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Chromosome 9 is one of the 23 pairs of chromosomes in humans.Humans normally have two copies of this chromosome, as they normally do with all chromosomes. Chromosome 9 spans about 138 million base pairs of nucleic acids (the building blocks of DNA) and represents between 4.0 and 4.5% of the total DNA in cells.
Human chromosome 9 gene stubs (289 P) Pages in category "Genes on human chromosome 9" The following 200 pages are in this category, out of approximately 515 total.
Full trisomy 9 is a rare and fatal chromosomal disorder caused by having three copies of chromosome number 9.It can be a viable condition if the trisomic component affects only part of the cells of the body or in cases of partial trisomy of the short arm (trisomy 9p) in which cells have a normal set of two entire chromosomes 9 plus part of a third copy of the short arm ("p") of the chromosome.
80908 Ensembl ENSG00000175164 ENSG00000281879 ENSMUSG00000015787 UniProt P16442 P38649 RefSeq (mRNA) NM_020469 NM_030718 NM_001290444 RefSeq (protein) NP_065202 NP_001277373 NP_109643 Location (UCSC) Chr 9: 133.23 – 133.28 Mb Chr 2: 26.73 – 26.75 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Histo-blood group ABO system transferase is an enzyme with glycosyltransferase activity ...
Tyrosine-protein kinase ABL1 also known as ABL1 is a protein that, in humans, is encoded by the ABL1 gene (previous symbol ABL) located on chromosome 9. [5] c-Abl is sometimes used to refer to the version of the gene found within the mammalian genome, while v-Abl refers to the viral gene, which was initially isolated from the Abelson murine leukemia virus.
Monosomy 9p (also known as Alfi's Syndrome, 9p Minus or simply 9P-) is a rare chromosomal disorder in which some DNA is missing or has been deleted on the short arm region, "p", of one copy of chromosome 9 (9p22.2-p23). [1] [2] This deletion either happens de novo or as a result of a parent having the chromosome abnormality. [3]
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66902 Ensembl ENSG00000099810 ENSMUSG00000062937 UniProt Q13126 Q9CQ65 RefSeq (mRNA) NM_002451 NM_024433 RefSeq (protein) NP_002442 NP_077753 Location (UCSC) Chr 9: 21.8 – 21.94 Mb Chr 4: 89.06 – 89.1 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse S-methyl-5'-thioadenosine phosphorylase (MTAP) is an enzyme responsible for polyamine metabolism. In humans, it is encoded by the ...