|
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 |
| 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
|
|
|
|
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 |
|