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: slc1a7b ENSDARG00000026248

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Description

solute carrier family 1 member 7b [Source:NCBI gene (formerly Entrezgene);Acc:100463517]

Gene Synonyms

si:ch73-116b16.2

Location

Chromosome 23: 41,949,575-42,093,537 reverse strand.

GRCz11:CM002907.2

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000122074.3	slc1a7b-201	1783	580aa	ENSDARP00000111235.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D7RVS5	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,
ENSDART00000144183.3	slc1a7b-202	532	166aa	ENSDARP00000119371.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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