Gene: Slc9a3 ENSRNOG00000015159

Description

solute carrier family 9 member A3 [Source:RGD Symbol;Acc:3720]

Gene Synonyms

NHE-3, Nhe3

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 234 orthologues, 10 paralogues and is associated with 15 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094251.2	Slc9a3-202	6399	831aa	ENSRNOP00000083053.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZZ59 A6JUV3	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,
ENSRNOT00000020711.5	Slc9a3-201	5201	831aa	ENSRNOP00000020711.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JUV3 G3V7Y7 P26433	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,

Summary