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: BCL7C ENSSSCG00000007776

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Description

BAF chromatin remodeling complex subunit BCL7C [Source:VGNC Symbol;Acc:VGNC:85786]

Location

Primary_assembly 3: 17,547,582-17,551,853 forward strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 1 transcript (splice variant), 105 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000008523.4	BCL7C-201	878	217aa	ENSSSCP00000008304.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1TMW7 F1RG97	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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