NKRF NFKB repressing factor

Information
Symbol
NKRF
Type
protein-coding
Description
NFKB repressing factor
Entrez Gene ID
55922
Genome
hg19
Position
chrX:118,723,315-118,739,958
Genome
hg38
Position
chrX:119,589,352-119,605,995
MIM
300440 OMIM
HGNC
HGNC:19374 HGNC
Ensembl
ENSG00000186416 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 12
not provided 6 0
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
58
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
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 ITBA4
SYNONYM NRF
MIM 300440 OMIM
HGNC HGNC:19374 HGNC
Ensembl ENSG00000186416 Ensembl
AllianceGenome HGNC:19374
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000304449.8 hg38 chrX 119,588,337 119,606,443 18,107
ENST00000688521.1 hg38 chrX 119,589,352 119,605,995 16,644
ENST00000542113.3 hg38 chrX 119,588,341 119,605,883 17,543
ENST00000304449.8 hg19 chrX 118,722,300 118,740,406 18,107
ENST00000542113.3 hg19 chrX 118,722,304 118,739,846 17,543
ENST00000688521.1 hg19 chrX 118,723,315 118,739,958 16,644
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