FAT3 FAT atypical cadherin 3

Information
Symbol
FAT3
Type
protein-coding
Description
FAT atypical cadherin 3
Entrez Gene ID
120114
Genome
hg19
Position
chr11:91,957,984-92,629,639
Genome
hg38
Position
chr11:92,224,818-92,896,473
MIM
612483 OMIM
HGNC
HGNC:23112 HGNC
Ensembl
ENSG00000165323 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 90
Likely benign 0 136
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 434
Ranking
ClinVar
0
0
58
590
2
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 CDHF15
SYNONYM CDHR10
SYNONYM hFat3
MIM 612483 OMIM
HGNC HGNC:23112 HGNC
Ensembl ENSG00000165323 Ensembl
AllianceGenome HGNC:23112
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409404.6 hg38 chr11 92,352,096 92,896,452 544,357
ENST00000533797.1 hg38 chr11 92,844,340 92,896,305 51,966
ENST00000525166.6 hg38 chr11 92,224,818 92,896,473 671,656
ENST00000525166.6 hg19 chr11 91,957,984 92,629,639 671,656
ENST00000409404.6 hg19 chr11 92,085,262 92,629,618 544,357
ENST00000533797.1 hg19 chr11 92,577,506 92,629,471 51,966
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