Gene Gene information from NCBI Gene database.
Entrez ID 23648
Gene name Single stranded DNA binding protein 3
Gene symbol SSBP3
Synonyms (NCBI Gene)
CSDPSSDPSSDP1
Chromosome 1
Chromosome location 1p32.3
miRNA miRNA information provided by mirtarbase database.
79
miRTarBase ID miRNA Experiments Reference
MIRT622040 hsa-miR-29b-1-5p HITS-CLIP 23824327
MIRT622040 hsa-miR-29b-1-5p HITS-CLIP 23824327
MIRT622040 hsa-miR-29b-1-5p HITS-CLIP 23824327
MIRT622040 hsa-miR-29b-1-5p HITS-CLIP 23824327
MIRT622040 hsa-miR-29b-1-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0002244 Process Hematopoietic progenitor cell differentiation IEA
GO:0003677 Function DNA binding IEA
GO:0003697 Function Single-stranded DNA binding IEA
GO:0003713 Function Transcription coactivator activity IEA
GO:0005515 Function Protein binding IPI 18330356, 20211142, 25416956, 30833792, 32296183, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607390 15674 ENSG00000157216
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BWW4
Protein name Single-stranded DNA-binding protein 3 (Sequence-specific single-stranded-DNA-binding protein)
Protein function May be involved in transcription regulation of the alpha 2(I) collagen gene where it binds to the single-stranded polypyrimidine sequences in the promoter region.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04503 SSDP 81 365 Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in all hematopoietic tissues, including spleen, lymph node, peripheral blood, bone marrow, thymus, and fetal liver, with highest expression in thymus and fetal liver. Expression is also high in heart, brain, kidney, an
Sequence
Sequence length 388
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEVELOPMENTAL DISABILITIES Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Jervell Lange Nielsen Syndrome Associate 31570892
★☆☆☆☆
Found in Text Mining only
Medulloblastoma Associate 36273157
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 36273157
★☆☆☆☆
Found in Text Mining only