Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HNRNPR ENSOCUG00000006686

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Description

heterogeneous nuclear ribonucleoprotein R [Source:HGNC Symbol;Acc:HGNC:5047]

Location

Chromosome 13: 129,867,826-129,900,657 forward strand.

OryCun2.0:CM000802.1

About this gene

This gene has 2 transcripts (splice variants), 236 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000006685.4	HNRNPR-201	3226	635aa	ENSOCUP00000005778.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SRH9	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,
ENSOCUT00000061950.1	HNRNPR-202	3103	594aa	ENSOCUP00000040540.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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