FCER2 Fc epsilon receptor II

Information
Symbol
FCER2
Type
protein-coding
Description
Fc epsilon receptor II
Entrez Gene ID
2208
Genome
hg19
Position
chr19:7,753,662-7,767,032
Genome
hg38
Position
chr19:7,688,776-7,702,146
MIM
151445 OMIM
HGNC
HGNC:3612 HGNC
Ensembl
ENSG00000104921 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
50
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 BLAST-2
SYNONYM CD23
SYNONYM CD23A
SYNONYM CLEC4J
SYNONYM FCE2
SYNONYM FCErII
SYNONYM IGEBF
MIM 151445 OMIM
HGNC HGNC:3612 HGNC
Ensembl ENSG00000104921 Ensembl
AllianceGenome HGNC:3612
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000346664.9 hg38 chr19 7,688,776 7,702,146 13,371
ENST00000597921.6 hg38 chr19 7,688,776 7,702,131 13,356
ENST00000360067.8 hg38 chr19 7,688,758 7,699,479 10,722
ENST00000360067.8 hg19 chr19 7,753,644 7,764,365 10,722
ENST00000597921.6 hg19 chr19 7,753,662 7,767,017 13,356
ENST00000346664.9 hg19 chr19 7,753,662 7,767,032 13,371
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