NANOGNB NANOG neighbor homeobox

Information
Symbol
NANOGNB
Type
protein-coding
Description
NANOG neighbor homeobox
Entrez Gene ID
360030
Genome
hg19
Position
chr12:7,917,812-7,926,717
Genome
hg38
Position
chr12:7,765,216-7,774,121
MIM
620692 OMIM
HGNC
HGNC:24958 HGNC
Ensembl
ENSG00000205857 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
20
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
MIM 620692 OMIM
HGNC HGNC:24958 HGNC
Ensembl ENSG00000205857 Ensembl
AllianceGenome HGNC:24958
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000382119.1 hg38 chr12 7,765,216 7,774,121 8,906
ENST00000640040.1 hg38 chr12 7,766,082 7,774,121 8,040
ENST00000382119.1 hg19 chr12 7,917,812 7,926,717 8,906
ENST00000640040.1 hg19 chr12 7,918,678 7,926,717 8,040
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