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
External references
Supporting evidence
ID History
- Gene history

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Gene: Fam228a ENSRNOG00000050114

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Description

family with sequence similarity 228, member A [Source:RGD Symbol;Acc:1359275]

Gene Synonyms

LOC313936

Location

Primary_assembly 6: 33,447,427-33,468,989 reverse strand.

GRCr8:CM070396.1

About this gene

This gene has 2 transcripts (splice variants), 99 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094984.2	Fam228a-202	1218	306aa	ENSRNOP00000091169.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AD49	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,
ENSRNOT00000070908.4	Fam228a-201	1132	282aa	ENSRNOP00000065885.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XIN5	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,

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Summary

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