Gene Gene information from NCBI Gene database.
Entrez ID 51097
Gene name Saccharopine dehydrogenase (putative)
Gene symbol SCCPDH
Synonyms (NCBI Gene)
CGI-49CGI49NET11
Chromosome 1
Chromosome location 1q44
miRNA miRNA information provided by mirtarbase database.
59
miRTarBase ID miRNA Experiments Reference
MIRT046432 hsa-miR-15b-5p CLASH 23622248
MIRT1328712 hsa-miR-144 CLIP-seq
MIRT1328713 hsa-miR-1470 CLIP-seq
MIRT1328714 hsa-miR-2053 CLIP-seq
MIRT1328715 hsa-miR-299-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region TAS
GO:0005634 Component Nucleus HDA 21630459
GO:0005739 Component Mitochondrion HDA 20833797
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005811 Component Lipid droplet IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620831 24275 ENSG00000143653
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NBX0
Protein name Saccharopine dehydrogenase-like oxidoreductase (EC 1.-.-.-)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03435 Sacchrp_dh_NADP 10 149 Saccharopine dehydrogenase NADP binding domain Family
PF16653 Sacchrp_dh_C 153 419 Saccharopine dehydrogenase C-terminal domain Domain
Sequence
Sequence length 429
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Platelet degranulation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
VASCULAR DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations