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Genes search result for Homo sapiens
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2 records found for search term Ift88
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1320207IFT88intraflagellar transport 88This gene encodes a member of the tetratrico peptide repeat (TPR) family. The encoded protein is involved in cilium biogenesis. Mutations of a similar gene in mouse can cause polycystic kidney disease. Several transcript variants encoding distinct isoforms have been identified for this gene. [provid132056715720691444Human235symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
16568078AL590096.1novel transcript, antisense to IFT88Humannamegene, lncrna