FOXL2NB FOXL2 neighbor

Information
Symbol
FOXL2NB
Type
protein-coding
Description
FOXL2 neighbor
Entrez Gene ID
401089
Genome
hg19
Position
chr3:138,666,059-138,672,832
Genome
hg38
Position
chr3:138,947,217-138,953,990
HGNC
HGNC:34428 HGNC
Ensembl
ENSG00000206262 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
22
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 C3orf72
HGNC HGNC:34428 HGNC
Ensembl ENSG00000206262 Ensembl
AllianceGenome HGNC:34428
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000383165.4 hg38 chr3 138,947,217 138,953,990 6,774
ENST00000383165.4 hg19 chr3 138,666,059 138,672,832 6,774
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