1. Gene
  2. C1QTNF1 - C1q and TNF related 1 Gene

C1QTNF1 - C1q and TNF related 1 Gene

Homo sapiens

Also known as GIP; CTRP1; ZSIG37

Gene ID: 114897 | Gene type: protein coding

About C1QTNF1

Cytogenetic location: 17q25.3 Genomic coordinates (GRCh38): 17:79,022,934-79,049,788 (from NCBI)

This gene has 12 transcripts (splice variants), 160 orthologues and 23 paralogues. Broad expression in fat (RPKM 33.8), placenta (RPKM 15.4) and 21 other tissues.

Summary

Enables collagen binding activity. Involved in several processes, including negative regulation of platelet aggregation; positive regulation of aldosterone secretion; and positive regulation of cytosolic calcium ion concentration. Located in extracellular space. Is integral component of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

C1QTNF1 Products(4)

mRNA Protein Name
NM_030968.5 NP_112230.1 complement C1q tumor necrosis factor-related protein 1 isoform 1 precursor
NM_153372.3 NP_699203.1 complement C1q tumor necrosis factor-related protein 1 isoform 1 precursor
NM_198593.4 NP_940995.1 complement C1q tumor necrosis factor-related protein 1 isoform 1 precursor
NM_198594.4 NP_940996.1 complement C1q tumor necrosis factor-related protein 1 isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables collagen binding IDA
IDA: Inferred from direct assay
16195328 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12409230 GOA
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of platelet activation IDA
IDA: Inferred from direct assay
16195328 GOA
involved in negative regulation of platelet aggregation IDA
IDA: Inferred from direct assay
16195328 GOA
involved in positive regulation of aldosterone secretion IDA
IDA: Inferred from direct assay
18171693 GOA
involved in positive regulation of cytosolic calcium ion concentration IDA
IDA: Inferred from direct assay
18171693 GOA
involved in positive regulation of gene expression IDA
IDA: Inferred from direct assay
18171693 GOA
Cellular Component GO Annotation Evidence Reference Source
located in extracellular space IDA
IDA: Inferred from direct assay
18171693 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
12409230 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

C1QTNF1 Protein Structure

Collagen

Collagen: Collagen triple helix repeat (20 copies) (99 - 140)

C1q

C1q: C1q domain (147 - 275)

  • 0
  • 100
  • 200
  • 281 a.a.
Protein Preferred Names Protein Names

complement C1q tumor necrosis factor-related protein 1

C1q and tumor necrosis factor related protein 1

Recombinant C1QTNF1 Proteins

Cat. No. Product Name Accession Purity
HY-P7693 C1QTNF1/CTRP1 Protein, Human (HEK293, His) Q9BXJ1-1 (R26-P281) ≥95%

Related Diseases

Diseases Alias
Granulomatous Disease, Chronic, Autosomal Recessive, 2

Chronic Granulomatous Disease Due To Deficiency Of Ncf-2

CGD2

Ncf2 Deficiency

P67-Phox Deficiency

Autosomal Recessive Chronic Granulomatous Disease Cytochrome B-Positive Type Ii

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type 2

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii

Cgd, Autosomal Recessive Cytochrome B-Positive, Type Ii

Granulomatous Disease, Chronic, Due To Ncf2 Deficiency

Neutrophil Cytosol Factor 2 Deficiency

Chronic Granulomatous Disease 2, Autosomal Recessive

Autosomal Recessive Chronic Granulomatous Disease 2

Cdg2

Deficiency Of Ncf2

Deficiency Of P67-Phox

Chronic Granulomatous Disease Autosomal Recessive Cytochrome B-Positive Type Ii

Deficiency Of Neutrophil Cytosol Factor 2

Avellino Corneal Dystrophy

Chorioangioma

Placental Hemangioma

Late-Onset Retinal Degeneration

LORD

Retinal Degeneration, Late-Onset, Autosomal Dominant

Autosomal Dominant Late-Onset Retinal Degeneration

Pigmentary Retinopathy

Retinal Degeneration, Late-Onset

Retinitis Pigmentosa

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus C1QTNF1 RGD RGD:1359204
Mus musculus C1QTNF1 MGD MGI:1919254
Canis familiaris C1QTNF1 VGNC VGNC:51925
Macaca mulatta C1QTNF1 VGNC VGNC:70311
Felis catus C1QTNF1 VGNC VGNC:60221
Bos taurus C1QTNF1 VGNC VGNC:26622
Others C1QTNF1 NCBI