FAM9A family with sequence similarity 9 member A

Information
Symbol
FAM9A
Type
protein-coding
Description
family with sequence similarity 9 member A
Entrez Gene ID
171482
Genome
hg19
Position
chrX:8,758,836-8,769,424
Genome
hg38
Position
chrX:8,790,795-8,801,383
MIM
300477 OMIM
HGNC
HGNC:18403 HGNC
Ensembl
ENSG00000183304 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
not provided 7 0
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
38
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 :
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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 TEX39A
MIM 300477 OMIM
HGNC HGNC:18403 HGNC
Ensembl ENSG00000183304 Ensembl
AllianceGenome HGNC:18403
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000381003.7 hg38 chrX 8,790,795 8,801,383 10,589
ENST00000543214.1 hg38 chrX 8,790,795 8,801,337 10,543
ENST00000543214.1 hg19 chrX 8,758,836 8,769,378 10,543
ENST00000381003.7 hg19 chrX 8,758,836 8,769,424 10,589
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