RERGL RERG like

Information
Symbol
RERGL
Type
protein-coding
Description
RERG like
Entrez Gene ID
79785
Genome
hg19
Position
chr12:18,233,803-18,243,127
Genome
hg38
Position
chr12:18,080,869-18,090,193
HGNC
HGNC:26213 HGNC
Ensembl
ENSG00000111404 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
22
2
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
HGNC HGNC:26213 HGNC
Ensembl ENSG00000111404 Ensembl
AllianceGenome HGNC:26213
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000536890.1 hg38 chr12 18,081,337 18,090,141 8,805
ENST00000229002.6 hg38 chr12 18,080,869 18,090,193 9,325
ENST00000538724.6 hg38 chr12 18,080,869 18,090,193 9,325
ENST00000229002.6 hg19 chr12 18,233,803 18,243,127 9,325
ENST00000538724.6 hg19 chr12 18,233,803 18,243,127 9,325
ENST00000536890.1 hg19 chr12 18,234,271 18,243,075 8,805
Genome browser