C2orf88 chromosome 2 open reading frame 88

Information
Symbol
C2orf88
Type
protein-coding
Description
chromosome 2 open reading frame 88
Entrez Gene ID
84281
Genome
hg19
Position
chr2:191,045,589-191,068,210
Genome
hg38
Position
chr2:190,180,863-190,203,484
MIM
615117 OMIM
HGNC
HGNC:28191 HGNC
Ensembl
ENSG00000187699 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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 :
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 smAKAP
MIM 615117 OMIM
HGNC HGNC:28191 HGNC
Ensembl ENSG00000187699 Ensembl
AllianceGenome HGNC:28191
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409870.1 hg38 chr2 190,180,482 190,200,209 19,728
ENST00000443551.2 hg38 chr2 190,180,955 190,200,214 19,260
ENST00000396974.2 hg38 chr2 190,137,760 190,200,479 62,720
ENST00000340623.4 hg38 chr2 190,180,863 190,203,484 22,622
ENST00000396974.2 hg19 chr2 191,002,486 191,065,205 62,720
ENST00000409870.1 hg19 chr2 191,045,208 191,064,935 19,728
ENST00000340623.4 hg19 chr2 191,045,589 191,068,210 22,622
ENST00000443551.2 hg19 chr2 191,045,681 191,064,940 19,260
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