SUMF2 sulfatase modifying factor 2

Information
Symbol
SUMF2
Type
protein-coding
Description
sulfatase modifying factor 2
Entrez Gene ID
25870
Genome
hg19
Position
chr7:56,131,982-56,147,429
Genome
hg38
Position
chr7:56,064,289-56,079,736
MIM
607940 OMIM
HGNC
HGNC:20415 HGNC
Ensembl
ENSG00000129103 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 8
Likely benign 0 12
not provided 1 0
Uncertain significance 0 70
Ranking
ClinVar
0
0
4
86
2
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 :
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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 pFGE
MIM 607940 OMIM
HGNC HGNC:20415 HGNC
Ensembl ENSG00000129103 Ensembl
AllianceGenome HGNC:20415
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000395435.7 hg38 chr7 56,064,254 56,080,187 15,934
ENST00000395436.7 hg38 chr7 56,064,002 56,080,124 16,123
ENST00000651586.1 hg38 chr7 56,064,224 56,080,669 16,446
ENST00000342190.11 hg38 chr7 56,064,255 56,080,670 16,416
ENST00000413756.5 hg38 chr7 56,064,289 56,079,736 15,448
ENST00000652303.1 hg38 chr7 56,064,224 56,080,669 16,446
ENST00000434526.8 hg38 chr7 56,064,286 56,080,670 16,385
ENST00000650735.1 hg38 chr7 56,064,224 56,080,669 16,446
ENST00000651354.1 hg38 chr7 56,064,224 56,080,669 16,446
ENST00000437307.6 hg38 chr7 56,064,284 56,079,832 15,549
ENST00000275607.13 hg38 chr7 56,064,224 56,080,669 16,446
ENST00000395436.7 hg19 chr7 56,131,695 56,147,817 16,123
ENST00000275607.13 hg19 chr7 56,131,917 56,148,362 16,446
ENST00000395435.7 hg19 chr7 56,131,947 56,147,880 15,934
ENST00000342190.11 hg19 chr7 56,131,948 56,148,363 16,416
ENST00000437307.6 hg19 chr7 56,131,977 56,147,525 15,549
ENST00000434526.8 hg19 chr7 56,131,979 56,148,363 16,385
ENST00000413756.5 hg19 chr7 56,131,982 56,147,429 15,448
ENST00000650735.1 hg19 chr7 56,131,917 56,148,362 16,446
ENST00000652303.1 hg19 chr7 56,131,917 56,148,362 16,446
ENST00000651586.1 hg19 chr7 56,131,917 56,148,362 16,446
ENST00000651354.1 hg19 chr7 56,131,917 56,148,362 16,446
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