FMNL1 formin like 1

Information
Symbol
FMNL1
Type
protein-coding
Description
formin like 1
Entrez Gene ID
752
Genome
hg19
Position
chr17:43,299,176-43,324,685
Genome
hg38
Position
chr17:45,221,809-45,247,318
MIM
604656 OMIM
HGNC
HGNC:1212 HGNC
Ensembl
ENSG00000184922 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 112
Ranking
ClinVar
0
0
0
120
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
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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 C17orf1
SYNONYM C17orf1B
SYNONYM FHOD4
SYNONYM FMNL
SYNONYM KW-13
MIM 604656 OMIM
HGNC HGNC:1212 HGNC
Ensembl ENSG00000184922 Ensembl
AllianceGenome HGNC:1212
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000587489.6 hg38 chr17 45,221,809 45,247,318 25,510
ENST00000331495.8 hg38 chr17 45,221,885 45,247,318 25,434
ENST00000587489.6 hg19 chr17 43,299,176 43,324,685 25,510
ENST00000331495.8 hg19 chr17 43,299,252 43,324,685 25,434
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