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RIT1

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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)
Chromosome 1 (human)Genomic location for RIT1Genomic location for RIT1
Band1q22Start155,897,808 bp
End155,911,404 bp
Gene location (Mouse)
Chromosome 3 (mouse)
Chr.Chromosome 3 (mouse)
Chromosome 3 (mouse)Genomic location for RIT1Genomic location for RIT1
Band3|3 F1Start88,624,145 bp
End88,638,356 bp
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
Cellular component
Biological process
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
Wikidata
View/Edit HumanView/Edit Mouse

GTP-binding protein Rit1 is a protein that in humans is encoded by the RIT1 gene.

Function

RIT belongs to the RAS (HRAS; MIM 190020) subfamily of small GTPases (Hynds et al., 2003).

Clinical significance

Mutations in RIT1 are associated to Noonan syndrome.

Interactions

RIT1 has been shown to interact with KLHL12 and Merlin.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000143622Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000028057Ensembl, 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. ^ "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


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