MED29 mediator complex subunit 29

Information
Symbol
MED29
Type
protein-coding
Description
mediator complex subunit 29
Entrez Gene ID
55588
Genome
hg19
Position
chr19:39,882,018-39,891,281
Genome
hg38
Position
chr19:39,391,378-39,400,641
MIM
612914 OMIM
HGNC
HGNC:23074 HGNC
Ensembl
ENSG00000063322 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
26
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 IXL
SYNONYM MED2
MIM 612914 OMIM
HGNC HGNC:23074 HGNC
Ensembl ENSG00000063322 Ensembl
AllianceGenome HGNC:23074
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000615911.4 hg38 chr19 39,391,323 39,400,561 9,239
ENST00000315588.11 hg38 chr19 39,391,378 39,400,641 9,264
ENST00000594368.5 hg38 chr19 39,391,393 39,398,607 7,215
ENST00000615911.4 hg19 chr19 39,881,963 39,891,201 9,239
ENST00000315588.11 hg19 chr19 39,882,018 39,891,281 9,264
ENST00000594368.5 hg19 chr19 39,882,033 39,889,247 7,215
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