Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: slc41a2b ENSDARG00000073881

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Description

solute carrier family 41 member 2 [Source:HGNC Symbol;Acc:HGNC:31045]

Location

Chromosome 4: 9,055,488-9,094,690 forward strand.

GRCz11:CM002888.2

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000155385.3	slc41a2b-202	2275	555aa	ENSDARP00000127955.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F597	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,
ENSDART00000113867.4	slc41a2b-201	2016	555aa	ENSDARP00000100886.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F597	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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