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*  Chromosome 13 (human)
The following is a partial list of genes on human chromosome 5. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 13. Because researchers use different approaches to ... People normally have two copies of this chromosome. Chromosome 13 spans about 114 million base pairs (the building material of ... International Standing Committee on Human Cytogenetic Nomenclature (2013). ISCN 2013: An International System for Human ...
*  Robertsonian translocation
In humans, Robertsonian translocations generally occur in the five acrocentric chromosome pairs, namely 13, 14, 15, 21 and 22. ... or non-homologous chromosomes (i.e. two different chromosomes, not belonging to a homologous pair). A feature of chromosomes ... This type of translocation is cytologically visible, and can reduce chromosome number (from 23 to 22 pairs, in humans) if the ... In humans, when a Robertsonian translocation joins the long arm of chromosome 21 with the long arm of chromosomes 14 or 15, the ...
*  Eukaryotic chromosome fine structure
The repeats are normally several thousand base pairs in length. These sequences constitute about 21% of the human genome. Both ... Eukaryotic chromosome fine structure refers to the structure of sequences for eukaryotic chromosomes. Some fine sequences are ... They may also be involved in fillers for increasing chromosome size to some minimum threshold level necessary for chromosome ... Typical eukaryotic chromosomes contain much more DNA than is classified in the categories above. The DNA may be used as spacing ...
*  Wellcome Sanger Institute
The Institute was engaged in collaborations to sequence 8 of the 23 human pairs of chromosomes (1, 6, 9, 10, 13, 20, 22, and X ... "International Human Genome Sequencing Consortium Announces "Working Draft" of Human Genome". National Human Genome Research ... Human Genome Sequencing Consortium (2004). "Finishing the euchromatic sequence of the human genome". Nature. 431 (7011): 931- ... The Institute's research in human genetics focuses on the characterisation of human genetic variation in health and disease. ...
*  ALOX15
In humans, it is encoded by the ALOX15 gene located on chromosome 17p13.3. This 11 kilobase pair gene consists of 14 exons and ... 1992) demonstrated that genes for 12-lipoxygenase and 15-lipoxygenase are located on human chromosome 17, whereas the most ... Consequently, human ALOX15 is now referred to as arachidonate-15-lipoxygenase-1, 15-lipoxygenase-1, 15-LOX-1, 15-LO-1, human 12 ... The distribution of Alox15 in sub-human primates and, in particular, rodents differs significantly from that of human ALOX15; ...
*  C12orf40
In humans, the gene for C12orf40 is located on chromosome 12. There are 13 exons in the highest quality isoform, forming an ... mRNA of 2797 base pairs. Three other isoforms have been isolated. Homologs exist as distant as the green sea turtle and ... The human C12orf40 protein is 652 amino acids in length. Its molecular weight is predicted to be 74.52 kDa, and its isoelectric ... Kenta Nakai, Human Genome Center, Institute for Medical Science, University of Tokyo, Japan.[2] Edgar, R. (1 January 2002). " ...
*  Arachidonate 5-lipoxygenase
The ALOX5 gene, which occupies 71.9 kilobase pairs (kb) on chromosome 10 (all other human lipoxygenases are clustered together ... Aberrant expression of LOX5 is seen in various types of human cancer tumors in vivo as well as in various types of human cancer ... Studies with cultured human cells have found that there are a large number of ALOX5 mRNA splice variants due to Alternative ... Human ALOX5 is a soluble, monomeric protein consisting of 673 amino acids with a molecular weight of ~78 kDa. Structurally, ...
*  CCDC47
The CCDC47 gene itself is located on the minus strand of human chromosome 17 and contains 13 exon splice sites and 14 distinct ... In regards to the mRNA, translation begins at base pair 337 and ends at 1728. There is a strong stem loop located in the 5' UTR ... Coiled-coil domain 47 (CCDC47) is a gene located on human chromosome 17, specifically locus 17q23.3 which encodes for the ... Percent identity of human CCDC47 to a specific ortholog declines with increasing years of divergence, as expected. Homologous ...
*  BRCA2
The ssDNA complexed with DMC1 can pair with homologous ssDNA from another chromosome during the synopsis stage of meiosis to ... BRCA2 is a human tumor suppressor gene (specifically, a caretaker gene), found in all humans; its protein, also called by the ... The human reference BRCA 2 gene contains 27 exons, and the cDNA has 10,254 base pairs coding for a protein of 3418 amino acids ... In mice and humans, BRCA2 primarily mediates orderly assembly of RAD51 on single-stranded (ss) DNA, the form that is active for ...
*  Human genetic variation
Chromosome abnormalities are detected in 1 of 160 live human births. Apart from sex chromosome disorders, most cases of ... The human nucleotide diversity is estimated to be 0.1% to 0.4% of base pairs. A difference of 1 in 1,000 amounts to ... According to a 2000 study of Y-chromosome sequence variation, human Y-chromosomes trace ancestry to Africa, and the descendants ... No two humans are genetically identical. On average, in DNA sequence, each human is 99.5% similar to any other human. Even ...
*  Dopamine receptor D4
The 48-base pair VNTR has been the subject of much speculation about its evolution and role in human behaviors cross-culturally ... The human protein is coded by the DRD4 on chromosome 11 located in 11p15.5.[citation needed] There are slight variations ( ... mutations/polymorphisms) in the human gene: A 48-base pair VNTR in exon 3 C-521T in the promoter 13-base pair deletion of bases ... "The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus". American Journal of Human Genetics ...
*  C21orf59
... is a gene found on the 21st chromosome at 21q22.1. A total of thirteen splice variants have been found, but only ... The most common form of C21orf59 mRNA has 1427 base pairs broken into seven exons. Its closest neighbors on the chromosome are ... 2006). "Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins ... "Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins". BMC ...
*  Proser1
"Human PubMed Reference:". "GeneCards". Human Gene Database. "BioCompare". BioCompare. "Ensembl". Ensembl. "GeneCards". Human ... It spans from 39,009,865 base pairs from the pter to 39,038,095 bp from the pter, with a size of 28,231 bases. PROSER1 has a ... Genes STOML3 and NHLRC3 neighbor PROSER1 on chromosome 13. Expressed Sequence Tag mapping of PROSER1 expression shows that it ... According to the Human Protein Atlas, PROSER1 has general cytoplasmic expression and is expressed in all RNA tissue categories ...
*  Takifugu rubripes
... that of the human genome, although the number of chromosomes (22) is comparable to that of humans (23). This makes it ... It remains among the smallest known vertebrate genomes; its number of base pairs is ~6% and the number of previously known ... Current estimates show a total of 392,376,244 base pairs, 1,138 known and 18,093 novel protein-coding genes, and 593 RNA genes ... After being initiated in 1989, it was the first vertebrate genome after the human genome to be made publicly available. ...
*  Smith-Lemli-Opitz syndrome
It is 14100 base pairs of DNA in length, and contains nine exons, the corresponding mRNA is 2786 base pairs in length (the ... they present lower levels of 7-DHC and 8-DHC than are seen in humans. This can be explained by the fact that humans experience ... Given that SLOS is an autosomal recessive disorder, mutations in DHCR7 on both copies of chromosome 11 are necessary to have ... The human version of this enzyme is predicted to have a molecular weight of 54,489 kDa, and an isoelectric point of 9.05. The ...
*  KIAA0895
... is a human gene that encodes a protein known as KIAA0895 protein or hypothetical protein LOC23366. Other known aliases ... The genomic DNA is 65,976 [base pair]s long, while the longest mRNA that it produces is 4463 bases long. KIAA0895 is surrounded ... The KIAA0895 gene is located at p14.2 on chromosome 7. It can be transcribed into 15 transcript variants, which in turn can ... KIAA0895 has one paralog in humans known as KIAA0895L. Orthologs have been found in all mammals, and eukaryotes through T. ...
*  RUFY2
The human RUFY2 gene is located on the long (q) arm of chromosome 10 at region 21 band 3, from base pair 70,100,864 to base ... The gene produces a 2,080 base pair mRNA. There are 18 predicted exons in the human gene with 13 alternative transcripts. 8,180 ... RUN and FYVE domain containing 2 (RUFY2) is a protein that in humans is encoded by the RUFY2 gene. The RUFY2 gene is named for ... While 6,770 base pairs downstream from RUFY2 is a DNA2 conserved helicase/nuclease involved in the maintenance of mitochondrial ...
*  Cell (biology)
... including 22 homologous chromosome pairs and a pair of sex chromosomes. The mitochondrial genome is a circular DNA molecule ... In humans the nuclear genome is divided into 46 linear DNA molecules called chromosomes, ... The DNA of a prokaryotic cell consists of a single chromosome that is in direct contact with the cytoplasm. The nuclear region ... It houses the cell's chromosomes, and is the place where almost all DNA replication and RNA synthesis (transcription) occur. ...
*  NDUFA13
The NDUFA13 gene is located on the p arm of chromosome 19 in position 13.2 and spans 11,995 base pairs. The gene produces a 17 ... The human NDUFA13 gene codes for a subunit of Complex I of the respiratory chain, which transfers electrons from NADH to ... Chidambaram NV, Angell JE, Ling W, Hofmann ER, Kalvakolanu DV (2000). "Chromosomal localization of human GRIM-19, a novel IFN- ... Ton C, Hwang DM, Dempsey AA, Liew CC (Jan 1998). "Identification and primary structure of five human NADH-ubiquinone ...
*  HIST1H2BO
2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805-11. doi:10.1038/nature02055. PMID ... "A novel divergently transcribed human histone H2A/H2B gene pair". DNA Seq. 1 (6): 409-13. doi:10.3109/10425179109020799. PMID ... Histone H2B type 1-O is a protein that in humans is encoded by the HIST1H2BO gene. Histones are basic nuclear proteins that are ... 2006). "Monoubiquitination of human histone H2B: the factors involved and their roles in HOX gene regulation". Mol. Cell. 20 (4 ...
*  HIST1H2AM
2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805-11. doi:10.1038/nature02055. PMID ... "A novel divergently transcribed human histone H2A/H2B gene pair". DNA Seq. 1 (6): 409-13. doi:10.3109/10425179109020799. PMID ... 1999). "The human H2A and H2B histone gene complement". Biol. Chem. 380 (1): 7-18. doi:10.1515/BC.1999.002. PMID 10064132. Deng ... Histone H2A type 1 is a protein that in humans is encoded by the HIST1H2AM gene. Histones are basic nuclear proteins that are ...
*  C10orf67
The gene spans 142,366 base pairs and is located at the 10p12.2 locus on the minus (-) or sense strand of chromosome 10. It is ... "C10orf67 chromosome 10 open reading frame 67 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2017-04-30 ... Chromosome 10 open reading frame 67 (C10orf67), also known as C10orf115, LINC01552, and BA215C7.4, is an un-characterized human ... "Homo sapiens chromosome 10 open reading frame 67 (C10orf67), mRNA". www.ncbi.nlm.nih.gov. Retrieved 2017-02-05. Database, ...
*  PITX1
... maps to human chromosome 5 (BFT) and mouse chromosome 13 (Bft)". Genomics. 40 (1): 108-13. doi:10.1006/geno.1996.4558. PMID ... paired-like homeodomain 1 is a protein that in humans is encoded by the PITX1 gene. This gene encodes a member of the RIEG/PITX ... "Identification of PITX1 as a TERT suppressor gene located on human chromosome 5". Molecular and Cellular Biology. 31 (8): 1624- ... "Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a ...
*  COX5A
The COX5A gene, located on the q arm of chromosome 15 in position 24.1, is made up of 5 exons and is 17,880 base pairs in ... Cytochrome c oxidase subunit 5a is a protein that in humans is encoded by the COX5A gene. Cytochrome c oxidase 5A is a subunit ... Human COX5A genome location and COX5A gene details page in the UCSC Genome Browser. Mass spectrometry characterization of COX5A ... Rizzuto R, Nakase H, Zeviani M, DiMauro S, Schon EA (Sep 1988). "Subunit Va of human and bovine cytochrome c oxidase is highly ...
*  UBE3A
... from base pair 23,133,488 to base pair 23,235,220. Mutations within the UBE3A gene are responsible for some cases of Angelman ... Lu Z, Hu X, Li Y, Zheng L, Zhou Y, Jiang H, Ning T, Basang Z, Zhang C, Ke Y (August 2004). "Human papillomavirus 16 E6 ... Other abnormalities in this region of chromosome 15 can also cause Angelman syndrome. These chromosomal changes include ... Anan T, Nagata Y, Koga H, Honda Y, Yabuki N, Miyamoto C, Kuwano A, Matsuda I, Endo F, Saya H, Nakao M (November 1998). "Human ...
*  TENM3
Odz1 to Mouse Chromosome 11; and ODZ3 to Human Chromosome Xq25". Genomics. 58 (1): 102-3. doi:10.1006/geno.1999.5798. PMID ... Levine A, Bashan-Ahrend A, Budai-Hadrian O, Gartenberg D, Menasherow S, Wides R (May 1994). "odd Oz: A novel Drosophila pair ... Odz1to Mouse Chromosome 11; and ODZ3 to Human Chromosome Xq25". Genomics. 58 (1): 102-103. doi:10.1006/geno.1999.5798. PMID ... Ben-Zur, T.; Feige, E.; Motro, B.; Wides, R. (2000). "The Mammalian Odz Gene Family: Homologs of a Drosophila Pair-Rule Gene ...