NARF nuclear prelamin A recognition factor

Information
Symbol
NARF
Type
protein-coding
Description
nuclear prelamin A recognition factor
Entrez Gene ID
26502
Genome
hg19
Position
chr17:80,416,617-80,448,413
Genome
hg38
Position
chr17:82,458,741-82,490,537
MIM
605349 OMIM
HGNC
HGNC:29916 HGNC
Ensembl
ENSG00000141562 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 60
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 :
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 IOP2
MIM 605349 OMIM
HGNC HGNC:29916 HGNC
Ensembl ENSG00000141562 Ensembl
AllianceGenome HGNC:29916
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000345415.11 hg38 chr17 82,458,649 82,488,262 29,614
ENST00000457415.7 hg38 chr17 82,458,703 82,488,215 29,513
ENST00000390006.8 hg38 chr17 82,458,185 82,488,255 30,071
ENST00000309794.16 hg38 chr17 82,458,741 82,490,537 31,797
ENST00000390006.8 hg19 chr17 80,416,061 80,446,131 30,071
ENST00000309794.16 hg19 chr17 80,416,617 80,448,413 31,797
ENST00000345415.11 hg19 chr17 80,416,525 80,446,138 29,614
ENST00000457415.7 hg19 chr17 80,416,579 80,446,091 29,513
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