C1QTNF5
Sign in to saveAlso known as CTRP5, C1q and tumor necrosis factor related protein 5, C1q and TNF related 5, MFRP
== Protein Summary ==
In the Vinony graph
Vinony's link graph records 3 inbound references to C1QTNF5, and connects out to PubMed, Ensembl genome database project and protein.
It is catalogued under the topic Genes on human chromosome 11.
Vinony links it to 5 Wikipedia language editions.
Gene data
C1QTNF5- Name
- C1q and TNF related 5
- Type
- protein-coding
- Position
- 119,338,942–119,340,940 (−)
- Aliases
- CTRP5, MFRP
- Ensembl
- ENSG00000223953
- RefSeq RNA
- NM_001278431.2, NM_015645.5
- RefSeq protein
- NP_001265360.1, NP_056460.1
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].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
C1q and TNF related 5
- Symbol
- C1QTNF5
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 11:119,338,942-119,340,940
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 9227
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/114902
- chromosome
- human chromosome 11
- genomic start
- 119338942
- genomic end
- 119217383
- cytogenetic location
- 11q23.3
- expressed in
- myometrium
Sources (4)
via Wikidata · CC0
~3 min read
Encyclopedic overview
9 sectionsContents
- Protein Summary
- Function
- Clinical significance
- Origin
- Structure
- Crystal structure
- References
- Further reading
- External links
== Protein Summary ==
C1q and tumor necrosis factor related protein 5, also known as C1QTNF5, is a protein which in humans is encoded by the C1QTNF5 gene, associated with late-onset retinal degeneration( otherwise known as L-ORD). The C1QTNF5 gene secreted and membrane-linked to a protein which is strongly expressed in retinal pigment epithelium cells.
Excerpted from Wikipedia’s “C1QTNF5” article, available under the CC BY-SA 4.0 licence.