CHRDL1 chordin like 1

Information
Symbol
CHRDL1
Type
protein-coding
Description
chordin like 1
Entrez Gene ID
91851
Genome
hg19
Position
chrX:109,917,084-110,039,045
Genome
hg38
Position
chrX:110,673,856-110,795,817
MIM
300350 OMIM
HGNC
HGNC:29861 HGNC
Ensembl
ENSG00000101938 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 26
Likely pathogenic 0 6
Benign 0 22
Likely benign 0 12
Conflicting classifications of pathogenicity 0 2
not provided 7 0
Uncertain significance 0 32
Ranking
ClinVar
0
0
8
78
10
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 CHL
SYNONYM MGC1
SYNONYM MGCN
SYNONYM NRLN1
SYNONYM VOPT
SYNONYM dA141H5.1
MIM 300350 OMIM
HGNC HGNC:29861 HGNC
Ensembl ENSG00000101938 Ensembl
AllianceGenome HGNC:29861
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000444321.2 hg38 chrX 110,676,057 110,795,819 119,763
ENST00000482160.5 hg38 chrX 110,675,941 110,795,819 119,879
ENST00000372042.6 hg38 chrX 110,673,856 110,795,817 121,962
ENST00000372045.5 hg38 chrX 110,673,856 110,795,765 121,910
ENST00000394797.8 hg38 chrX 110,675,245 110,795,765 120,521
ENST00000372045.5 hg19 chrX 109,917,084 110,038,993 121,910
ENST00000372042.6 hg19 chrX 109,917,084 110,039,045 121,962
ENST00000394797.8 hg19 chrX 109,918,473 110,038,993 120,521
ENST00000482160.5 hg19 chrX 109,919,169 110,039,047 119,879
ENST00000444321.2 hg19 chrX 109,919,285 110,039,047 119,763
Genome browser