Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
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ID History
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Gene: Fam8a1 ENSRNOG00000026120

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Description

family with sequence similarity 8, member A1 [Source:RGD Symbol;Acc:1307845]

Gene Synonyms

LOC291031, Rbm24

Location

Primary_assembly 17: 18,232,834-18,241,703 reverse strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant) and 262 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000060500.7	Fam8a1-201	3792	384aa	ENSRNOP00000057242.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J712 D4ACR7	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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