FCRL2 Fc receptor like 2

Information
Symbol
FCRL2
Type
protein-coding
Description
Fc receptor like 2
Entrez Gene ID
79368
Genome
hg19
Position
chr1:157,715,523-157,746,922
Genome
hg38
Position
chr1:157,745,733-157,777,132
MIM
606509 OMIM
HGNC
HGNC:14875 HGNC
Ensembl
ENSG00000132704 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
64
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 CD307b
SYNONYM FCRH2
SYNONYM IFGP4
SYNONYM IRTA4
SYNONYM SPAP1
SYNONYM SPAP1A
SYNONYM SPAP1B
SYNONYM SPAP1C
MIM 606509 OMIM
HGNC HGNC:14875 HGNC
Ensembl ENSG00000132704 Ensembl
AllianceGenome HGNC:14875
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000469986.1 hg38 chr1 157,766,614 157,767,774 1,161
ENST00000361516.8 hg38 chr1 157,745,733 157,777,132 31,400
ENST00000368181.4 hg38 chr1 157,745,735 157,777,132 31,398
ENST00000361516.8 hg19 chr1 157,715,523 157,746,922 31,400
ENST00000368181.4 hg19 chr1 157,715,525 157,746,922 31,398
ENST00000469986.1 hg19 chr1 157,736,404 157,737,564 1,161
Genome browser