Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55851
Gene name Gene Name - the full gene name approved by the HGNC.
Presenilin enhancer, gamma-secretase subunit
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PSENEN
Synonyms (NCBI Gene) Gene synonyms aliases
ACNINV2, MDS033, MSTP064, PEN-2, PEN2
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.12
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607632 30100 ENSG00000205155
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Acne Inversa Acne inversa, familial, 2 rs1555738903, rs1555738836, rs1555738837, rs1555738943, rs1555738763, rs1555738906 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Dowling-Degos Disease Dowling-Degos disease N/A N/A GenCC
Associations from Text Mining Disease 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