ATOH7 atonal bHLH transcription factor 7

Information
Symbol
ATOH7
Type
protein-coding
Description
atonal bHLH transcription factor 7
Entrez Gene ID
220202
Genome
hg19
Position
chr10:69,990,352-69,991,870
Genome
hg38
Position
chr10:68,230,595-68,232,113
MIM
609875 OMIM
HGNC
HGNC:13907 HGNC
Ensembl
ENSG00000179774 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Benign 0 14
Likely benign 0 46
Uncertain significance 0 188
Ranking
ClinVar
0
0
16
234
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
[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 Math5
SYNONYM NCRNA
SYNONYM PHPVAR
SYNONYM RNANC
SYNONYM bHLHa13
MIM 609875 OMIM
HGNC HGNC:13907 HGNC
Ensembl ENSG00000179774 Ensembl
AllianceGenome HGNC:13907
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000373673.5 hg38 chr10 68,230,595 68,232,113 1,519
ENST00000373673.5 hg19 chr10 69,990,352 69,991,870 1,519
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