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

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Gene: BLEC1 ENSGALG00010002955

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Description

c-type lectin like 1, MHCB region [Source:NCBI gene (formerly Entrezgene);Acc:404776]

Gene Synonyms

B-LEC, Blec, CLEC2D, TCLEC2D

Location

Primary_assembly 16: 2,174,268-2,185,542 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028497.1

About this gene

This gene has 2 transcripts (splice variants), 342 orthologues and 30 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010006881.1	BLEC1-201	1168	191aa	ENSGALP00010004197.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0XC06	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,
ENSGALT00010006878.1	BLEC1-202	2673	188aa	ENSGALP00010004195.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A5HUL1	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,

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Summary

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