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WormBase Tree Display for Gene: HGNC:29262

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Name Class

HGNC:29262IdentityNameCGC_nameIft80Inferred_automaticallyAGR_import
Other_name (12)
Public_nameIft80
DB_infoDatabaseHGNCid29262
AGRcURIHGNC:29262
EnsEMBLENSEMBL_geneIDENSG00000068885
UniProtUniProt_ACQ9P2H3
OMIMgene611177
DOidDOID:0110086
SpeciesHomo sapiens
StatusLive
Gene_infoBiotypeSO:0001217
OrthologWBGene00000484Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
Structured_descriptionAutomated_descriptionThe protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]Inferred_automaticallyAGR_import