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

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Gene: lin28aa ENSDARG00000004328

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Description

lin-28 homolog A [Source:HGNC Symbol;Acc:HGNC:15986]

Location

Chromosome 16: 4,654,333-4,686,245 forward strand.

GRCz11:CM002900.2

About this gene

This gene has 2 transcripts (splice variants), 262 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000167665.2	lin28aa-202	783	193aa	ENSDARP00000138197.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IRA3	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,
ENSDART00000006212.7	lin28aa-201	891	191aa	ENSDARP00000015591.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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