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

Configure this page

Share this page

Bookmark this page

.

Gene: SLC22A25 ENSPTRG00000024251

.

Description

solute carrier family 22 member 25 [Source:VGNC Symbol;Acc:VGNC:7753]

Location

Chromosome 11: 63,172,803-63,238,178 reverse strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 2 transcripts (splice variants), 845 orthologues and 24 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000007073.5	SLC22A25-201	1641	546aa	ENSPTRP00000006525.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2Q3X6	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,
ENSPTRT00000088707.1	SLC22A25-202	486	161aa	ENSPTRP00000066252.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RNL6	-

.

Summary

.

.