SELENOH selenoprotein H

Information
Symbol
SELENOH
Type
protein-coding
Description
selenoprotein H
Entrez Gene ID
280636
Genome
hg19
Position
chr11:57,508,963-57,511,022
Genome
hg38
Position
chr11:57,741,491-57,743,550
MIM
607914 OMIM
HGNC
HGNC:18251 HGNC
Ensembl
ENSG00000211450 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
4
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
SYNONYM C11orf31
SYNONYM C17orf10
SYNONYM SELH
MIM 607914 OMIM
HGNC HGNC:18251 HGNC
Ensembl ENSG00000211450 Ensembl
AllianceGenome HGNC:18251
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000534355.6 hg38 chr11 57,741,491 57,743,550 2,060
ENST00000388857.8 hg38 chr11 57,741,572 57,742,657 1,086
ENST00000534355.6 hg19 chr11 57,508,963 57,511,022 2,060
ENST00000388857.8 hg19 chr11 57,509,044 57,510,129 1,086
Genome browser