*  Gene dosage - Wikipedia
2014). "Chromosome position effects on gene expression in Escherichia coli K-12". Nucleic Acids Research. 42 (18): 11383-11392 ... The bacterial chromosome is present only in one copy per cell, but there can still be variation in gene dosage due to DNA ... slight gene dosage differences are responsible for variation in gene expression depending on the position on the chromosome. ... In Down syndrome, the gene expression on chromosome 21 has increased 50%, and this results in significant health and mental ...
  https://en.wikipedia.org/wiki/Gene_dosage
*  Haplogroup G-P303 - Wikipedia
L660 is found at position 12511525 on the Y chromosome and is a change from C to A. L662 is found at position 16446702 and is a ... Z1903 is found at chromosome position 15106340 and represents a mutation from A to G. Z724 is found at position 6895545 and ... L1264 is at position 7704368, mutation A to G; L1265 at position 12741229, mutation A to G; and L1268 at position 20081319, T ... It represents a mutation from A to G and is found at position 16903082 on the Y chromosome. Most, if not all, these L640+ men ...
  https://en.wikipedia.org/wiki/Haplogroup_G-P303
*  Gerald Schatten - Wikipedia
Luetjens CM, Payne C, Schatten G (April 1999). "Non-random chromosome positioning in human sperm and sex chromosome anomalies ... He successively occupied the following positions: 1976-1985: Assistant Professor, Associate Professor, Full Professor of ...
  https://en.wikipedia.org/wiki/Gerald_Schatten
*  Kinesin family member 11 - Wikipedia
The function of this gene product includes chromosome positioning, centrosome separation and establishing a bipolar spindle ... Recent data, however, finds that aspects of the 'force balance' model that posit spindle length and stability to be mediated by ... Sharp DJ, Yu KR, Sisson JC, Sullivan W, Scholey JM (May 1999). "Antagonistic microtubule-sliding motors position mitotic ... leaving centrally positioned centrosome pairs flanked by a radial array of microtubules with peripheral condensed chromosomes. ...
  https://en.wikipedia.org/wiki/Kinesin_family_member_11
*  Mir-15 microRNA precursor family - Wikipedia
In humans miR-15a and miR-16 are clustered within 0.5 kilobases at chromosome position 13q14. This region has been found to be ... The CHEK1 (checkpoint kinase 1) gene, located at chromosome position 11q24.2, is responsible for encoding the protein kinase ... These six highly conserved miRNAs are clustered on three separate chromosomes. ...
  https://en.wikipedia.org/wiki/Mir-15_microRNA_precursor_family
*  Thomas Cremer - Wikipedia
Cremer T, Cremer C, Schneider T, Baumann H, Hens L, Kirsch-Volders M (1982). "Analysis of chromosome positions in the ... Fall and resurrection of chromosome territories during the 1950s to 1980s. Part III. Chromosome territories and the functional ... "Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific ... "Specific staining of human chromosomes in Chinese hamster x man hybrid cell lines demonstrates interphase chromosome ...
  https://en.wikipedia.org/wiki/Thomas_Cremer
*  Notch 2 - Wikipedia
... and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated ... identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of ...
  https://en.wikipedia.org/wiki/Notch_2
*  Notch 3 - Wikipedia
Larsson C, Lardelli M, White I, Lendahl U (1994). "The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, ... "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12". Nat. ...
  https://en.wikipedia.org/wiki/Notch_3
*  Notch proteins - Wikipedia
Larsson C, Lardelli M, White I, Lendahl U (Nov 1994). "The human NOTCH1, 2, and 3 genes are located at chromosome positions ...
  https://en.wikipedia.org/wiki/Notch_proteins
*  OPN1LW - Wikipedia
OPN1LW and OPN1MW are on the X chromosome at position Xq28. They are in a tandem array, composed of a single OPN1LW gene which ... OPN1LW have tyrosine at position 277 and 309, and threonine at position 285. The identity of the amino acids at these positions ... OPN1LW is a gene on the X chromosome that encodes for long wave sensitive (LWS) opsin, or red cone photopigment. It is ... This would create colour vision deficiencies if either chromosome were passed onto a male offspring. The LWS type I opsin is a ...
  https://en.wikipedia.org/wiki/OPN1LW
*  Cistron - Wikipedia
... on one chromosome and has the mutation at position y {\displaystyle y} on the paired chromosome exhibits the recessive trait ... For example, suppose a mutation at a chromosome position x {\displaystyle x} is responsible for a recessive trait in a diploid ... unless both chromosomes of a pair have the mutation (homozygous mutation). Similarly, suppose a mutation at another position, y ... The positions x {\displaystyle x} and y {\displaystyle y} are said to be within the same cistron when an organism that has the ...
  https://en.wikipedia.org/wiki/Cistron
*  Haplogroup G-FGC7535 - Wikipedia
L293 is found at chromosome position 10595022 and represents a mutation from G to C. The forward primer is ... The Y Chromosome Consortium (2002). "A Nomenclature System for the Tree of Human Y-Chromosomal Binary Haplogroups". Genome ... Haplogroup G-FGC7535, also known as Haplogroup G2a1 (and formerly G-L293), is a Y-chromosome haplogroup. It is an immediate ... June 2000). "Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes". Proc. ...
  https://en.wikipedia.org/wiki/Haplogroup_G-FGC7535
*  Mir-143 - Wikipedia
mir- 143 is located on chromosome 5 position 33 in the human genome. mir-143 is located very close to mir-145 in the genome and ...
  https://en.wikipedia.org/wiki/Mir-143
*  List of MeSH codes (G04) - Wikipedia
... chromosome positioning MeSH G04.335.130.107 --- blood cell count MeSH G04.335.130.107.330 --- erythrocyte count MeSH G04.335. ... chromosome segregation MeSH G04.335.134.220.220.687 --- meiosis MeSH G04.335.134.220.220.687.444 --- meiotic prophase i MeSH ... chromosome segregation MeSH G04.335.233.750.500.220.718 --- meiosis MeSH G04.335.233.750.500.220.718.500 --- meiotic prophase i ... chromosome pairing MeSH G04.335.233.750.500.220.875.500.299.500 --- synaptonemal complex MeSH G04.335.233.750.500.220.875.500. ...
  https://en.wikipedia.org/wiki/List_of_MeSH_codes_(G04)
*  Condensin - Wikipedia
Jeppsson K, Kanno T, Shirahige K, Sjögren C (2014). "The maintenance of chromosome structure: positioning and functioning of ... In Drosophila, condensin II subunits contribute to the dissolution of polytene chromosomes and the formation of chromosome ... "Condensin II promotes the formation of chromosome territories by inducing axial compaction of polyploid interphase chromosomes ... On the other hand, condensin I is present in the cytoplasm during interphase, and gains access to chromosomes only after the ...
  https://en.wikipedia.org/wiki/Condensin
*  Epigenetics of human development - Wikipedia
Another part of the RNA binds to the X-chromosome positioning PRC2 such that it can methylate various regions on the X- ... In human cells with more than one X chromosome, two long non-coding RNAs are produced: Tsix is produced by one X chromosome, ... or on a different chromosome from a separate chromosome pair. An example of this is a long non coding RNA from Hox gene C ... chromosome. This methylation causes other factors like histone deacetylases (HDACs) to bind to the chromosome and propagate ...
  https://en.wikipedia.org/wiki/Epigenetics_of_human_development
*  PEDF - Wikipedia
The gene encoding human PEDF was localized to the 17th chromosome at position 17p13.1. The human PEDF gene is around 15.6kb, ... The gene most homologous to PEDF is its adjacent neighbor on chromosome 17, SerpinF2. The PEDF protein is a secreted protein of ... to chromosome 17p13.1 and expression in cultured human retinoblastoma cells". Genomics. 19 (2): 266-72. doi:10.1006/geno. ...
  https://en.wikipedia.org/wiki/PEDF
*  Haplogroup G-M406 - Wikipedia
It was found at chromosome position 2948673 and represents a mutation from A to C. There is a cluster of G-M406 men not ... M406 is located on the Y chromosome at position 2809995, reference SNP ID i4000120. The mutation involves a change from T to G ... In human genetics, Haplogroup G-M406 is a Y-chromosome haplogroup. G-M406 is a branch of Haplogroup G Y-DNA (M201). More ... Its location on the Y chromosome is given as 20087688, reference number rs35169834. The mutation is a change from G to A. In ...
  https://en.wikipedia.org/wiki/Haplogroup_G-M406
*  CAPZA2 - Wikipedia
CAPZA2 is located on human chromosome 7, position q31.2-q31.3. The primary sequence of CapZ-alpha2 contains three C-terminal, ... regularly spaced leucines at positions 258, 262 and 266 found in consensus sequence of KxxxLxxE/DLxxALxxK/R that are critical ...
  https://en.wikipedia.org/wiki/CAPZA2
*  TMCO6 - Wikipedia
The human TMCO6 is found on chromosome 5 (position 5q31.3). The entire gene spans 5568 base pairs on the positive strand of ... chromosome 5 (140019113-140024689bp) but is alternately spliced into different variants. There are three known variants for ...
  https://en.wikipedia.org/wiki/TMCO6
*  Serpin - Wikipedia
... with the remaining 16 organised into five gene clusters that occur at chromosome positions 28D (2 serpins), 42D (5 serpins), ... and instead a nomenclature system has been adopted that is based on the position of serpin genes on the Drosophila chromosomes ... Chromosomes & Cancer. 22 (3): 179-85. doi:10.1002/(SICI)1098-2264(199807)22:3. 3.0.CO;2-T. PMID 9624529. Loftus SK, Cannons JL ...
  https://en.wikipedia.org/wiki/Serpin
*  Centimorgan - Wikipedia
It is defined as the distance between chromosome positions (also termed loci or markers) for which the expected average number ... It is often used to infer distance along a chromosome. However, It is not a true physical distance. The number of base-pairs to ... Note that non-syntenic genes (genes residing on different chromosomes) are inherently unlinked, and cM distances have no ... which it corresponds varies widely across the genome (different regions of a chromosome have different propensities towards ...
  https://en.wikipedia.org/wiki/Centimorgan
*  C6orf62 - Wikipedia
It is located on chromosome 6 on position 22.3 (6q22.3). The mature mRNA sequence is 2498 base-pairs long with 5 exons and 4 ... Chromosome 6 open reading frame 62 (C6orf62), also known as X-trans-activated protein 12 (XTP12), is a gene that encodes a ... "C6orf62 chromosome 6 open reading frame 62 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2017-05-08. ... There is a domain of unknown function (DUF4566) present in all three variants and spans positions 1-226 on the main transcript ...
  https://en.wikipedia.org/wiki/C6orf62
*  Leukodystrophy - Wikipedia
The GALC gene, found on chromosome 14 at position 31 (14q31), codes for the enzyme beta-galactocerebrosidase (GALC). GALC is a ... The X chromosome is a sex chromosome, and since women have two "chances" of acquiring a normal X chromosome (one maternal, one ... MLD is found on human chromosome 22 at position q13.31. Another type of inherited leukodystrophy is X-linked ... To date, there have been no found cases of a leukodystrophy carried on the Y chromosome. MLD Foundation provides updates on MLD ...
  https://en.wikipedia.org/wiki/Leukodystrophy
*  Dynein - Wikipedia
Dynein is involved in the movement of chromosomes and positioning the mitotic spindles for cell division. Dynein carries ... Cytoplasmic dynein positions the spindle at the site of cytokinesis by anchoring to the cell cortex and pulling on astral ... Cytoplasmic dynein helps to position the Golgi complex and other organelles in the cell. It also helps transport cargo needed ... Proper segregation is essential for producing haploid meiotic products with a normal complement of chromosomes. The formation ...
  https://en.wikipedia.org/wiki/Dynein