Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: R3hcc1l ENSRNOG00000051256

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Description

R3H domain and coiled-coil containing 1-like [Source:RGD Symbol;Acc:1307934]

Gene Synonyms

LOC293953, RGD1307934

Location

Primary_assembly 1: 251,266,493-251,344,495 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 190 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000081765.3	R3hcc1l-201	3407	775aa	ENSRNOP00000071099.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JZM0	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,
ENSRNOT00000110075.2	R3hcc1l-202	3389	769aa	ENSRNOP00000080786.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZR31	-
ENSRNOT00000119667.2	R3hcc1l-203	1338	195aa	ENSRNOP00000094769.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AK93	-

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Summary

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