Chromosome 3

Number of genes The following are some of the gene count estimates of human chromosome 3. Because researchers use different approaches to genome annotation their predictions of the number of genes on each chromosome varies (for technical details, see gene prediction). Among various projects, the collaborative consensus coding sequence project (CCDS) takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes. List of genes The following is a partial list of genes on human chromosome 3. For complete list, see the link in the infobox on the right. p-arm Partial list of the genes located on p-arm (short arm) of human chromosome 3: q-arm Partial list of the genes located on q-arm (long arm) of human chromosome 3: ==Diseases and disorders==

The following diseases and disorders are some of those related to genes on chromosome 3: • 3-Methylcrotonyl-CoA carboxylase deficiency • 3q29 microdeletion syndrome • Acute myeloid leukemia (AML) • Alkaptonuria • Arrhythmogenic right ventricular dysplasia • Atransferrinemia • Autism • Autosomal dominant optic atrophy • ADOA plus syndrome • Biotinidase deficiency • Blepharophimosis, epicanthus inversus and ptosis type 1 • Breast/colon/lung/pancreatic cancer • Brugada syndrome • Castillo fever • Carnitine-acylcarnitine translocase deficiency • Cataracts • Cerebral cavernous malformation • Charcot–Marie–Tooth disease, type 2 • Charcot–Marie–Tooth disease • Chromosome 3q duplication syndrome • Coproporphyria • A location on human chromosome 3 is associated with respiratory failure and possibly with increased severity in COVID-19 • Dandy–Walker syndrome • Deafness • Diabetes • Dystrophic epidermolysis bullosa • Endplate acetylcholinesterase deficiency • Essential tremors • Ectrodactyly, Case 4 • Glaucoma, primary open angle • Glycogen storage disease • Hailey–Hailey disease • Harderoporphyrinuria • Heart block, progressive/nonprogressive • Hereditary coproporphyria • Hereditary nonpolyposis colorectal cancer • HIV infection, susceptibility/resistance to • Hypobetalipoproteinemia, familial • Hypothermia • Leukoencephalopathy with vanishing white matter • Long QT syndrome • Lymphomas • Malignant hyperthermia susceptibility • Metaphyseal chondrodysplasia, Murk Jansen type • Microcoria • Möbius syndrome • Moyamoya disease • Mucopolysaccharidosis • Muir–Torre family cancer syndrome • Myotonic dystrophy • Neuropathy, hereditary motor and sensory, Okinawa type • Night blindness • Nonsyndromic deafness • Ovarian cancer • Porphyria • Propionic acidemia • Protein S deficiency • Pseudocholinesterase deficiency • Pseudo-Zellweger syndrome • Retinitis pigmentosa • Romano–Ward syndrome • Seckel syndrome • Sensenbrenner syndrome • Septo-optic dysplasia • Short stature • Spinocerebellar ataxia • Sucrose intolerance • T-cell leukemia translocation altered gene • Usher syndrome • von Hippel–Lindau syndrome • Waardenburg syndrome • Xeroderma pigmentosum, complementation group c ==Cytogenetic band==