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: Fam216a ENSRNOG00000031731

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Description

family with sequence similarity 216, member A [Source:RGD Symbol;Acc:1310861]

Gene Synonyms

LOC288667, MGC105520, RGD1310861

Location

Primary_assembly 12: 39,859,172-39,868,442 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 1 transcript (splice variant), 93 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000050398.4	Fam216a-201	1275	261aa	ENSRNOP00000046271.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J1A2 Q5U1Y9	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,

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Summary

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