RETSAT retinol saturase

Information
Symbol
RETSAT
Type
protein-coding
Description
retinol saturase
Entrez Gene ID
54884
Genome
hg19
Position
chr2:85,569,078-85,581,651
Genome
hg38
Position
chr2:85,341,955-85,354,528
MIM
617597 OMIM
HGNC
HGNC:25991 HGNC
Ensembl
ENSG00000042445 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 6
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
108
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
MIM 617597 OMIM
HGNC HGNC:25991 HGNC
Ensembl ENSG00000042445 Ensembl
AllianceGenome HGNC:25991
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000295802.9 hg38 chr2 85,341,955 85,354,528 12,574
ENST00000295802.9 hg19 chr2 85,569,078 85,581,651 12,574
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