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    IFT22 intraflagellar transport 22 [ Homo sapiens (human) ]

    Gene ID: 64792, updated on 10-Dec-2024

    Summary

    Official Symbol
    IFT22provided by HGNC
    Official Full Name
    intraflagellar transport 22provided by HGNC
    Primary source
    HGNC:HGNC:21895
    See related
    Ensembl:ENSG00000128581 MIM:620505; AllianceGenome:HGNC:21895
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    FAP9; CFAP9; RABL5
    Summary
    Predicted to enable GTPase activity. Predicted to be involved in intracellular protein transport. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Broad expression in testis (RPKM 22.2), thyroid (RPKM 11.1) and 21 other tissues See more
    Orthologs
    NEW
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    Try the new Transcript table

    Genomic context

    See IFT22 in Genome Data Viewer
    Location:
    7q22.1
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (101310914..101321823, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (102634389..102645291, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (100954195..100965104, complement)

    Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100933165-100933715 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26406 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100934773-100935682 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100935683-100936592 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100936593-100937501 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100937502-100938411 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:100940231-100941139 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100943223-100943888 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100945388-100946089 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100946090-100946792 Neighboring gene AZGP1 pseudogene 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:100952259-100953086 Neighboring gene lncRNA p53 regulated and ESC associated 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18483 Neighboring gene E2F1 mRNA stabilizing lncRNA Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18484 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101015900-101016438 Neighboring gene collagen type XXVI alpha 1 chain Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101029559-101030174 Neighboring gene Sharpr-MPRA regulatory region 586 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:101041899-101042500 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101044285-101044812 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101054568-101055111 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:101063681-101064232 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:101064233-101064784 Neighboring gene NANOG hESC enhancer GRCh37_chr7:101065582-101066107 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101079627-101080270 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101080271-101080912 Neighboring gene H3K27ac hESC enhancer GRCh37_chr7:101081787-101082746 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101104635-101105147 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101128605-101129258 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101129259-101129911 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101137182-101137752 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101137753-101138322 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101146871-101147560 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101147561-101148250 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101150569-101151328 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:101185407-101186075 Neighboring gene Sharpr-MPRA regulatory region 7535 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:101207140-101208002 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:101208003-101208864 Neighboring gene long intergenic non-protein coding RNA 1007

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • FLJ13225, FLJ14117, DKFZp761N0823

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables GTP binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables GTPase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Process Evidence Code Pubs
    involved_in cilium assembly NAS
    Non-traceable Author Statement
    more info
    PubMed 
    involved_in intracellular protein transport IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in intraciliary anterograde transport NAS
    Non-traceable Author Statement
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in centrosome IEA
    Inferred from Electronic Annotation
    more info
     
    located_in ciliary tip TAS
    Traceable Author Statement
    more info
     
    located_in cilium NAS
    Non-traceable Author Statement
    more info
    PubMed 
    located_in cilium TAS
    Traceable Author Statement
    more info
     
    is_active_in endomembrane system IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    part_of intraciliary transport particle B IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    part_of intraciliary transport particle B ISS
    Inferred from Sequence or Structural Similarity
    more info
     

    General protein information

    Preferred Names
    intraflagellar transport protein 22 homolog
    Names
    RAB, member RAS oncogene family-like 5
    RAB, member of RAS oncogene family-like 5
    intraflagellar transport 22 homolog
    rab-like protein 5

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_001130820.3NP_001124292.1  intraflagellar transport protein 22 homolog isoform b

      See identical proteins and their annotated locations for NP_001124292.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (2) lacks an alternate in-frame exon in the 5' coding region, compared to variant 1. It encodes isoform b, which is shorter than isoform a.
      Source sequence(s)
      AC006329, BC004522, CA841889, DA709553
      Consensus CDS
      CCDS47670.1
      UniProtKB/TrEMBL
      A8K889
      Related
      ENSP00000390770.2, ENST00000437644.2
      Conserved Domains (1) summary
      cl38936
      Location:591
      P-loop_NTPase; P-loop containing Nucleoside Triphosphate Hydrolases
    2. NM_001130821.3NP_001124293.1  intraflagellar transport protein 22 homolog isoform c

      See identical proteins and their annotated locations for NP_001124293.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at a downstream start codon, compared to variant 1. Variants 3 through 6 encode the same isoform (c), which is shorter at the N-terminus, compared to isoform a.
      Source sequence(s)
      AC006329, BC004522, CA841889, DA709553, DN993868
      Consensus CDS
      CCDS47671.1
    3. NM_001130822.3NP_001124294.1  intraflagellar transport protein 22 homolog isoform c

      See identical proteins and their annotated locations for NP_001124294.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at a downstream start codon, compared to variant 1. Variants 3 through 6 encode the same isoform (c), which is shorter at the N-terminus, compared to isoform a.
      Source sequence(s)
      AC006329, AK298888, CA841889, DA709553
      Consensus CDS
      CCDS47671.1
      Related
      ENSP00000429648.1, ENST00000498704.6
    4. NM_001287525.2NP_001274454.1  intraflagellar transport protein 22 homolog isoform c

      See identical proteins and their annotated locations for NP_001274454.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at a downstream start codon, compared to variant 1. Variants 3 through 6 encode the same isoform (c), which is shorter at the N-terminus, compared to isoform a.
      Source sequence(s)
      AC006329, AU133515, BC009823, CA841889, DA709553
      Consensus CDS
      CCDS47671.1
      Related
      ENSP00000429202.1, ENST00000517481.5
    5. NM_001287526.1NP_001274455.1  intraflagellar transport protein 22 homolog isoform c

      See identical proteins and their annotated locations for NP_001274455.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at a downstream start codon, compared to variant 1. Variants 3 through 6 encode the same isoform (c), which is shorter at the N-terminus, compared to isoform a.
      Source sequence(s)
      AC006329, CA841889, DA700693, DA709553
      Consensus CDS
      CCDS47671.1
      Related
      ENSP00000478948.1, ENST00000621899.4
    6. NM_022777.4NP_073614.1  intraflagellar transport protein 22 homolog isoform a

      See identical proteins and their annotated locations for NP_073614.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) encodes the longest isoform (a).
      Source sequence(s)
      AC006329, BC009823, CA841889, DA709553
      Consensus CDS
      CCDS5719.1
      UniProtKB/Swiss-Prot
      Q49AG1, Q69YV5, Q9BSW4, Q9H7X7
      UniProtKB/TrEMBL
      A8K889
      Related
      ENSP00000320359.4, ENST00000315322.10
      Conserved Domains (1) summary
      COG1100
      Location:1104
      Gem1; GTPase SAR1 family domain [General function prediction only]

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

      Range
      101310914..101321823 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060931.1 Alternate T2T-CHM13v2.0

      Range
      102634389..102645291 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)