LUM lumican

Information
Symbol
LUM
Type
protein-coding
Description
lumican
Entrez Gene ID
4060
Genome
hg19
Position
chr12:91,496,406-91,505,271
Genome
hg38
Position
chr12:91,102,629-91,111,494
MIM
600616 OMIM
HGNC
HGNC:6724 HGNC
Ensembl
ENSG00000139329 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 10
Uncertain significance 0 20
Ranking
ClinVar
0
0
2
38
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 LDC
SYNONYM SLRR2D
MIM 600616 OMIM
HGNC HGNC:6724 HGNC
Ensembl ENSG00000139329 Ensembl
AllianceGenome HGNC:6724
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000266718.5 hg38 chr12 91,102,629 91,111,494 8,866
ENST00000266718.5 hg19 chr12 91,496,406 91,505,271 8,866
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