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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SYT9 ENSG00000170743

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Description

synaptotagmin IX [Source:HGNC Symbol;Acc:19265]

Location

Chromosome 11: 7,260,009-7,490,273 forward strand.

GRCh37:CM000673.1

About this gene

This gene has 4 transcripts (splice variants) and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000318881.6	SYT9-001	3955	491aa	ENSP00000324419.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS7778	Q86SS6	NM_175733.3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000396716.2	SYT9-201	960	319aa	ENSP00000379944.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PDN4	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000532592.1	SYT9-002	3183	173aa	ENSP00000434558.1	Nonsense mediated decay		B3KNT7	-	-
ENST00000524820.2	SYT9-003	2094	319aa	ENSP00000432141.2	Nonsense mediated decay		E9PDN4	-	-

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Summary

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