ATG9A autophagy related 9A

Information
Symbol
ATG9A
Type
protein-coding
Description
autophagy related 9A
Entrez Gene ID
79065
Genome
hg19
Position
chr2:220,084,104-220,094,090
Genome
hg38
Position
chr2:219,219,382-219,229,368
MIM
612204 OMIM
HGNC
HGNC:22408 HGNC
Ensembl
ENSG00000198925 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
80
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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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 APG9L1
SYNONYM MGD3208
SYNONYM mATG9
MIM 612204 OMIM
HGNC HGNC:22408 HGNC
Ensembl ENSG00000198925 Ensembl
AllianceGenome HGNC:22408
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361242.9 hg38 chr2 219,219,380 219,229,636 10,257
ENST00000409618.5 hg38 chr2 219,219,382 219,229,368 9,987
ENST00000409422.5 hg38 chr2 219,220,447 219,229,629 9,183
ENST00000396761.6 hg38 chr2 219,219,380 219,229,717 10,338
ENST00000361242.9 hg19 chr2 220,084,102 220,094,358 10,257
ENST00000396761.6 hg19 chr2 220,084,102 220,094,439 10,338
ENST00000409618.5 hg19 chr2 220,084,104 220,094,090 9,987
ENST00000409422.5 hg19 chr2 220,085,169 220,094,351 9,183
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