RLBP1

3HX3, 3HY5, 4CIZ, 4CJ6

RLBP1
RLBP1
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauRLBP1, CRALBP, retinaldehyde binding protein 1
Dynodwyr allanolOMIM: 180090 HomoloGene: 68046 GeneCards: RLBP1
Patrwm RNA pattern
Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000326

n/a

RefSeq (protein)

NP_000317

n/a

Lleoliad (UCSC)n/an/a
PubMed search[1]n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn y corff dynol gan y genyn RLBP1 yw RLBP1 a elwir hefyd yn Retinaldehyde binding protein 1 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 15, band 15q26.1.[2]

Cyfystyron

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn RLBP1.

  • CRALBP

Llyfryddiaeth

  • "Molecular clues to Bothnia-type retinal dystrophy. ". Adv Exp Med Biol. 2012. PMID 22183382.
  • "Clinical features of a Japanese case with Bothnia dystrophy. ". Ophthalmic Genet. 2012. PMID 22171637.
  • "Phenotype variations of retinal dystrophies caused by mutations in the RLBP1 gene. ". Acta Ophthalmol. 2015. PMID 25429852.
  • "Early-onset foveal involvement in retinitis punctata albescens with mutations in RLBP1. ". JAMA Ophthalmol. 2013. PMID 23929416.
  • "Genotype-phenotype correlations in Bothnia dystrophy caused by RLBP1 gene sequence variations.". Acta Ophthalmol. 2013. PMID 22551409.

Cyfeiriadau

  1. "Human PubMed Reference:".
  2. RLBP1 - Cronfa NCBI

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