Alpha-tocopherol transfer protein

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TTPA
5mug.jpg
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTTPA, ATTP, AVED, TTP1, alphaTTP, tocopherol (alpha) transfer protein, alpha tocopherol transfer protein
External IDsMGI: 1354168 HomoloGene: 37295 GeneCards: TTPA
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)[1]
Chromosome 8 (human)
Genomic location for TTPA
Genomic location for TTPA
Band8q12.3Start63,048,553 bp[1]
End63,086,053 bp[1]
RNA expression pattern
PBB GE TTPA 210614 at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000370

NM_015767
NM_001317723

RefSeq (protein)

NP_000361

NP_001304652
NP_056582

Location (UCSC)Chr 8: 63.05 – 63.09 MbChr 4: 20.01 – 20.03 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Alpha-tocopherol transfer protein is a protein that in humans is encoded by the TTPA gene.[5][6][7]

See also[edit]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000137561 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000073988 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:".
  4. ^ "Mouse PubMed Reference:".
  5. ^ Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M (1995). "Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein". Nat Genet. 9 (2): 141–145. doi:10.1038/ng0295-141. PMID 7719340.
  6. ^ Arita M, Sato Y, Miyata A, Tanabe T, Takahashi E, Kayden HJ, Arai H, Inoue K (1995). "Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization". Biochem J. 306 (2): 437–443. PMC 1136538. PMID 7887897.
  7. ^ "Entrez Gene: TTPA tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency)".

Further reading[edit]

External links[edit]