| 2008 |
THM1/TTC21B encodes a tetratricopeptide repeat-containing protein that localizes to primary cilia and is required for retrograde intraflagellar transport (IFT). Loss of THM1 in mouse (alien mutant) causes bulb-like structures at cilia tips where IFT proteins (e.g., IFT88) are sequestered, characteristic of retrograde IFT failure. RNAi knockdown of Ttc21b in IMCD cells expressing IFT88-EYFP recapitulated the cilial phenotype, and live imaging confirmed impaired retrograde IFT velocity. |
ENU mutagenesis (aln mouse), RNAi knockdown, live fluorescence imaging of IFT88-EYFP, immunolocalization |
Nature genetics |
High |
18327258
|
| 2008 |
THM1/TTC21B negatively modulates Sonic Hedgehog (SHH) signaling. In aln mutant cilia lacking functional THM1, Smoothened and full-length GLI proteins accumulate in cilia, and SHH pathway is overactivated. This uncouples anterograde IFT (required for GLI activation) from retrograde IFT (which modulates/restrains GLI activation), positioning TTC21B as a retrograde IFT-dependent negative modulator of SHH signaling. |
ENU mutagenesis mouse model, immunofluorescence localization of Smoothened and GLI proteins in cilia, pathway reporter assays |
Nature genetics |
High |
18327258
|
| 2009 |
Loss of Ttc21b in mouse causes elevated SHH signaling in the rostral forebrain, including near the zona limitans intrathalamica. Reducing Shh ligand levels genetically ameliorated the forebrain patterning defects, establishing that the Ttc21b brain phenotype is caused by excessive SHH signaling downstream of impaired retrograde IFT. |
ENU mutant mouse, genetic epistasis (reducing Shh dosage), in situ hybridization, immunohistochemistry |
Developmental biology |
High |
19732765
|
| 2011 |
TTC21B encodes the retrograde IFT protein IFT139. Mutations in TTC21B cause both isolated nephronophthisis and syndromic Jeune asphyxiating thoracic dystrophy. In vivo (zebrafish) and in vitro functional evaluations showed that a significant enrichment of pathogenic alleles from ciliopathy cases were functionally deleterious, establishing TTC21B as both a causal ciliopathy gene and a modifier allele contributor across the ciliopathy spectrum. |
Resequencing of a large ciliopathy cohort, zebrafish in vivo complementation assays, in vitro functional evaluation of variants |
Nature genetics |
High |
21258341
|
| 2014 |
IFT139 (TTC21B protein) localizes to the base of the primary cilium in developing/undifferentiated podocytes, and relocates along extended microtubule networks in non-ciliated adult/differentiated podocytes. Knockdown of IFT139 in podocytes causes primary cilia defects, abnormal cell migration, and cytoskeleton alterations. The p.P209L mutation partially rescues these defects, demonstrating its hypomorphic nature. |
Immunofluorescence localization in human fetal tissue and cultured podocytes, siRNA knockdown, cell migration assay, rescue by overexpression of wild-type and mutant constructs |
Journal of the American Society of Nephrology : JASN |
High |
24876116
|
| 2017 |
In the developing cerebellum, Ttc21b ablation in Bergmann glia (not just neurons) causes accumulation of ectopic granule cells and, unexpectedly, a reduction in SHH signaling—indicating that in some cellular contexts Ttc21b augments rather than attenuates SHH signaling. This context-dependent role was confirmed by cell-type-specific conditional ablation. |
Conditional (Cre-mediated) knockout in Bergmann glia and Purkinje cells, immunohistochemistry, cerebellar histology |
Journal of developmental biology |
Medium |
29615573
|
| 2019 |
Gpr63, an orphan GPCR, is a genetic modifier of Ttc21b microcephaly. GPR63 can localize to primary cilia, and alleles affecting its ciliary localization genetically interact with Ttc21b null alleles to cause spina bifida aperta and earlier embryonic lethality, linking ciliary GPR63 function to TTC21B-dependent neural development. |
QTL mapping, congenic strain construction, CRISPR-Cas9 allele generation, in vitro ciliary localization assay, genetic interaction (double mutant phenotype analysis) |
PLoS genetics |
Medium |
31730647
|
| 2021 |
THM2 (paralog of THM1/TTC21B) localizes to primary cilia and genetically interacts with Thm1: compound Thm2-/-; Thm1aln/+ mice exhibit impaired chondrocyte differentiation and increased Hedgehog signaling in the growth plate, with defective bone nodule formation in osteoblasts. Deletion of one Gli2 allele exacerbated the small phenotype, suggesting Thm2 and Thm1 interact in the Hedgehog pathway during skeletogenesis. |
Mouse genetics (double/triple mutant), micro-CT, radiography, immunohistochemistry, primary osteoblast cultures, genetic epistasis with Gli2 |
Cellular and molecular life sciences : CMLS |
Medium |
33683377
|
| 2022 |
Deletion of Ttc21b in adult (but not juvenile) ADPKD mice markedly attenuates kidney cystogenesis and reduces cilia length, inflammation, and O-GlcNAc levels, revealing that the IFT-A component TTC21B is required for pathological cilia maintenance in mature kidney tubules and that its effect on ADPKD severity is development-stage-specific. |
Conditional/global Ttc21b deletion in juvenile and adult Pkd1 mutant ADPKD mouse models, kidney histology, cilia length measurement, O-GlcNAc immunoblot, inflammatory marker analysis |
Kidney international |
Medium |
35644283
|
| 2025 |
TTC21B compound heterozygous mutations (p.C299R and p.C518R) disrupt ciliogenesis and shorten ciliary length in renal podocytes in vitro. Wild-type TTC21B fully rescues podocyte morphology defects caused by TTC21B knockdown, while each mutant only partially rescues, confirming their hypomorphic/loss-of-function effect on ciliogenesis. |
In vitro rescue experiments in podocytes (TTC21B knockdown + overexpression of wild-type or mutant), ciliogenesis assay (cilia number/length measurement), morphology quantification; bioinformatics structural analysis of mutants |
Frontiers in genetics |
Medium |
41378128
|
| 2025 |
Ttc21b null mouse embryos exhibit microcephaly caused by disrupted neural progenitor proliferation and differentiation in the forebrain: enlarged ventricular zone, reduced cortical plate, fewer TBR2-positive intermediate progenitors, altered mitotic spindle angles (symmetric vs. asymmetric division defects), and shortened neuronal processes in the cortical plate. Early embryonic Ttc21b expression in neural precursors is required for perdurant TTC21B protein to sustain later progenitor proliferation. |
Ttc21b null mouse (alien allele), immunohistochemistry (TBR2, TBR1, mitotic markers), histology, progenitor proliferation kinetics (BrdU/EdU labeling), spindle angle measurement |
Disease models & mechanisms |
Medium |
41384431
|
| 2025 |
SPECC1L and TTC21B/THM1 genetically interact: double or compound heterozygotes for Specc1l and Thm1 exhibit higher penetrance of cleft palate than Specc1l heterozygotes alone. Elevated F-actin caused by Specc1l loss negatively regulates primary cilia length, and reduced F-actin at the ciliary base in Specc1l mutant cells accompanies cilia shortening, suggesting cytoskeletal-ciliary crosstalk converges on Thm1-dependent IFT-A function. |
Double heterozygous mouse genetics, F-actin staining, cilia length measurement, F-actin depolymerization rescue experiment |
bioRxivpreprint |
Low |
41278885
|