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
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Ontologies
Phenotypes
Genetic Variation
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External references
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ID History
- Gene history

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Gene: Erich6b ENSMUSG00000022002

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Description

glutamate rich 6B [Source:MGI Symbol;Acc:MGI:1922522]

Gene Synonyms

4930564B18Rik, Gm46471

Location

Chromosome 14: 75,879,689-75,934,157 forward strand.

GRCm39:CM001007.3

About this gene

This gene has 2 transcripts (splice variants), 71 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000238633.2	Erich6b-202	1961	574aa	ENSMUSP00000158673.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A571BEV3	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,
ENSMUST00000022579.2	Erich6b-201	869	220aa	ENSMUSP00000022579.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS56969	Q9D4S6	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

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Summary

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