Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: LINS1 ENSBTAG00000016495

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Description

lines homolog 1 [Source:VGNC Symbol;Acc:VGNC:30903]

Location

Primary_assembly 21: 6,034,990-6,056,488 forward strand.

ARS-UCD1.3:CM008188.2

About this gene

This gene has 2 transcripts (splice variants) and 189 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000021928.3	LINS1-202	2584	758aa	ENSBTAP00000021928.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BNP0	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,
ENSBTAT00000063961.3	LINS1-201	2494	728aa	ENSBTAP00000054328.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MXR0	-

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Summary

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