FAM89A family with sequence similarity 89 member A

Information
Symbol
FAM89A
Type
protein-coding
Description
family with sequence similarity 89 member A
Entrez Gene ID
375061
Genome
hg19
Position
chr1:231,154,704-231,176,000
Genome
hg38
Position
chr1:231,018,958-231,040,254
HGNC
HGNC:25057 HGNC
Ensembl
ENSG00000182118 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
24
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 C1orf153
HGNC HGNC:25057 HGNC
Ensembl ENSG00000182118 Ensembl
AllianceGenome HGNC:25057
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000366654.5 hg38 chr1 231,018,958 231,040,254 21,297
ENST00000366654.5 hg19 chr1 231,154,704 231,176,000 21,297
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