Gene Gene information from NCBI Gene database.
Entrez ID 55851
Gene name Presenilin enhancer, gamma-secretase subunit
Gene symbol PSENEN
Synonyms (NCBI Gene)
ACNINV2MDS033MSTP064PEN-2PEN2
Chromosome 19
Chromosome location 19q13.12
Summary Presenilins, which are components of the gamma-secretase protein complex, are required for intramembranous processing of some type I transmembrane proteins, such as the Notch proteins and the beta-amyloid precursor protein. Signaling by Notch receptors me
miRNA miRNA information provided by mirtarbase database.
60
miRTarBase ID miRNA Experiments Reference
MIRT1269636 hsa-miR-1182 CLIP-seq
MIRT1269637 hsa-miR-1275 CLIP-seq
MIRT1269638 hsa-miR-1302 CLIP-seq
MIRT1269639 hsa-miR-1915 CLIP-seq
MIRT1269640 hsa-miR-214 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
48
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane NAS 15274632
GO:0005515 Function Protein binding IPI 15322109, 16641999, 18201567, 23685131, 30559186, 32296183, 32814053
GO:0005783 Component Endoplasmic reticulum IDA 15274632
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607632 30100 ENSG00000205155
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NZ42
Protein name Gamma-secretase subunit PEN-2 (Presenilin enhancer protein 2)
Protein function Essential subunit of the gamma-secretase complex, an endoprotease complex that catalyzes the intramembrane cleavage of integral membrane proteins such as Notch receptors and APP (amyloid-beta precursor protein) (PubMed:12522139, PubMed:12679784,
PDB 5A63 , 5FN2 , 5FN3 , 5FN4 , 5FN5 , 6IDF , 6IYC , 6LQG , 6LR4 , 7C9I , 7D8X , 7Y5T , 7Y5X , 7Y5Z , 8IM7 , 8K8E , 8KCO , 8KCP , 8KCS , 8KCT , 8KCU , 8OQY , 8OQZ , 8X52 , 8X53 , 8X54
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10251 PEN-2 7 99 Presenilin enhancer-2 subunit of gamma secretase Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Expressed in leukocytes, lung, placenta, small intestine, liver, kidney, spleen thymus, skeletal muscle, heart and brain. {ECO:0000269|PubMed:12110170, ECO:0000269|PubMed:12740439}.
Sequence
Sequence length 101
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Notch signaling pathway
Alzheimer disease
  Nuclear signaling by ERBB4
Regulated proteolysis of p75NTR
NRIF signals cell death from the nucleus
Constitutive Signaling by NOTCH1 PEST Domain Mutants
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
EPH-ephrin mediated repulsion of cells
NOTCH3 Activation and Transmission of Signal to the Nucleus
Noncanonical activation of NOTCH3
Amyloid fiber formation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
11
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acne inversa, familial, 2 Pathogenic rs1555738837, rs1555738943, rs1555738763, rs1555738906, rs1555738903, rs1555738836 RCV000023658
RCV000023659
RCV000515755
RCV000515757
RCV000515753
RCV000515756
RCV000515758
Squamous cell lung carcinoma Pathogenic rs1555738837 RCV005867794
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
PSENEN-related disorder Likely benign rs535099488 RCV003951994
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 12639958
Comedones Familial Dyskeratotic Associate 27900998
Dowling Degos Disease Associate 27900998
Hidradenitis Suppurativa Associate 27900998
Hidradenitis suppurativa familial Associate 27900998
Immunologic Deficiency Syndromes Inhibit 15286082
Neoplasms Associate 24223915
Neurodegenerative Diseases Associate 34964690