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

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Gene: Fas ENSRNOG00000019142

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Description

Fas cell surface death receptor [Source:RGD Symbol;Acc:619831]

Gene Synonyms

Tnfrsf6

Location

Primary_assembly 1: 231,798,960-231,832,591 forward strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 5 transcripts (splice variants), 178 orthologues, 20 paralogues and is associated with 165 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025928.6	Fas-201	2545	324aa	ENSRNOP00000025928.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LWQ2	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSRNOT00000119978.1	Fas-205	2488	305aa	ENSRNOP00000082757.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G9W1	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,
ENSRNOT00000112109.1	Fas-203	2141	317aa	ENSRNOP00000096262.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ALF0	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,
ENSRNOT00000114760.1	Fas-204	942	313aa	ENSRNOP00000089144.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AC34	-
ENSRNOT00000094083.1	Fas-202	249	63aa	ENSRNOP00000079622.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZN15	-

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Summary

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