LEPROT leptin receptor overlapping transcript

Information
Symbol
LEPROT
Type
protein-coding
Description
leptin receptor overlapping transcript
Entrez Gene ID
54741
Genome
hg19
Position
chr1:65,886,399-65,901,690
Genome
hg38
Position
chr1:65,420,716-65,436,007
MIM
613461 OMIM
HGNC
HGNC:29477 HGNC
Ensembl
ENSG00000213625 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Conflicting classifications of pathogenicity 0 2
not provided 1 0
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
24
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
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 LEPR
SYNONYM OB-RGRP
SYNONYM OBRGRP
SYNONYM VPS55
MIM 613461 OMIM
HGNC HGNC:29477 HGNC
Ensembl ENSG00000213625 Ensembl
AllianceGenome HGNC:29477
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000484243.1 hg38 chr1 65,420,710 65,430,303 9,594
ENST00000613538.1 hg38 chr1 65,420,716 65,436,007 15,292
ENST00000488747.5 hg38 chr1 65,420,708 65,431,920 11,213
ENST00000371065.9 hg38 chr1 65,420,668 65,436,007 15,340
ENST00000475108.5 hg38 chr1 65,420,587 65,432,064 11,478
ENST00000475108.5 hg19 chr1 65,886,270 65,897,747 11,478
ENST00000371065.9 hg19 chr1 65,886,351 65,901,690 15,340
ENST00000488747.5 hg19 chr1 65,886,391 65,897,603 11,213
ENST00000484243.1 hg19 chr1 65,886,393 65,895,986 9,594
ENST00000613538.1 hg19 chr1 65,886,399 65,901,690 15,292
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