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

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Gene: LOC120096281 ENSRNOG00000011100

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Description

heterogeneous nuclear ribonucleoprotein A3-like [Source:RGD Symbol;Acc:41086608]

Gene Synonyms

AABR07040947.1

Location

Primary_assembly 13: 68,489,590-68,493,283 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 64 orthologues and 35 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000121297.1	LOC120096281-202	3694	357aa	ENSRNOP00000106923.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000014756.9	LOC120096281-201	1989	348aa	ENSRNOP00000014756.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M6C7	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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