SLC39A10 solute carrier family 39 member 10

Information
Symbol
SLC39A10
Type
protein-coding
Description
solute carrier family 39 member 10
Entrez Gene ID
57181
Genome
hg19
Position
chr2:196,521,471-196,602,426
Genome
hg38
Position
chr2:195,656,747-195,737,702
MIM
608733 OMIM
HGNC
HGNC:20861 HGNC
Ensembl
ENSG00000196950 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
54
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 LZT-Hs2
SYNONYM ZIP10
MIM 608733 OMIM
HGNC HGNC:20861 HGNC
Ensembl ENSG00000196950 Ensembl
AllianceGenome HGNC:20861
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409086.7 hg38 chr2 195,656,747 195,737,702 80,956
ENST00000359634.10 hg38 chr2 195,657,226 195,737,700 80,475
ENST00000409086.7 hg19 chr2 196,521,471 196,602,426 80,956
ENST00000359634.10 hg19 chr2 196,521,950 196,602,424 80,475
Genome browser