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

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Gene: CSTF2 ENSBTAG00000003547

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Description

cleavage stimulation factor subunit 2 [Source:VGNC Symbol;Acc:VGNC:27781]

Location

Primary_assembly X: 51,346,938-51,381,374 reverse strand.

ARS-UCD2.0:CM008197.2

About this gene

This gene has 4 transcripts (splice variants), 203 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000123805.1	CSTF2-201	4773	614aa	ENSBTAP00000103329.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TXF0	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,
ENSBTAT00000045511.3	CSTF2-202	4707	592aa	ENSBTAP00000042892.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MVI1	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,
ENSBTAT00000004619.7	CSTF2-203	2023	594aa	ENSBTAP00000004619.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6YL13	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,
ENSBTAT00000131175.1	CSTF2-204	1927	562aa	ENSBTAP00000077076.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RX58	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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