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RIPOR2

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Protein-coding gene in humans
RIPOR2
Identifiers
AliasesRIPOR2, C6orf32, DIFF40, DIFF48, MYONAP, PL48, FAM65B, DFNB104, family with sequence similarity 65 member B, RHO family interacting cell polarization regulator 2, DFNA21
External IDsOMIM: 611410; MGI: 2444879; HomoloGene: 9284; GeneCards: RIPOR2; OMA:RIPOR2 - orthologs
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)
Chromosome 6 (human)Genomic location for RIPOR2Genomic location for RIPOR2
Band6p22.3Start24,804,282 bp
End25,042,170 bp
Gene location (Mouse)
Chromosome 13 (mouse)
Chr.Chromosome 13 (mouse)
Chromosome 13 (mouse)Genomic location for RIPOR2Genomic location for RIPOR2
Band13|13 A3.1Start24,685,508 bp
End24,917,799 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • blood

  • monocyte

  • granulocyte

  • bronchial epithelial cell

  • spleen

  • appendix

  • lymph node

  • bone marrow cells

  • epithelium of nasopharynx

  • body of uterus
Top expressed in
  • lateral septal nucleus

  • granulocyte

  • subiculum

  • lymph node

  • nucleus accumbens

  • spleen

  • mesenteric lymph nodes

  • blood

  • medial dorsal nucleus

  • Region I of hippocampus proper
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

9750

193385

Ensembl

ENSG00000111913

ENSMUSG00000036006

UniProt

Q9Y4F9

Q80U16

RefSeq (mRNA)
NM_001286445
NM_001286446
NM_001286447
NM_014722
NM_015864

NM_001346031
NM_001346032

NM_001080381
NM_001286100
NM_001286101
NM_029679
NM_178658

RefSeq (protein)
NP_001273374
NP_001273375
NP_001273376
NP_001332960
NP_001332961

NP_055537
NP_056948

NP_001073850
NP_001273029
NP_001273030
NP_083955
NP_848773

NP_001389841
NP_001389842
NP_001389843
NP_001389844
NP_001389845
NP_001389846
NP_001389847
NP_001389848

Location (UCSC)Chr 6: 24.8 – 25.04 MbChr 13: 24.69 – 24.92 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

RHO family interacting cell polarization regulator 2 is a protein that in humans is encoded by the RIPOR2 gene.

Function

The protein encoded by this gene stimulates the formation of a non-mitotic multinucleate syncytium from proliferative cytotrophoblasts during trophoblast differentiation. Alternative splicing of this gene results in multiple transcript variants. .

Clinical significance

Mutations in RIPOR2 are associated to hearing loss.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000111913Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000036006Ensembl, 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. "Entrez Gene: Family with sequence similarity 65, member B".
  6. Diaz-Horta O, Subasioglu-Uzak A, Grati M, DeSmidt A, Foster J, Cao L, Bademci G, Tokgoz-Yilmaz S, Duman D, Cengiz FB, Abad C, Mittal R, Blanton S, Liu XZ, Farooq A, Walz K, Lu Z, Tekin M (July 2014). "FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing". Proceedings of the National Academy of Sciences of the United States of America. 111 (27): 9864–8. Bibcode:2014PNAS..111.9864D. doi:10.1073/pnas.1401950111. PMC 4103326. PMID 24958875.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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