EIF1AX
genyn codio-protien yn y rhywogaeth Homo sapiens
Protein sy'n cael ei godio yn y corff dynol gan y genyn EIF1AX yw EIF1AX a elwir hefyd yn Eukaryotic translation initiation factor 1A, X-linked (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 X dynol, band Xp22.12.[2]
EIF1AX | |||||||||||||||||
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Dynodwyr | |||||||||||||||||
Cyfenwau | EIF1AX, EIF1A, EIF1AP1, EIF4C, eIF-1A, eIF-4C, eukaryotic translation initiation factor 1A, X-linked, eukaryotic translation initiation factor 1A X-linked | ||||||||||||||||
Dynodwyr allanol | OMIM: 300186 HomoloGene: 20364 GeneCards: EIF1AX | ||||||||||||||||
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Orthologau | |||||||||||||||||
Species | Bod dynol | Llygoden | |||||||||||||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Lleoliad (UCSC) | n/a | n/a | |||||||||||||||
PubMed search | [1] | n/a | |||||||||||||||
Wicidata | |||||||||||||||||
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Cyfystyron golygu
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 EIF1AX.
- EIF1A
- EIF4C
- eIF-1A
- eIF-4C
- EIF1AP1
Llyfryddiaeth golygu
- "Prevalence and phenotypic correlations of EIF1AX mutations in thyroid nodules. ". Endocr Relat Cancer. 2016. PMID 26911375.
- "Efficiency of the elongation factor-1alpha promoter in mammalian embryonic stem cells using lentiviral gene delivery systems. ". Stem Cells Dev. 2007. PMID 17784828.
- "EIF1AXand NRASMutations Co-occur and Cooperate in Low-Grade Serous Ovarian Carcinomas. ". Cancer Res. 2017. PMID 28646021.
- "eIF1A/eIF5B interaction network and its functions in translation initiation complex assembly and remodeling. ". Nucleic Acids Res. 2016. PMID 27325746.
- "SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas.". Acta Neuropathol Commun. 2016. PMID 26769193.