RAI2

Retinoic acid-induced protein 2 is a protein that in humans is encoded by the RAI2 gene.[5][6][7]

RAI2
Identifiers
AliasesRAI2, retinoic acid induced 2
External IDsOMIM: 300217 MGI: 1344378 HomoloGene: 11034 GeneCards: RAI2
Gene location (Human)
Chr.X chromosome (human)[1]
BandXp22.13Start17,800,049 bp[1]
End17,861,337 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

10742

24004

Ensembl

ENSG00000131831

ENSMUSG00000043518

UniProt

Q9Y5P3

Q9QVY8

RefSeq (mRNA)

NM_001172732
NM_001172739
NM_001172743
NM_021785

NM_001103367
NM_198409

RefSeq (protein)

NP_001096837
NP_940801

Location (UCSC)Chr X: 17.8 – 17.86 MbChr X: 161.72 – 161.78 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this intronless, retinoic acid-induced gene has not yet been determined; however, it has been suggested to play a role in development. Localization of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked mental retardation, oral-facial-digital syndrome, and Fried syndrome.[7]

References

  1. GRCh38: Ensembl release 89: ENSG00000131831 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000043518 - 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. Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JR, Sieving PA, Trump D (May 1999). "Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22". Genomics. 55 (3): 275–83. doi:10.1006/geno.1998.5667. PMID 10049581.
  6. Walpole SM, Ronce N, Grayson C, Dessay B, Yates JR, Trump D, Toutain A (Jul 1999). "Exclusion of RAI2 as the causative gene for Nance-Horan syndrome". Hum Genet. 104 (5): 410–1. doi:10.1007/s004390050976. PMID 10394933.
  7. "Entrez Gene: RAI2 retinoic acid induced 2".

Further reading


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