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Homo sapiens cDNA clone IMAGE:5285105, containing frame-shift errors

GenBank: BC036069.1

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Reference sequence information

More about the XYLT2 gene

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  • reagents [ExactAntigen/Labome]
    reagents
    ExactAntigen/Labome

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  • Homo sapiens cDNA clone IMAGE:5285105, containing frame-shift errors
    Homo sapiens cDNA clone IMAGE:5285105, containing frame-shift errors
    gi|23271284|gb|BC036069.1|
    Nucleotide
  • Netherton Syndrome
    Netherton Syndrome
    Rare autosomal recessive disease with variable expressions. Clinical features of the disease include variable ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; bamboo hair (trichorrhexi...<br/>Year introduced: 2010
    MeSH
  • Ichthyosiform Erythroderma, Congenital
    Ichthyosiform Erythroderma, Congenital
    Designation for several severe forms of ichthyosis, present at birth, that are characterized by hyperkeratotic scaling. Infants may be born encased in a collodion membrane whi...<br/>Year introduced: 1991
    MeSH
  • Focal Facial Dermal Dysplasias
    Focal Facial Dermal Dysplasias
    A heterogenous group of genetic disorders characterized by scar-like atrophic lesions on the temple region of the head including preauricular area. Location of skin defects is...<br/>Year introduced: 2022
    MeSH

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