intraflagellar transport protein 74 homolog isoform c [Homo sapiens]

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Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations. [Hum Mol Genet. 2023]
Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations.
Fassad MR, Rumman N, Junger K, Patel MP, Thompson J, Goggin P, Ueffing M, Beyer T, Boldt K, Lucas JS, et al. Hum Mol Genet. 2023 Oct 17; 32(21):3090-3104.
Case Report: Second Report of Joubert Syndrome Caused by Biallelic Variants in IFT74. [Front Genet. 2021]
Case Report: Second Report of Joubert Syndrome Caused by Biallelic Variants in IFT74.
Zhongling K, Guoming L, Yanhui C, Xiaoru C. Front Genet. 2021; 12:738157. Epub 2021 Sep 1.
Third case of Bardet-Biedl syndrome caused by a biallelic variant predicted to affect splicing of IFT74. [Clin Genet. 2021]
Third case of Bardet-Biedl syndrome caused by a biallelic variant predicted to affect splicing of IFT74.
Mardy AH, Hodoglugil U, Yip T, Slavotinek AM. Clin Genet. 2021 Jul; 100(1):93-99. Epub 2021 Mar 27.

RefSeq genomic sequence
See the genomic reference sequence for the IFT74 gene (NG_053083.1).
RefSeq mRNA
See reference mRNA sequence for the IFT74 gene (NM_001349928.2).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the IFT74 gene.

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Protein