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

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Gene: Fchsd1 ENSRNOG00000039415

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Description

FCH and double SH3 domains 1 [Source:RGD Symbol;Acc:1308240]

Gene Synonyms

LOC307482

Location

Primary_assembly 18: 30,045,106-30,055,673 reverse strand.

GRCr8:CM070408.1

About this gene

This gene has 1 transcript (splice variant), 174 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026381.9	Fchsd1-201	2616	690aa	ENSRNOP00000026381.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J3E2 D4AD36	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,

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Summary

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