RTKN rhotekin

Information
Symbol
RTKN
Type
protein-coding
Description
rhotekin
Entrez Gene ID
6242
Genome
hg19
Position
chr2:74,652,962-74,669,064
Genome
hg38
Position
chr2:74,425,835-74,441,937
MIM
602288 OMIM
HGNC
HGNC:10466 HGNC
Ensembl
ENSG00000114993 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 86
Ranking
ClinVar
0
0
0
88
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
SYNONYM RTKN-1
MIM 602288 OMIM
HGNC HGNC:10466 HGNC
Ensembl ENSG00000114993 Ensembl
AllianceGenome HGNC:10466
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000305557.9 hg38 chr2 74,425,836 74,440,583 14,748
ENST00000640304.2 hg38 chr2 74,426,180 74,442,300 16,121
ENST00000272430.10 hg38 chr2 74,425,835 74,441,937 16,103
ENST00000233330.6 hg38 chr2 74,425,883 74,440,631 14,749
ENST00000272430.10 hg19 chr2 74,652,962 74,669,064 16,103
ENST00000305557.9 hg19 chr2 74,652,963 74,667,710 14,748
ENST00000233330.6 hg19 chr2 74,653,010 74,667,758 14,749
ENST00000640304.2 hg19 chr2 74,653,307 74,669,427 16,121
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