FAM89B family with sequence similarity 89 member B

Information
Symbol
FAM89B
Type
protein-coding
Description
family with sequence similarity 89 member B
Entrez Gene ID
23625
Genome
hg19
Position
chr11:65,340,009-65,341,661
Genome
hg38
Position
chr11:65,572,538-65,574,190
MIM
616128 OMIM
HGNC
HGNC:16708 HGNC
Ensembl
ENSG00000176973 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
22
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 :
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 LRAP25
SYNONYM MTVR
SYNONYM MTVR1
MIM 616128 OMIM
HGNC HGNC:16708 HGNC
Ensembl ENSG00000176973 Ensembl
AllianceGenome HGNC:16708
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000449319.2 hg38 chr11 65,572,462 65,574,190 1,729
ENST00000530349.2 hg38 chr11 65,572,538 65,574,190 1,653
ENST00000316409.2 hg38 chr11 65,572,349 65,574,198 1,850
ENST00000316409.2 hg19 chr11 65,339,820 65,341,669 1,850
ENST00000449319.2 hg19 chr11 65,339,933 65,341,661 1,729
ENST00000530349.2 hg19 chr11 65,340,009 65,341,661 1,653
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