F11R F11 receptor

Information
Symbol
F11R
Type
protein-coding
Description
F11 receptor
Entrez Gene ID
50848
Genome
hg19
Position
chr1:160,965,001-160,990,942
Genome
hg38
Position
chr1:160,995,211-161,021,152
MIM
605721 OMIM
HGNC
HGNC:14685 HGNC
Ensembl
ENSG00000158769 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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 :
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 CD321
SYNONYM JAM
SYNONYM JAM1
SYNONYM JAMA
SYNONYM JCAM
SYNONYM KAT
SYNONYM PAM-1
MIM 605721 OMIM
HGNC HGNC:14685 HGNC
Ensembl ENSG00000158769 Ensembl
AllianceGenome HGNC:14685
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000368026.11 hg38 chr1 160,995,211 161,021,152 25,942
ENST00000537746.1 hg38 chr1 160,998,402 161,021,096 22,695
ENST00000368026.11 hg19 chr1 160,965,001 160,990,942 25,942
ENST00000537746.1 hg19 chr1 160,968,192 160,990,886 22,695
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