APLN apelin

Information
Symbol
APLN
Type
protein-coding
Description
apelin
Entrez Gene ID
8862
Genome
hg19
Position
chrX:128,779,236-128,788,933
Genome
hg38
Position
chrX:129,645,259-129,654,956
MIM
300297 OMIM
HGNC
HGNC:16665 HGNC
Ensembl
ENSG00000171388 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
not provided 6 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
18
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM APEL
SYNONYM XNPEP2
MIM 300297 OMIM
HGNC HGNC:16665 HGNC
Ensembl ENSG00000171388 Ensembl
AllianceGenome HGNC:16665
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000429967.3 hg38 chrX 129,645,259 129,654,956 9,698
ENST00000429967.3 hg19 chrX 128,779,236 128,788,933 9,698
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