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

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Gene: BCL7A ENSBTAG00000032517

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Description

BAF chromatin remodeling complex subunit BCL7A [Source:VGNC Symbol;Acc:VGNC:53891]

Location

Primary_assembly 17: 53,301,513-53,332,694 reverse strand.

ARS-UCD2.0:CM008184.2

About this gene

This gene has 5 transcripts (splice variants), 219 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000094262.1	BCL7A-204	1992	263aa	ENSBTAP00000081140.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S7D9	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,
ENSBTAT00000125971.1	BCL7A-201	1971	256aa	ENSBTAP00000092117.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T5V5	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,
ENSBTAT00000131671.1	BCL7A-203	1896	231aa	ENSBTAP00000102646.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9U0N3	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,
ENSBTAT00000099724.1	BCL7A-202	1875	224aa	ENSBTAP00000098340.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TIQ3	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,
ENSBTAT00000005481.6	BCL7A-205	853	218aa	ENSBTAP00000005481.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MST5	-

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Summary

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