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

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Gene: LIN28B ENSBTAG00000043973

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Description

lin-28 homolog B [Source:VGNC Symbol;Acc:VGNC:108131]

Location

Primary_assembly 9: 44,947,436-45,086,340 reverse strand.

ARS-UCD1.3:CM008176.2

About this gene

This gene has 4 transcripts (splice variants), 228 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000061356.4	LIN28B-203	1854	276aa	ENSBTAP00000053651.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N777	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,
ENSBTAT00000123716.1	LIN28B-201	2035	261aa	ENSBTAP00000092232.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000096065.1	LIN28B-204	2010	269aa	ENSBTAP00000075334.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000092997.1	LIN28B-202	1993	247aa	ENSBTAP00000084030.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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