Gene Gene information from NCBI Gene database.
Entrez ID 6954
Gene name T-complex 11
Gene symbol TCP11
Synonyms (NCBI Gene)
D6S230EFPPR
Chromosome 6
Chromosome location 6p21.31
miRNA miRNA information provided by mirtarbase database.
7
miRTarBase ID miRNA Experiments Reference
MIRT023346 hsa-miR-122-5p Microarray 17612493
MIRT1416684 hsa-miR-3921 CLIP-seq
MIRT1416685 hsa-miR-4303 CLIP-seq
MIRT1416686 hsa-miR-4537 CLIP-seq
MIRT1416687 hsa-miR-4653-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0001669 Component Acrosomal vesicle IBA
GO:0001669 Component Acrosomal vesicle IDA 21597245
GO:0001669 Component Acrosomal vesicle IEA
GO:0001669 Component Acrosomal vesicle ISS
GO:0005515 Function Protein binding IPI 21597245, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
186982 11658 ENSG00000124678
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8WWU5
Protein name T-complex protein 11 homolog
Protein function Plays a role in the process of sperm capacitation and acrosome reactions. Probable receptor for the putative fertilization-promoting peptide (FPP) at the sperm membrane that may modulate the activity of the adenylyl cyclase cAMP pathway. {ECO:00
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05794 Tcp11 58 487 T-complex protein 11 Family
Tissue specificity TISSUE SPECIFICITY: Isoform 2 and isoform 3 are expressed in sperm. Isoform 1 is not detected in sperm (at protein level) (PubMed:21597245). Testis-specific (PubMed:11756566). Isoform 1, isoform 2 and isoform 3 are expressed in sperm (PubMed:21597245). {E
Sequence
Sequence length 503
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
13
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHILDHOOD ONSET ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHRONIC RHINOSINUSITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GRAVES DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Lupus Erythematosus, Systemic Lupus Erythematosus GWASCAT_DG 28714469
★☆☆☆☆
Found in Text Mining only
Sarcoma Sarcoma Pubtator 28088687 Associate
★☆☆☆☆
Found in Text Mining only
Uterine Cervical Neoplasms Uterine neoplasm Pubtator 37697257 Associate
★☆☆☆☆
Found in Text Mining only