PHF21B PHD finger protein 21B

Information
Symbol
PHF21B
Type
protein-coding
Description
PHD finger protein 21B
Entrez Gene ID
112885
Genome
hg19
Position
chr22:45,277,042-45,405,886
Genome
hg38
Position
chr22:44,881,162-45,010,005
MIM
616727 OMIM
HGNC
HGNC:25161 HGNC
Ensembl
ENSG00000056487 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
54
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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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 :
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 BHC80L
SYNONYM PHF4
MIM 616727 OMIM
HGNC HGNC:25161 HGNC
Ensembl ENSG00000056487 Ensembl
AllianceGenome HGNC:25161
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000414269.2 hg38 chr22 44,883,086 45,009,999 126,914
ENST00000629843.3 hg38 chr22 44,881,162 45,010,005 128,844
ENST00000420689.2 hg38 chr22 44,882,881 45,008,986 126,106
ENST00000313237.10 hg38 chr22 44,881,162 45,010,005 128,844
ENST00000313237.10 hg19 chr22 45,277,042 45,405,886 128,845
ENST00000629843.3 hg19 chr22 45,277,042 45,405,886 128,845
ENST00000420689.2 hg19 chr22 45,278,761 45,404,867 126,107
ENST00000414269.2 hg19 chr22 45,278,966 45,405,880 126,915
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