Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Slc18b1 ENSRNOG00000016371

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Description

solute carrier family 18 member B1 [Source:RGD Symbol;Acc:1306962]

Gene Synonyms

LOC309570, RGD1306962, VPAT

Location

Primary_assembly 1: 23,447,462-23,489,962 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 213 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021944.9	Slc18b1-201	2549	470aa	ENSRNOP00000021944.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A9K4	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,
ENSRNOT00000118149.2	Slc18b1-202	2358	421aa	ENSRNOP00000092228.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GK33	-
ENSRNOT00000130741.1	Slc18b1-203	1414	410aa	ENSRNOP00000105802.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Paralogues

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