Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Sp2 ENSRNOG00000010492

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Description

Sp2 transcription factor [Source:RGD Symbol;Acc:1592078]

Gene Synonyms

Sp2_mapped

Location

Primary_assembly 10: 82,437,029-82,467,651 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 3 transcripts (splice variants), 210 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000155912.1	Sp2-203	3262	636aa	ENSRNOP00000110364.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000068083.3	Sp2-201	3200	616aa	ENSRNOP00000059769.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZSM5	-
ENSRNOT00000087322.3	Sp2-202	3040	612aa	ENSRNOP00000072347.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B5DEH3	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,

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Summary

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