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

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Gene: FAS ENSBTAG00000010785

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Description

Fas cell surface death receptor [Source:VGNC Symbol;Acc:VGNC:28869]

Location

Primary_assembly 26: 10,678,448-10,712,480 forward strand.

ARS-UCD1.3:CM008193.2

About this gene

This gene has 3 transcripts (splice variants), 178 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000014282.7	FAS-203	2804	323aa	ENSBTAP00000014282.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A5D7R0	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000121211.1	FAS-201	3018	295aa	ENSBTAP00000078369.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000086406.2	FAS-202	1179	323aa	ENSBTAP00000059383.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MVY3	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,

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Summary

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