Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,
ENSRNOT00000070908.4	Fam228a-201	1132	282aa	ENSRNOP00000065885.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XIN5	-

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Summary

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