Entity Details

Primary name TTC21A
Entity type gene
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Details

PrimaryID199223
RefseqGene
SymbolTTC21A
Nametetratricopeptide repeat domain 21A
Chromosome3
Location3p22.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-04-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTT21A_HUMAN

GO terms

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GOName
GO:0005929 cilium
GO:0007286 spermatid development
GO:0030317 flagellated sperm motility
GO:0030991 intraciliary transport particle A
GO:0035721 intraciliary retrograde transport
GO:0061512 protein localization to cilium

Diseases

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Disease IDSourceNameDescription
618429 OMIMSpermatogenic failure 37 (SPGF37)An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities, primarily consisting of short or absent flagella, and neck defects at the head-tail junction. The disease is caused by variants affecting the gene represented in this entry.