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ATXN2L

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Protein-coding gene in the species Homo sapiens
ATXN2L
Identifiers
AliasesATXN2L, A2D, A2LG, A2LP, A2RP, ataxin 2 like
External IDsOMIM: 607931; MGI: 2446242; HomoloGene: 16513; GeneCards: ATXN2L; OMA:ATXN2L - orthologs
Gene location (Human)
Chromosome 16 (human)
Chr.Chromosome 16 (human)
Chromosome 16 (human)Genomic location for ATXN2LGenomic location for ATXN2L
Band16p11.2Start28,823,035 bp
End28,837,237 bp
Gene location (Mouse)
Chromosome 7 (mouse)
Chr.Chromosome 7 (mouse)
Chromosome 7 (mouse)Genomic location for ATXN2LGenomic location for ATXN2L
Band7|7 F3Start126,491,708 bp
End126,503,437 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • left testis

  • right testis

  • right hemisphere of cerebellum

  • anterior pituitary

  • granulocyte

  • beta cell

  • olfactory bulb

  • body of uterus

  • left lobe of thyroid gland

  • right lobe of thyroid gland
Top expressed in
  • zygote

  • secondary oocyte

  • Rostral migratory stream

  • tail of embryo

  • genital tubercle

  • neural layer of retina

  • granulocyte

  • spermatocyte

  • spermatid

  • primary visual cortex
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

11273

233871

Ensembl

ENSG00000168488

ENSMUSG00000032637

UniProt

Q8WWM7

Q7TQH0

RefSeq (mRNA)
NM_001308230
NM_007245
NM_017492
NM_145714
NM_148414

NM_148415
NM_148416

NM_183020
NM_001347658
NM_001361487

RefSeq (protein)
NP_001295159
NP_009176
NP_059867
NP_663760
NP_680780

NP_680781
NP_680782

NP_001334587
NP_898841
NP_001348416

Location (UCSC)Chr 16: 28.82 – 28.84 MbChr 7: 126.49 – 126.5 Mb
PubMed search
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.

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.

Interactions

ATXN2L has been shown to interact with Myeloproliferative leukemia virus oncogene.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000168488Ensembl, May 2017
  2. ^ 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. ^ Meunier C, Bordereaux D, Porteu F, Gisselbrecht S, Chretien S, Courtois G (Mar 2002). "Cloning and characterization of a family of proteins associated with Mpl". J Biol Chem. 277 (11): 9139–47. doi:10.1074/jbc.M105970200. PMID 11784712.
  6. Figueroa KP, Pulst SM (Feb 2004). "Identification and expression of the gene for human ataxin-2-related protein on chromosome 16". Exp Neurol. 184 (2): 669–78. doi:10.1016/S0014-4886(03)00287-5. PMID 14769358. S2CID 10975750.
  7. ^ "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. doi:10.1038/ng1196-269. PMID 8896555. S2CID 12365475.

External links

Further reading


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