NUFIP1

Nuclear fragile X mental retardation-interacting protein 1 is a protein that in humans is encoded by the NUFIP1 gene.[5][6][7]

NUFIP1
Identifiers
AliasesNUFIP1, NUFIP, bA540M5.1, FMR1 interacting protein 1, nuclear FMR1 interacting protein 1, Rsa1
External IDsOMIM: 604354 MGI: 1351474 HomoloGene: 8216 GeneCards: NUFIP1
Gene location (Human)
Chr.Chromosome 13 (human)[1]
Band13q14.12Start44,939,249 bp[1]
End44,989,471 bp[1]
RNA expression pattern




More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

26747

27275

Ensembl

ENSG00000083635

ENSMUSG00000022009

UniProt

Q9UHK0

Q9QXX8

RefSeq (mRNA)

NM_012345

NM_013745

RefSeq (protein)

NP_036477

NP_038773

Location (UCSC)Chr 13: 44.94 – 44.99 MbChr 14: 76.11 – 76.14 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Interactions

NUFIP1 has been shown to interact with:

References

  1. GRCh38: Ensembl release 89: ENSG00000083635 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000022009 - 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. Bardoni B, Schenck A, Mandel JL (Jan 2000). "A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein". Hum Mol Genet. 8 (13): 2557–66. doi:10.1093/hmg/8.13.2557. PMID 10556305.
  6. Bardoni B, Giglio S, Schenck A, Rocchi M, Mandel JL (Aug 2000). "Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12". Cytogenet Cell Genet. 89 (1–2): 11–3. doi:10.1159/000015580. PMID 10894927.
  7. "Entrez Gene: NUFIP1 nuclear fragile X mental retardation protein interacting protein 1".
  8. Cabart P, Chew HK, Murphy S (Jul 2004). "BRCA1 cooperates with NUFIP and P-TEFb to activate transcription by RNA polymerase II". Oncogene. 23 (31): 5316–29. doi:10.1038/sj.onc.1207684. PMID 15107825.
  9. Bardoni B, Castets M, Huot ME, Schenck A, Adinolfi S, Corbin F, Pastore A, Khandjian EW, Mandel JL (Jul 2003). "82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization". Hum. Mol. Genet. 12 (14): 1689–98. doi:10.1093/hmg/ddg181. PMID 12837692.

Further reading


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