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Gene Gene information from NCBI Gene database.
Entrez ID 196463
Gene name Phospholipase B domain containing 2
Gene symbol PLBD2
Synonyms (NCBI Gene)
P76
Chromosome 12
Chromosome location 12q24.13
miRNA miRNA information provided by mirtarbase database.
323 Show/Hide all (323)
miRTarBase ID miRNA Experiments Reference
MIRT039950 hsa-miR-615-3p CLASH 23622248
MIRT531418 hsa-miR-3607-3p PAR-CLIP 22012620
MIRT531417 hsa-miR-4284 PAR-CLIP 22012620
MIRT531416 hsa-miR-4437 PAR-CLIP 22012620
MIRT531414 hsa-miR-3686 PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11 Show/Hide all (11)
GO ID Ontology Definition Evidence Reference
GO:0004620 Function Phospholipase activity IBA
GO:0004620 Function Phospholipase activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IBA
GO:0005764 Component Lysosome IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620097 27283 ENSG00000151176
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NHP8
Protein name Putative phospholipase B-like 2 (EC 3.1.1.-) (76 kDa protein) (p76) (LAMA-like protein 2) (Lamina ancestor homolog 2) (Phospholipase B domain-containing protein 2) [Cleaved into: Putative phospholipase B-like 2 32 kDa form; Putative phospholipase B-like 2
Protein function Putative phospholipase.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04916 Phospholip_B 55 → 586 Phospholipase B Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed, with highest levels in heart, brain and liver. {ECO:0000269|PubMed:17105447}.
Sequence
Sequence length 589
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
Familial cancer of breast Uncertain significance ClinVar —
★★★★★
★★☆☆☆
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
Ulcerative Colitis Ulcerative colitis BEFREE 18488086
★★★★★
★☆☆☆☆
Found in Text Mining only