FAM168A family with sequence similarity 168 member A

Information
Symbol
FAM168A
Type
protein-coding
Description
family with sequence similarity 168 member A
Entrez Gene ID
23201
Genome
hg19
Position
chr11:73,111,532-73,309,234
Genome
hg38
Position
chr11:73,400,487-73,598,189
MIM
616316 OMIM
HGNC
HGNC:28999 HGNC
Ensembl
ENSG00000054965 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
14
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 KIAA0280
SYNONYM TCRP1
MIM 616316 OMIM
HGNC HGNC:28999 HGNC
Ensembl ENSG00000054965 Ensembl
AllianceGenome HGNC:28999
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000450446.6 hg38 chr11 73,405,983 73,598,098 192,116
ENST00000064778.8 hg38 chr11 73,400,487 73,598,189 197,703
ENST00000356467.5 hg38 chr11 73,400,487 73,598,112 197,626
ENST00000356467.5 hg19 chr11 73,111,532 73,309,157 197,626
ENST00000064778.8 hg19 chr11 73,111,532 73,309,234 197,703
ENST00000450446.6 hg19 chr11 73,117,028 73,309,143 192,116
Genome browser