Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: NR2C2AP ENSSSCG00000023658

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Description

nuclear receptor 2C2 associated protein [Source:VGNC Symbol;Acc:VGNC:90877]

Location

Primary_assembly 2: 58,675,990-58,678,130 forward strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 3 transcripts (splice variants) and 194 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000023414.3	NR2C2AP-202	1249	140aa	ENSSSCP00000022715.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U2U3 I3LF75	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,
ENSSSCT00000076297.2	NR2C2AP-203	1250	74aa	ENSSSCP00000061931.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QUT4	-
ENSSSCT00000078801.1	NR2C2AP-201	635	120aa	ENSSSCP00000060569.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U2U8 A0A5G2QAX6	-

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Summary

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