C1QTNF1

C1QTNF1

Identifiers

C1QTNF1, CTRP1, GIP, ZSIG37, C1q and tumor necrosis factor related protein 1

External IDs

MGI: 1919254 HomoloGene: 10548 GeneCards: C1QTNF1

Gene ontology
Molecular function	• protein binding • collagen binding
Cellular component	• extracellular space • extracellular region • collagen trimer • integral component of plasma membrane
Biological process	• positive regulation of cytosolic calcium ion concentration • negative regulation of platelet activation • protein heterotrimerization • regulation of glucose metabolic process • positive regulation of gene expression • positive regulation of protein kinase B signaling • positive regulation of aldosterone secretion • protein homooligomerization • negative regulation of platelet aggregation • positive regulation of MAPK cascade
Sources:Amigo / QuickGO

RNA expression pattern

More reference expression data

Orthologs

Species

Human

Mouse


114897


56745


ENSG00000173918


ENSMUSG00000017446


Q9BXJ1


Q9QXP7

RefSeq (mRNA)


NM_030968 NM_153372 NM_198593 NM_198594


NM_001204129 NM_001204130 NM_019959

RefSeq (protein)


NP_112230.1 NP_699203.1 NP_940995.1 NP_940996.1


NP_001191058.1 NP_001191059.1 NP_064343.1

Location (UCSC)

Chr 17: 79.02 – 79.05 Mb

Chr 11: 118.43 – 118.45 Mb

PubMed search

^[1]

^[2]

View/Edit Human

View/Edit Mouse

Complement C1q tumor necrosis factor-related protein 1 is a protein that in humans is encoded by the C1QTNF1 gene.^[3]^[4]

Interactions

C1QTNF1 has been shown to interact with Arginine vasopressin receptor 2.^[5]

References

↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Innamorati G, Whang MI, Molteni R, Le Gouill C, Birnbaumer M (Oct 2002). "GIP, a G-protein-coupled receptor interacting protein". Regul Pept. 109 (1–3): 173–9. doi:10.1016/S0167-0115(02)00201-X. PMID 12409230.
↑ "Entrez Gene: C1QTNF1 C1q and tumor necrosis factor related protein 1".
↑ Innamorati, Giulio; Whang Michael Insuk; Molteni Raffaella; Le Gouill Christian; Birnbaumer Mariel (Nov 2002). "GIP, a G-protein-coupled receptor interacting protein". Regul. Pept. Netherlands. 109 (1–3): 173–9. doi:10.1016/S0167-0115(02)00201-X. ISSN 0167-0115. PMID 12409230.

Further reading

Innamorati G, Bianchi E, Whang MI (2006). "An intracellular role for the C1q-globular domain". Cell Signal. 18 (6): 761–70. doi:10.1016/j.cellsig.2005.11.004. PMID 16386877.

Kim KY, Kim HY, Kim JH, et al. (2006). "Tumor necrosis factor-alpha and interleukin-1beta increases CTRP1 expression in adipose tissue". FEBS Lett. 580 (16): 3953–60. doi:10.1016/j.febslet.2006.06.034. PMID 16806199.
Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. 12 (2): 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.

This article is issued from Wikipedia - version of the 6/6/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.