HOXA4 homeobox A4

Information
Symbol
HOXA4
Type
protein-coding
Description
homeobox A4
Entrez Gene ID
3201
Genome
hg19
Position
chr7:27,168,144-27,170,376
Genome
hg38
Position
chr7:27,128,525-27,130,757
MIM
142953 OMIM
HGNC
HGNC:5105 HGNC
Ensembl
ENSG00000197576 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 20
Likely benign 0 14
Uncertain significance 0 74
Ranking
ClinVar
0
0
2
106
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 HOX1
SYNONYM HOX1D
MIM 142953 OMIM
HGNC HGNC:5105 HGNC
Ensembl ENSG00000197576 Ensembl
AllianceGenome HGNC:5105
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000360046.10 hg38 chr7 27,128,525 27,130,757 2,233
ENST00000610970.1 hg38 chr7 27,128,507 27,130,780 2,274
ENST00000610970.1 hg19 chr7 27,168,126 27,170,399 2,274
ENST00000360046.10 hg19 chr7 27,168,144 27,170,376 2,233
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