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Gene : C1QTNF5 Homo sapiens

Name  ? C1q and TNF related 5 Cytological Location  11q23.3
Brief Description  C1q and TNF related 5
Description  This gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late-onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled-related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter. [provided by RefSeq, Jun 2013]
  • synonyms:
  • CTRP5,
  • uc058iiv.2,
  • MFRP,
  • LORD,
  • DKFZp586B0621,
  • NM_015645,
  • AF329841,
  • myonectin,
  • complement-c1q tumor necrosis factor-related protein 5,
  • CTRP5,
  • C1q and tumor necrosis factor related protein 5,
  • HGNC:14344,
  • OTTHUMG00000166198,
  • C1QTNF5
  • identifiers:
  • 114902,
  • ENSG00000223953,
  • C1QTNF5

Genome feature

Region: gene ? Length: 7764  
Location: 11:119338942-119346705 reverse strand Cyto location: 11q23.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

2 SNPs

5 Cross References

16 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results