Lamin B receptor

Source: Wikipedia, the free encyclopedia.
LBR
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_002296
NM_194442

NM_133815

RefSeq (protein)

NP_002287
NP_919424

NP_598576

Location (UCSC)Chr 1: 225.4 – 225.43 MbChr 1: 181.64 – 181.67 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Lamin-B receptor is a protein, and in humans, it is encoded by the LBR gene.[5][6][7]

Function

The protein encoded by this gene belongs to the

lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.[7]

Clinical significance

There is evidence tying it to

Interactions

Lamin B receptor has been shown to

interact with CBX3[10] and CBX5.[10] LBR also interacts with long non-coding RNA XIST in mouse cells and potentially assist the spreading XIST across X chromosome in differentiating female embryonic stem cells,[11] but it might be redundant for correct XCI in vivo.[12]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000143815Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000004880Ensembl, 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. PMID 8157663
    .
  6. .
  7. ^ a b "Entrez Gene: LBR lamin B receptor".
  8. ^ Online Mendelian Inheritance in Man (OMIM): 215140
  9. ^ Online Mendelian Inheritance in Man (OMIM): 169400
  10. ^
    PMID 8663349
    .
  11. .
  12. .

Further reading

External links