WormBase Tree Display for Gene: HGNC:29262
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HGNC:29262 | Identity | Name | CGC_name | Ift80 | Inferred_automatically | AGR_import |
---|---|---|---|---|---|---|
Other_name (12) | ||||||
Public_name | Ift80 | |||||
DB_info | Database | HGNC | id | 29262 | ||
AGR | cURI | HGNC:29262 | ||||
EnsEMBL | ENSEMBL_geneID | ENSG00000068885 | ||||
UniProt | UniProt_AC | Q9P2H3 | ||||
OMIM | gene | 611177 | ||||
DO | id | DOID:0110086 | ||||
Species | Homo sapiens | |||||
Status | Live | |||||
Gene_info | Biotype | SO:0001217 | ||||
Ortholog | WBGene00000484 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
Hieranoid | ||||||
Inparanoid | ||||||
OMA | ||||||
OrthoFinder | ||||||
OrthoInspector | ||||||
Panther | ||||||
PhylomeDB | ||||||
SonicParanoid | ||||||
Structured_description | Automated_description | The 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_automatically | AGR_import |