ATXN2L

Source: Wikipedia, the free encyclopedia.
ATXN2L
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_183020
NM_001347658
NM_001361487

RefSeq (protein)

NP_001334587
NP_898841
NP_001348416

Location (UCSC)Chr 16: 28.82 – 28.84 MbChr 7: 126.49 – 126.5 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Ataxin-2-like protein was initially identified in 1996 and designated Ataxin-2 Related protein (A2RP) as the search for the gene causing SCA2 lead to the identification of 2 cDNA clones with high similarity to ATXN2 (Pulst et al, 1996). It was later renamed as ATXN2L. It is a protein that in humans is encoded by the ATXN2L gene.[5][6][7]

This gene encodes an ataxin type 2 related protein of unknown function. This protein is a member of the spinocerebellar ataxia (SCAs) family, which is associated with a complex group of neurodegenerative disorders. Several alternatively spliced transcripts encoding different isoforms have been found for this gene.[7]

Interactions

ATXN2L has been shown to

Myeloproliferative leukemia virus oncogene.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000168488Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032637Ensembl, 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 11784712
    .
  6. .
  7. ^ a b "Entrez Gene: ATXN2L ataxin 2-like".
  • Pulst SM, Nechiporuk A, Nechiporuk T, et al. (1996). "Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2". Nat. Genet. 14 (3): 269–76.
    S2CID 12365475
    .

External links

Further reading


This page is based on the copyrighted Wikipedia article: ATXN2L. Articles is available under the CC BY-SA 3.0 license; additional terms may apply.Privacy Policy