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Chromosome 4 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 4 spans more than 190 million base pairs (the building material of DNA ) and represents between 6 and 6.5 percent of the total DNA in cells .
Normally, chromosomes are visible under a light microscope only during the metaphase of cell division, where all chromosomes are aligned in the center of the cell in their condensed form. [4] Before this stage occurs, each chromosome is duplicated , and the two copies are joined by a centromere—resulting in either an X-shaped structure if the ...
In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation, with two main types: reciprocal , and Robertsonian translocation.
The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living organisms.This number, along with the visual appearance of the chromosome, is known as the karyotype, [1] [2] [3] and can be found by looking at the chromosomes through a microscope.
Human chromosome 4 gene stubs (298 P) Pages in category "Genes on human chromosome 4" The following 200 pages are in this category, out of approximately 529 total.
15194 Ensembl ENSG00000197386 ENSMUSG00000029104 UniProt P42858 P42859 RefSeq (mRNA) NM_002111 NM_001388492 NM_010414 RefSeq (protein) NP_002102 NP_034544 Location (UCSC) Chr 4: 3.04 – 3.24 Mb Chr 5: 34.92 – 35.07 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Huntingtin (Htt) is the protein coded for in humans by the HTT gene, also known as the IT15 ("interesting transcript 15 ...
The Utah Hockey Club has chosen three finalists for the permanent team name it will adopt beginning with the 2025-26 NHL season. The franchise will use a final round of fan voting to decide among ...
The chromosomal basis of Wolf-Hirschhorn syndrome (WHS) consists of a deletion of the most terminal portion of the short arm of chromosome 4. The deleted segment of reported individuals represent about one half of the p arm, occurring distal to the bands 4p15.1-p15.2. The proximal boundary of the WHSCR was defined by a 1.9 megabase terminal ...