Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Fcer1g ENSRNOG00000024159

.

Description

Fc epsilon receptor Ig [Source:RGD Symbol;Acc:2599]

Gene Synonyms

MGC188226

Location

Primary_assembly 13: 86,181,908-86,186,859 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 5 transcripts (splice variants), 103 orthologues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000098830.2	Fcer1g-202	1000	169aa	ENSRNOP00000077355.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YBS0	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,
ENSRNOT00000103864.2	Fcer1g-203	817	108aa	ENSRNOP00000096825.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ARQ1	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,
ENSRNOT00000029179.5	Fcer1g-201	702	91aa	ENSRNOP00000036716.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QIN1	-
ENSRNOT00000103998.2	Fcer1g-204	555	87aa	ENSRNOP00000088147.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AI77	-
ENSRNOT00000140295.1	Fcer1g-205	342	86aa	ENSRNOP00000102941.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.