LMAN2L lectin, mannose binding 2 like

Information
Symbol
LMAN2L
Type
protein-coding
Description
lectin, mannose binding 2 like
Entrez Gene ID
81562
Genome
hg19
Position
chr2:97,372,077-97,405,801
Genome
hg38
Position
chr2:96,706,340-96,740,064
MIM
609552 OMIM
HGNC
HGNC:19263 HGNC
Ensembl
ENSG00000114988 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 2
Benign 0 2
Likely benign 0 26
not provided 2 0
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
92
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 MRD69
SYNONYM MRT52
SYNONYM VIPL
MIM 609552 OMIM
HGNC HGNC:19263 HGNC
Ensembl ENSG00000114988 Ensembl
AllianceGenome HGNC:19263
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000377079.8 hg38 chr2 96,706,340 96,740,064 33,725
ENST00000264963.9 hg38 chr2 96,705,929 96,740,064 34,136
ENST00000264963.9 hg19 chr2 97,371,666 97,405,801 34,136
ENST00000377079.8 hg19 chr2 97,372,077 97,405,801 33,725
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