Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Sncg ENSRNOG00000058006

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Description

synuclein, gamma [Source:RGD Symbol;Acc:70996]

Location

Primary_assembly 16: 9,706,753-9,712,076 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 4 transcripts (splice variants), 258 orthologues, 2 paralogues and is associated with 25 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000143530.1	Sncg-204	836	182aa	ENSRNOP00000109611.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000080635.3	Sncg-201	932	148aa	ENSRNOP00000075051.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KFR9 F1LQ96	-
ENSRNOT00000087150.3	Sncg-202	661	124aa	ENSRNOP00000071576.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K0T6	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSRNOT00000131287.1	Sncg-203	637	126aa	ENSRNOP00000102366.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data