MAP7D2 MAP7 domain containing 2

Information
Symbol
MAP7D2
Type
protein-coding
Description
MAP7 domain containing 2
Entrez Gene ID
256714
Genome
hg19
Position
chrX:20,024,831-20,135,025
Genome
hg38
Position
chrX:20,006,713-20,116,907
HGNC
HGNC:25899 HGNC
Ensembl
ENSG00000184368 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
not provided 8 0
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
104
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
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
HGNC HGNC:25899 HGNC
Ensembl ENSG00000184368 Ensembl
AllianceGenome HGNC:25899
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000379651.7 hg38 chrX 20,006,713 20,116,898 110,186
ENST00000452324.3 hg38 chrX 20,008,339 20,116,632 108,294
ENST00000443379.7 hg38 chrX 20,008,038 20,116,904 108,867
ENST00000379643.10 hg38 chrX 20,006,713 20,116,907 110,195
ENST00000379651.7 hg19 chrX 20,024,831 20,135,016 110,186
ENST00000379643.10 hg19 chrX 20,024,831 20,135,025 110,195
ENST00000443379.7 hg19 chrX 20,026,156 20,135,022 108,867
ENST00000452324.3 hg19 chrX 20,026,457 20,134,750 108,294
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