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: SMARCE1 ENSPTRG00000022902

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Description

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 [Source:VGNC Symbol;Acc:VGNC:9635]

Location

Chromosome 17: 16,949,980-16,974,363 forward strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 3 transcripts (splice variants), 277 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000079689.1	SMARCE1-201	6593	411aa	ENSPTRP00000068187.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RU20 A0A6D2W080	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,
ENSPTRT00000092152.1	SMARCE1-202	6487	376aa	ENSPTRP00000085756.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T941 A0A6D2XFX6	-
ENSPTRT00000044181.4	SMARCE1-203	987	328aa	ENSPTRP00000046617.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WMB5 H2R455	-

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Summary

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