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

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Gene: APLN ENSG00000171388

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Description

apelin [Source:HGNC Symbol;Acc:16665]

Gene Synonyms

APEL, XNPEP2, apelin

Location

Chromosome X: 128,779,240-128,788,933 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000307484.6	APLN-201	3220	77aa	ENSP00000305464.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS48165	Q9ULZ1	NM_017413.4	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000429967.1	APLN-001	2655	122aa	ENSP00000391800.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		B2R550 D3DTF8	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000427399.1	APLN-202	387	122aa	ENSP00000390834.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		B2R550 D3DTF8	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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