RHOU ras homolog family member U

Information
Symbol
RHOU
Type
protein-coding
Description
ras homolog family member U
Entrez Gene ID
58480
Genome
hg19
Position
chr1:228,871,226-228,882,411
Genome
hg38
Position
chr1:228,735,479-228,746,664
MIM
606366 OMIM
HGNC
HGNC:17794 HGNC
Ensembl
ENSG00000116574 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
20
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 ARHU
SYNONYM CDC42L1
SYNONYM G28K
SYNONYM WRCH1
SYNONYM hG28K
MIM 606366 OMIM
HGNC HGNC:17794 HGNC
Ensembl ENSG00000116574 Ensembl
AllianceGenome HGNC:17794
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000366691.4 hg38 chr1 228,735,479 228,746,664 11,186
ENST00000366691.4 hg19 chr1 228,871,226 228,882,411 11,186
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