SLC29A2 solute carrier family 29 member 2

Information
Symbol
SLC29A2
Type
protein-coding
Description
solute carrier family 29 member 2
Entrez Gene ID
3177
Genome
hg19
Position
chr11:66,129,994-66,139,685
Genome
hg38
Position
chr11:66,362,523-66,372,214
MIM
602110 OMIM
HGNC
HGNC:11004 HGNC
Ensembl
ENSG00000174669 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
48
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 DER12
SYNONYM ENT2
SYNONYM HNP36
SYNONYM hENT2
MIM 602110 OMIM
HGNC HGNC:11004 HGNC
Ensembl ENSG00000174669 Ensembl
AllianceGenome HGNC:11004
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000546034.1 hg38 chr11 66,362,523 66,372,214 9,692
ENST00000619145.4 hg38 chr11 66,362,522 66,371,820 9,299
ENST00000311161.11 hg38 chr11 66,362,521 66,372,099 9,579
ENST00000357440.7 hg38 chr11 66,362,521 66,371,760 9,240
ENST00000544554.5 hg38 chr11 66,362,522 66,372,174 9,653
ENST00000357440.7 hg19 chr11 66,129,992 66,139,231 9,240
ENST00000311161.11 hg19 chr11 66,129,992 66,139,570 9,579
ENST00000619145.4 hg19 chr11 66,129,993 66,139,291 9,299
ENST00000544554.5 hg19 chr11 66,129,993 66,139,645 9,653
ENST00000546034.1 hg19 chr11 66,129,994 66,139,685 9,692
Genome browser