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

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Gene: lrrc14b ENSDARG00000060788

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Description

leucine rich repeat containing 14B [Source:NCBI gene;Acc:566643]

Gene Synonyms

si:dkey-231l1.3

Location

Chromosome 19: 44,039,849-44,047,176 forward strand.

GRCz11:CM002903.2

About this gene

This gene has 1 transcript (splice variant), 190 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000086040.4	lrrc14b-201	1687	526aa	ENSDARP00000080475.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1L8H0	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,

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Summary

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