Gene Gene information from NCBI Gene database.
Entrez ID 126402
Gene name Tektin like 1
Gene symbol TEKTL1
Synonyms (NCBI Gene)
CCDC105
Chromosome 19
Chromosome location 19p13.12
miRNA miRNA information provided by mirtarbase database.
3
miRTarBase ID miRNA Experiments Reference
MIRT867331 hsa-miR-374a CLIP-seq
MIRT867332 hsa-miR-374b CLIP-seq
MIRT867333 hsa-miR-944 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005856 Component Cytoskeleton IEA
GO:0005929 Component Cilium IEA
GO:0030317 Process Flagellated sperm motility IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IYK2
Protein name Tektin-like protein 1 (Coiled-coil domain-containing protein 105)
Protein function Microtubule inner protein (MIP) part of the dynein-decorated doublet microtubules (DMTs) in sperm flagellar axoneme, which is required for motile flagellum beating (By similarity). Forms an extensive interaction network cross-linking the lumen o
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03148 Tektin 115 468 Family
Sequence
Sequence length 499
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
BRONCHIAL DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BRONCHITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations