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: SP2 ENSPTRG00000009342

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Description

Sp2 transcription factor [Source:VGNC Symbol;Acc:VGNC:9644]

Location

Chromosome 17: 9,914,099-9,946,971 reverse strand.

Pan_tro_3.0:CM000331.3

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000017155.5	SP2-201	3165	613aa	ENSPTRP00000015881.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WP36 H2QDB1	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,
ENSPTRT00000017154.5	SP2-202	759	252aa	ENSPTRP00000015880.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QDB0	-

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Summary

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