dbo:abstract |
El cromosoma 3 és un dels 23 parells de cromosomes en humans. Té uns 200 milions de parells de bases i representa aproximadament el 6,5% de l'ADN. Conté entre 1.100 i 1.500 gens. (ca) الصبغي البشري الثالث (بالإنجليزية: Chromosome 3) هو أحد 23 زوجاً صبغياً بشرياً، والشخص الطبيعي يملك زوجاً من هذا الصبغي، ويحوي الصبغي 200 مليون زوجاً من أسسس الدنا ويشكل حوالي 6.5% من دنا الخلية وقد يحوي من 1100 إلى 1500 مورثة. (ar) Chromosom 3 ist eines von 23 Chromosomen-Paaren des Menschen. Ein normaler Mensch hat in den meisten seiner Zellen zwei weitgehend identische Kopien dieses Chromosoms. (de) Chromosome 3 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 3 spans almost 200 million base pairs (the building material of DNA) and represents about 6.5 percent of the total DNA in cells. (en) [[İmage:Chromosome 3.svg|125px |
dbo:thumbnail |
wiki-commons:Special:FilePath/Human_male_karyotpe_h..._-_Chromosome_3_cropped.png?width=300 |
dbo:wikiPageExternalLink |
http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo03.shtml%7Ctitle=Chromosome https://web.archive.org/web/20100408061926/http:/ghr.nlm.nih.gov/chromosome=3 http://ghr.nlm.nih.gov/chromosome=3 |
dbo:wikiPageID |
3402407 (xsd:integer) |
dbo:wikiPageLength |
33574 (xsd:nonNegativeInteger) |
dbo:wikiPageRevisionID |
1108874684 (xsd:integer) |
dbo:wikiPageWikiLink |
dbr:Cataracts dbr:AZI2 dbr:BRK1 dbr:Propionic_acidemia dbr:Epidermolysis_bullosa_dystrophica dbr:FAM107A dbr:FAM43A dbr:FBXL2 dbr:Moyamoya_disease dbr:Mab-21_domain_containing_2 dbr:NBEAL2 dbr:Coproporphyria dbr:Biotinidase_deficiency dbr:Alkaptonuria dbr:Human dbr:Hypothermia dbr:Arrhythmogenic_right_ventricular_dysplasia dbr:DNA dbr:UniProt dbr:Usher_syndrome dbr:VHL dbr:C3orf14-Chromosome_3_open_reading_frame_14 dbr:C3orf62 dbr:C3orf67 dbr:C3orf70 dbr:CD200R1 dbr:Deafness dbr:Carbohydrate_(chondroitin_4)_sulfotransferase_13 dbr:Doublecortin_like_kinase_3 dbr:EFCC1 dbr:LARS2 dbr:GMPPB dbr:SETD5 dbr:KIAA1257 dbr:Pseudogene dbr:SYNPR dbr:LINC01279 dbr:SERP1 dbr:Nucleolus_and_neural_progenitor_protein dbr:Zinc_finger_protein_502 dbr:Gene_prediction dbr:Telokin dbr:MLH1 dbr:QRICH1 dbr:RTP3_(gene) dbr:Zinc_finger_bed-type_containing_2 dbr:Ensembl_genome_database_project dbr:Enzyme dbr:Myotonic_dystrophy dbr:Consensus_CDS_Project dbr:Coproporphyrinogen_III_oxidase dbr:Brpf1 dbr:LMLN dbr:LNCR5 dbr:LOC105377021 dbr:LZTFL1 dbr:Teratocarcinoma-derived_growth_factor_1 dbr:LIMD1 dbr:TCAIM dbr:TEX55 dbr:TIMMDC1 dbr:TMPRSS7_(gene) dbr:Leukoencephalopathy_with_vanishing_white_matter dbr:Lymphomas dbr:Hailey–Hailey_disease dbr:Daz_interacting_zinc_finger_protein_3 dbr:Developmental_pluripotency_associated_2 dbr:Protein_S_deficiency dbr:Microcoria dbr:Autism dbr:COVID-19 dbr:Cell_(biology) dbr:GRCh38 dbr:G_banding dbr:Cklf_like_marvel_transmembrane_domain_containing_7 dbr:Glaucoma dbr:HIV dbr:DTX3L dbr:Family_with_sequence_similarity_19_member_A4,_C-C_motif_chemokine_like dbr:NKTR dbr:TM4SF1 dbr:NPRL2 dbr:Vestigial-like_family_member_3 dbr:LSG1 dbr:3-Methylcrotonyl-CoA_carboxylase_deficiency dbr:Acute_myeloid_leukemia dbr:3q29_microdeletion_syndrome dbr:Dandy–Walker_syndrome dbr:Essential_tremor dbr:Base_pair dbr:Night_blindness dbr:Nonsyndromic_deafness dbr:Centromere dbc:Chromosomes_(human) dbr:Chromosome dbr:Glycogen_storage_disease dbr:Glycogenin-1 dbr:Ensembl dbr:Protein dbr:Respiratory_failure dbr:ALAS1 dbr:AMOTL2 dbr:APEH_(gene) dbr:ARPP-21 dbr:HUGO_Gene_Nomenclature_Committee dbr:Hereditary_nonpolyposis_colorectal_cancer dbr:Atransferrinemia dbr:EAF1 dbr:EAF2 dbr:ENTPD3 dbr:ETM1 dbr:Ferm_domain_containing_4b dbr:Rhodopsin dbr:TTLL3 dbr:ARHGAP31 dbr:Charcot–Marie–Tooth_disease dbr:Collagen,_type_VII,_alpha_1 dbr:Hereditary_coproporphyria dbr:Homogentisate_1,2-dioxygenase dbr:Mitosis dbr:SRPRB dbr:Zinc_finger_protein_621 dbr:Diabetes dbr:3-hydroxyacyl-CoA_dehydratase_2 dbr:Autosome dbr:CACNA2D3 dbr:CCDC80 dbr:CCR5 dbc:Genes_on_human_chromosome_3 dbr:Porphyria dbr:Spinocerebellar_ataxia dbr:HEMK1 dbr:HIGD1A dbr:DNA_binding_protein dbr:FAM19A1 dbr:Metaphyseal_chondrodysplasia,_Murk_Jansen_type dbr:Brugada_syndrome dbr:National_Center_for_Biotechnology_Information dbr:Camptodactyly dbr:Carnitine-acylcarnitine_translocase_deficiency dbr:CGGBP1 dbr:CLDND1 dbr:CNTN4 dbr:CPN2 dbr:Long_QT_syndrome dbr:Long_intergenic_non-protein_coding_rna_312 dbr:Long_non-coding_RNA dbr:Mucopolysaccharidosis dbr:Retinitis_pigmentosa dbr:SFMBT1 dbr:Seckel_syndrome dbr:Septo-optic_dysplasia dbr:Short_stature dbr:UCN2 dbr:ULK4 dbr:Waardenburg_syndrome dbr:Sodium_channel dbr:UCSC_Genome_Browser dbr:Ets_variant_5 dbr:FAM162A dbr:FAM3D dbr:FOXP1 dbr:FRA3A dbr:SENP7 dbr:ZMYND10 dbr:PDCD10 dbr:SOX2OT dbr:SELT dbr:Sensenbrenner_syndrome dbr:Transmembrane_protein_44 dbr:TUSC2 dbr:Möbius_syndrome dbr:STT3B dbr:Myosin_viia_and_rab_interacting_protein dbr:NDUFAF3 dbr:Von_Hippel–Lindau_syndrome dbr:Poly(adp-ribose)_polymerase_family_member_14 dbr:TRAT1 dbr:Sucrose_intolerance dbr:Non-coding_RNA dbr:Romano–Ward_syndrome dbr:RBM6 dbr:RETNLB dbr:PHD_finger_protein_7 dbr:NFKBIZ dbr:PISRT1 dbr:RPP14 dbr:SPG14 dbr:Ovarian_cancer dbr:TMEM158 dbr:TRAK1 dbr:SCN5A dbr:SOX2 dbr:TRANK1 dbr:TP63 dbr:Proser1 dbr:RIOX2 dbr:Leucine_rich_repeat_containing_15 dbr:BTD dbr:Protein-coding_genes dbr:USH3A dbr:Hypobetalipoproteinemia,_familial dbr:PCCB dbr:PIK3CA dbr:PTHR1 dbr:SLC25A20 dbr:Charcot–Marie–Tooth_disease,_type_2 dbr:Cavernous_angioma dbr:Karyogram dbr:MCCC1 dbr:RAB7 dbr:ADIPOQ dbr:Genome_annotation dbr:Number_of_genes dbr:OXTR dbr:COL7A1 dbr:CRBN dbr:ZNF9 dbr:MITF dbr:Xeroderma_pigmentosum,_complementation_group_c dbr:ADOA_plus_syndrome dbr:Autosomal_dominant_optic_atrophy dbr:Blepharophimosis,_epicanthus_inversus_and_ptosis_type_1 dbr:Breast/colon/lung/pancreatic_cancer dbr:CAMPD1 dbr:Castillo_fever dbr:Chromosome_3q_duplication_syndrome dbr:Ectrodactyly,_Case_4 dbr:Endplate_acetylcholinesterase_deficiency dbr:Harderoporphyrinuria dbr:Heart_block,_progressive/nonprogressive dbr:IFT122 dbr:Malignant_hyperthermia_susceptibility dbr:Muir–Torre_family_cancer_syndrome dbr:Neuropathy,_hereditary_motor_and_sensory,_Okinawa_type dbr:Pseudo-Zellweger_syndrome dbr:T-cell_leukemia_translocation_altered_gene dbr:TMIE |
dbp:caption |
Chromosome 3 pair (en) in human male karyogram. (en) G-banding ideogram of human chromosome 3 in resolution 850 bphs. Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers . (en) Human chromosome 3 pair after G-banding. One is from mother, one is from father. (en) G-banding patterns of human chromosome 3 in three different resolutions . Band length in this diagram is based on the ideograms from ISCN . This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process. (en) |
dbp:centromerePosition |
dbr:Centromere (en) |
dbp:chr |
3 (xsd:integer) |
dbp:ensemblId |
3 (xsd:integer) |
dbp:entrezId |
3 (xsd:integer) |
dbp:genbankId |
CM000665 (en) |
dbp:genes |
1024 (xsd:integer) |
dbp:header |
G-banding ideograms of human chromosome 3 (en) |
dbp:height |
1125 (xsd:integer) 2801 (xsd:integer) |
dbp:image |
Human chromosome 03 - 400 550 850 bphs.png (en) Human chromosome 3 ideogram vertical.svg (en) Human male karyotpe high resolution - Chromosome 3.png (en) |
dbp:lengthBp |
198295559 (xsd:integer) (en) |
dbp:ncbiId |
3 (xsd:integer) |
dbp:refseqId |
NC_000003 (en) |
dbp:totalWidth |
400 (xsd:integer) |
dbp:type |
dbr:Autosome |
dbp:ucscId |
3 (xsd:integer) |
dbp:width |
216 (xsd:integer) 1003 (xsd:integer) |
dbp:wikiPageUsesTemplate |
dbt:Cite_web dbt:Columns-list dbt:Commons_category dbt:Div_col dbt:Div_col_end dbt:Expand_list dbt:Multiple_image dbt:Reflist dbt:Short_description dbt:Val dbt:Infobox_chromosome dbt:Category_see_also dbt:Chromosome_genetics dbt:Chromosomes |
dcterms:subject |
dbc:Chromosomes_(human) dbc:Genes_on_human_chromosome_3 |
rdfs:comment |
El cromosoma 3 és un dels 23 parells de cromosomes en humans. Té uns 200 milions de parells de bases i representa aproximadament el 6,5% de l'ADN. Conté entre 1.100 i 1.500 gens. (ca) الصبغي البشري الثالث (بالإنجليزية: Chromosome 3) هو أحد 23 زوجاً صبغياً بشرياً، والشخص الطبيعي يملك زوجاً من هذا الصبغي، ويحوي الصبغي 200 مليون زوجاً من أسسس الدنا ويشكل حوالي 6.5% من دنا الخلية وقد يحوي من 1100 إلى 1500 مورثة. (ar) Chromosom 3 ist eines von 23 Chromosomen-Paaren des Menschen. Ein normaler Mensch hat in den meisten seiner Zellen zwei weitgehend identische Kopien dieses Chromosoms. (de) Chromosome 3 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 3 spans almost 200 million base pairs (the building material of DNA) and represents about 6.5 percent of the total DNA in cells. (en) Le chromosome 3 constitue l'une des 23 paires de chromosomes humains. C'est l'un des 22 autosomes. (fr) 3번 염색체는 인간의 염색체 중 하나이며 인간의 염색체들 중에서 길이가 세 번째로 길다. (ko) Con il nome di cromosoma 3 si indica, per convenzione, il terzo più grande cromosoma umano. Le persone presentano solitamente due copie del cromosoma 3, come di ogni autosoma. Il cromosoma 3 possiede quasi 200 milioni di nucleotidi. I due cromosomi 3 rappresentano all'incirca il 6,5% del DNA totale nelle cellule umane. Il cromosoma 3 contiene di certo oltre 1300 geni, ma si ritiene possa contenerne fino a 1500. Il numero di polimorfismi a singolo nucleotide (SNP) individuati è di oltre 700.000. (it) Chromosom 3 – jeden z 23 parzystych chromosomów człowieka. DNA chromosomu 3 liczy około 200 milionów par nukleotydów, co stanowi około 6,5% materiału genetycznego ludzkiej komórki. Liczbę genów mających swoje locus na chromosomie 3 szacuje się na 1100–1500. (pl) O cromossoma 3 é um dos 23 pares de cromossomas do cariótipo humano. Tem aproximadamente 200 milhões de pares de bases, representando 6,5 % da totalidade de DNA presente na célula. Contém entre 1100 e 1500 genes. (pt) Chromosoom 3 is een chromosoom in het menselijk lichaam dat ongeveer 199 miljoen basenparen DNA bevat. Het staat voor 6 tot 6,5 procent van het totale DNA in cellen. Op chromosoom 3 bevinden zich naar wordt aangenomen anno 2008 ongeveer 80 genen die de oorzaak van een ziekte kunnen vormen. (nl) Хромосома 3 – одна з 23 пар хромосом людини. За нормальних умов у людей дві копії цієї хромосоми. 3-та хромосома має в своєму складі 200 млн пар основ або 6.5% від загальної кількості нуклеотидів в ДНК клітинІдентифікація генів кожної хромосоми є пріоритетним напрямком наукових досліджень в генетиці. Проте, дослідники застосовують різні підходи щодо визначення кількості генів в кожній хромосомі, внаслідок цього дані щодо їх кількості демонструють різні цифри. Це також стосується і хромосоми 3, в якій налічують до 1926 генів (станом на 2012р.) . (uk) 3-я хромосо́ма челове́ка — одна из 23 пар человеческих хромосом, одна из 22 аутосом человека. Хромосома содержит почти 200 млн пар оснований, что составляет примерно 6,5 % всего материала ДНК человеческой клетки. В настоящее время считается, что на 3-й хромосоме находятся 1960 генов. (ru) 3號染色體是人類基因組中的24種染色體(並組成23對)的其中之一。對一般人來說,細胞中會有1對3號染色體,分別來自父親與母親。這條染色體也是人體中第3大的染色體,擁有大約2億個鹼基對,約佔人類DNA的6.5%。 和其他的染色體一樣,3號染色體所擁有的基因數目並不確定,不同的研究中會有一些差異。根據NCBI資料庫的紀錄,現在已知位在3號染色體的基因有1469個,其中有8個基因尚未確定位置。 (zh) [[İmage:Chromosome 3.svg|125px |
rdfs:label |
صبغي 3 (ar) Cromosoma 3 (ca) Chromosom 3 (Mensch) (de) Chromosome 3 (en) Cromosoma 3 (humano) (es) Chromosome 3 humain (fr) Cromosoma 3 (it) 3번 염색체 (ko) Chromosom 3 (pl) Chromosoom 3 (nl) Cromossoma 3 (pt) 3-я хромосома человека (ru) 3號染色體 (zh) Хромосома 3 (людина) (uk) |
owl:sameAs |
wikidata:Chromosome 3 dbpedia-ar:Chromosome 3 dbpedia-bg:Chromosome 3 http://bn.dbpedia.org/resource/৩_নং_ক্রোমোজোম_(মানবদেহ) http://bs.dbpedia.org/resource/Hromosom_3 dbpedia-ca:Chromosome 3 dbpedia-da:Chromosome 3 dbpedia-de:Chromosome 3 dbpedia-es:Chromosome 3 dbpedia-et:Chromosome 3 dbpedia-fa:Chromosome 3 dbpedia-fi:Chromosome 3 dbpedia-fr:Chromosome 3 dbpedia-gl:Chromosome 3 dbpedia-he:Chromosome 3 dbpedia-hr:Chromosome 3 dbpedia-hu:Chromosome 3 http://hy.dbpedia.org/resource/3-րդ_քրոմոսոմ_(մարդ) dbpedia-it:Chromosome 3 dbpedia-ko:Chromosome 3 dbpedia-la:Chromosome 3 dbpedia-mk:Chromosome 3 dbpedia-nl:Chromosome 3 dbpedia-no:Chromosome 3 dbpedia-pl:Chromosome 3 dbpedia-pt:Chromosome 3 dbpedia-ro:Chromosome 3 dbpedia-ru:Chromosome 3 dbpedia-sh:Chromosome 3 dbpedia-sr:Chromosome 3 http://tl.dbpedia.org/resource/Kromosomang_3_(tao) dbpedia-tr:Chromosome 3 dbpedia-uk:Chromosome 3 dbpedia-vi:Chromosome 3 dbpedia-zh:Chromosome 3 https://global.dbpedia.org/id/4qgud |
prov:wasDerivedFrom |
wikipedia-en:Chromosome_3?oldid=1108874684&ns=0 |
foaf:depiction |
wiki-commons:Special:FilePath/Human_male_karyotpe_high_resolution_-_Chromosome_3_cropped.png wiki-commons:Special:FilePath/Human_chromosome_03_-_400_550_850_bphs.png wiki-commons:Special:FilePath/Human_chromosome_3_ideogram_vertical.svg wiki-commons:Special:FilePath/Human_male_karyotpe_high_resolution_-_Chromosome_3.png |
foaf:isPrimaryTopicOf |
wikipedia-en:Chromosome_3 |
is dbo:wikiPageRedirects of |
dbr:Chromosome_3_(human) dbr:Chromosome_3q dbr:Chromosomes,_human,_pair_3 dbr:List_of_human_genes_on_chromosome_3 dbr:Human_Chromosome_3 dbr:Human_chromosome_3 |
is dbo:wikiPageWikiLink of |
dbr:Endolymphatic_sac_tumor dbr:FAM43A dbr:MRE11A dbr:Moyamoya_disease dbr:Megakaryocyte dbr:Methylcrotonyl-CoA_carboxylase dbr:MCOLN3 dbr:Hyaluronidase dbr:Renal_cell_carcinoma dbr:DNAJC19 dbr:Usher_syndrome dbr:Uveal_melanoma dbr:C3orf70 dbr:Von_Hippel–Lindau_disease dbr:DecisionDx-UM dbr:Dyslexia_research dbr:Dystroglycan dbr:EEM_syndrome dbr:Innate_resistance_to_HIV dbr:Leukonychia dbr:Geminin_coiled-coil_domain-containing_protein_1 dbr:RIDDLE_syndrome dbr:RTP3_(gene) dbr:Chromosome_3_(human) dbr:Gillespie_syndrome dbr:Coproporphyrinogen_III_oxidase dbr:LOC105377021 dbr:Teratocarcinoma-derived_growth_factor_1 dbr:TCAIM dbr:TEX55 dbr:TIMMDC1 dbr:TMEM212 dbr:Emberger_syndrome dbr:Hailey–Hailey_disease dbr:Protein_S_deficiency dbr:Thrombopoietin dbr:Thyroid_hormone_receptor dbr:Microphthalmia,_syndromic_12_(MCOPS12) dbr:Wilms'_tumor dbr:GATA1 dbr:GATA2 dbr:GATA2_deficiency dbr:GHRLOS dbr:HIDEA_syndrome dbr:Oxytocin_receptor dbr:PTX3 dbr:Acute_megakaryoblastic_leukemia dbr:Acute_myeloid_leukemia dbr:Aminoacylase_1_deficiency dbr:3q29_microdeletion_syndrome dbr:5-HT3_receptor dbr:Familial_hypocalciuric_hypercalcemia dbr:Bart_syndrome dbr:Osteogenesis_imperfecta dbr:Pachydermoperiostosis dbr:Cavernous_hemangioma dbr:Dibucaine_number dbr:Dilated_cardiomyopathy_with_ataxia_syndrome dbr:Familial_episodic_pain_syndrome dbr:Familial_thoracic_aortic_aneurysm_and_aortic_dissection dbr:Glycogenin-1 dbr:Histidine-rich_glycoprotein dbr:Isolated_hyperCKemia dbr:APEH_(gene) dbr:Hereditary_sensory_and_autonomic_neuropathy_type_I dbr:Atelosteogenesis_type_I dbr:Isolated_congenital_asplenia dbr:ACY1 dbr:Acral_myxoinflammatory_fibroblastic_sarcoma dbr:Cole–Carpenter_syndrome dbr:Collagen,_type_VI,_alpha_5 dbr:Collagen,_type_VII,_alpha_1 dbr:Hereditary_coproporphyria dbr:TRAIL dbr:CCBP2 dbr:CD80 dbr:CKLF-like_MARVEL_transmembrane_domain-containing_family dbr:CKLF_like_MARVEL_transmembrane_domain-containing_8 dbr:CKLF_like_MARVEL_transmembrane_domain_containing_6 dbr:CKLF_like_MARVEL_transmembrane_domain_containing_7 dbr:CXC_chemokine_receptors dbr:Fibro-adipose_vascular_anomaly dbr:Contactin_4 dbr:Human_Endogenous_Retrovirus-W dbr:Human_blood_group_systems dbr:Human_identical_sequence dbr:ZNF385D dbr:CGGBP1 dbr:CPA3 dbr:Kjer's_optic_neuropathy dbr:Kleine–Levin_syndrome dbr:Roundabout_family dbr:SDHD dbr:Uridine_monophosphate_synthase dbr:FERM_domain_Containing_4B dbr:Sensenbrenner_syndrome dbr:Mycophenolic_acid_acyl-glucuronide_esterase dbr:NAALADL2 dbr:NDUFB4 dbr:NDUFB5 dbr:Polysomy dbr:Severe_intellectual_disability-progressive_spastic_diplegia_syndrome dbr:Naa80 dbr:Peroxisome_proliferator-activated_receptor dbr:Rev-ErbA_alpha dbr:PET100 dbr:PRR23C dbr:Tumor_marker dbr:SOFT_syndrome dbr:Spondylometaphyseal_dysplasia_with_cone-rod_dystrophy dbr:Chromosome_3q dbr:Chromosomes,_human,_pair_3 dbr:List_of_human_genes_on_chromosome_3 dbr:Human_Chromosome_3 dbr:Human_chromosome_3 |
is foaf:primaryTopic of |
wikipedia-en:Chromosome_3 |