Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Erhl1 ENSRNOG00000011239

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Description

ERH, mRNA splicing and mitosis factor like 1 [Source:RGD Symbol;Acc:1307595]

Gene Synonyms

LOC295019, RGD1307595

Location

Primary_assembly 2: 134,629,172-134,645,681 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 178 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000126154.1	Erhl1-202	3301	138aa	ENSRNOP00000107918.1	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,
ENSRNOT00000014928.7	Erhl1-201	998	138aa	ENSRNOP00000014928.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A5C2	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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