FMNL3 formin like 3

Information
Symbol
FMNL3
Type
protein-coding
Description
formin like 3
Entrez Gene ID
91010
Genome
hg19
Position
chr12:50,030,282-50,101,188
Genome
hg38
Position
chr12:49,636,499-49,707,405
MIM
616288 OMIM
HGNC
HGNC:23698 HGNC
Ensembl
ENSG00000161791 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 1 0
Uncertain significance 0 160
Ranking
ClinVar
0
0
0
164
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
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 FHOD3
SYNONYM FRL2
SYNONYM WBP-3
SYNONYM WBP3
MIM 616288 OMIM
HGNC HGNC:23698 HGNC
Ensembl ENSG00000161791 Ensembl
AllianceGenome HGNC:23698
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335154.10 hg38 chr12 49,636,499 49,707,405 70,907
ENST00000352151.9 hg38 chr12 49,644,953 49,707,393 62,441
ENST00000550488.5 hg38 chr12 49,644,931 49,707,220 62,290
ENST00000335154.10 hg19 chr12 50,030,282 50,101,188 70,907
ENST00000550488.5 hg19 chr12 50,038,714 50,101,003 62,290
ENST00000352151.9 hg19 chr12 50,038,736 50,101,176 62,441
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