Gene Gene information from NCBI Gene database.
Entrez ID 131368
Gene name Zona pellucida like domain containing 1
Gene symbol ZPLD1
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3q12.3
miRNA miRNA information provided by mirtarbase database.
45
miRTarBase ID miRNA Experiments Reference
MIRT018809 hsa-miR-335-5p Microarray 18185580
MIRT019492 hsa-miR-148b-3p Microarray 17612493
MIRT1543377 hsa-miR-153 CLIP-seq
MIRT1543378 hsa-miR-19a CLIP-seq
MIRT1543379 hsa-miR-19b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0009986 Component Cell surface IBA
GO:0016020 Component Membrane IEA
GO:0030659 Component Cytoplasmic vesicle membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
615915 27022 ENSG00000170044
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TCW7
Protein name Zona pellucida-like domain-containing protein 1 (ZP domain-containing protein 1) (Cupulin) [Cleaved into: Zona pellucida-like domain-containing protein 1, secreted form]
Protein function Glycoprotein which is a component of the gelatinous extracellular matrix in the cupulae of the vestibular organ.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00100 Zona_pellucida 44 314 Zona pellucida-like domain Family
Tissue specificity TISSUE SPECIFICITY: Detected in placenta, kidney, lung, pancreas and at very low level in other tissues. {ECO:0000269|PubMed:18632209}.
Sequence
Sequence length 415
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
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
AMBLYOPIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Hepatocellular carcinoma Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Hypesthesia Associate 23834954
★☆☆☆☆
Found in Text Mining only
Obesity Associate 20950786
★☆☆☆☆
Found in Text Mining only
Paresthesia Associate 23834954
★☆☆☆☆
Found in Text Mining only