FGD6 FYVE, RhoGEF and PH domain containing 6

Information
Symbol
FGD6
Type
protein-coding
Description
FYVE, RhoGEF and PH domain containing 6
Entrez Gene ID
55785
Genome
hg19
Position
chr12:95,470,525-95,611,243
Genome
hg38
Position
chr12:95,076,749-95,217,467
MIM
613520 OMIM
HGNC
HGNC:21740 HGNC
Ensembl
ENSG00000180263 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 16
Uncertain significance 0 122
Ranking
ClinVar
0
0
0
146
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 :
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 ZFYVE24
MIM 613520 OMIM
HGNC HGNC:21740 HGNC
Ensembl ENSG00000180263 Ensembl
AllianceGenome HGNC:21740
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000343958.9 hg38 chr12 95,076,749 95,217,467 140,719
ENST00000546711.5 hg38 chr12 95,085,543 95,217,464 131,922
ENST00000549499.1 hg38 chr12 95,092,828 95,217,379 124,552
ENST00000343958.9 hg19 chr12 95,470,525 95,611,243 140,719
ENST00000546711.5 hg19 chr12 95,479,319 95,611,240 131,922
ENST00000549499.1 hg19 chr12 95,486,604 95,611,155 124,552
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