Gene Gene information from NCBI Gene database.
Entrez ID 81619
Gene name Tetraspanin 14
Gene symbol TSPAN14
Synonyms (NCBI Gene)
DC-TM4F2TM4SF14tspan-14
Chromosome 10
Chromosome location 10q23.1
miRNA miRNA information provided by mirtarbase database.
1102
miRTarBase ID miRNA Experiments Reference
MIRT020709 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT025376 hsa-miR-34a-5p Sequencing 20371350
MIRT027896 hsa-miR-96-5p Sequencing 20371350
MIRT030452 hsa-miR-24-3p Microarray 19748357
MIRT039092 hsa-miR-769-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 23091066, 26686862
GO:0005788 Component Endoplasmic reticulum lumen TAS
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 23091066
GO:0005886 Component Plasma membrane 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.
Q8NG11
Protein name Tetraspanin-14 (Tspan-14) (DC-TM4F2) (Transmembrane 4 superfamily member 14)
Protein function Part of TspanC8 subgroup, composed of 6 members that interact with the transmembrane metalloprotease ADAM10. This interaction is required for ADAM10 exit from the endoplasmic reticulum and for enzymatic maturation and trafficking to the cell sur
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00335 Tetraspanin 15 260 Tetraspanin family Family
Sequence
Sequence length 270
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Neutrophil degranulation
Amyloid fiber formation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
20
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ALZHEIMERS DISEASE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANKYLOSING SPONDYLITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 36951251, 37735198
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Breast Neoplasms Associate 34930307
★☆☆☆☆
Found in Text Mining only
Embolic Stroke Associate 35075378
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 34930307
★☆☆☆☆
Found in Text Mining only