DLX4 distal-less homeobox 4

Information
Symbol
DLX4
Type
protein-coding
Description
distal-less homeobox 4
Entrez Gene ID
1748
Genome
hg19
Position
chr17:48,046,554-48,052,323
Genome
hg38
Position
chr17:49,969,190-49,974,959
MIM
601911 OMIM
HGNC
HGNC:2917 HGNC
Ensembl
ENSG00000108813 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 4
Likely benign 0 24
Uncertain significance 0 48
Ranking
ClinVar
0
0
8
62
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 BP1
SYNONYM DLX7
SYNONYM DLX8
SYNONYM DLX9
SYNONYM OFC15
MIM 601911 OMIM
HGNC HGNC:2917 HGNC
Ensembl ENSG00000108813 Ensembl
AllianceGenome HGNC:2917
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000411890.3 hg38 chr17 49,972,766 49,974,600 1,835
ENST00000240306.5 hg38 chr17 49,969,190 49,974,959 5,770
ENST00000611342.1 hg38 chr17 49,972,939 49,974,600 1,662
ENST00000240306.5 hg19 chr17 48,046,554 48,052,323 5,770
ENST00000411890.3 hg19 chr17 48,050,130 48,051,964 1,835
ENST00000611342.1 hg19 chr17 48,050,303 48,051,964 1,662
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