SLC39A7 solute carrier family 39 member 7

Information
Symbol
SLC39A7
Type
protein-coding
Description
solute carrier family 39 member 7
Entrez Gene ID
7922
Genome
hg19
Position
chr6:33,168,644-33,172,214
Genome
hg38
Position
chr6:33,200,867-33,204,437
MIM
601416 OMIM
HGNC
HGNC:4927 HGNC
Ensembl
ENSG00000112473 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 8
Benign 0 22
Likely benign 0 152
Conflicting classifications of pathogenicity 0 4
not provided 3 2
Uncertain significance 0 182
Ranking
ClinVar
0
0
30
330
6
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 AGM9
SYNONYM D6S115E
SYNONYM D6S2244E
SYNONYM H2-KE4
SYNONYM HKE4
SYNONYM KE4
SYNONYM RING5
SYNONYM ZIP7
MIM 601416 OMIM
HGNC HGNC:4927 HGNC
Ensembl ENSG00000112473 Ensembl
AllianceGenome HGNC:4927
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000374675.7 hg38 chr6 33,200,826 33,204,439 3,614
ENST00000374677.8 hg38 chr6 33,200,867 33,204,437 3,571
ENST00000698687.1 hg38 chr6 33,200,887 33,204,415 3,529
ENST00000698680.1 hg38 chr6 33,200,826 33,204,376 3,551
ENST00000698680.1 hg19 chr6 33,168,603 33,172,153 3,551
ENST00000374675.7 hg19 chr6 33,168,603 33,172,216 3,614
ENST00000374677.8 hg19 chr6 33,168,644 33,172,214 3,571
ENST00000698687.1 hg19 chr6 33,168,664 33,172,192 3,529
Genome browser