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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Eml2 ENSRNOG00000030127

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Description

EMAP like 2 [Source:RGD Symbol;Acc:621066]

Gene Synonyms

Emap, Emap-2, Eml1

Location

Primary_assembly 1: 87,955,606-87,987,366 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 6 transcripts (splice variants), 191 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000041215.7	Eml2-201	2988	841aa	ENSRNOP00000046691.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QPN8	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000111912.2	Eml2-204	2832	794aa	ENSRNOP00000096567.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6API3	-
ENSRNOT00000107022.2	Eml2-203	2788	837aa	ENSRNOP00000097902.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6B6G9	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000113449.2	Eml2-205	2777	795aa	ENSRNOP00000096394.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AQQ2	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000115540.2	Eml2-206	2162	628aa	ENSRNOP00000090007.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ACZ3	-
ENSRNOT00000078336.3	Eml2-202	2071	587aa	ENSRNOP00000075212.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2RA46	-

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Summary

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