Gene Gene information from NCBI Gene database.
Entrez ID 6291
Gene name Serum amyloid A4, constitutive
Gene symbol SAA4
Synonyms (NCBI Gene)
C-SAACSAA
Chromosome 11
Chromosome location 11p15.1
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT1324598 hsa-miR-1343 CLIP-seq
MIRT1324599 hsa-miR-3144-5p CLIP-seq
MIRT1324600 hsa-miR-3191 CLIP-seq
MIRT1324601 hsa-miR-4652-5p CLIP-seq
MIRT1324602 hsa-miR-4667-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region NAS 14718574
GO:0006953 Process Acute-phase response IEA
GO:0034364 Component High-density lipoprotein particle IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
104752 10516 ENSG00000148965
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P35542
Protein name Serum amyloid A-4 protein (Constitutively expressed serum amyloid A protein) (C-SAA)
Protein function Major acute phase reactant.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00277 SAA 22 130 Serum amyloid A protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed by the liver; secreted in plasma.
Sequence
Sequence length 130
Interactions View interactions
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
AA amyloidosis AA amyloidosis BEFREE 20536400
★☆☆☆☆
Found in Text Mining only
Amyloidosis Amyloidosis BEFREE 20536400
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 28505104 Stimulate
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 30662913 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Carcinoma BEFREE 16116035
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 38300370 Associate
★☆☆☆☆
Found in Text Mining only
Glioma Glioma BEFREE 25220188
★☆☆☆☆
Found in Text Mining only
Lymphohistiocytosis Hemophagocytic Hemophagocytic lymphohistiocytosis Pubtator 37653176 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of ovary Ovarian cancer BEFREE 20713982
★☆☆☆☆
Found in Text Mining only
Osteosarcoma Osteosarcoma BEFREE 17849429
★☆☆☆☆
Found in Text Mining only