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

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Gene: EGFLAM ENSBTAG00000019595

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Description

EGF like, fibronectin type III and laminin G domains [Source:VGNC Symbol;Acc:VGNC:55044]

Location

Primary_assembly 20: 35,967,740-36,161,759 reverse strand.

ARS-UCD2.0:CM008187.2

About this gene

This gene has 6 transcripts (splice variants), 204 orthologues and 28 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000106912.1	EGFLAM-203	4174	1048aa	ENSBTAP00000080655.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S607	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,
ENSBTAT00000074054.1	EGFLAM-204	4084	1018aa	ENSBTAP00000062240.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N606	-
ENSBTAT00000026111.7	EGFLAM-205	4084	1018aa	ENSBTAP00000026111.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N606	-
ENSBTAT00000131710.1	EGFLAM-206	4081	1017aa	ENSBTAP00000085427.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SGV8	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,
ENSBTAT00000069022.2	EGFLAM-202	4024	1006aa	ENSBTAP00000058765.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LPC1	-
ENSBTAT00000103818.1	EGFLAM-201	3331	775aa	ENSBTAP00000086892.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SKM6	-

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Summary

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