FOXQ1 forkhead box Q1

Information
Symbol
FOXQ1
Type
protein-coding
Description
forkhead box Q1
Entrez Gene ID
94234
Genome
hg19
Position
chr6:1,312,333-1,314,993
Genome
hg38
Position
chr6:1,312,098-1,314,758
MIM
612788 OMIM
HGNC
HGNC:20951 HGNC
Ensembl
ENSG00000164379 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 84
Ranking
ClinVar
0
0
0
96
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 :
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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 :
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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 HFH1
MIM 612788 OMIM
HGNC HGNC:20951 HGNC
Ensembl ENSG00000164379 Ensembl
AllianceGenome HGNC:20951
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000296839.5 hg38 chr6 1,312,098 1,314,758 2,661
ENST00000296839.5 hg19 chr6 1,312,333 1,314,993 2,661
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