All strawberry (Fragaria) species have a base haploid count of seven chromosomes; Fragaria vesca is diploid, having two pairs ... Evidence from archaeological excavations suggests that Fragaria vesca has been consumed by humans since the Stone Age. Woodland ... Mayrose, Itay; Lysak, Martin A (2020). "The Evolution of Chromosome Numbers: Mechanistic Models and Experimental Approaches". ... Renner, Susanne S.; Müller, Niels A. (2021). "Plant sex chromosomes defy evolutionary models of expanding recombination ...

The leaves are arranged alternately along the stem, are up to about 9 cm long, have 2-3 pairs of leaflets, and end in branched ... Vicia bithynica is not cultivated for human or livestock consumption. The seeds contain high levels of vicine, which causes ... The flowers are arranged in pairs (although sometimes solitary) on long (5 cm) peduncles branching from the leaf axils. The ...

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; ...

The gene paralog FAM71F1 and the gene LINC01000 directly neighbor FAM71F2 on chromosome 7. The gene spans 30,627 base pairs and ... FAM71F2 gene is located on chromosome 7 in humans (7q32.1), starting at 128,671,636 and ending at 128,702,262 on the positive ... The time of divergence between eight orthologs from the human FAM71F2 is shown in Figure 5. It is not found in birds or in ... Isoform a is the longest of the mRNA transcripts and spans 5,775 base pairs that translates into a 309 amino acids sequence. It ...

The TMEM251 gene is located on human chromosome 14, at 14q32.12, on the plus strand. The gene size is 1,277 base pairs. It ... The promoter region starts 500 base pairs upstream of the 5 UTR of TMEM251 mRNA transcript and contains part of this 5 UTR. ... "Q8N6I4 - TM251_HUMAN". UniProt. UnitProt. Retrieved 9 May 2015. "Human BLAT Search". UCSC Genome Browser. UCSC. Retrieved 9 May ... EST Profile data shows the tissue expression of TMEM251 in humans. TMEM251 has no paralogs in humans. It does have orthologs ...

The MORN1 gene is located on Chromosome 1 at locus 1p36.33 and contains 7 MORN repeats. It has 1641 base pairs in 14 exons in ... CS1 errors: missing periodical, Articles with short description, Short description matches Wikidata, Genes on human chromosome ... 2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315-21. Bibcode:2006Natur.441.. ... MORN1 containing repeat 1, also known as Morn1, is a protein that in humans is encoded by the MORN1 gene. The function of Morn1 ...

It is located on the human chromosome 4 at 4q35.1. The function of the protein encoded by this gene is not well understood, but ... The total span of the gene, including 5 and 3 UTR, is 3149 base pairs. The gene is flanked on the left by NUDT13 (nudix ... Overall in the human body, this gene is expressed at levels slightly below the average human gene expression level. The protein ... A Systematic Exploration of the Human Interactome. Cell, 162(2), 425-440. doi:10.1016/j.cell.2015.06.043 "ABHD8_HUMAN". UniProt ...

Chromosome 18 open reading frame 63 is a protein which in humans is encoded by the C18orf63 gene. This protein is not yet well ... This gene is located at band 22, sub-band 3, on the long arm of chromosome 18. It is composed of 5065 base pairs spanning from ... "C18orf63 chromosome 18 open reading frame 63 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2018-02-19 ... CS1 errors: generic name, Articles with short description, Short description matches Wikidata, Genes on human chromosome 18, ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 20, Genes, Human proteins). ... with the cDNA being 204,000 base pairs orientated on the plus strand. This codes for a protein of 408 amino acids with a ... The SLX4IP gene is located on the short arm (p) of chromosome 20 at position 12.2 (20p12.2). The human SLX4IP gene contains 14 ... Orthologs for the human SLX4IP gene have also been identified in 283 other organisms. The SLX4IP protein is expressed at its ...

This gene is found on the plus strand of chromosome 17 at locus 17q11.2. It spans from base pairs 31,254,928 to 31,272,124. ... CS1 errors: missing periodical, Articles with short description, Short description matches Wikidata, Genes on human chromosome ... "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome ... This missing region corresponds to 85 base pairs near the end of the 5 UTR. Variant one is more abundant than Variant two with ...

The SLC66A3 is a gene consisting of 26,831 base pairs spanning from 11,155,467 to 11,178,856 on chromosome 2. SLC66A3 mapped to ... Solute carrier family 66 member 3 is a gene in humans that encodes the protein SLC66A3. The function of the SLC66A3 protein is ... The promoter of SLC66A3 is 1,169 base pairs long and is located 1000 base pairs upstream of the 5 UTR. Many different ... "AceView: Gene:PQLC3, a comprehensive annotation of human, mouse and worm genes with mRNAs or ESTsAceView". www.ncbi.nlm.nih.gov ...

Articles with short description, Short description is different from Wikidata, Genes on human chromosome X). ... The first ninety base pairs compose the five prime untranslated region and the last 1913 base pairs compose the three prime ... The isoelectric point of EFHC2 is estimated to be 7.13 in humans. Relative to other proteins expressed in humans, EFHC2 has ... EFHC2 is located on the negative strand (sense strand) of the X chromosome at p11.3. EFHC2 is one of a few, select number of ...

"MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice". ... Genes on human chromosome 1, Webarchive template wayback links). ... MutS protein homolog 4 is a protein that in humans is encoded ... indicating that it is not needed for establishing the preceding stages of pairing and synapsis of homologous chromosomes. In an ... Yi W, Wu X, Lee TH, Doggett NA, Her C (Jul 2005). "Two variants of MutS homolog hMSH5: prevalence in humans and effects on ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 22). ... "Structural basis for octameric ring formation and DNA interaction of the human homologous-pairing protein Dmc1". Mol. Cell. 14 ... "The DNA sequence of human chromosome 22". Nature. 402 (6761): 489-95. Bibcode:1999Natur.402..489D. doi:10.1038/990031. PMID ... Habu T, Taki T, West A, Nishimune Y, Morita T (1996). "The mouse and human homologs of DMC1, the yeast meiosis-specific ...

Uncharacterized protein C14orf80 is a protein which in humans is encoded by the chromosome 14 open reading frame 80, C14orf80, ... Of the mRNA variants that have been found experimentally, the longest is 1,719 base pairs and produces a protein with 426 amino ... C14orf80 is 9,393 base pairs long and contains 11 exons that can be alternatively spliced to form different mRNA variants. ... Behrends C, Sowa ME, Gygi SP, Harper JW (July 2010). "Network organization of the human autophagy system". Nature. 466 (7302): ...

Covering a total of 45,038 base pairs (bp) along the chromosome, the TMEM229B gene has a total of 3 exons in its primary ... Human genes, Proteins, Genes on human chromosome 14). ... "Human Gene TMEM229B (uc001xjk.2) Description and Page Index". ... Transmembrane protein 229b is a protein that in humans is encoded by the TMEM229b gene. The TMEM229B gene is also known as ... "Genecards". The Human Gene Compendium. Weizmann Institute of Science with Xennex Inc. Retrieved 24 April 2011. "Chromosomal ...

Genes on human chromosome X, Pages using multiple image with auto scaled images, Human proteins). ... Including 5 and 3 untranslated regions, isoform 1 is 18,515 base pairs long, spanning chromosome X at 40,626,921 - 40,647,554 ... Chromosome X Open Reading Frame 38 (CXorf38) is a protein which, in humans, is encoded by the CXorf38 gene. CXorf38 appears in ... UCSC entry on CXorf38 variant 1 "CXorf38 chromosome X open reading frame 38 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm ...

Uncharacterized protein Chromosome 1 Open Reading Frame 27 is a protein in humans, encoded by the C1orf27 gene. It is accession ... This is a membrane protein that is 3926 base pairs long with the most extensive string of amino acids being 454aa long. C1orf27 ... The primary encoded protein of C1orf27 consists of 454 amino acid residues and is 3926 base pairs long. It consists of 14 total ... Expression was also localized to the nucleoplasm and plasma membrane in humans but is localized to the cytosol in mice. There ...

If two given DNA markers are far apart on the initial chromosome, then it is likely that they will appear in distinct fragments ... Radiation hybrid mapping was also used in constructing early physical maps of the human genome. Deloukas, Panos (23 September ... A radiation hybrid is "a cell or organism that contains fragments of chromosomes from a second organism".: 82 Radiation hybrids ... Radiation hybrid mapping (also known as RH mapping) is a technique for mapping mammalian chromosomes. Radiation hybrid mapping ...

The SLC2A1 gene is located on the p arm of chromosome 1 in position 34.2 and has 10 exons spanning 33,802 base pairs. The gene ... GLUT 1 of humans and mice have 98% identity at the amino acid level. GLUT 1 is encoded by the SLC2 gene and is one of a family ... S2CID 18128118.*Lay summary in: "How Humans Make Up For An Inborn Vitamin C Deficiency". ScienceDaily. March 21, 2008. Uldry ... "SLC2A1 - Solute carrier family 2, facilitated glucose transporter member 1 - Homo sapiens (Human) - SLC2A1 gene & protein". www ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 14, Wikipedia articles ... is 5,687 base pairs long. The NDUFB1 protein weighs 7 kDa and is composed of 58 amino acids. NDUFB1 is a subunit of the enzyme ... The human NDUFB1 gene codes for a subunit of Complex I of the respiratory chain, which transfers electrons from NADH to ... NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 1 is an enzyme that in humans is encoded by the NDUFB1 gene. NADH ...

In humans, CHST14 is positioned on the long arm (q) of chromosome 15 at position 15.1, from base pair 40,470,961 to base pair ... Genes on human chromosome 15, All stub articles, Human chromosome 15 gene stubs). ... Human CHST14 genome location and CHST14 gene details page in the UCSC Genome Browser. Otsuki T, Ota T, Nishikawa T, Hayashi K, ... August 2010). "Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome". Human Mutation. 31 (8): 966-74. ...

... in the SLC39A9 gene can occur due to genetic deletion of the q24.1-24.3 band of base pairs within the human chromosome 14. This ... Genes on human chromosome 14, G protein-coupled receptors, Solute carrier family). ... ZIP9 influxes zinc ions into the cytosol and its gene is expressed almost in every tissue of human body. The sub-cellular ... Role of human ZIP9 in testosterone-induced prostate and breast cancer cell apoptosis". Endocrinology. 155 (11): 4250-65. doi: ...

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 ... Human CCDC47 genome location and CCDC47 gene details page in the UCSC Genome Browser. (All articles with dead external links, ...

Genes on human chromosome 7, All stub articles, Human chromosome 7 gene stubs). ... a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the ... "Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers". Proceedings of the National ... Stromal antigen 3 is a protein that in humans is encoded by the STAG3 gene. STAG3 protein is a component of a cohesin complex ...

Articles with short description, Short description matches Wikidata, Human genes, Genes on human chromosome 1, Human proteins, ... HSPB7 and its gene pair SRARP are located 5 kb apart on the opposite strands of chromosome 1p36.13. HSPB7 is widely expressed ... in humans is a protein encoded by a gene of the same name with four exons that is located on chromosome 1p36.13.,. HSPB7 ... "HSPB7_HUMAN". UniProt. Vos MJ, Kanon B, Kampinga HH (August 2009). "HSPB7 is a SC35 speckle resident small heat shock protein ...

Paired box gene 9, also known as PAX9, is a protein which in humans is encoded by the PAX9 gene. It is also found in other ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 14, Wikipedia articles ... In humans, a frameshift mutation in the paired domain of PAX9 was discovered in those affected with oligodontia. Multiple ... "A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia". Human Genetics. 114 (3): 242-9. doi: ...

It contains approximately 1 Gbp (giga base pairs) or 109 base pairs. This genome size is close to the average observed for ... Jha, A. N.; Hutchinson, T. H.; Mackay, J. M.; Elliott, B. M.; Pascoe, P. L.; Dixon, D. R. (1995). "The chromosomes Of ... The ciliary photoreceptor cells resemble molecularly and morphologically the rods and cones of the human eye. Additional, they ... A pair of these eyes mediate phototaxis in the early Platynereis dumerilii trochophore larva. In the later nectochaete larva, ...

For example, diploid human cells contain 23 pairs of chromosomes including 1 pair of sex chromosomes (46 total), half of ... Recombination among the 23 pairs of human chromosomes is responsible for redistributing not just the actual chromosomes, but ... The paired and replicated chromosomes are called bivalents (two chromosomes) or tetrads (four chromatids), with one chromosome ... The paired chromosomes are called bivalent or tetrad chromosomes. The pachytene stage (/ˈpækɪtiːn/ PAK-i-teen), also known as ...

Paired box protein Pax-1 is a protein that in humans is encoded by the PAX1 gene. This gene is a member of the paired box (PAX ... v t e (Articles with short description, Short description is different from Wikidata, Genes on human chromosome 20, Wikipedia ... 1989). "Conservation of the paired domain in metazoans and its structure in three isolated human genes". EMBO J. 8 (4): 1183-90 ... 2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865-71. Bibcode:2001Natur.414.. ...