LOC561429

Ensembl ID:
ENSDARG00000063568
Human Orthologue:
SYT7
Human Description:
synaptotagmin VII [Source:HGNC Symbol;Acc:11514]
Mouse Orthologue:
Syt7
Mouse Description:
synaptotagmin VII Gene [Source:MGI Symbol;Acc:MGI:1859545]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa44221 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa44221
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000093003 Essential Splice Site 118 653 5 13
Genomic Location (Zv9):
Chromosome 25 (position 4521227)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 4175249
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTCTCTCATTCCTTTGCATCTCCGCGGCTCTCTTTCTCGCGGACCCCTCA[G/A]TGGGACGGTTCACGGGGGCCAGAAAGGGGCCGCGGGGTGTGTATTGGGGG
Associated Phenotype:
Not determined

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

Short-link