FCAR Fc alpha receptor

Information
Symbol
FCAR
Type
protein-coding
Description
Fc alpha receptor
Entrez Gene ID
2204
Genome
hg19
Position
chr19:55,385,691-55,402,786
Genome
hg38
Position
chr19:54,874,235-54,891,420
MIM
147045 OMIM
HGNC
HGNC:3608 HGNC
Ensembl
ENSG00000186431 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
46
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 CD89
SYNONYM CTB-61M7.2
SYNONYM FcalphaR
SYNONYM FcalphaRI
MIM 147045 OMIM
HGNC HGNC:3608 HGNC
Ensembl ENSG00000186431 Ensembl
AllianceGenome HGNC:3608
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000391724.3 hg38 chr19 54,874,290 54,889,863 15,574
ENST00000391723.7 hg38 chr19 54,874,290 54,889,863 15,574
ENST00000391726.7 hg38 chr19 54,874,248 54,889,890 15,643
ENST00000391725.7 hg38 chr19 54,874,285 54,889,890 15,606
ENST00000359272.8 hg38 chr19 54,874,290 54,889,863 15,574
ENST00000345937.8 hg38 chr19 54,874,285 54,889,890 15,606
ENST00000353758.8 hg38 chr19 54,874,290 54,889,863 15,574
ENST00000355524.8 hg38 chr19 54,874,235 54,891,420 17,186
ENST00000469767.5 hg38 chr19 54,874,280 54,889,067 14,788
ENST00000355524.8 hg19 chr19 55,385,691 55,402,786 17,096
ENST00000391726.7 hg19 chr19 55,385,704 55,401,256 15,553
ENST00000469767.5 hg19 chr19 55,385,736 55,400,434 14,699
ENST00000345937.8 hg19 chr19 55,385,741 55,401,256 15,516
ENST00000391725.7 hg19 chr19 55,385,741 55,401,256 15,516
ENST00000353758.8 hg19 chr19 55,385,746 55,401,229 15,484
ENST00000359272.8 hg19 chr19 55,385,746 55,401,229 15,484
ENST00000391723.7 hg19 chr19 55,385,746 55,401,229 15,484
ENST00000391724.3 hg19 chr19 55,385,746 55,401,229 15,484
Genome browser