CRNN cornulin

Information
Symbol
CRNN
Type
protein-coding
Description
cornulin
Entrez Gene ID
49860
Genome
hg19
Position
chr1:152,381,719-152,386,739
Genome
hg38
Position
chr1:152,409,243-152,414,263
MIM
611312 OMIM
HGNC
HGNC:1230 HGNC
Ensembl
ENSG00000143536 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 12
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
70
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 :
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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 :
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 C1orf10
SYNONYM DRC1
SYNONYM PDRC1
SYNONYM SEP53
MIM 611312 OMIM
HGNC HGNC:1230 HGNC
Ensembl ENSG00000143536 Ensembl
AllianceGenome HGNC:1230
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000271835.3 hg38 chr1 152,409,243 152,414,263 5,021
ENST00000271835.3 hg19 chr1 152,381,719 152,386,739 5,021
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