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Fig. 4 | Orphanet Journal of Rare Diseases

Fig. 4

From: Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease

Fig. 4

Localization of identified IFT140 variants (Refseq NM_014714.4). Schematic representation of the gene structure of IFT140. Light grey blocks represent the exons (upper panel). The lower panel shows a schematic of IFT140 protein. The protein contains five WD repeats and nine tetratricopeptide (TRP) repeats. Stars and lines indicate the positions of the detected IFT140 variants

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172