Gilbert F, Kauff N (2000). "Disease genes and chromosomes: disease maps of the human genome.Chromosome 12". Genet Test. 4 (3): ... Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19. "Human chromosome 12: entries, gene ... 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 ...

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 ...

"Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector ... Cosmid End-sequence profiling Fosmid Human artificial chromosome Secondary chromosome Yeast artificial chromosome O'Connor M, ... BACs can also be utilized to detect genes or large sequences of interest and then used to map them onto the human chromosome ... "Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the ...

... six pairs) of chromosomes, i.e. 2n = 12. The draft genome and transcriptomes were published in 2014. Its genome is 634.5 MB in ... 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 ...

"Homologous expressed genes in the human sex chromosome pairing region". Nature. 317 (6039): 739-41. Bibcode:1985Natur.317..739B ... CD99+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Human CD99 genome location and ... 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. ... Genes on human chromosome X, Clusters of differentiation). ... Unusually for a gene present on the X chromosome, the CD99 gene ...

In humans, the gene for C12orf40 is located on chromosome 12. There are 13 exons in the canonical isoform that is transcribed ... into an mRNA of 2797 base pairs. Three other isoforms have been isolated. Homologs exist as distant as the green sea turtle and ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 12, Chromosomes, ... The human C12orf40 protein is 652 amino acids in length. Its molecular weight is predicted to be 74.52 kDa, and its isoelectric ...

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 alike. The primary difference is that humans have one fewer pair of chromosomes than ... producing human chromosome 2. There are nine other major chromosomal differences between chimpanzees and humans: chromosome ... Results from the human and chimpanzee genome analyses should help in understanding some human diseases. Humans appear to have ...

Chromosome 11 open reading frame 86, also known as C11orf86, is a protein-coding gene in humans. It encodes for a protein known ... 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 ... "C11orf86 chromosome 11 open reading frame 86 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2016-05-09 ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 11, Uncharacterized proteins). ...

v t e (Articles with short description, Short description is different from Wikidata, Genes on human chromosome 12, Wikipedia ... Homeobox protein DBX2, also known as developing brain homeobox protein 2, is a protein that in humans is encoded by the DBX2 ... DBX2 is located on chromosome 12 and is approximately 36,000 base pairs long. DBX2 is predicted to enable DNA-binding ... articles incorporating text from the United States National Library of Medicine, All stub articles, Human chromosome 12 gene ...

The human β-dystrobrevin gene was localized to the short arm of chromosome 2. Pair-wise comparison between α- and β- ... Genes on human chromosome 18, Genes on human chromosome 2). ... The human α-dystrobrevin gene is localized to chromosome 18 and ... In human, the Duchenne muscular dystrophy is a well-known muscle disease which highlights the importance of dystrophin/ ... In humans, there are at least two isoforms of dystrobrevin, dystrobrevin alpha and dystrobrevin beta. Dystrobrevins are members ...

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 ...

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 ...

Genes on human chromosome 1, All articles with unsourced statements, Articles with unsourced statements from January 2021, ... The mouse gene has two exons (100 and 1064 nucleotides in length), separated by a 461 base pair intron. In the mouse DARC is ... is located on the long arm of chromosome 1 (1.q22-1.q23) and was cloned in 1993. The gene was first localised to chromosome 1 ... DARC+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Duffy at BGMUT Blood Group Antigen ...

The CTNS gene 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, ... Human models for cystinosin are typically derived from cystinotic renal tubular cell lines. Non-human protein homologs for ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 17). ... The most common mutation is a 57,257 base pair deletion commonly referred to as the 57 kb deletion. This was formally known as ...

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. 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 235 to ... Genes on human chromosome 11, Wikipedia articles needing clarification from December 2018, Wikipedia articles incorporating ...

... 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 ...

In humans c12orf71 has shown an intermediate expression level in testis and low expression in the bone marrow, skin, spleen, ... The DNA sequence of the c12orf71 gene is 3071 base pairs long and 8 significant structural variations have been identified ... Chromosome 12 open reading frame 71 (c12orf71) is a protein which in humans is encoded by c12orf71 gene. The protein is also ... Additionally, the human protein also contains a vacuolar domain, which is mammal specific and may be modulated by ...

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 ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 12, Proteins). ... The promoter region of SMCO3 is 1,100 base pairs long and begins 961 base pairs upstream of the 5' UTR with the end of the ... The mRNA transcript of SMCO3 is 2,104 base pair long. There are no mRNA variants of SMCO3. The SMCO3 promoter has many ... Single-pass membrane and coiled-coil domain-containing protein 3 is a protein that is encoded in humans by the SMCO3 gene. ...

... is a protein in humans that is encoded by the chromosome 4 open reading frame 47 (c4orf47) gene. The c4orf47 gene is ... positioned at 4q35.1 on the plus strand and spans 44,602 base pairs in length (185,405,227...185,449,828). The gene is made up ... "C4orf47 chromosome 4 open reading frame 47 [Homo sapiens (human)] - Gene". National Center for Biotechnology Information. "Homo ... "Homo sapiens chromosome 4 open reading frame 47 (C4orf47), transcript variant 2, mRNA". National Center for Biotechnology ...

Parthenogenesis appears to involve initial meiotic chromosome pairing. During both cyclic and obligate parthenogenesis a polar ... Its genome contains 31,000 genes - 8,000 more than are present in the human genome - as a result of extensive gene duplication ... It bears the mouthparts, and two pairs of antennae, the second pair of which is enlarged into powerful organs used for swimming ... It can only be recognised by its appendages (only ever one pair per segment), and by studying its internal anatomy. The head is ...

Chromosome 15 open reading frame 52 is a human protein encoded by the C15orf52 gene, its function is poorly understood. ... 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 ... Glycine and Arginine were found at higher frequencies than other proteins in humans. The isoelectric point of the protein is ...

Source attribution, Articles with imported Creative Commons Attribution 4.0 text, Genes on human chromosome 12, Wikipedia ... The SLC25A3 gene is located on the q arm of chromosome 12 in position 23.1 and spans 8,376 base pairs. The gene has 9 exons and ... Phosphate carrier protein, mitochondrial is a protein that in humans is encoded by the SLC25A3 gene. The encoded protein is a ... Huizing M, Ruitenbeek W, van den Heuvel LP, Dolce V, Iacobazzi V, Smeitink JA, Palmieri F, Trijbels JM (June 1998). "Human ...

... is a protein that in human is encoded by the C1orf159 gene located on chromosome 1. This gene is also found to be an ... The gene is 34,247 base pairs in length, located at Chromosome 1 position 1,081,818 to 1,116,089 on the reverse strand. The ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 1, All articles with ... The isoelectric point of the human C1orf159 protein is 10.07, which is more basic than the average human proteomic protein pI ...

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 ...

Aldehyde dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ALDH2 gene located on chromosome 12. This ... ALDH2 protein, human at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Human ALDH2 genome location and ... Portal: Biology (Articles with short description, Short description is different from Wikidata, Genes on human chromosome 12, ... "The structural gene for the mitochondrial aldehyde dehydrogenase maps to human chromosome 12". Hum. Genet. 73 (4): 365-7. doi: ...

Animals Plants Other Eukaryotes Karyotype of a human being. It shows 22 homologous autosomal chromosome pairs, both the female ... Stebbins GL (1950). "Chapter XII: The Karyotype". Variation and evolution in plants. Columbia University Press. King RC, ... As other non-human extant hominidae have 48 chromosomes it is believed that the human chromosome 2 is the result of the merging ... Shared synteny of human chromosome 17 loci in Canids (archived 24 September 2015) An atlas of the chromosome numbers in animals ...

... 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 ... Genes on human chromosome 12, Wikipedia articles incorporating text from the United States National Library of Medicine, ... Human BHLHE41 genome location and BHLHE41 gene details page in the UCSC Genome Browser. This article incorporates text from the ...

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 ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 12, Wikipedia articles ... 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 ...