NBPF14 NBPF member 14

Information
Symbol
NBPF14
Type
protein-coding
Description
NBPF member 14
Entrez Gene ID
25832
Genome
hg38
Position
chr1:148,531,385-148,596,011
MIM
614003 OMIM
HGNC
HGNC:25232 HGNC
Ensembl
ENSG00000270629 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 3
Ranking
ClinVar
0
0
0
3
0
Frequency
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
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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 :
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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 :
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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 AE5
SYNONYM DJ328E19.C1.1
SYNONYM NBPF
MIM 614003 OMIM
HGNC HGNC:25232 HGNC
Ensembl ENSG00000270629 Ensembl
AllianceGenome HGNC:25232
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000611826.4 hg38 chr1 148,532,979 148,595,890 62,912
ENST00000616120.4 hg38 chr1 148,532,979 148,595,890 62,912
ENST00000619423.4 hg38 chr1 148,531,385 148,596,011 64,627
ENST00000614999.4 hg38 chr1 148,531,385 148,595,717 64,333
ENST00000621070.4 hg38 chr1 148,532,979 148,595,890 62,912
ENST00000621066.4 hg38 chr1 148,532,118 148,593,685 61,568
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