LGALS12 galectin 12

Information
Symbol
LGALS12
Type
protein-coding
Description
galectin 12
Entrez Gene ID
85329
Genome
hg19
Position
chr11:63,273,835-63,284,246
Genome
hg38
Position
chr11:63,506,363-63,516,774
MIM
606096 OMIM
HGNC
HGNC:15788 HGNC
Ensembl
ENSG00000133317 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
52
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 GAL12
SYNONYM GRIP1
MIM 606096 OMIM
HGNC HGNC:15788 HGNC
Ensembl ENSG00000133317 Ensembl
AllianceGenome HGNC:15788
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000394618.9 hg38 chr11 63,506,084 63,516,772 10,689
ENST00000255684.10 hg38 chr11 63,506,084 63,516,767 10,684
ENST00000674247.1 hg38 chr11 63,506,052 63,516,774 10,723
ENST00000425950.2 hg38 chr11 63,507,987 63,516,767 8,781
ENST00000340246.10 hg38 chr11 63,506,363 63,516,774 10,412
ENST00000415491.6 hg38 chr11 63,507,987 63,516,767 8,781
ENST00000674247.1 hg19 chr11 63,273,524 63,284,246 10,723
ENST00000255684.10 hg19 chr11 63,273,556 63,284,239 10,684
ENST00000394618.9 hg19 chr11 63,273,556 63,284,244 10,689
ENST00000340246.10 hg19 chr11 63,273,835 63,284,246 10,412
ENST00000415491.6 hg19 chr11 63,275,459 63,284,239 8,781
ENST00000425950.2 hg19 chr11 63,275,459 63,284,239 8,781
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