CD59 CD59 molecule (CD59 blood group)

Information
Symbol
CD59
Type
protein-coding
Description
CD59 molecule (CD59 blood group)
Entrez Gene ID
966
Genome
hg19
Position
chr11:33,724,556-33,757,969
Genome
hg38
Position
chr11:33,703,010-33,736,423
MIM
107271 OMIM
HGNC
HGNC:1689 HGNC
Ensembl
ENSG00000085063 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Benign 0 10
Likely benign 0 102
Conflicting classifications of pathogenicity 0 4
not provided 1 0
Uncertain significance 0 58
Ranking
ClinVar
0
0
10
164
4
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 16.3A5
SYNONYM 1F5
SYNONYM EJ16
SYNONYM EJ30
SYNONYM EL32
SYNONYM G344
SYNONYM HRF-20
SYNONYM HRF20
SYNONYM MAC-IP
SYNONYM MACIF
SYNONYM MEM43
SYNONYM MIC11
SYNONYM MIN1
SYNONYM MIN2
SYNONYM MIN3
SYNONYM MIRL
SYNONYM MSK21
SYNONYM p18-20
MIM 107271 OMIM
HGNC HGNC:1689 HGNC
Ensembl ENSG00000085063 Ensembl
AllianceGenome HGNC:1689
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000351554.8 hg38 chr11 33,709,996 33,736,479 26,484
ENST00000643183.1 hg38 chr11 33,710,099 33,736,423 26,325
ENST00000426650.7 hg38 chr11 33,709,470 33,736,422 26,953
ENST00000642928.2 hg38 chr11 33,703,010 33,736,423 33,414
ENST00000651785.1 hg38 chr11 33,703,010 33,736,423 33,414
ENST00000445143.6 hg38 chr11 33,709,798 33,722,727 12,930
ENST00000527577.5 hg38 chr11 33,710,005 33,736,425 26,421
ENST00000437761.6 hg38 chr11 33,709,929 33,722,726 12,798
ENST00000533403.6 hg38 chr11 33,709,556 33,736,408 26,853
ENST00000652086.1 hg38 chr11 33,709,439 33,736,427 26,989
ENST00000652678.1 hg38 chr11 33,703,012 33,722,952 19,941
ENST00000415002.7 hg38 chr11 33,709,635 33,722,710 13,076
ENST00000706436.1 hg38 chr11 33,703,010 33,736,423 33,414
ENST00000395850.9 hg38 chr11 33,708,715 33,736,422 27,708
ENST00000395850.9 hg19 chr11 33,730,261 33,757,968 27,708
ENST00000527577.5 hg19 chr11 33,731,551 33,757,971 26,421
ENST00000642928.2 hg19 chr11 33,724,556 33,757,969 33,414
ENST00000351554.8 hg19 chr11 33,731,542 33,758,025 26,484
ENST00000426650.7 hg19 chr11 33,731,016 33,757,968 26,953
ENST00000415002.7 hg19 chr11 33,731,181 33,744,256 13,076
ENST00000437761.6 hg19 chr11 33,731,475 33,744,272 12,798
ENST00000445143.6 hg19 chr11 33,731,344 33,744,273 12,930
ENST00000533403.6 hg19 chr11 33,731,102 33,757,954 26,853
ENST00000643183.1 hg19 chr11 33,731,645 33,757,969 26,325
ENST00000652086.1 hg19 chr11 33,730,985 33,757,973 26,989
ENST00000652678.1 hg19 chr11 33,724,558 33,744,498 19,941
ENST00000706436.1 hg19 chr11 33,724,556 33,757,969 33,414
ENST00000651785.1 hg19 chr11 33,724,556 33,757,969 33,414
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