Gene: Slc25a38 ENSRNOG00000018552

Description

solute carrier family 25, member 38 [Source:RGD Symbol;Acc:1311914]

Gene Synonyms

LOC301067, MGC124671, RGD1311914

Location

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 279 orthologues, 54 paralogues and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025142.8	Slc25a38-201	1715	326aa	ENSRNOP00000025142.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QD79 Q499U1	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,
ENSRNOT00000083329.3	Slc25a38-202	1715	305aa	ENSRNOP00000071588.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K0U7	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