كروموسوم 3
كروموسوم 3 | |
---|---|
السمات | |
Length (bp) | 201,105,948 bp (CHM13) |
No. of genes | 1,024 (CCDS)[1] |
Type | Autosome |
Centromere position | Metacentric[2] (90.9 Mbp[3]) |
قوائم الجينات الكاملة | |
CCDS | Gene list |
HGNC | Gene list |
UniProt | Gene list |
NCBI | Gene list |
متصفحات الخرائط الخارجية | |
Ensembl | Chromosome 3 |
Entrez | Chromosome 3 |
NCBI | Chromosome 3 |
UCSC | Chromosome 3 |
تسلسلات الدنا الكاملة | |
RefSeq | NC_000003 (FASTA) |
GenBank | CM000665 (FASTA) |
كروموسوم 3 Chromosome 3، هو واحد من 23 زوج من الكروموسومات البشرية. عادة ما يمتلك البشر زوجان من هذا الكروموسوم. يحتوي الكروموسوم 3 على 200 مليون زوج قاعدي (مادة بناء الدنا) ويمثل حوالي 6.5% من إجمالي الدنا في الخلايا.
نظراً لاختلاف المناهج التي يستخدمها الباحثون في التنبؤ بعدد الجينات في كل كروموسوم، فهناك تباين في أعداد الجينات المقدرة. على الأرجح يحتوي الكروموسوم 2 ما بين 1.100 و1500 جين.
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الجينات
الجينات الموجودة على الكروموسوم 2:
الذراع-پ
- ALAS1: aminolevulinate, delta-, synthase 1
- BTD: biotinidase
- CCR5: كيموكين (C-C motif) مستقبل 5
- CNTN4: كونتاسين 4
- COL7A1: كولاجين النوع 7، الفا 1 (epidermolysis bullosa, dystrophic, dominant and recessive)
- C3orf14-Chromosome 3 open reading frame 14: predicted DNA binding protein.
- MITF: microphthalmia-associated transcription factor
- MLH1: mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
- OXTR: oxytocin receptor
- PTHR1: parathyroid hormone receptor 1
- SCN5A: sodium channel, voltage-gated, type V, alpha (long QT syndrome 3)
- SLC25A20: solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
- TMIE: transmembrane inner ear
- VHL: von Hippel-Lindau tumor suppressor
- FOXP1: Forkhead Box Protein P1
- CRBN: Cereblon protein[4]
الذراع-كيو
- ADIPOQ: adiponectin
- CPOX: coproporphyrinogen oxidase (coproporphyria, harderoporphyria)
- HGD: homogentisate 1,2-dioxygenase (homogentisate oxidase)
- IFT122: intraflagellar transport gene 122
- MCCC1: methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)
- PCCB: propionyl Coenzyme A carboxylase, beta polypeptide
- PDCD10: programmed cell death 10
- PIK3CA: phosphoinositide-3-kinase, catalytic, alpha polypeptide
- RAB7: RAB7, member RAS oncogene family
- RHO: rhodopsin visual pigment
- SOX2: transcription factor
- USH3A: Usher syndrome 3A
- ZNF9: zinc finger protein 9 (a cellular retroviral nucleic acid binding protein)
الأمراض والاضطرابات
القائمة التالية لبعض الأمراض المتعلقة بالكروموسوم 3:
- 3-methylcrotonyl-CoA carboxylase deficiency
- 3q29 microdeletion syndrome
- Alkaptonuria
- Arrhythmogenic right ventricular dysplasia
- Atransferrinemia
- التوحد
- Biotinidase deficiency
- Blepharophimosis, epicanthus inversus and ptosis type 1
- Breast/colon/lung/pancreatic cancer
- Brugada syndrome
- حمى كاستيلو
- Carnitine-acylcarnitine translocase deficiency
- الساد
- Cerebral cavernous malformation
- Charcot-Marie-Tooth disease, type 2
- Charcot-Marie-Tooth disease
- Chromosome 3q duplication syndrome
- Coproporphyria
- Dandy Walker Syndrome
- الصمم
- مرض السكري
- مستقبل الدومپامين
- Dystrophic epidermolysis bullosa
- Endplate acetlycholinesterase deficiency
- الرعاش المجهول
- Glaucoma, primary open angle
- Glycogen storage disease
- مرض هايلي-هايلي
- Harderoporphyrinuria
- Heart block, progressive/nonprogressive
- Hereditary coproporphyria
- Hereditary nonpolyposis colorectal cancer
- HIV infection, susceptibility/resistance to
- Hypobetalipoproteinemia, familial
- هبوط الحرارة
- Leukoencephalopathy with vanishing white matter
- Long QT syndrome
- Lymphomas
- Malignant hyperthermia susceptibility
- Metaphyseal chondrodysplasia, Murk Jansen type
- Microcoria
- Moebius syndrome
- Moyamoya disease
- Mucopolysaccharidosis
- Muir-Torre family cancer syndrome
- Myotonic dystrophy, type 2
- Myotonic dystrophy
- Neuropathy, hereditary motor and sensory, Okinawa type
- Night blindness
- Nonsyndromic deafness, autosomal recessive
- Nonsyndromic deafness
- سرطان المبضين
- Porphyria
- Propionic acidemia
- نقص الپروتين إس
- Pseudo-Zellweger syndrome
- Retinitis pigmentosa
- Romano-Ward syndrome
- متلازمة سكل
- متلازمة سنسنبرنر
- Septo-optic dysplasia
- Short stature
- Spinocerebellar ataxia
- Sucrose intolerance
- T-cell leukemia translocation altered gene
- Usher syndrome type III
- متلازمة آشر (فنلندا)
- متلازمة آشر
- von Hippel-Lindau syndrome
- Waardenburg syndrome
- Xeroderma pigmentosum, complementation group c
Cytogenetic band
Chr. | Arm[9] | Band[10] | ISCN start[11] |
ISCN stop[11] |
Basepair start |
Basepair stop |
Stain[12] | Density |
---|---|---|---|---|---|---|---|---|
3 | p | 26.3 | 0 | 175 | 1 | 2,800,000 | gpos | 50 |
3 | p | 26.2 | 175 | 263 | 2,800,001 | 4,000,000 | gneg | |
3 | p | 26.1 | 263 | 408 | 4,000,001 | 8,100,000 | gpos | 50 |
3 | p | 25.3 | 408 | 642 | 8,100,001 | 11,600,000 | gneg | |
3 | p | 25.2 | 642 | 759 | 11,600,001 | 13,200,000 | gpos | 25 |
3 | p | 25.1 | 759 | 963 | 13,200,001 | 16,300,000 | gneg | |
3 | p | 24.3 | 963 | 1269 | 16,300,001 | 23,800,000 | gpos | 100 |
3 | p | 24.2 | 1269 | 1357 | 23,800,001 | 26,300,000 | gneg | |
3 | p | 24.1 | 1357 | 1561 | 26,300,001 | 30,800,000 | gpos | 75 |
3 | p | 23 | 1561 | 1751 | 30,800,001 | 32,000,000 | gneg | |
3 | p | 22.3 | 1751 | 1926 | 32,000,001 | 36,400,000 | gpos | 50 |
3 | p | 22.2 | 1926 | 2013 | 36,400,001 | 39,300,000 | gneg | |
3 | p | 22.1 | 2013 | 2188 | 39,300,001 | 43,600,000 | gpos | 75 |
3 | p | 21.33 | 2188 | 2451 | 43,600,001 | 44,100,000 | gneg | |
3 | p | 21.32 | 2451 | 2626 | 44,100,001 | 44,200,000 | gpos | 50 |
3 | p | 21.31 | 2626 | 3239 | 44,200,001 | 50,600,000 | gneg | |
3 | p | 21.2 | 3239 | 3385 | 50,600,001 | 52,300,000 | gpos | 25 |
3 | p | 21.1 | 3385 | 3676 | 52,300,001 | 54,400,000 | gneg | |
3 | p | 14.3 | 3676 | 3910 | 54,400,001 | 58,600,000 | gpos | 50 |
3 | p | 14.2 | 3910 | 4143 | 58,600,001 | 63,800,000 | gneg | |
3 | p | 14.1 | 4143 | 4362 | 63,800,001 | 69,700,000 | gpos | 50 |
3 | p | 13 | 4362 | 4566 | 69,700,001 | 74,100,000 | gneg | |
3 | p | 12.3 | 4566 | 4814 | 74,100,001 | 79,800,000 | gpos | 75 |
3 | p | 12.2 | 4814 | 4946 | 79,800,001 | 83,500,000 | gneg | |
3 | p | 12.1 | 4946 | 5077 | 83,500,001 | 87,100,000 | gpos | 75 |
3 | p | 11.2 | 5077 | 5135 | 87,100,001 | 87,800,000 | gneg | |
3 | p | 11.1 | 5135 | 5266 | 87,800,001 | 90,900,000 | acen | |
3 | q | 11.1 | 5266 | 5427 | 90,900,001 | 94,000,000 | acen | |
3 | q | 11.2 | 5427 | 5602 | 94,000,001 | 98,600,000 | gvar | |
3 | q | 12.1 | 5602 | 5762 | 98,600,001 | 100,300,000 | gneg | |
3 | q | 12.2 | 5762 | 5850 | 100,300,001 | 101,200,000 | gpos | 25 |
3 | q | 12.3 | 5850 | 5996 | 101,200,001 | 103,100,000 | gneg | |
3 | q | 13.11 | 5996 | 6229 | 103,100,001 | 106,500,000 | gpos | 75 |
3 | q | 13.12 | 6229 | 6361 | 106,500,001 | 108,200,000 | gneg | |
3 | q | 13.13 | 6361 | 6594 | 108,200,001 | 111,600,000 | gpos | 50 |
3 | q | 13.2 | 6594 | 6682 | 111,600,001 | 113,700,000 | gneg | |
3 | q | 13.31 | 6682 | 6871 | 113,700,001 | 117,600,000 | gpos | 75 |
3 | q | 13.32 | 6871 | 6973 | 117,600,001 | 119,300,000 | gneg | |
3 | q | 13.33 | 6973 | 7148 | 119,300,001 | 122,200,000 | gpos | 75 |
3 | q | 21.1 | 7148 | 7294 | 122,200,001 | 124,100,000 | gneg | |
3 | q | 21.2 | 7294 | 7440 | 124,100,001 | 126,100,000 | gpos | 25 |
3 | q | 21.3 | 7440 | 7674 | 126,100,001 | 129,500,000 | gneg | |
3 | q | 22.1 | 7674 | 7936 | 129,500,001 | 134,000,000 | gpos | 25 |
3 | q | 22.2 | 7936 | 8053 | 134,000,001 | 136,000,000 | gneg | |
3 | q | 22.3 | 8053 | 8228 | 136,000,001 | 139,000,000 | gpos | 25 |
3 | q | 23 | 8228 | 8461 | 139,000,001 | 143,100,000 | gneg | |
3 | q | 24 | 8461 | 8811 | 143,100,001 | 149,200,000 | gpos | 100 |
3 | q | 25.1 | 8811 | 9001 | 149,200,001 | 152,300,000 | gneg | |
3 | q | 25.2 | 9001 | 9162 | 152,300,001 | 155,300,000 | gpos | 50 |
3 | q | 25.31 | 9162 | 9264 | 155,300,001 | 157,300,000 | gneg | |
3 | q | 25.32 | 9264 | 9366 | 157,300,001 | 159,300,000 | gpos | 50 |
3 | q | 25.33 | 9366 | 9453 | 159,300,001 | 161,000,000 | gneg | |
3 | q | 26.1 | 9453 | 9803 | 161,000,001 | 167,900,000 | gpos | 100 |
3 | q | 26.2 | 9803 | 9949 | 167,900,001 | 171,200,000 | gneg | |
3 | q | 26.31 | 9949 | 10183 | 171,200,001 | 176,000,000 | gpos | 75 |
3 | q | 26.32 | 10183 | 10329 | 176,000,001 | 179,300,000 | gneg | |
3 | q | 26.33 | 10329 | 10489 | 179,300,001 | 183,000,000 | gpos | 75 |
3 | q | 27.1 | 10489 | 10620 | 183,000,001 | 184,800,000 | gneg | |
3 | q | 27.2 | 10620 | 10737 | 184,800,001 | 186,300,000 | gpos | 25 |
3 | q | 27.3 | 10737 | 10883 | 186,300,001 | 188,200,000 | gneg | |
3 | q | 28 | 10883 | 11175 | 188,200,001 | 192,600,000 | gpos | 75 |
3 | q | 29 | 11175 | 11700 | 192,600,001 | 198,295,559 | gneg |
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انظر أيضاً
المصادر
- ^ خطأ استشهاد: وسم
<ref>
غير صحيح؛ لا نص تم توفيره للمراجع المسماةCCDS
- ^ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
- ^ أ ب ت Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
- ^ http://www.ncbi.nlm.nih.gov/gene/51185
- ^ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
- ^ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
- ^ 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.
- ^ 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.
- ^ "p": Short arm; "q": Long arm.
- ^ For cytogenetic banding nomenclature, see article locus.
- ^ أ ب These 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.
- ^ gpos: Region which is positively stained by G banding, generally AT-rich and gene poor; gneg: Region which is negatively stained by G banding, generally CG-rich and gene rich; acen Centromere. var: Variable region; stalk: Stalk.
وصلات خارجية
- National Institutes of Health. "Chromosome 3". Genetics Home Reference. Archived from the original on 2010-04-08. Retrieved 2017-05-06.
- "Chromosome 3". Human Genome Project Information Archive 1990–2003. Retrieved 2017-05-06.