Gene Gene information from NCBI Gene database.
Entrez ID 114900
Gene name C1q and TNF related 4
Gene symbol C1QTNF4
Synonyms (NCBI Gene)
CTRP4ZACRP4
Chromosome 11
Chromosome location 11p11.2
miRNA miRNA information provided by mirtarbase database.
4
miRTarBase ID miRNA Experiments Reference
MIRT842335 hsa-miR-4645-5p CLIP-seq
MIRT842336 hsa-miR-4673 CLIP-seq
MIRT842337 hsa-miR-4783-5p CLIP-seq
MIRT2385129 hsa-miR-4532 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0002023 Process Reduction of food intake in response to dietary excess IEA
GO:0005125 Function Cytokine activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614911 14346 ENSG00000172247
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BXJ3
Protein name Complement C1q tumor necrosis factor-related protein 4 (C1q/TNF-related protein 4)
Protein function May be involved in the regulation of the inflammatory network. Its role as pro- or anti-inflammatory seems to be context dependent (PubMed:21658842, PubMed:27086950). Seems to have some role in regulating food intake and energy balance when admi
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00386 C1q 31 156 C1q domain Domain
PF00386 C1q 178 311 C1q domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed at low levels (PubMed:21658842). Highest levels in adipocyte tissue and brain (PubMed:24366864). {ECO:0000269|PubMed:21658842, ECO:0000269|PubMed:24366864}.
Sequence
Sequence length 329
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
CARDIOVASCULAR DISEASE 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
Autoimmune Diseases Autoimmune disease Pubtator 33676896 Associate
★☆☆☆☆
Found in Text Mining only
Cardiovascular Diseases Cardiovascular Diseases GWASCAT_DG 30595370
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Diabetes mellitus, type 2 Pubtator 38286878 Associate
★☆☆☆☆
Found in Text Mining only
Lupus Erythematosus Systemic Systemic lupus erythematosus Pubtator 29177435, 33676896 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 21658842, 30885436
★☆☆☆☆
Found in Text Mining only
Osteopenia Osteopenia BEFREE 30885436
★☆☆☆☆
Found in Text Mining only
Osteoporosis Osteoporosis BEFREE 30885436
★☆☆☆☆
Found in Text Mining only