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

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Gene: NHERF2 ENSSSCG00000008038

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Description

NHERF family PDZ scaffold protein 2 [Source:VGNC Symbol;Acc:VGNC:93185]

Location

Primary_assembly 3: 39,942,367-39,952,825 reverse strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 2 transcripts (splice variants), 270 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000067185.2	NHERF2-201	2224	361aa	ENSSSCP00000061879.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QIN1 A0A8D1SEU1	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,
ENSSSCT00000008809.4	NHERF2-202	1870	337aa	ENSSSCP00000008585.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0R8F9 B6EAV5	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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