GenAge entry for SPRTN (Homo sapiens)
Gene name (HAGRID: 302)
- HGNC symbol
- SPRTN
- Aliases
- DKFZP547N043; Spartan; DVC1; C1orf124
- Common name
- SprT-like N-terminal domain
Potential relevance to the human ageing process
- Main reason for selection
- Entry selected based on indirect or inconclusive evidence linking the gene product to ageing in humans or in one or more model systems
- Description
SPRTN may play a role in DNA repair during replication of damaged DNA and in G2/M-checkpoint regulation. Mutations in SPRTN have been associated with Ruijs-Aalfs segmental progeroid syndrome, causing early onset hepatocellular carcinoma, genomic instability and progeroid features [3644]. Many of the displayed features resembled those seen during normal ageing/progeroid syndromes, including: short stature and low weight, delayed bone age, thoracic kyphosis and kyphoscoliosis, cataracts, muscular atrophy, graying of hair, lipodystrophy [3644]. All reported cases so far (N=3) developed hepatocellular carcinoma at an early age (14-17 years old).
Cytogenetic information
- Cytogenetic band
- 1q42-q43
- Location
- 231,337,936 bp to 231,355,027 bp
- Orientation
- Plus strand
Protein information
- Gene Ontology
-
Process: GO:0006974; cellular response to DNA damage stimulus
GO:0009411; response to UV
GO:0019985; translesion synthesis
GO:0031398; positive regulation of protein ubiquitination
GO:0070987; error-free translesion synthesis
Cellular component: GO:0005634; nucleus
GO:0005654; nucleoplasm
GO:0005694; chromosome
GO:0016607; nuclear speck
Function: GO:0003677; DNA binding
GO:0005515; protein binding
GO:0043130; ubiquitin binding
GO:0046872; metal ion binding
GO:0070530; K63-linked polyubiquitin binding
Protein interactions and network
- Protein-protein interacting partners in GenAge
- UBB, RPA1, VCP, PCNA, POLD1, HSPA9, HSPA1A, LMNB1, HSPA8, MLH1
- STRING interaction network
Retrieve sequences for SPRTN
Homologs in model organisms
Selected references
External links
- EPD
- ORF Accession
- NM_032018
- CDS Accession
- NP_114407
- OMIM
- 616086
- HPRD
- 13164
- Ensembl
- SPRTN
- UniProt/Swiss-Prot
- SPRTN_HUMAN
- GeneCards
- SPRTN
- Entrez Gene
- 83932
- UniGene
- GenAtlas
- SPRTN
- Internet
- Search Google