CNIH4 cornichon family member 4

Information
Symbol
CNIH4
Type
protein-coding
Description
cornichon family member 4
Entrez Gene ID
29097
Genome
hg19
Position
chr1:224,544,581-224,567,154
Genome
hg38
Position
chr1:224,356,879-224,379,452
MIM
617483 OMIM
HGNC
HGNC:25013 HGNC
Ensembl
ENSG00000143771 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
10
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 CNIH-4
SYNONYM CNIH2
SYNONYM HSPC163
MIM 617483 OMIM
HGNC HGNC:25013 HGNC
Ensembl ENSG00000143771 Ensembl
AllianceGenome HGNC:25013
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000366857.9 hg38 chr1 224,356,871 224,379,452 22,582
ENST00000366856.3 hg38 chr1 224,356,893 224,379,452 22,560
ENST00000366858.7 hg38 chr1 224,356,858 224,379,452 22,595
ENST00000465271.6 hg38 chr1 224,356,879 224,379,452 22,574
ENST00000366858.7 hg19 chr1 224,544,560 224,567,154 22,595
ENST00000366857.9 hg19 chr1 224,544,573 224,567,154 22,582
ENST00000465271.6 hg19 chr1 224,544,581 224,567,154 22,574
ENST00000366856.3 hg19 chr1 224,544,595 224,567,154 22,560
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