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

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Gene: Slc5a1l1 ENSRNOG00000029979

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Description

solute carrier family 5 member 1 like 1 [Source:RGD Symbol;Acc:1563815]

Gene Synonyms

LOC100909546, LOC365549, RGD1563815

Location

Primary_assembly 20: 12,663,826-12,713,142 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 1 transcript (splice variant), 520 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000058343.6	Slc5a1l1-201	2833	671aa	ENSRNOP00000055145.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZEM7	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,

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Summary

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