Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Fam222a ENSRNOG00000001198

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Description

family with sequence similarity 222, member A [Source:RGD Symbol;Acc:1565883]

Gene Synonyms

LOC498193, RGD1565883

Location

Primary_assembly 12: 47,647,405-47,693,703 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 249 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095969.2	Fam222a-202	2574	457aa	ENSRNOP00000089749.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ALN9	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,
ENSRNOT00000001588.6	Fam222a-201	2808	452aa	ENSRNOP00000001588.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J1Z5 D3ZY38	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,

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Summary

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