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Benjamin Lewin is a molecular biologist who founded the journal Cell [1] and authored the textbook Genes. [2] He is credited with building Cell into a recognized journal of cellular biology in a short period of time to rival Nature and Science .
Human chromosome 13 gene stubs (132 P) Pages in category "Genes on human chromosome 13" The following 200 pages are in this category, out of approximately 214 total.
13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Depending upon the size and location of the deletion on chromosome 13, the physical and mental manifestations will vary. It has the potential to cause intellectual disability and congenital malformations that affect a ...
Retinoblastoma: A small percentage of retinoblastoma cases are caused by deletions in the region of chromosome 13 (13q14) containing the RB1 gene. [11] Children with these chromosomal deletions may also have intellectual disability, slow growth, and characteristic facial features (such as prominent eyebrows, a broad nasal bridge, a short nose ...
268379 Ensembl ENSG00000179869 ENSMUSG00000004668 UniProt Q86UQ4 Q5SSE9 RefSeq (mRNA) NM_152701 NM_152555 NM_178259 RefSeq (protein) NP_689914 NP_839990 Location (UCSC) Chr 7: 48.17 – 48.65 Mb Chr 11: 9.14 – 9.63 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse ATP-binding cassette sub-family A member 13 also known as ABCA13 is a protein that in humans is encoded by the ABCA13 ...
Short interspersed nuclear elements (SINEs) are non-autonomous, non-coding transposable elements (TEs) that are about 100 to 700 base pairs in length. [1] They are a class of retrotransposons, DNA elements that amplify themselves throughout eukaryotic genomes, often through RNA intermediates. SINEs compose about 13% of the mammalian genome. [2]
6137 100040416 Ensembl ENSG00000167526 ENSMUSG00000059776 UniProt P26373 n/a RefSeq (mRNA) NM_033251 NM_000977 NM_001243130 NM_001243131 XM_036163486 RefSeq (protein) NP_000968 NP_001230060 NP_150254 n/a Location (UCSC) Chr 16: 89.56 – 89.56 Mb Chr 3: 58.89 – 58.9 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse 60S ribosomal protein L13 is a protein that in humans is encoded by ...
This gene and other HOXB genes form a gene cluster on chromosome 17 in the 17q21.32 region. [6] Men who inherit a rare (<0.1% in a selected group of patients without clinical signs of prostate cancer ) genetic variant in HOXB13 (G84E or rs138213197) have a 10-20-fold increased risk of prostate cancer.