ZNFX1 zinc finger NFX1-type containing 1

Information
Symbol
ZNFX1
Type
protein-coding
Description
zinc finger NFX1-type containing 1
Entrez Gene ID
57169
Genome
hg19
Position
chr20:47,862,434-47,894,602
Genome
hg38
Position
chr20:49,245,897-49,278,065
MIM
618931 OMIM
HGNC
HGNC:29271 HGNC
Ensembl
ENSG00000124201 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 2
Benign 0 30
Likely benign 0 34
Conflicting classifications of pathogenicity 0 2
not provided 1 0
Uncertain significance 0 236
Ranking
ClinVar
0
0
12
288
8
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 IMD91
MIM 618931 OMIM
HGNC HGNC:29271 HGNC
Ensembl ENSG00000124201 Ensembl
AllianceGenome HGNC:29271
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000371752.5 hg38 chr20 49,245,897 49,278,065 32,169
ENST00000371754.8 hg38 chr20 49,237,946 49,278,426 40,481
ENST00000396105.6 hg38 chr20 49,245,900 49,278,057 32,158
ENST00000371754.8 hg19 chr20 47,854,483 47,894,963 40,481
ENST00000371752.5 hg19 chr20 47,862,434 47,894,602 32,169
ENST00000396105.6 hg19 chr20 47,862,437 47,894,594 32,158
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