Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: slc44a1a ENSDARG00000015946

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Description

solute carrier family 44 member 1a [Source:ZFIN;Acc:ZDB-GENE-050417-204]

Gene Synonyms

cdw92, slc44a1, zgc:112201

Location

Chromosome 1: 52,632,856-52,652,163 forward strand.

GRCz11:CM002885.2

About this gene

This gene has 2 transcripts (splice variants), 145 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000011725.10	slc44a1a-201	2752	651aa	ENSDARP00000007186.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q9M4	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,
ENSDART00000134658.3	slc44a1a-202	2220	645aa	ENSDARP00000121604.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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