PROM2 prominin 2

Information
Symbol
PROM2
Type
protein-coding
Description
prominin 2
Entrez Gene ID
150696
Genome
hg19
Position
chr2:95,940,197-95,957,050
Genome
hg38
Position
chr2:95,274,449-95,291,302
MIM
617160 OMIM
HGNC
HGNC:20685 HGNC
Ensembl
ENSG00000155066 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
Uncertain significance 0 102
Ranking
ClinVar
0
0
0
114
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 PROML2
MIM 617160 OMIM
HGNC HGNC:20685 HGNC
Ensembl ENSG00000155066 Ensembl
AllianceGenome HGNC:20685
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000317620.14 hg38 chr2 95,274,449 95,291,302 16,854
ENST00000403131.6 hg38 chr2 95,274,453 95,291,306 16,854
ENST00000317668.8 hg38 chr2 95,274,453 95,291,308 16,856
ENST00000317620.14 hg19 chr2 95,940,197 95,957,050 16,854
ENST00000403131.6 hg19 chr2 95,940,201 95,957,054 16,854
ENST00000317668.8 hg19 chr2 95,940,201 95,957,056 16,856
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