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MGI:Ift88

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Ift88 ( synonyms: fxo, IFT88, Oak Ridge polycystic kidneys, orpk, polaris, Tg737, Tg737Rpw, TgN737Rpw, Ttc10 )
Protein Name(s) intraflagellar transport 88 homolog (Chlamydomonas),
External Links
MGI MGI:98715

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001701

in utero embryonic development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0001701

in utero embryonic development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0003382

epithelial cell morphogenesis

MGI:MGI:4940123
PMID:21285373[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0005515

protein binding

MGI:MGI:1926671
PMID:11062270[3]

IPI: Inferred from Physical Interaction

UniProtKB:Q6VH22

F

From MGI

GO:0005737

cytoplasm

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0963

C

From MGI

GO:0005814

centriole

MGI:MGI:4457459
PMID:20230748[4]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005856

cytoskeleton

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0206

C

From MGI

GO:0005929

cilium

MGI:MGI:3692156
PMID:16254602[5]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005929

cilium

MGI:MGI:4457459
PMID:20230748[4]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005930

axoneme

MGI:MGI:2664063
PMID:11251073[6]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005932

microtubule basal body

MGI:MGI:2158985
PMID:11854326[7]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005932

microtubule basal body

MGI:MGI:2664063
PMID:11251073[6]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005932

microtubule basal body

MGI:MGI:4457459
PMID:20230748[4]

IDA: Inferred from Direct Assay

C

From MGI

GO:0007224

smoothened signaling pathway

MGI:MGI:3579954
PMID:15930098[8]

IGI: Inferred from Genetic Interaction

MGI:MGI:98297

P

From MGI

GO:0007224

smoothened signaling pathway

MGI:MGI:3579954
PMID:15930098[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0007224

smoothened signaling pathway

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0007368

determination of left/right symmetry

MGI:MGI:1855904
PMID:10804177[9]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1859153

P

From MGI

GO:0007368

determination of left/right symmetry

MGI:MGI:3577662
PMID:15755804[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0007399

nervous system development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0007399

nervous system development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0007420

brain development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0009887

organ morphogenesis

MGI:MGI:3045643
PMID:15226261[11]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0009952

anterior/posterior pattern specification

MGI:MGI:2660994
PMID:12701101[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0009952

anterior/posterior pattern specification

MGI:MGI:3579954
PMID:15930098[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0009953

dorsal/ventral pattern formation

MGI:MGI:3577662
PMID:15755804[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0009953

dorsal/ventral pattern formation

MGI:MGI:3579954
PMID:15930098[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0016485

protein processing

MGI:MGI:3692156
PMID:16254602[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1859153

P

From MGI

GO:0019861

flagellum

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0282

C

From MGI

GO:0021537

telencephalon development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0030030

cell projection organization

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0970

P

From MGI

GO:0030324

lung development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0031512

motile primary cilium

MGI:MGI:3806189
PMID:18590716[13]

IDA: Inferred from Direct Assay

C

From MGI

GO:0031512

motile primary cilium

MGI:MGI:5009180
PMID:12802074[14]

IDA: Inferred from Direct Assay

C

From MGI

GO:0032391

photoreceptor connecting cilium

MGI:MGI:3839506
PMID:19208653[15]

IDA: Inferred from Direct Assay

C

From MGI

GO:0032391

photoreceptor connecting cilium

MGI:MGI:4460838
PMID:20368623[16]

IDA: Inferred from Direct Assay

C

From MGI

GO:0035085

cilium axoneme

MGI:MGI:4460838
PMID:20368623[16]

IDA: Inferred from Direct Assay

C

From MGI

GO:0035085

cilium axoneme

MGI:MGI:5009180
PMID:12802074[14]

IDA: Inferred from Direct Assay

C

From MGI

GO:0042487

regulation of odontogenesis of dentin-containing tooth

MGI:MGI:2660994
PMID:12701101[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:2660994
PMID:12701101[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:3577662
PMID:15755804[10]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:3579954
PMID:15930098[8]

IGI: Inferred from Genetic Interaction

MGI:MGI:98297

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:3579954
PMID:15930098[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:3692156
PMID:16254602[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0042733

embryonic digit morphogenesis

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0042995

cell projection

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0966

C

From MGI

GO:0045177

apical part of cell

MGI:MGI:5009180
PMID:12802074[14]

IDA: Inferred from Direct Assay

C

From MGI

GO:0045862

positive regulation of proteolysis

MGI:MGI:3579954
PMID:15930098[8]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3027342

P

From MGI

GO:0048568

embryonic organ development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0048598

embryonic morphogenesis

MGI:MGI:3579954
PMID:15930098[8]

IGI: Inferred from Genetic Interaction

MGI:MGI:98297

P

From MGI

GO:0048853

forebrain morphogenesis

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0060271

cilium morphogenesis

MGI:MGI:1926671
PMID:11062270[3]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0060271

cilium morphogenesis

MGI:MGI:3692156
PMID:16254602[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:1859153

P

From MGI

GO:0060271

cilium morphogenesis

MGI:MGI:4940123
PMID:21285373[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2157527

P

From MGI

GO:0060411

cardiac septum morphogenesis

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI

GO:0060426

lung vasculature development

MGI:MGI:3821634
PMID:19036983[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3823090

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 Willaredt MA et al. (2008) A crucial role for primary cilia in cortical morphogenesis. J Neurosci 28: 12887-900 PubMed GONUTS page
  2. 2.0 2.1 Blitzer AL et al. (2011) Primary cilia dynamics instruct tissue patterning and repair of corneal endothelium. Proc Natl Acad Sci U S A 108: 2819-24 PubMed GONUTS page
  3. 3.0 3.1 Pazour GJ et al. (2000) Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J Cell Biol 151: 709-18 PubMed GONUTS page
  4. 4.0 4.1 4.2 Singla V et al. (2010) Ofd1, a human disease gene, regulates the length and distal structure of centrioles. Dev Cell 18: 410-24 PubMed GONUTS page
  5. 5.0 5.1 5.2 5.3 Haycraft CJ et al. (2005) Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet 1: e53 PubMed GONUTS page
  6. 6.0 6.1 Taulman PD et al. (2001) Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia. Mol Biol Cell 12: 589-99 PubMed GONUTS page
  7. Hou X et al. (2002) Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. J Clin Invest 109: 533-40 PubMed GONUTS page
  8. 8.0 8.1 8.2 8.3 8.4 8.5 8.6 8.7 Liu A et al. (2005) Mouse intraflagellar transport proteins regulate both the activator and repressor functions of Gli transcription factors. Development 132: 3103-11 PubMed GONUTS page
  9. Murcia NS et al. (2000) The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. Development 127: 2347-55 PubMed GONUTS page
  10. 10.0 10.1 10.2 García-García MJ et al. (2005) Analysis of mouse embryonic patterning and morphogenesis by forward genetics. Proc Natl Acad Sci U S A 102: 5913-9 PubMed GONUTS page
  11. Cano DA et al. (2004) Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization. Development 131: 3457-67 PubMed GONUTS page
  12. 12.0 12.1 12.2 Zhang Q et al. (2003) Loss of the Tg737 protein results in skeletal patterning defects. Dev Dyn 227: 78-90 PubMed GONUTS page
  13. Cho A et al. (2008) FKBP8 cell-autonomously controls neural tube patterning through a Gli2- and Kif3a-dependent mechanism. Dev Biol 321: 27-39 PubMed GONUTS page
  14. 14.0 14.1 14.2 Perrone CA et al. (2003) A novel dynein light intermediate chain colocalizes with the retrograde motor for intraflagellar transport at sites of axoneme assembly in chlamydomonas and Mammalian cells. Mol Biol Cell 14: 2041-56 PubMed GONUTS page
  15. Jiang ST et al. (2009) Essential role of nephrocystin in photoreceptor intraflagellar transport in mouse. Hum Mol Genet 18: 1566-77 PubMed GONUTS page
  16. 16.0 16.1 Sedmak T & Wolfrum U (2010) Intraflagellar transport molecules in ciliary and nonciliary cells of the retina. J Cell Biol 189: 171-86 PubMed GONUTS page
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