Humans normally have two copies of this chromosome, as they normally do with all chromosomes. Chromosome 9 spans about 150 ... million base pairs of nucleic acids (the building blocks of DNA) and represents between 4.0 and 4.5% of the total DNA in cells ... Gilbert F, Kauff N (2001). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 9". Genet Test. 5 (2): ... locus to chromosome 9q33-34". Am. J. Hum. Genet. 61 (suppl): A30. Wikimedia Commons has media related to Human chromosome 9. ...

Human gene SIGIRR is localized on chromosome 11. It is composed of 10 exons spanning about 11 700 base pairs. In mouse, this ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 11). ... In human cells from colonic cancer, there was observed an increased expression of one variant of SIGIRR. This variant lacks its ... Human and mouse SIGIRR protein sequences are 82%, identical and they are overall 23% identical with IL-1R1. SIGIRR is ...

"one mutation in every 30 million base pairs" Karmin; et al. (2015). "A recent bottleneck of Y chromosome diversity coincides ... In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non-recombining portions of ... 2016). "The Divergence of Neandertal and Modern Human Y Chromosomes". The American Journal of Human Genetics. 98 (4): 728-34. ... Y-chromosome DNA (Y-DNA) haplogroups are the major branches on the human paternal family tree. Each haplogroup has many ...

The molecular location of the gene is from base pair 133,189,767 to base pair 133,192,979 on chromosome 9 for an mRNA length of ... Articles with short description, Short description matches Wikidata, Human genes, Genes on human chromosome 9, Proteins). ... The human LOC101928193 gene is located on the long (q) arm of chromosome 9 with a cytogenic location at 9q34.2. ... and it is 1101 nucleotides long on the positive strand from base pairs 133,188,767 to 133,189,867 on chromosome 9. The ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 8, All pages needing factual ... The two genes show 93% homology to each other and are both encoded on the same chromosome. Research has shown that calcium ions ... May 1997). "CMO I deficiency caused by a point mutation in exon 8 of the human CYP11B2 gene encoding steroid 18-hydroxylase ( ... It is the sole enzyme capable of synthesizing aldosterone in humans and plays an important role in electrolyte balance and ...

The human gene TMEM8A is found on chromosome 16 at the band 16p13.3. The span of this gene on chromosome 16 spans from base ... pair 420,773 to 437,113 making this gene 16,340 base pairs in length. This gene is found on the minus strand of the chromosome ... There are two paralogs for TMEM8A found in humans, C9orf127 and TMEM8C. Both of these paralogs are found on Chromosome 9. The ... December 2004). "The sequence and analysis of duplication-rich human chromosome 16" (PDF). Nature. 432 (7020): 988-94. Bibcode: ...

It encodes for a transmembrane protein that is 338 amino acids long, and is located on human chromosome 9. Aliases associated ... It starts at base pair 35,814,451, and ends at 35,865,518, and contains 19 exons. There are 13 transcript variants that are ... Genes on human chromosome 9, All articles with unsourced statements, Articles with unsourced statements from January 2023). ... One human paralog was found when this protein was sequenced in BLAST. It is 416 amino acids long, with 40% sequence identity, ...

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 ...

... spanning the chromosomal locus from base pair 34,502,909 to 34,398,027. The span of the gene is 104,882 base pairs In humans ... In humans, C9orf25 is located at the 9p13.3 position on chromosome 9. The gene is encoded on the sense strand (-) ... Chromosome 9 open reading frame 25 (C9orf25) is a domain that encodes the FAM219A gene. The terms FAM219A and C9orf25 are ... C9orf25 has a paralog FAM219B which is located on the long arm of chromosome 9 and is 198 amino acids long. The C9orf25 and ...

... is located at 15q21.3-q22.1, spanning 90,707 base pairs on chromosome 15. The full name of FAM63B is family with ... FAM63B is a protein which in humans is encoded by the gene FAM63B. This gene is highly expressed in humans. The FAM63B gene is ... FAM63B variant a is the most common isoform found in humans. FAM63B is a member of the Pfam super family, and contains a domain ... The discovered function of FAM63B protein is a transporter of vaccinia virus in the human genome. FAM63B contains a bipartite ...

The RAB7A gene is located on chromosome 3 in humans, specifically on the long q arm from base pair 128,726,135 to 128,814,797. ... in 1997 to map the RAB7A gene to chromosome 3 using PCR analysis. In 1995 it had been mapped to chromosome 9 in mice by Barbosa ... "NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia ... Ras-related protein Rab-7a is a protein that in humans is encoded by the RAB7A gene. Ras-related protein Rab-7a is involved in ...

Articles with short description, Short description matches Wikidata, Genes on human chromosome 9). ... The promoter region of C9orf43 predicted by Genomatix ElDorado is 1199 base pairs long and contains a CpG island and part of ... Chromosome 9 open reading frame 43 is a protein that in humans is encoded by the C9orf43 gene. The gene is also known as ... "Entrez Gene: Chromosome 9 open reading frame 43". Butland SL, Devon RS, Huang Y, Mead CL, Meynert AM, Neal SJ, Lee SS, ...

The human gene C9orf152 is located on the long (q) arm of Chromosome 9. Its cytogenetic location is 9q31.1. It has one known ... The final mRNA consists of 2698 base pairs. Nucleotides 66-68 encode an upstream in frame stop codon. C9orf152 has orthologs in ... 2009 (GRCh37/hg19) Assembly". Human BLAT Search. University of California Santa Cruz. "Chromosome 9 Open Reading Frame 152". ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 9, Uncharacterized proteins). ...

In humans, aldolase B is encoded by the ALDOB gene located on chromosome 9. The gene is 14,500 base pairs long and contains 9 ... Mutant alleles are a result of a number different types of mutations including base pair substitutions and small deletions. The ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 9, CS1: long volume value, ... 1988). "Human aldolase B gene: characterization of the genomic aldolase B gene and analysis of sequences required for multiple ...

Genes on human chromosome 15, Developmental genes and proteins, MH1 domain, MH2 domain, R-SMAD, Transcription factors, Human ... the convex face of the DNA-binding hairpin dives into the concave major groove of the duplex DNA containing five base pairs ( ... The human SMAD3 gene is located on chromosome 15 on the cytogenic band at 15q22.33. The gene is composed of 9 exons over ... 129,339 base pairs. It is one of several human homologues of a gene that was originally discovered in the fruit fly Drosophila ...

This 1069 base pair promoter sequence spans 41936535-41937603 on human chromosome 4. The promoter sequence overlaps with the 5 ... In humans, this gene's DNA location is the short arm of chromosome 4, loci position: 4p13. The genomic range is 41937502- ... Transcripts a, b, and c have a 744 base pair long coding range and a particularly long 3' UTR that is 6000 base pairs long. In ... There is an experimentally determined acetylation point is at alanine, amino acid residue 2 in humans. Human TMEM33 has ...

In humans,TMEM106B is found on chromosome 7 at positions 12211270 - 12243367, totaling 32097 base pairs. The gene includes 9 ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 7). ... chromosome 7p21) as a genome-wide signal. Further studies have identified other SNPs that are associated with an increased risk ... "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine. "Mouse PubMed ...

It spans a total of 2,974 base pairs, between bases 46497976 and 46500950 on chromosome 3.[citation needed] There is only one ... RTP3 (receptor transporter protein 3) is a gene located on chromosome 3 in humans that encodes the RTP3 protein. Its expression ... RTP3 has several paralogs in humans, including other members of the RTP family. While there is experimental evidence RTP3 may ... "RTP3 receptor transporter protein 3 [Homo sapiens (human)] - Gene - NCBI". Fagerberg L, Hallström BM, Oksvold P, Kampf C, ...

9q34.11 in human from base pair 127,706,989 to base pair 127,716,002. The size of the gene is 9,013 bases, and the orientation ... Cilia and flagella associated protein 157 (CFAP157) also known as chromosome 9 open reading frame 117 (c9orf117) is a protein ... The most common variant of mRNAs of CFAP157 contains 1,722 base pairs. CFAP157 is expressed in many human body tissues such as ... There are 520 amino acids in CFAP157 in human. The protein is glutamine extremely rich, and glycine poor. The protein is quite ...

The CCDC142 gene is located on chromosome 2 (at 2p13), spans 4339 base pairs and contains 9 exons. The gene codes for the ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 2, Protein structural ... "Microarray Data :: Allen Brain Atlas: Human Brain". human.brain-map.org. Retrieved 2016-05-01. "EST Profile - Hs.430199". www. ... Allen Human Brain Atlas Expression of CCDC142 Lateral View Red=Low Expression11 Frontal View Green=High Expression11 Above are ...

The LENG9 gene is 1,930 base pairs in length and contains one exon. Genes LENG8-AS1 and CDC42EP5 neighbor LENG9 on chromosome ... human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2017-05-06. Database, GeneCards Human Gene. "LENG9 Gene - GeneCards , ... Human expression of LENG9 is observed in the cervix, lung, and placenta of adults. The gene is also expressed in disease states ... In humans, LENG9 has two mRNA unspliced transcript variants. Variant (1) is the longest and most conserved transcript of the ...

In humans, FAM166B has 10 transcript variants, which are all spliced. FAM166B transcript variant 1 is 1,092 bp in length and ... The FAM166B gene is located on the short arm of chromosome 9 at 9p13.3 on the minus strand. The genomic sequence spans 2,069 ... base pairs from 35563899 to 35561830. Gene neighbors are RUSC2, RPS29P17, and TESK1. FAM166B is expressed 0.5 times higher than ... It is known to have a higher than normal proline composition compared to other human proteins at 12.4%. The protein has a ...

In humans the gene is located on the negative strand at 9q34.11 and the coding sequence is 8,552 base pairs long. On human ... human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2019-02-25. "C9orf50 chromosome 9 open reading frame 50 [Homo sapiens ( ... In humans the gene coding sequence is 10,051 base pairs long, transcribing an mRNA of 1,624 bases that encodes a 431 amino acid ... RNA-seq data of C9orf50 has found a low expression level, 25-50th percentile, in most human tissues compared to all human ...

The human C9orf72 gene is located on the short (p) arm of chromosome 9 open reading frame 72, from base pair 27,546,546 to base ... base pairs 27,546,546 to 27,573,866 The mutation of C9ORF72 is a hexanucleotide repeat expansion of the six letter string of ... Genes on human chromosome 9, Commons category link is on Wikidata). ... Human C9orf72 genome location and C9orf72 gene details page in the UCSC Genome Browser. Wikimedia Commons has media related to ...

Transmembrane protein 261 is a protein that in humans is encoded by the TMEM261 gene located on chromosome 9. TMEM261 is also ... its length is 91,891 base pairs (bp) on the reverse strand. Its neighbouring gene is PTPRD located at 9p23-p24.3 also on the ... Articles with short description, Short description matches Wikidata, Genes on human chromosome 4, All articles with dead ... "9ORF123 chromosome 9 open reading frame 123". BioGRID: Database of Protein and Genetic Interactions. TyersLab. She X, Rohl CA, ...

The human TBR1 gene is located on the q arm of the positive strand of chromosome 2. It is 8,954 base pairs in length. TBR1 is ... Articles with short description, Short description is different from Wikidata, Good articles, Genes on human chromosome 2, ... "Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins". ... Orthologs of the human TBR1 gene have been identified in chimpanzee, dog, cow, rat, mouse, and zebrafish. In mice, TBR1 has ...

The human gene product is a 4,469 base pair mRNA with 25 predicted exons. There are 9 predicted splice isoforms of the gene, ... TMEM63A is located on the negative DNA strand of chromosome 1 at location 1q42.12, spanning base pairs 226,033,237 to ... The predicted promoter region spans 971 base pairs, from 226,070,920 to 226,069,950 on the negative strand of chromosome 1. ... 2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315-21. Bibcode:2006Natur.441.. ...

The gene locus is located on the long arm of chromosome 2 at 2q21.1, and spans 5991 base pairs. A common alternative alias is ... Articles with short description, Short description is different from Wikidata, Genes on human chromosome 2). ... In humans, CCDC74A has one important paralog, CCDC74B. Gene duplication is estimated to have occurred approximately 7 million ... Coiled-coil domain containing 74A is a protein that in humans is encoded by the CCDC74A gene. The protein is most highly ...

Schäfer BW, Mattei MG (July 1993). "The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2". Genomics. 17 (1 ... Paired box protein Pax-7 is a protein that in humans is encoded by the PAX7 gene. Pax-7 plays a role in neural crest ... "PAX7 - Paired box protein Pax-7 - Homo sapiens (Human) - PAX7 gene & protein". Aloisio, Gina M.; Nakada, Yuji; Saatcioglu, ... Pilz AJ, Povey S, Gruss P, Abbott CM (March 1993). "Mapping of the human homologs of the murine paired-box-containing genes". ...

... of the Y chromosome during meiosis. Additionally, 10-25% of human X chromosome genes, and 3-7% of mouse X chromosome genes ... with females possessing five pairs of X chromosomes as the homogametic sex, and males possessing five X and five Y chromosomes ... Specifically, platypus X1 shares homology with the chicken Z chromosome, and both share homology with the human chromosome 9. ... expressed X chromosome. Thus, human females have the same number of expressed X-linked genes per cell as do human males (XY), ...

"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 ...