NOB1 NIN1 (RPN12) binding protein 1 homolog

Information
Symbol
NOB1
Type
protein-coding
Description
NIN1 (RPN12) binding protein 1 homolog
Entrez Gene ID
28987
Genome
hg19
Position
chr16:69,775,774-69,788,829
Genome
hg38
Position
chr16:69,741,871-69,754,926
MIM
613586 OMIM
HGNC
HGNC:29540 HGNC
Ensembl
ENSG00000141101 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
64
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 :
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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 ART-4
SYNONYM MST158
SYNONYM MSTP158
SYNONYM NOB1P
SYNONYM PSMD8BP1
MIM 613586 OMIM
HGNC HGNC:29540 HGNC
Ensembl ENSG00000141101 Ensembl
AllianceGenome HGNC:29540
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000268802.10 hg38 chr16 69,741,871 69,754,926 13,056
ENST00000268802.10 hg19 chr16 69,775,774 69,788,829 13,056
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