Gene: Fcer2 ENSRNOG00000001005

Description

Fc epsilon receptor II [Source:RGD Symbol;Acc:619997]

Gene Synonyms

CD23, Fcer2a, MGC93219

Location

Primary_assembly 12: 6,540,703-6,549,374 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 5 transcripts (splice variants), 858 orthologues, 23 paralogues and is associated with 7 phenotypes.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000001333.6	Fcer2-202	2168	378aa	ENSRNOP00000001333.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V638	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,
ENSRNOT00000102279.2	Fcer2-203	2105	357aa	ENSRNOP00000085732.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A2A4	-
ENSRNOT00000119392.2	Fcer2-205	2105	357aa	ENSRNOP00000082891.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZUS9	-
ENSRNOT00000109939.2	Fcer2-204	2038	357aa	ENSRNOP00000081846.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTY3	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,
ENSRNOT00000001332.8	Fcer2-201	1976	331aa	ENSRNOP00000001332.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7EKM2 Q6AZ45	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,