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HXA11 Polyclonal Antibody, 100ul Gene Editing Defects in this gene are

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HXA11 Polyclonal Antibody, 100ul Gene Editing Defects in this gene areIn vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved

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Description

Defects in this gene are a cause of startle disease with epilepsy (STHEE)

subcellular location:Associated with the endoplasmic reticulum and nuclear

tumorigenesis

a region associated with Cornelia de Lange syndrome

HXA11 Polyclonal Antibody, 100ul Gene Editing Defects in this gene areIn vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved

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