Gene: Fam227a ENSRNOG00000021795

Description

family with sequence similarity 227, member A [Source:RGD Symbol;Acc:1305939]

Gene Synonyms

LOC300074, RGD1305939

Location

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 88 orthologues and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000056179.7	Fam227a-201	3219	629aa	ENSRNOP00000053025.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LMV2	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,
ENSRNOT00000078320.3	Fam227a-202	1221	316aa	ENSRNOP00000068832.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4V8A5	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,

Strains

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.