Number of genes

Gene list

• AASS: encodingenzymeAlpha-aminoadipic semialdehyde synthase, mitochondrial
• ACTR3B: actin-related protein 3B
• AEBP1: AE binding protein 1
• AGK: encodingenzyme mitochondrial acylglycerol kinase
• ARHGEF35: encodingprotein Rho guanine nucleotide exchange factor (GEF) 35
• AVL9: encoding protein Avl9 cell migration associated
• BCAP29: B-cell receptor-associated protein 29
• BCC6: encoding protein basal cell carcinoma, susceptibility to, 6
• BRAT1: BRCA1-associated ATM activator 1
• C7orf25: protein UPF0415
• C7orf31: chromosome 7 open reading frame 31
• CALU: Calumenin
• CCL24: encoding protein C-C motif chemokine ligand 24
• CDCA7L: Cell division cycle-associated 7-like protein
• CFTR: anion channel membrane protein
• CNOT4: CCR4-NOT transcription complex, subunit 4
• CPED1: cadherin like and PC-esterase domain containing 1
• CPVL: carboxypeptidase, vitellogenic like
• CROT: Peroxisomal carnitine O-octanoyltransferase
• DDX56: DEAD-box helicase 56
• DMTF1: Cyclin D binding myb like transcription factor 1
• ECOP: EGFR-coamplified and overexpressed protein
• EEPD1: encoding protein Endonuclease/exonuclease/phosphatase family domain containing 1
• EGFR-AS1: encoding protein EGFR antisense RNA 1
• EZH2: encodingenzymehistone-lysine N-methyltransferase for histone h3 lysine 27
• FAM71F2: family with sequence similarity 71 member F2
• FAM185A: family with sequence similarity 185 member A
• FAM200A: family with sequence similarity 200 member A
• FBXO24: F-box only protein 24
• GBAS: Glioblastoma amplified sequence; Protein NipSnap homolog 2
• GET4: encodingprotein GET4
• GLCCI1: Glucocorticoid-induced transcript 1 protein
• HOXA@: encoding protein Homeobox a cluster
• HOXA10-HOXA9: readthrough gene unlikely to produce a protein product
• HPC4: Prostate cancer, hereditary, 4
• ICA1: islet cell autoantigen 1
• ING3: inhibitor of growth protein 3
• INTS1: encodingprotein Integrator complex subunit 1
• IQCE: IQ domain-containing protein E
• KDM7A: encodingprotein Lysine demethylase 7A
• LCHN: protein encoded by the KIAA1147 gene
• LHFPL3: LHFPL tetraspan subfamily member 3
• LINC01003: encoding long intergenic non-protein coding RNA 1003
• LRRC17: leucine-rich repeat containing protein 17
• LRRC61: encoding protein Leucine rich repeat containing 61
• LRRD1: encoding protein Leucine-rich repeats and death domain containing 1
• LSM5: U6 small nuclear RNA and mRNA degradation associated
• LUC7L2: putative RNA-binding protein Luc7-like 2
• MACC1: encoding protein Macc1, met transcriptional regulator
• MAP11: encodingprotein Microtubule-associated protein 11
• MDFIC: MyoD family inhibitor domain containing
• METTL2B: methyltransferase-like protein 2B
• MINDY4: MINDY lysine 48 deubiquitinase 4
• MIR93: encoding protein MicroRNA 93
• MIR148A: encoding protein MicroRNA 148a
• MIR196B: encoding protein MicroRNA 196b
• MIR548F4: encoding protein MicroRNA 548f-4
• MIR96: microRNA 96
• MOSPD3: motile sperm domain containing 3
• MTERF: mitochondrial transcription termination factor 1
• MTRNR2L6: encoding protein MT-RNR2-like 6
• NOM1: nucleolar protein with MIF4G domain 1
• NUDCD3: NudC domain-containing protein 3
• NUPL2: nucleoporin-like 2
• NXPH1: neurexophilin-1
• OPN1SW: blue-sensitiveopsin
• PDAP1: PDGFA associated protein 1
• PHTF2: putative homeodomain transcription factor 2
• PLOD3: procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
• POM121: POM121 transmembrane nucleoporin
• POP7: ribonuclease P protein subunit p20
• PPP1R17: protein phosphatase 1 regulatory subunit 17
• PSPH: phosphoserine phosphatase
• PURB: purine-rich element binding protein B
• PVRIG: encodingprotein Poliovirus receptor related immunoglobulin domain containing
• RADIL: ras-associating and dilute domain-containing protein
• RASA4B: encoding protein RAS p21 protein activator 4B
• RCP9: DNA-directed RNA polymerase III subunit RCP9
• REPIN1: replication initiator 1
• RNF216-IT1: encodingprotein RNF216 intronic transcript 1
• SCIN: scinderin
• SCRN1: secernin 1
• SEMA3E: encoding protein Semaphorin 3E
• SOSTDC1: sclerostin domain containing 1
• SPDYE1: speedy/RINGO cell cycle regulator family member E1
• SSC4D: scavenger receptor cysteine rich family member with 4 domains
• STEAP1: six transmembrane epithelial antigen of the prostate 1
• STEAP2: six transmembrane epithelial antigen of the prostate 2
• STEAP4: six transmembrane epithelial antigen of the prostate 4
• STYXL1: serine/threonine/tyrosine-interacting-like protein 1
• SUMF2: sulatase-modifying factor 2
• SYPL1: synaptophysin-like protein 1
• TARP: TCR gamma alternate reading frame protein
• TBRG4: transforming growth factor beta regulator 4
• TECPR1 encodingprotein Tectonin beta-propeller repeat containing 1
• TMED4: transmembrane emp24 domain-containing protein 4
• TMEM130: transmembrane protein 130
• TMEM196 encodingprotein Transmembrane protein 196
• TMEM243: encoding protein Transmembrane protein 243
• TNRC18: encoding protein Trinucleotide repeat containing 18
• TRBC1 encodingprotein T cell receptor beta constant 1
• TRBC2 encodingprotein T cell receptor beta constant 2
• TRGV1: encoding protein T cell receptor gamma variable 1 (non-functional)
• TRIL: TRL4 interactor with leucine rich repeats
• UPK3B: encoding protein Uroplakin 3B
• URG4: up-regulated gene 4
• WBSCR17: polypeptide N-acetylgalactosaminyltransferase 17
• WDR91 encodingprotein WD repeat domain 91
• WEE2-AS1: encoding protein WEE2 antisense RNA 1
• XKR5: encoding protein XK, Kell blood group complex subunit-related family, member 5
• ZC3HAV1: zinc finger CCCH-type containing
• ZC3HC1: zinc finger C3HC-type containing 1
• ZNF106: encodingprotein Zinc finger protein 106
• ZNF117: encodingprotein Zinc finger protein 117
• ZNF394: zinc finger protein 394
• ZNF398: zinc finger protein 398
• ZNF679: encodingprotein Zinc finger protein 679
• ZNF716: encodingprotein Zinc finger protein 716
• ZNF727: encodingprotein Zinc finger protein 727
• ZNF786: encodingprotein Zinc finger protein 786
• ZNF853: encodingprotein Zinc finger protein 853
• ZKSCAN1: zinc finger protein with KRAB and SCAN domains 1
• ZKSCAN5: zinc finger protein with KRAB and SCAN domains 5
• ZMIZ2: zinc finger MIZ domain-containing protein 2
• ZNF277P: zinc finger protein 277
• ZRF1: DnaJ heat shock protein family (Hsp40) member C2
• ZSCAN21: zinc finger and SCAN domain-containing protein 21

• 7p22.1 microduplication syndrome^[12]
• argininosuccinic aciduria^[13][14][15]
• cerebral cavernous malformation^[13][15]
• Charcot–Marie–Tooth disease^[13]
• Cholestasis, progressive familial intrahepatic 3^[13]
• Citrullinemia, type II, adult-onset,^[13]
• congenital bilateral absence of vas deferens^[13]
• cystic fibrosis^[16][13][15]
• Developmental verbal dyspraxia^[17]
• distal spinal muscular atrophy, type V^{[citation needed]}
• Ehlers–Danlos syndrome
• hemochromatosis, type 3^[13]
• Hereditary nonpolyposis colorectal cancer HNPCC4^[13]
• Lissencephaly syndrome, norman-roberts type^[13]
• Marfan syndrome^[13]
• maple syrup urine disease^{[citation needed]}
• maturity onset diabetes of the young type 3^{[citation needed]}
• mucopolysaccharidosis type VII orSly syndrome^[13]
• Muscular dystrophy, limb-girdle, type 1D^[13]
• myelodysplastic syndrome^[18]
• Myotonia congenita^[13][19]
• nonsyndromic deafness^[13]
• osteogenesis imperfecta^{[citation needed]}
• p47-phox-deficient chronic granulomatous disease^{[citation needed]}
• Pectus excavatum
• Pendred syndrome^[13][20]
• Romano–Ward syndrome^{[citation needed]}
• Shwachman–Diamond syndrome^[13][15]
• Schizophrenia^{[citation needed]}
• Silver-Russell syndrome^[21]
• Specific language impairment^[13][17]
• Tritanopia or tritanomalycolor blindness^[13]
• Williams syndrome^[16][13][22]
• Zellweger syndrome^[23]

Novels

1. ^^ab"Search results - 1[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene".NCBI. CCDS Release 20 forHomo sapiens. 2016-09-08. Retrieved2017-05-28.
2. ^Tom Strachan; Andrew Read (2 April 2010).Human Molecular Genetics. Garland Science. p. 45.ISBN 978-1-136-84407-2.
3. ^^abcGenome Decoration Page, NCBI.Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
4. ^What is chromosome 7, "Genetics Home Reference" ofU.S. National Library of Medicine. April 2008. [2014-05-14].
5. ^Pertea M, Salzberg SL (2010)."Between a chicken and a grape: estimating the number of human genes".Genome Biol.11 (5): 206.doi:10.1186/gb-2010-11-5-206.PMC 2898077.PMID 20441615.
6. ^"Statistics & Downloads for chromosome 7".HUGO Gene Nomenclature Committee. 2017-05-12. Archived fromthe original on 2017-06-29. Retrieved2017-05-19.
7. ^"Chromosome 7: Chromosome summary - Homo sapiens".Ensembl Release 88. 2017-03-29. Retrieved2017-05-19.
8. ^"Human chromosome 7: entries, gene names and cross-references to MIM".UniProt. 2018-02-28. Retrieved2018-03-16.
9. ^"Search results - 7[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene".NCBI. 2017-05-19. Retrieved2017-05-20.
10. ^"Search results - 7[CHR] AND "Homo sapiens"[Organism] AND ( ("genetype miscrna"[Properties] OR "genetype ncrna"[Properties] OR "genetype rrna"[Properties] OR "genetype trna"[Properties] OR "genetype scrna"[Properties] OR "genetype snrna"[Properties] OR "genetype snorna"[Properties]) NOT "genetype protein coding"[Properties] AND alive[prop]) - Gene".NCBI. 2017-05-19. Retrieved2017-05-20.
11. ^"Search results - 7[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene".NCBI. 2017-05-19. Retrieved2017-05-20.
12. ^Caselli, Rossella; Ballarati, Lucia; Vignoli, Aglaia; Peron, Angela; Recalcati, Maria Paola; Catusi, Ilaria; Larizza, Lidia; Giardino, Daniela (November 2015)."7p22.1 microduplication syndrome: Clinical and molecular characterization of an adult case and review of the literature".European Journal of Medical Genetics.58 (11):578–583.doi:10.1016/j.ejmg.2015.08.003.ISSN 1878-0849.PMID 26297194.
13. ^^{abcdefghijklmnopqrst}Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, Herbrick JA, Carson AR, Parker-Katiraee L, Skaug J, Khaja R, Zhang J, Hudek AK, Li M, Haddad M, Duggan GE, Fernandez BA, Kanematsu E, Gentles S, Christopoulos CC, Choufani S, Kwasnicka D, Zheng XH, Lai Z, Nusskern D, Zhang Q, Gu Z, Lu F, Zeesman S, Nowaczyk MJ, Teshima I, Chitayat D, Shuman C, Weksberg R, Zackai EH, Grebe TA, Cox SR, Kirkpatrick SJ, Rahman N, Friedman JM, Heng HH, Pelicci PG, Lo-Coco F, Belloni E, Shaffer LG, Pober B, Morton CC, Gusella JF, Bruns GA, Korf BR, Quade BJ, Ligon AH, Ferguson H, Higgins AW, Leach NT, Herrick SR, Lemyre E, Farra CG, Kim HG, Summers AM, Gripp KW, Roberts W, Szatmari P, Winsor EJ, Grzeschik KH, Teebi A, Minassian BA, Kere J, Armengol L, Pujana MA, Estivill X, Wilson MD, Koop BF, Tosi S, Moore GE, Boright AP, Zlotorynski E, Kerem B, Kroisel PM, Petek E, Oscier DG, Mould SJ, Döhner H, Döhner K, Rommens JM, Vincent JB, Venter JC, Li PW, Mural RJ, Adams MD, Tsui LC (May 2003)."Human chromosome 7: DNA sequence and biology".Science.300 (5620):767–772.Bibcode:2003Sci...300..767S.doi:10.1126/science.1083423.PMC 2882961.PMID 12690205.
14. ^Nagamani SC, Erez A, Lee B (May 2012)."Argininosuccinate lyase deficiency".Genetics in Medicine.14 (5):501–507.doi:10.1038/gim.2011.1.PMC 3709024.PMID 22241104.
15. ^^abcdGilbert F (2002). "Chromosome 7".Genetic Testing.6 (2):141–161.doi:10.1089/10906570260199429.PMID 12215256.
16. ^^abHillier LW, Fulton RS, Fulton LA, Graves TA, Pepin KH, Wagner-McPherson C, Layman D, Maas J, Jaeger S, Walker R, Wylie K, Sekhon M, Becker MC, O'Laughlin MD, Schaller ME, Fewell GA, Delehaunty KD, Miner TL, Nash WE, Cordes M, Du H, Sun H, Edwards J, Bradshaw-Cordum H, Ali J, Andrews S, Isak A, Vanbrunt A, Nguyen C, Du F, Lamar B, Courtney L, Kalicki J, Ozersky P, Bielicki L, Scott K, Holmes A, Harkins R, Harris A, Strong CM, Hou S, Tomlinson C, Dauphin-Kohlberg S, Kozlowicz-Reilly A, Leonard S, Rohlfing T, Rock SM, Tin-Wollam AM, Abbott A, Minx P, Maupin R, Strowmatt C, Latreille P, Miller N, Johnson D, Murray J, Woessner JP, Wendl MC, Yang SP, Schultz BR, Wallis JW, Spieth J, Bieri TA, Nelson JO, Berkowicz N, Wohldmann PE, Cook LL, Hickenbotham MT, Eldred J, Williams D, Bedell JA, Mardis ER, Clifton SW, Chissoe SL, Marra MA, Raymond C, Haugen E, Gillett W, Zhou Y, James R, Phelps K, Iadanoto S, Bubb K, Simms E, Levy R, Clendenning J, Kaul R, Kent WJ, Furey TS, Baertsch RA, Brent MR, Keibler E, Flicek P, Bork P, Suyama M, Bailey JA, Portnoy ME, Torrents D, Chinwalla AT, Gish WR, Eddy SR, McPherson JD, Olson MV, Eichler EE, Green ED, Waterston RH, Wilson RK (Jul 2003)."The DNA sequence of human chromosome 7".Nature.424 (6945):157–164.Bibcode:2003Natur.424..157H.doi:10.1038/nature01782.PMID 12853948.</bn>Lichtenbelt KD, Hochstenbach R, van Dam WM, Eleveld MJ, Poot M, Beemer FA (Jan 2005)."Supernumerary ring chromosome 7 mosaicism: case report, investigation of the gene content, and delineation of the phenotype"(PDF).American Journal of Medical Genetics Part A.132A (1):93–100.doi:10.1002/ajmg.a.30408.PMID 15580634.S2CID 20178860. Archived fromthe original(PDF) on 2013-12-17. Retrieved2017-01-20.
17. ^^abNewbury DF, Monaco AP (Oct 2010)."Genetic advances in the study of speech and language disorders".Neuron.68 (2):309–320.doi:10.1016/j.neuron.2010.10.001.PMC 2977079.PMID 20955937.
18. ^Solé F, Espinet B, Sanz GF, Cervera J, Calasanz MJ, Luño E, Prieto F, Granada I, Hernández JM, Cigudosa JC, Diez JL, Bureo E, Marqués ML, Arranz E, Ríos R, Martínez Climent JA, Vallespí T, Florensa L, Woessner S (Feb 2000). "Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes. Grupo Cooperativo Español de Citogenética Hematológica".British Journal of Haematology.108 (2):346–356.doi:10.1046/j.1365-2141.2000.01868.x.PMID 10691865.S2CID 10149222.
19. ^Lossin C, George AL (2008).Chapter 2 Myotonia Congenita. Advances in Genetics. Vol. 63. pp. 25–55.doi:10.1016/S0065-2660(08)01002-X.ISBN 9780123745279.PMID 19185184.
20. ^Grimaldi R, Capuano P, Miranda N, Wagner C, Capasso G (2007). "[Pendrin: physiology, molecular biology and clinical importance]".Giornale Italiano di Nefrologia (in Italian).24 (4):288–294.PMID 17659500.
21. ^Eggermann T, Begemann M, Binder G, Spengler S (2010)."Silver-Russell syndrome: genetic basis and molecular genetic testing".Orphanet Journal of Rare Diseases.5: 19.doi:10.1186/1750-1172-5-19.PMC 2907323.PMID 20573229.
22. ^Zarchi O, Attias J, Gothelf D (2010). "Auditory and visual processing in Williams syndrome".The Israel Journal of Psychiatry and Related Sciences.47 (2):125–131.PMID 20733255.
23. ^Steinberg, Steven J; Raymond, Gerald V; Braverman, Nancy E; Moser, Ann B (2017)."Zellweger Spectrum Disorder".GeneReviews®. University of Washington, Seattle.PMID 20301621. Retrieved2019-09-17.
24. ^Velagaleti GV, Jalal SM, Kukolich MK, Lockhart LH, Tonk VS (Mar 2002). "De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature".Clinical Genetics.61 (3):202–206.doi:10.1034/j.1399-0004.2002.610306.x.PMID 12000362.S2CID 33574584.
25. ^Genome Decoration Page, NCBI.Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
26. ^Genome Decoration Page, NCBI.Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
27. ^International Standing Committee on Human Cytogenetic Nomenclature (2013).ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013). Karger Medical and Scientific Publishers.ISBN 978-3-318-02253-7.
28. ^Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012)."Estimation of band level resolutions of human chromosome images".2012 Ninth International Conference on Computer Science and Software Engineering (JCSSE). pp. 276–282.doi:10.1109/JCSSE.2012.6261965.ISBN 978-1-4673-1921-8.S2CID 16666470.
29. ^"p": Short arm; "q": Long arm.
30. ^For cytogenetic banding nomenclature, see articlelocus.
31. ^^abThese values (ISCN start/stop) are based on the length of bands/ideograms from the ISCN book, An International System for Human Cytogenetic Nomenclature (2013).Arbitrary unit.
32. ^gpos: Region which is positively stained byG banding, generallyAT-rich and gene poor;gneg: Region which is negatively stained by G banding, generallyCG-rich and gene rich;acenCentromere.var: Variable region;stalk: Stalk.
33. ^Lee, Victor Robert (2013-01-15).Performance Anomalies: A Novel. Perimeter Six Press.ISBN 9781938409202.

• Rodríguez L, López F, Paisán L, de la Red Mdel M, Ruiz AM, Blanco M, Antelo Cortizas J, Martínez-Frías ML (Nov 2002). "Pure partial trisomy 7q: two new patients and review".American Journal of Medical Genetics.113 (2):218–224.doi:10.1002/ajmg.10719.PMID 12407716.