... also known as chromosome 8 open reading frame 47 (C8orf47). The ERICH5 gene is located on human chromosome 8 at 8q22.2 and ... The second isoform lacks the third and final exon and is 596 base pairs long. ERICH5 contains one conserved domain, a domain of ... Database, GeneCards Human Gene. "ERICH5 Gene - GeneCards , ERIC5 Protein , ERIC5 Antibody". www.genecards.org. Retrieved 2018- ... November 2008). "A comprehensive functional analysis of tissue specificity of human gene expression". BMC Biology. 6: 49. doi: ...

Source attribution, Articles with short description, Short description matches Wikidata, Genes on human chromosome 5, Wikipedia ... "A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis". Human ... The UQCRQ gene is located on the q arm of chromosome 5 in position 31.1 and spans 2,217 base pairs. The gene produces a 9.9 kDa ... Ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa is a protein that in humans is encoded by the UQCRQ gene. ...

Human C5orf24 is a protein-coding gene 26,133 base pairs long (chr5:134,833,603-134,859,735) composed of two exons and one ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 5, Animal proteins). ... C5orf24 (chromosome 5 open reading frame 24) is a protein encoded by the C5orf24 gene (5q31.1) in humans. C5orf24 is primarily ... The human C5orf24 gene has three mRNA transcript variants. Both transcript variant 1 and 2 encode protein isoform 1 which is ...

In humans, FAM110A is located on the plus strand at 20p13. The gene transcript is found from base pairs 833,715 to 846,279, ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 20, Genetics, Protein ... All human FAM110A transcript variants encode the same protein, which is 295 amino acids in length. The human FAM110A protein is ... Human FAM110A is also predicted to contain a frequency of arginine residues two standard deviations higher than average. The ...

The human XRCC4 gene is located on chromosome 5, specifically at 5q14.2. This gene contains eight exons and three mRNA ... the DSB repair pathway will use homologous recombination by pairing with the newly synthesized daughter strand to repair the ... Giaccia AJ, Denko N, MacLaren R, Mirman D, Waldren C, Hart I, Stamato TD (September 1990). "Human chromosome 5 complements the ... Genes on human chromosome 5, Protein pages needing a picture, Wikipedia articles incorporating text from the United States ...

The human RAD21 (hRAD21) gene is located on the long (q) arm of chromosome 8 at position 24.11 (8q24.11). In 1997, RAD21 was ... The major role of Rad21L cohesin complex is in homologue pairing and synapsis, not in sister chromatid cohesion, whereas Rec8 ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 8, Wikipedia articles ... June 2012). "RAD21 mutations cause a human cohesinopathy". American Journal of Human Genetics. 90 (6): 1014-27. doi:10.1016/j. ...

... is located on the negative DNA strand of the short arm of chromosome 6 at locus 12. The gene is 28,744 base pairs long ... In humans, C5orf34 contains two domains of unknown function, DUF 4520 (pfam 15016) and DUF 4524 (pfam 150125), found between ... and spans from base pair 43,486,701 to base pair 43,515,445. The gene produces a single transcript of 2,540 base pairs long and ... C5orf34 (chromosome 5 open reading frame 34) is a protein that in humans is encoded by the C5orf34 gene (5p12). C5orf34 is ...

... arm of chromosome 11 at position 14.3 Molecular location: base pairs 22,192,485 to 22,283,367 on chromosome 11 (Homo sapiens ... ANO5_HUMAN anoctamin-5 GDD1 gnathodiaphyseal dysplasia 1 protein integral membrane protein GDD1 LGMD2L TMEM16E transmembrane ... American Journal of Human Genetics. 86 (2): 213-21. doi:10.1016/j.ajhg.2009.12.013. PMC 2820170. PMID 20096397. Jarmula A, ... is a protein that in humans is encoded by the ANO5 gene. The ANO5 gene provides instructions for making a protein called ...

UTR of 94 base pairs and a 3' UTR of 1273 base pairs. It is expressed at high levels in most tissues of the human body. It is ... Genes on human chromosome 5, All stub articles, Human chromosome 5 gene stubs). ... FAM114A2 (chromosome 5 open reading frame 3) is a gene on chromosome 5 in humans that encodes a protein FAM114A2. The protein ... 2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci ...

The human gene spans 30,775 base pairs over 4 exons and 3 introns for transcript variant 1, 5 exons and 4 introns for ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 1, Proteins). ... Human dendritic cells infected with Chlamydia pneumoniae showed an absence of TMED5 expression compared to uninfected dendritic ... Compared to the reference set of human proteins, TMED5 has fewer alanine and proline residues but more aspartic acid and ...

The gene that encodes the APOL1 protein is 14,522 base pairs long and found on the human chromosome 22, on the long arm at ... have been recently identified with relevance to human phenotypes. The G1 is a pair of two non-synonymous single nucleotide ... The existence of these variants are only found on African chromosomes and exist in people with recent African ancestry (. ... Apolipoprotein L1 is a protein that in humans is encoded by the APOL1 gene. Two transcript variants encoding two different ...

Genes on human chromosome 19, CS1: long volume value, All stub articles, Human chromosome 19 gene stubs). ... is encoded by six highly homologous and structurally similar genes that are arranged in tandem and inverted pairs on chromosome ... 1984). "The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19". Hum. Genet. 67 (2): 174-7. ... 1997). "Expression of the human chorionic gonadotropin-beta gene cluster in human pituitaries and alternate use of exon 1". J. ...

Genes on human chromosome 19, CS1: long volume value, All stub articles, Human chromosome 19 gene stubs). ... is encoded by six highly homologous and structurally similar genes that are arranged in tandem and inverted pairs on chromosome ... 1984). "The beta chorionic gonadotropin-beta luteinizing gene cluster maps to human chromosome 19". Hum. Genet. 67 (2): 174-177 ... 1997). "Expression of the human chorionic gonadotropin-beta gene cluster in human pituitaries and alternate use of exon 1". J. ...

Located on the negative strand of human DNA, TMEM143 spans 31,882 base pairs on human chromosome 19 (19q13.33), neighbored by ... human)]". NCBI. "Tmem143 (human)". NCBI. "TMEM143 Gene". GeneCards. "TMEM143 - Normal human tissue expression profiling". NCBI ... There are no known paralogs for the human TMEM143 sequence. Possible human expression of TMEM143 protein occurs in Jurkat cells ... Chromosome 14 open reading frame 28 (C14orf28), Chromosome 14 open reading frame 28 (TRIN71), and Cytoplasmic polyadenylation ...

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, ...

... encoded by six highly homologous genes that are arranged in tandem and inverted pairs on chromosome 19q13.3 - CGB (1, 2, 3, 5, ... Talwar GP (1997). "Fertility regulating and immunotherapeutic vaccines reaching human trials stage". Human Reproduction Update ... Genes on human chromosome 6, Pages using infobox protein with unknown parameters, Protein pages needing a picture, Genes on ... Human chorionic gonadotropin interacts with the LHCG receptor of the ovary and promotes the maintenance of the corpus luteum ...

The UBR1 gene is located on human chromosome 15. Johanson-Blizzard Syndrome may be diagnosed based on the identification of ... 161,000 base pairs) in length and contains 47 exons expressed as mRNA. In comparison, mouse 120kb UBR1 is in the middle of ... chromosome 2 and shows homology of synteny (co-localized loci in same chromosome) with its human counterpart through its 50 ... specifically at a fixed chromosomal position known as locus 15q15.2 or human chromosome 15, q-arm region 1, band 5, sub-band 2 ...

The human LECT2 gene, LECT2, is located on the long, i.e, "q", arm of chromosome 5 at position q31.1 (notated as 5q31.1). This ... Human LECT2 is composed of 4 exons, 3 introns, and ~8,000 base pairs. The gene has numerous single nucleotide variants as well ... 2004). "The DNA sequence and comparative analysis of human chromosome 5". Nature. 431 (7006): 268-74. doi:10.1038/nature02919. ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 5). ...

The human LECT2 gene, LECT2, is located on the long, i.e, "q", arm of chromosome 5 at position q31.1 (notated as 5q31.1). This ... Human LECT2 is composed of 4 exons, 3 introns, and ~8,000 base pairs. The gene has numerous single nucleotide variants as well ... Human LECT2 has several different transcriptional initiation sights and codes for a mRNA composed of 1,000 to 1,300 ... "Crystal Structure of Human Leukocyte Cell-derived Chemotaxin 2 (LECT2) Reveals a Mechanistic Basis of Functional Evolution in a ...

Structural maintenance of chromosomes protein 6 is a protein that in humans is encoded by the SMC6 gene. The SMC6 was ... Once localized to the DNA, the SCM5/6 complex non-specifically binds to ~20 DNA base pairs. Smc6 and Smc5 proteins form a ... In humans, a chromosome breakage syndrome characterized by severe lung disease in early childhood is associated with a mutation ... 2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4". Nature. 434 (7034): 724-31. Bibcode: ...

Genes on human chromosome 6, All stub articles, Human chromosome 6 gene stubs). ... Dobner T, Wolf I, Mai B, Lipp M (Feb 1992). "A novel divergently transcribed human histone H2A/H2B gene pair". DNA Seq. 1 (6): ... 2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805-11. Bibcode:2003Natur.425..805M. doi: ... Histone H2B type 1-O is a protein that in humans is encoded by the HIST1H2BO gene. Histones are basic nuclear proteins that are ...

Chromosome 15 open reading frame 52 is a human protein encoded by the C15orf52 gene, its function is poorly understood. ... untranslated region of 15 base pairs and a long 3' untranslated region of 3782 base pairs. In the long 3' untranslated region, ... C15orf52 is a gene located on the reverse strand of chromosome 15 in the species Homo sapiens at locus 15q15.1. The gene is ... Glycine and Arginine were found at higher frequencies than other proteins in humans. The isoelectric point of the protein is ...

Partial monosomy occurs when a portion of one chromosome in a pair is missing. Human conditions due to monosomy: Turner ... Monosomy is a form of aneuploidy with the presence of only one chromosome from a pair. ... People with Turner syndrome typically have one X chromosome instead of the usual two X chromosomes. Turner syndrome is the only ... a partial monosomy caused by a deletion of the end of the short arm of chromosome 5 1p36 deletion syndrome - a partial monosomy ...

Genes on human chromosome 5). ... meaning it has length of 40,927 base pairs. TMEM267 produces 13 ... TMEM267 was shown to be one of 26 over-expressed genes on chromosome 5p, meaning it belongs to a group of genes which likely ... TMEM267 is a protein that in humans is encoded by the TMEM267 gene. It is a possible oncogene which encodes a transmembrane ... TMEM267 is expressed at 1.6 times the average gene on chromosome 5. The table below describes a curated set of transcription ...

In humans, FAM71D codes for an mRNA strand that is 1790 base pairs long. The human mRNA is composed of a 5' untranslated region ... FAM71D, also known as chromosome 14 open reading frame 54 (C14orf54), is a protein that in humans is encoded by the FAM71D gene ... In humans, FAM71D is located at 14q23.3 and stretches between positions 67189393 and 67228550 (span 39157 bp). It codes for at ... GEO microarray data also supports the expression of FAM71D in humans No studies have directly associated FAM71D protein with ...

December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". ... "Y-chromosome diversity is inversely associated with language affiliation in paired Austronesian- and Papuan-speaking ... November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358-361. doi: ... 1 July 2001). "Hierarchical Patterns of Global Human Y-Chromosome Diversity". Molecular Biology and Evolution. 18 (7): 1189- ...

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; ...

Among the 23 pairs of chromosomes, there are 22 pairs of autosomes and one pair of sex chromosomes. Like other mammals, humans ... chromosome 2 was formed from the joining of two other chromosomes, leaving humans with only 23 pairs of chromosomes, compared ... MacAndrew A. "Human Chromosome 2 is a fusion of two ancestral chromosomes". Evolution pages. Archived from the original on 9 ... the eight richest humans are worth the same monetary value as the poorest half of all the human population. Humans commit ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 19, Wikipedia articles ... the first of which encodes a 66 base pair 5'-untranslated sequence, the second of which has an intronless open reading frame ... Bao L, Gerard NP, Eddy RL, Shows TB, Gerard C (Jun 1992). "Mapping of genes for the human C5a receptor (C5AR), human FMLP ... Bao L, Gerard NP, Eddy RL, Shows TB, Gerard C (Jun 1992). "Mapping of genes for the human C5a receptor (C5AR), human FMLP ...

In humans, a chromosome breakage syndrome characterized by severe lung disease in early childhood is associated with a mutation ... Once localized to the DNA, the SCM5/6 complex non-specifically binds to ~20 DNA base pairs Smc5 and Smc6 proteins form a ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 9). ... In humans the complex is localized to viral DNA sequences using SMC5/6 localization factors 1 and 2 (SLF1 and SLF2) which ...

Normal human sex cells have 23 chromosomes. Other human cells have 46 chromosomes, arranged in 23 pairs. Scientific notation ... "Human genetics and disease: Human cytogenetics: 46 chromosomes, 46 years and counting" Nature Reviews Genetics 3 (2002): 769. " ... "Human cytogenetics was born in 1956 with the fundamental, but empowering, discovery that normal human cells contain 46 ... "Chromosome analysis of human oocytes recovered from preovulatory follicles in stimulated cycles" New England Journal of ...

Genes on human chromosome 17, Protein pages needing a picture, Human gene pages with Wikidata item, All stub articles, Human ... The gene has a size of 5961 base pairs and contains five exons. PRR29 is located on the long arm of chromosome 17 (17q23.3), ... "C21orf58 chromosome 21 open reading frame 58 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-04-28 ... PRR29 (proline-rich protein 29) is a protein encoded by the PRR29 gene located in humans on chromosome 17 at 17q23. Its ...