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

Configure this page

Share this page

Bookmark this page

.

Gene: FCHSD1 ENSPTRG00000023689

.

Description

FCH and double SH3 domains 1 [Source:VGNC Symbol;Acc:VGNC:6873]

Location

Chromosome 5: 141,678,349-141,690,528 reverse strand.

Pan_tro_3.0:CM000319.3

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
ENSPTRT00000046182.5	FCHSD1-201	4359	690aa	ENSPTRP00000045350.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XC71 K7B8F9	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,
ENSPTRT00000109661.1	FCHSD1-202	1929	642aa	ENSPTRP00000092500.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TTB8	-
ENSPTRT00000081817.1	FCHSD1-203	1797	598aa	ENSPTRP00000072889.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S766 A0A6D2X457	-

.

Summary

.

.