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

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Gene: r3hcc1 ENSDARG00000099593

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Description

R3H domain and coiled-coil containing 1 [Source:ZFIN;Acc:ZDB-GENE-091204-146]

Gene Synonyms

si:dkey-191l12.1

Location

Chromosome 10: 20,392,083-20,402,161 forward strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 191 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000166867.2	r3hcc1-202	2082	404aa	ENSDARP00000137545.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IN15	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,
ENSDART00000160803.2	r3hcc1-201	2286	385aa	ENSDARP00000139628.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IWG5	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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