ALX4 ALX homeobox 4

Information
Symbol
ALX4
Type
protein-coding
Description
ALX homeobox 4
Entrez Gene ID
60529
Genome
hg19
Position
chr11:44,281,990-44,331,689
Genome
hg38
Position
chr11:44,260,440-44,310,139
MIM
605420 OMIM
HGNC
HGNC:450 HGNC
Ensembl
ENSG00000052850 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 32
Likely pathogenic 0 8
Benign 6 166
Likely benign 0 96
Conflicting classifications of pathogenicity 0 6
risk factor 0 4
Uncertain significance 0 244
Ranking
ClinVar
0
0
76
430
30
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
SYNONYM CRS5
SYNONYM FND2
MIM 605420 OMIM
HGNC HGNC:450 HGNC
Ensembl ENSG00000052850 Ensembl
AllianceGenome HGNC:450
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000652299.1 hg38 chr11 44,260,440 44,310,139 49,700
ENST00000652299.1 hg19 chr11 44,281,990 44,331,689 49,700
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