LRCH2 leucine rich repeats and calponin homology domain containing 2

Information
Symbol
LRCH2
Type
protein-coding
Description
leucine rich repeats and calponin homology domain containing 2
Entrez Gene ID
57631
Genome
hg19
Position
chrX:114,345,179-114,468,659
Genome
hg38
Position
chrX:115,110,616-115,234,096
HGNC
HGNC:29292 HGNC
Ensembl
ENSG00000130224 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely benign 0 50
Conflicting classifications of pathogenicity 0 6
not provided 7 0
Uncertain significance 0 284
Ranking
ClinVar
0
0
0
334
2
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 dA204F4.4
HGNC HGNC:29292 HGNC
Ensembl ENSG00000130224 Ensembl
AllianceGenome HGNC:29292
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000538422.2 hg38 chrX 115,110,626 115,234,072 123,447
ENST00000317135.13 hg38 chrX 115,110,616 115,234,096 123,481
ENST00000317135.13 hg19 chrX 114,345,179 114,468,659 123,481
ENST00000538422.2 hg19 chrX 114,345,189 114,468,635 123,447
Genome browser