAATGGTTACTTTTCGGCTCAATGTTGCCAGATTTAGCAAAACGCTGCAAAAAAAAAAAATAAATAAATCATATCGGCTTTTTACAGTCTACACATAGCCATGATCAATGTGACCTGTTTTCAGGAAAATGCGCTGAAAGTTTAACAAAAGTAAGCATTACATATACCCTTCTTTGTTCTCCCTCCTCTAGCTTTTTGGATTCCTGAACCTGATTCTGTGGGCAGGGAACTGCTG[G/A]TTCATCTACAAGGAGACTCCGTTTCACAAGCCGGCAAACCCACCAGTAAACGCAGAAGAAGGAGTTTCCTCTTCCTAATCAGACAAAAGCGGCTCCTTCCTCTCCTCTCCACACATCCATACAGCAGAGGACATCACCGTTTGTTCATGTCCACACACACACACACACTGAAGAGAAACTACACTTTAATATGCAAAAGCTTCATGCAATGCAGTTCACTACTTATAAATGCAATAAGCTGAATTCATCATTTCTAGATGTTTGTTTTATCATTATTATTTTAGTGTCTGCTTGAAGGCACTGACAAAAGCAGGTCGTAAAAAAAATTGTATTTGATCATAGGTCTCCAACTTAAGTCCTGGAGGGCTGCAGCTCTGCGCAGTTTTGCTCCAACCCTAATCAAACTAATTAAGGTGTTTAAGACTACTTTTGAACGCCTTGATTAGTTGGATCGGCTGTGTTGGAATACGCTTATCTGCGGCCCTCAGGGAATTGAGTTT
Associated Phenotype:
Not determined