NOG noggin

Information
Symbol
NOG
Type
protein-coding
Description
noggin
Entrez Gene ID
9241
Genome
hg19
Position
chr17:54,671,060-54,672,972
Genome
hg38
Position
chr17:56,593,699-56,595,611
MIM
602991 OMIM
HGNC
HGNC:7866 HGNC
Ensembl
ENSG00000183691 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 5 54
Likely pathogenic 2 26
Benign 0 18
Likely benign 0 80
Conflicting classifications of pathogenicity 0 6
Uncertain significance 0 174
Ranking
ClinVar
0
0
18
298
30
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 :
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 SYM1
SYNONYM SYNS1
SYNONYM SYNS1A
MIM 602991 OMIM
HGNC HGNC:7866 HGNC
Ensembl ENSG00000183691 Ensembl
AllianceGenome HGNC:7866
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000332822.6 hg38 chr17 56,593,699 56,595,611 1,913
ENST00000332822.6 hg19 chr17 54,671,060 54,672,972 1,913
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