LCN6 lipocalin 6

Information
Symbol
LCN6
Type
protein-coding
Description
lipocalin 6
Entrez Gene ID
158062
Genome
hg19
Position
chr9:139,638,469-139,642,977
Genome
hg38
Position
chr9:136,744,017-136,748,525
MIM
609379 OMIM
HGNC
HGNC:17337 HGNC
Ensembl
ENSG00000267206 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
36
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 LCN5
SYNONYM UNQ643
SYNONYM hLcn5
MIM 609379 OMIM
HGNC HGNC:17337 HGNC
Ensembl ENSG00000267206 Ensembl
AllianceGenome HGNC:17337
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000341206.9 hg38 chr9 136,744,017 136,748,525 4,509
ENST00000476567.1 hg38 chr9 136,744,017 136,746,022 2,006
ENST00000476567.1 hg19 chr9 139,638,469 139,640,474 2,006
ENST00000341206.9 hg19 chr9 139,638,469 139,642,977 4,509
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