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  2. XY sex-determination system - Wikipedia

    en.wikipedia.org/wiki/XY_sex-determination_system

    Other species (including most Drosophila species) use the presence of two X chromosomes to determine femaleness: one X chromosome gives putative maleness, but the presence of Y chromosome genes is required for normal male development. In the fruit fly individuals with XY are male and individuals with XX are female; however, individuals with XXY ...

  3. Sexual differentiation in humans - Wikipedia

    en.wikipedia.org/wiki/Sexual_differentiation_in...

    In the absence of a Y chromosome, the fetus will undergo female development. This is because of the presence of the sex-determining region of the Y chromosome, also known as the SRY gene. [5] Thus, male mammals typically have an X and a Y chromosome (XY), while female mammals typically have two X chromosomes (XX).

  4. Lists of human genes - Wikipedia

    en.wikipedia.org/wiki/Lists_of_human_genes

    •List of human protein-coding genes page 4 covers genes SLC17A8–ZZZ3 NB: Each list page contains 5000 human protein-coding genes, sorted alphanumerically by the HGNC-approved gene symbol. Follow the Python code link for information about updates to the list of genes on these pages.

  5. Sex chromosome - Wikipedia

    en.wikipedia.org/wiki/Sex_chromosome

    Females therefore have 23 homologous chromosome pairs, while males have 22. The X and Y chromosomes have small regions of homology called pseudoautosomal regions. An X chromosome is always present as the 23rd chromosome in the ovum, while either an X or Y chromosome may be present in an individual sperm. [4]

  6. Acetylserotonin O-methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Acetylserotonin_O-methyl...

    N-Acetylserotonin O-methyltransferase is an enzyme that is coded for by genes located on the pseudoautosomal region of the X and Y chromosome, and is most abundantly found in the pineal gland and retina of humans. [8] The structure of N- Acetylserotonin O-methyltransferase has been determined by X-ray diffraction. [9]

  7. Pseudoautosomal region - Wikipedia

    en.wikipedia.org/wiki/Pseudoautosomal_region

    The SHOX gene in the PAR1 region is the gene most commonly associated with and well understood with regards to disorders in humans, [17] but all pseudoautosomal genes escape X-inactivation and are therefore candidates for having gene dosage effects in sex chromosome aneuploidy conditions (45,X, 47,XXX, 47,XXY, 47,XYY, etc.).

  8. Chromosome 4 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_4

    The chromosome is ~193 megabases in length. In a 2012 paper, 775 protein-encoding genes were identified on this chromosome. [4] 211 (27.9%) of these coding sequences did not have any experimental evidence at the protein level, in 2012. 271 appear to be membrane proteins. 54 have been classified as cancer-associated proteins.

  9. Amelogenin - Wikipedia

    en.wikipedia.org/wiki/Amelogenin

    The amelogenin gene has been most widely studied in humans, where it is a single copy gene, located on the X and Y chromosomes at Xp22.1–Xp22.3 and Yp 11.2 [5]. [3] The amelogenin gene's location on sex chromosomes has implications for variability both between the X chromosome form and the Y chromosome form (), and between alleles of AMELY among different populations.