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
External references
Supporting evidence
ID History
- Gene history

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Gene: SREBF2 ENSPTRG00000014439

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Description

sterol regulatory element binding transcription factor 2 [Source:VGNC Symbol;Acc:VGNC:6008]

Location

Chromosome 22: 28,493,092-28,567,054 forward strand.

Pan_tro_3.0:CM000335.3

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000026976.5	SREBF2-201	5254	1142aa	ENSPTRP00000024869.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WKS3 K7D4A6	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSPTRT00000106076.1	SREBF2-202	2058	685aa	ENSPTRP00000065035.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RK58 A0A6D2X1E9	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,

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Summary

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