Gene Gene information from NCBI Gene database.
Entrez ID 26472
Gene name Protein phosphatase 1 regulatory inhibitor subunit 14B
Gene symbol PPP1R14B
Synonyms (NCBI Gene)
PHI-1PLCB3NPNGSOM172
Chromosome 11
Chromosome location 11q13.1
miRNA miRNA information provided by mirtarbase database.
73
miRTarBase ID miRNA Experiments Reference
MIRT029319 hsa-miR-26b-5p Microarray 19088304
MIRT040374 hsa-miR-615-3p CLASH 23622248
MIRT1255918 hsa-miR-1275 CLIP-seq
MIRT1255919 hsa-miR-1914 CLIP-seq
MIRT1255920 hsa-miR-219-5p 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:0004864 Function Protein phosphatase inhibitor activity IEA
GO:0004865 Function Protein serine/threonine phosphatase inhibitor activity IBA
GO:0005515 Function Protein binding IPI 32707033, 33961781
GO:0005737 Component Cytoplasm IEA
GO:0019212 Function Phosphatase inhibitor activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601140 9057 ENSG00000173457
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96C90
Protein name Protein phosphatase 1 regulatory subunit 14B (Phospholipase C-beta-3 neighbouring gene protein)
Protein function Inhibitor of PPP1CA. Has over 50-fold higher inhibitory activity when phosphorylated (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05361 PP1_inhibitor 38 147 PKC-activated protein phosphatase-1 inhibitor Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Expressed at low levels. {ECO:0000269|PubMed:8838322}.
Sequence
Sequence length 147
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
Familial cancer of breast Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MELANOMA CTD
★★☆☆☆
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
Endometrial Neoplasms Endometrial neoplasm Pubtator 36824011 Associate
★☆☆☆☆
Found in Text Mining only
Endometriosis Endometriosis Pubtator 26059197 Stimulate
★☆☆☆☆
Found in Text Mining only
melanoma Melanoma CTD_human_DG 22535842
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Ovarian Neoplasms Ovarian neoplasm Pubtator 26059197 Stimulate
★☆☆☆☆
Found in Text Mining only
Triple Negative Breast Neoplasms Triple negative breast cancer Pubtator 36484700 Stimulate
★☆☆☆☆
Found in Text Mining only