FXR2 FMR1 autosomal homolog 2

Information
Symbol
FXR2
Type
protein-coding
Description
FMR1 autosomal homolog 2
Entrez Gene ID
9513
Genome
hg19
Position
chr17:7,494,548-7,518,215
Genome
hg38
Position
chr17:7,591,230-7,614,897
MIM
605339 OMIM
HGNC
HGNC:4024 HGNC
Ensembl
ENSG00000129245 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 8
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
84
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 :
Search word :
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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 FMR1L2
SYNONYM FXR2P
MIM 605339 OMIM
HGNC HGNC:4024 HGNC
Ensembl ENSG00000129245 Ensembl
AllianceGenome HGNC:4024
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000250113.12 hg38 chr17 7,591,230 7,614,897 23,668
ENST00000704984.1 hg38 chr17 7,591,230 7,614,897 23,668
ENST00000250113.12 hg19 chr17 7,494,548 7,518,215 23,668
ENST00000704984.1 hg19 chr17 7,494,548 7,518,215 23,668
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