TTC21B

TTC21B

tetratricopeptide repeat domain 21B

HCNC Approved Symbol: TTC21B (HGNC:25660)
Genomic Coordinates: 2:165,873,362 - 165,953,776 (2q24.3)
Synonyms: FLJ11457, JBTS11, NPHP12, IFT139B, THM1, FAP60, FLA17, IFT139, CFAP60
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the TTC21B gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

02
Patient count

End stage renal disease: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Abnormal renal morphology: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)
Kidney malformation: 1 (50.0%)
Patient Count: 1 (50.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (50.0%)

Last updated: 2024-06-30