IFT22 intraflagellar transport 22

Information
Symbol
IFT22
Type
protein-coding
Description
intraflagellar transport 22
Entrez Gene ID
64792
Genome
hg19
Position
chr7:100,954,195-100,965,093
Genome
hg38
Position
chr7:101,310,914-101,321,812
MIM
620505 OMIM
HGNC
HGNC:21895 HGNC
Ensembl
ENSG00000128581 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
28
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 CFAP9
SYNONYM FAP9
SYNONYM RABL5
MIM 620505 OMIM
HGNC HGNC:21895 HGNC
Ensembl ENSG00000128581 Ensembl
AllianceGenome HGNC:21895
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000315322.10 hg38 chr7 101,310,914 101,321,812 10,899
ENST00000621899.4 hg38 chr7 101,313,367 101,321,823 8,457
ENST00000498704.6 hg38 chr7 101,314,753 101,321,764 7,012
ENST00000517481.5 hg38 chr7 101,314,175 101,321,776 7,602
ENST00000437644.2 hg38 chr7 101,314,795 101,321,777 6,983
ENST00000315322.10 hg19 chr7 100,954,195 100,965,093 10,899
ENST00000621899.4 hg19 chr7 100,956,648 100,965,104 8,457
ENST00000517481.5 hg19 chr7 100,957,456 100,965,057 7,602
ENST00000498704.6 hg19 chr7 100,958,034 100,965,045 7,012
ENST00000437644.2 hg19 chr7 100,958,076 100,965,058 6,983
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