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*  Chromosome 12 (human)
Gilbert F, Kauff N (2000). "Disease genes and chromosomes: disease maps of the human genome.Chromosome 12". Genet Test. 4 (3): ... The following is a partial list of genes on human chromosome 12. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 12. Because researchers use different approaches to ... People normally have two copies of this chromosome. Chromosome 12 spans about 133 million base pairs (the building material of ...
*  CTNS (gene)
CTNS is located on the p arm of human chromosome 17, at position 13.2. It spans base pairs 3,636,468 and 3,661,542, and ... Human models for cystinosin are typically derived from cystinotic renal tubular cell lines. Non-human protein homologs for ... Human Mutation. 20 (3): 237. doi:10.1002/humu.9063. PMID 12204010. GeneReviews/NCBI/NIH/UW entry on Cystinosis Human CTNS ... The most common mutation is a 57,257 base pair deletion commonly referred to as the 57 kb deletion. This was formally known as ...
*  ERBB3
The human ERBB3 gene is located on the long arm of chromosome 12 (12q13). It is encoded by 23,651 base pairs and translates ... During human development, ERBB3 is expressed in skin, bone, muscle, nervous system, heart, lungs, and intestinal epithelium. ... Receptor tyrosine-protein kinase erbB-3, also known as HER3 (human epidermal growth factor receptor 3), is a membrane bound ... ERBB3 is expressed in normal adult human gastrointestinal tract, reproductive system, skin, nervous system, urinary tract, and ...
*  GLIPR1
... in human it is in chromosome 12q21 and in chromosome 10D1 in mouse (Figs. 1A and 1B). In human GLIPR1 gene is located on the ... Human GLIPR1, was initially identified in human glioblastoma and was called as GLIPR1 (glioma pathogenesis-related protein 1) ... "Human PubMed Reference:". "Mouse PubMed Reference:". Murphy EV, Zhang Y, Zhu W, Biggs J (June 1995). "The human glioma ... Study showed human GLIPR1 promoter to be highly methylated in prostate cancer tissues compared to the normal prostate tissue ...
*  BHLHE41
... was mapped to human chromosome 12: 26,120,026-26-125-127 reverse strand and has a total length of 5,101 base pairs. The ... BHLHE41-001 contains 5 coding exons, has a transcript length of 3,837 base pairs, and encodes the 482 amino acid BHLHE41 ... "Human PubMed Reference:". "Mouse PubMed Reference:". "BHLHE41 basic helix-loop-helix family, member e41 [ Homo sapiens (human ... Human BHLHE41 genome location and BHLHE41 gene details page in the UCSC Genome Browser. This article incorporates text from the ...
*  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). " ...
*  CD99
"Homologous expressed genes in the human sex chromosome pairing region". Nature. 317 (6039): 739-41. doi:10.1038/317739a0. PMID ... CD99 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) Human CD99 genome location and CD99 ... a gene shared by the human X and Y chromosomes". Cold Spring Harb. Symp. Quant. Biol. 51 (1): 205-12. doi:10.1101/SQB.1986.051. ... Unusually for a gene present on the X chromosome, the CD99 gene does not undergo X inactivation, and it was the first such ...
*  PRNP
The human PRNP gene is located on the short (p) arm of chromosome 20 between the end (terminus) of the arm and position 12, ... from base pair 4,615,068 to base pair 4,630,233. PrP is highly conserved through mammals, lending credence to application of ... of a human gene homologous to the PrP gene on the p arm of chromosome 20 and detection of PrP-related antigens in normal human ... "Assignment of the human and mouse prion protein genes to homologous chromosomes". Proc. Natl. Acad. Sci. U.S.A. 83 (19): 7358- ...
*  FAM71F2
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 ...
*  Duffy antigen system
DARC protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) Duffy at BGMUT Blood Group Antigen ... The gene was first localised to chromosome 1 in 1968, and was the first blood system antigen to be localised. It is a single ... The mouse gene has two exons (100 and 1064 nucleotides in length respectively), separated by a 461 base pair intron. In the ... The ancestral form of extant DARC alleles in humans appears to be the FY*B allele. The gene appears to be under strong ...
*  Coiled-coil domain-containing 37 (FLJ40083)
The human gene CCDC37 is found on chromosome 3 at the band 3q21.3. It extends from base pairs 90,403,731 to 90,429,231, making ... There is only one paralog for CCDC37 found in humans, CCDC38. CCDC38 is located on chromosome 12. The ortholog space of CCDC37 ... Coiled-coil domain-containing 37, also known as FLJ40083, is a protein that in humans is encoded by the CCDC37 gene (3q21.3). ... "CCDC38 coiled-coil domain containing 38 [Homo sapiens (human)] - Gene". Ncbi.nlm.nih.gov. Retrieved 2015-03-07. Dinkel, H. The ...
*  Chromothripsis
When multiple chromosomes are involved in chromothripsis, fragments of both chromosomes are joined together by paired end ... using genome-wide paired-end sequencing and SNP array analysis have found similar patterns of chromothripsis in various human ... Cells with defective chromosome segregation will form micronuclei which contain whole chromosomes or fragments of chromosomes. ... Through paired end sequencing, 42 chromosomal rearrangements were found in the long arm of chromosome 4 and a significant ...
*  C15orf52
Chromosome 15 open reading frame 52 is a protein which in humans is encoded by the C15orf52 gene. This protein has a function ... The linear mRNA is 5344 base pairs long. The mRNA contains a short 5' untranslated region of 15 base pairs and a long 3' ... C15orf52 is a gene located on the reverse strand of chromosome 15 in the species Homo sapiens at locus 15q15.1. The gene is ... "A human interactome in three quantitative dimensions organized by stoichiometries and abundances." Cell 163.3 (2015): 712-723. ...
*  Opisthorchis viverrini
... viverrini have twelve (six pairs of) chromosomes, i.e. 2n = 12. The draft genome and transcriptomes was published in 2014. Its ... In humans,O. viverrini inhabits mainly the bile ducts and, rarely, the gall bladder and pancreatic duct. Heavy infection can ... The first human specimen was described by a British parasitologist Robert Thomson Leiper in 1915, but without knowing the exact ... The first human case was discovered by Robert Thomson Leiper in 1915. O. viverrini (together with Clonorchis sinensis and ...
*  Dopamine receptor D4
... in the human gene: A 48-base pair VNTR in exon 3 C-521T in the promoter 13-base pair deletion of bases 235 to 247 in exon 1 12 ... The human protein is coded by the DRD4 on chromosome 11 located in 11p15.5.[citation needed] There are slight variations ( ... The 48-base pair VNTR has been the subject of much speculation about its evolution and role in human behaviors cross-culturally ... "The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus". American Journal of Human Genetics ...
*  PRR29
... is a protein located on human chromosome 17 that in humans is encoded by the PRR29 gene. It is also commonly known as ... 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 ... The gene spans 5961 base pairs and is oriented on the plus strand. Genes SNHG25 and LOC105371858 neighbor PRR29 on chromosome ...
*  Chimpanzee genome project
Humans have 23 pairs of chromosomes and other great apes have 24 pairs of chromosomes. In the human evolutionary lineage, two ... Human and chimpanzee chromosomes are very similar. The primary difference is that humans have one fewer pair of chromosomes ... Human evolutionary genetics Human chromosome 2 Human Genome Project McConkey EH (2004). "Orthologous numbering of great ape and ... producing human chromosome 2. There are nine other major chromosomal differences between chimpanzees and humans: chromosome ...
*  C11orf86
"Human PubMed Reference:". "Mouse PubMed Reference:". "C11orf86 chromosome 11 open reading frame 86 [Homo sapiens (human)] - ... C11orf86 is located on the long arm of chromosome 11 at 11q13.2. It consists of 1732 base pairs, and is found on the plus ... Chromosome 11 open reading frame 86, also known as C11orf86, is a protein-coding gene in humans. It encodes for a protein known ... The transcript used for this article is made up of two exons, amounting to 1185 base pairs, and has the reference number NM_ ...
*  C12orf66
... variant 1 is 36 Mbp in length spanning the base pairs 64,186,312 - 64,222,296 on chromosome 12. There are 3 total ... The human C12orf66 protein is 446 amino acids in length with a molecular weight of 50kdal . C12orf66 contains the domain of ... C12orf66 is a protein that in humans is encoded by the C12orf66 gene. The C12orf66 protein is one of four proteins in the ... "C12orf66 chromosome 12 open reading frame 66 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2017-02-25 ...
*  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. ...
*  NDUFA4L2
The human NDUFA4L2 gene codes for a subunit of Complex I of the respiratory chain, which transfers electrons from NADH to ... The NDUFA4L2 gene is located on the long q arm of chromosome 12 at position 13.3 and it spans 5,860 base pairs. NDUFA4L2 is a ... NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 is a protein that in humans is encoded by the NDUFA4L2 gene. The ... "Human PubMed Reference:". "Mouse PubMed Reference:". "Entrez Gene: NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 ...
*  List of organisms by chromosome count
1992). "Evidence for an ancestral alphoid domain on the long arm of human chromosome 2". Human Genetics. 89 (2): 247-9. doi: ... Crosland, M.W.J., Crozier, R.H. (1986). "Myrmecia pilosula, an ant with only one pair of chromosomes". Science. 231 (4743): ... Concise Oxford Dictionary White 1973, p. 28 Stebbins, G.L. (1950). "Chapter XII: The Karyotype". Variation and evolution in ... Russian bionet site The dog through evolution Shared synteny of human chromosome 17 loci in Canids An atlas of the chromosome ...
*  Mouse
The mouse has approximately 2.7 billion base pairs and 20 chromosomes. They can also be manipulated in ways that are illegal ... Humans have eaten mice since prehistoric times and still eat them as a delicacy throughout eastern Zambia and northern Malawi, ... Mice are generally very docile if raised from birth and given sufficient human contact. However, certain strains have been ... Mice are no longer routinely consumed by humans elsewhere. However in Victorian Britain, fried mice were still given to ...
*  Monosomy
Human conditions due to monosomy: Turner syndrome - People with Turner syndrome typically have one X chromosome instead of the ... Monosomy is a form of aneuploidy with the presence of only one chromosome from a pair. Partial monosomy occurs when only a ... usual two sex chromosomes. Turner syndrome is the only full monosomy that is seen in humans-all other cases of full monosomy ... arm of chromosome 5 1p36 deletion syndrome - a partial monosomy caused by a deletion at the end of the short p arm of ...
*  H2AFJ
Histone H2A.J is a protein that in humans is encoded by the H2AFJ gene. Histones are basic nuclear proteins that are ... This gene is located on chromosome 12 and encodes a variant H2A histone. The protein is divergent at the C-terminus compared to ... Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core ... 2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci ...
*  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 ...