Gene: Slc39a14 ENSRNOG00000009832

Description

solute carrier family 39 member 14 [Source:RGD Symbol;Acc:1307026]

Gene Synonyms

LOC306009

Location

GRCr8:CM070405.1

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues, 6 paralogues and is associated with 7 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000105917.2	Slc39a14-202	4720	490aa	ENSRNOP00000091533.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABU1	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 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,
ENSRNOT00000013067.5	Slc39a14-201	4720	490aa	ENSRNOP00000013066.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HTK2 D3ZZM0	APPRIS ALT1: 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 is conserved in at least 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 ALT1,

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