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

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Gene: FCHSD1 ENSSSCG00000014390

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Description

FCH and double SH3 domains 1 [Source:VGNC Symbol;Acc:VGNC:88067]

Location

Primary_assembly 2: 143,289,859-143,301,900 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 3 transcripts (splice variants), 175 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000015727.4	FCHSD1-203	4377	692aa	ENSSSCP00000015312.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RMS3	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,
ENSSSCT00000069467.2	FCHSD1-202	1769	579aa	ENSSSCP00000073841.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R9W9 A0A8D0S5D4	-
ENSSSCT00000084573.2	FCHSD1-201	785	243aa	ENSSSCP00000067557.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QRZ4 A0A8D0W136	-

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Paralogues

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