NR2F6 nuclear receptor subfamily 2 group F member 6

Information
Symbol
NR2F6
Type
protein-coding
Description
nuclear receptor subfamily 2 group F member 6
Entrez Gene ID
2063
Genome
hg19
Position
chr19:17,342,692-17,356,728
Genome
hg38
Position
chr19:17,231,883-17,245,919
MIM
132880 OMIM
HGNC
HGNC:7977 HGNC
Ensembl
ENSG00000160113 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
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 EAR-2
SYNONYM EAR2
SYNONYM ERBAL2
MIM 132880 OMIM
HGNC HGNC:7977 HGNC
Ensembl ENSG00000160113 Ensembl
AllianceGenome HGNC:7977
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000291442.4 hg38 chr19 17,231,883 17,245,919 14,037
ENST00000291442.4 hg19 chr19 17,342,692 17,356,728 14,037
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