GLIPR1L2 GLIPR1 like 2

Information
Symbol
GLIPR1L2
Type
protein-coding
Description
GLIPR1 like 2
Entrez Gene ID
144321
Genome
hg19
Position
chr12:75,784,869-75,826,468
Genome
hg38
Position
chr12:75,391,089-75,432,688
MIM
610394 OMIM
HGNC
HGNC:28592 HGNC
Ensembl
ENSG00000180481 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 50
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 :
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
MIM 610394 OMIM
HGNC HGNC:28592 HGNC
Ensembl ENSG00000180481 Ensembl
AllianceGenome HGNC:28592
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000550916.6 hg38 chr12 75,391,089 75,432,688 41,600
ENST00000547164.1 hg38 chr12 75,391,117 75,422,932 31,816
ENST00000378692.7 hg38 chr12 75,391,101 75,431,883 40,783
ENST00000320460.8 hg38 chr12 75,391,109 75,424,040 32,932
ENST00000550916.6 hg19 chr12 75,784,869 75,826,468 41,600
ENST00000378692.7 hg19 chr12 75,784,881 75,825,663 40,783
ENST00000320460.8 hg19 chr12 75,784,889 75,817,820 32,932
ENST00000547164.1 hg19 chr12 75,784,897 75,816,712 31,816
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