REN renin

Information
Symbol
REN
Type
protein-coding
Description
renin
Entrez Gene ID
5972
Genome
hg19
Position
chr1:204,123,947-204,135,465
Genome
hg38
Position
chr1:204,154,819-204,166,337
MIM
179820 OMIM
HGNC
HGNC:9958 HGNC
Ensembl
ENSG00000143839 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 4 18
Likely pathogenic 0 12
Benign 0 52
Likely benign 0 78
Conflicting classifications of pathogenicity 0 30
not provided 1 0
Uncertain significance 0 146
Ranking
ClinVar
0
0
58
218
18
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 ADTKD4
SYNONYM HNFJ2
SYNONYM RTD
MIM 179820 OMIM
HGNC HGNC:9958 HGNC
Ensembl ENSG00000143839 Ensembl
AllianceGenome HGNC:9958
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000272190.9 hg38 chr1 204,154,819 204,166,337 11,519
ENST00000638118.1 hg38 chr1 204,154,938 204,190,324 35,387
ENST00000272190.9 hg19 chr1 204,123,947 204,135,465 11,519
ENST00000638118.1 hg19 chr1 204,124,066 204,159,452 35,387
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