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

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Gene: FCHSD2 ENSDARG00000091428

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Description

FCH and double SH3 domains 2 [Source:HGNC Symbol;Acc:HGNC:29114]

Location

Chromosome 10: 36,741,502-36,778,514 forward strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 210 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSDART00000155687.3	FCHSD2-201	2199	732aa	ENSDARP00000127514.1	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, 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,
ENSDART00000181690.1	FCHSD2-202	360	119aa	ENSDARP00000147789.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-

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Summary

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