FCGR1BP Fc gamma receptor Ib, pseudogene

Information
Symbol
FCGR1BP
Type
pseudo
Description
Fc gamma receptor Ib, pseudogene
Entrez Gene ID
2210
Genome
hg38
Position
chr1:121,087,298-121,097,161
MIM
601502 OMIM
HGNC
HGNC:3614 HGNC
Ensembl
ENSG00000291135 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
0
Frequency
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
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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 :
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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 :
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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 CD34
SYNONYM CD64b
SYNONYM FCG1
SYNONYM FCGR1
SYNONYM FCGR1B
SYNONYM FcRI
SYNONYM FcgammaRIa
SYNONYM IGFR1
SYNONYM IGFRB
MIM 601502 OMIM
HGNC HGNC:3614 HGNC
Ensembl ENSG00000291135 Ensembl
AllianceGenome HGNC:3614
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000369384.10 hg38 chr1 121,087,298 121,097,161 9,864
ENST00000697335.1 hg38 chr1 121,087,311 121,091,051 3,741
ENST00000702854.1 hg38 chr1 121,087,345 121,096,310 8,966
ENST00000700943.1 hg38 chr1 121,087,368 121,096,308 8,941
ENST00000701628.1 hg38 chr1 121,087,334 121,096,312 8,979
ENST00000369383.9 hg38 chr1 121,087,316 121,097,157 9,842
ENST00000701453.1 hg38 chr1 121,087,372 121,096,307 8,936
ENST00000700986.1 hg38 chr1 121,087,331 121,096,318 8,988
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