RIT1

Protein-coding gene in the species Homo sapiens
RIT1
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

4KLZ

Identifiers
AliasesRIT1, NS8, RIBB, RIT, ROC1, Ras like without CAAX 1
External IDsOMIM: 609591; MGI: 108053; HomoloGene: 56003; GeneCards: RIT1; OMA:RIT1 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for RIT1
Genomic location for RIT1
Band1q22Start155,897,808 bp[1]
End155,911,404 bp[1]
Gene location (Mouse)
Chromosome 3 (mouse)
Chr.Chromosome 3 (mouse)[2]
Chromosome 3 (mouse)
Genomic location for RIT1
Genomic location for RIT1
Band3|3 F1Start88,624,145 bp[2]
End88,638,356 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • monocyte

  • amniotic fluid

  • Achilles tendon

  • stromal cell of endometrium

  • islet of Langerhans

  • blood

  • ventricular zone

  • vagina

  • palpebral conjunctiva

  • granulocyte
Top expressed in
  • granulocyte

  • saccule

  • stroma of bone marrow

  • seminal vesicula

  • lip

  • ectoderm

  • otic vesicle

  • esophagus

  • lacrimal gland

  • otic placode
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
  • nucleotide binding
  • protein binding
  • calmodulin binding
  • GTP binding
  • GTPase activity
  • GDP binding
Cellular component
  • membrane
  • plasma membrane
  • intracellular anatomical structure
Biological process
  • Ras protein signal transduction
  • signal transduction
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

6016

19769

Ensembl

ENSG00000143622

ENSMUSG00000028057

UniProt

Q92963

P70426

RefSeq (mRNA)

NM_006912
NM_001256820
NM_001256821

NM_001163310
NM_009069

RefSeq (protein)

NP_001243749
NP_001243750
NP_008843

NP_001156782
NP_033095
NP_001390950
NP_001390951
NP_001390958

NP_001390959
NP_001390960
NP_001390962
NP_001390963
NP_001390964
NP_001390965

Location (UCSC)Chr 1: 155.9 – 155.91 MbChr 3: 88.62 – 88.64 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

GTP-binding protein Rit1 is a protein that in humans is encoded by the RIT1 gene.[5][6][7]

Function

RIT belongs to the RAS (HRAS; MIM 190020) subfamily of small GTPases (Hynds et al., 2003).[supplied by OMIM][7]

Clinical significance

Mutations in RIT1 are associated to Noonan syndrome.[8]

Interactions

RIT1 has been shown to interact with KLHL12[9] and Merlin.[10]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000143622 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028057 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lee CH, Della NG, Chew CE, Zack DJ (November 1996). "Rin, a neuron-specific and calmodulin-binding small G-protein, and Rit define a novel subfamily of ras proteins". The Journal of Neuroscience. 16 (21): 6784–94. doi:10.1523/JNEUROSCI.16-21-06784.1996. PMC 6579259. PMID 8824319.
  6. ^ Wes PD, Yu M, Montell C (November 1996). "RIC, a calmodulin-binding Ras-like GTPase". The EMBO Journal. 15 (21): 5839–48. doi:10.1002/j.1460-2075.1996.tb00971.x. PMC 452332. PMID 8918462.
  7. ^ a b "Entrez Gene: RIT1 Ras-like without CAAX 1".
  8. ^ Gos M, Fahiminiya S, Poznański J, Klapecki J, Obersztyn E, Piotrowicz M, Wierzba J, Posmyk R, Bal J, Majewski J (September 2014). "Contribution of RIT1 mutations to the pathogenesis of Noonan syndrome: four new cases and further evidence of heterogeneity". American Journal of Medical Genetics. Part A. 164A (9): 2310–6. doi:10.1002/ajmg.a.36646. PMID 24939608. S2CID 2005508.
  9. ^ Rondou P, Haegeman G, Vanhoenacker P, Van Craenenbroeck K (April 2008). "BTB Protein KLHL12 targets the dopamine D4 receptor for ubiquitination by a Cul3-based E3 ligase". The Journal of Biological Chemistry. 283 (17): 11083–96. doi:10.1074/jbc.M708473200. PMC 2431063. PMID 18303015.
  10. ^ Huang J, Chen J (July 2008). "VprBP targets Merlin to the Roc1-Cul4A-DDB1 E3 ligase complex for degradation". Oncogene. 27 (29): 4056–64. doi:10.1038/onc.2008.44. PMID 18332868.

Further reading

  • Shao H, Kadono-Okuda K, Finlin BS, Andres DA (November 1999). "Biochemical characterization of the Ras-related GTPases Rit and Rin". Archives of Biochemistry and Biophysics. 371 (2): 207–19. doi:10.1006/abbi.1999.1448. PMID 10545207.
  • Shao H, Andres DA (September 2000). "A novel RalGEF-like protein, RGL3, as a candidate effector for rit and Ras". The Journal of Biological Chemistry. 275 (35): 26914–24. doi:10.1074/jbc.M002241200. PMID 10869344.
  • Hynds DL, Spencer ML, Andres DA, Snow DM (May 2003). "Rit promotes MEK-independent neurite branching in human neuroblastoma cells". Journal of Cell Science. 116 (Pt 10): 1925–35. doi:10.1242/jcs.00401. PMID 12668729.
  • Li JT, Liu W, Kuang ZH, Zhang RH, Chen HK, Feng QS (February 2004). "[Mutation and amplification of RIT1 gene in hepatocellular carcinoma]". Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 21 (1): 43–6. PMID 14767908.
  • Shi GX, Andres DA (January 2005). "Rit contributes to nerve growth factor-induced neuronal differentiation via activation of B-Raf-extracellular signal-regulated kinase and p38 mitogen-activated protein kinase cascades". Molecular and Cellular Biology. 25 (2): 830–46. doi:10.1128/MCB.25.2.830-846.2005. PMC 543422. PMID 15632082.
  • Barrios-Rodiles M, Brown KR, Ozdamar B, Bose R, Liu Z, Donovan RS, Shinjo F, Liu Y, Dembowy J, Taylor IW, Luga V, Przulj N, Robinson M, Suzuki H, Hayashizaki Y, Jurisica I, Wrana JL (March 2005). "High-throughput mapping of a dynamic signaling network in mammalian cells". Science. 307 (5715): 1621–5. Bibcode:2005Sci...307.1621B. doi:10.1126/science.1105776. PMID 15761153. S2CID 39457788.
  • Benmaamar R, Pagano M (September 2005). "Involvement of the SCF complex in the control of Cdh1 degradation in S-phase". Cell Cycle. 4 (9): 1230–2. doi:10.4161/cc.4.9.2048. PMID 16123585.


  • v
  • t
  • e