Chromosome 3
Human chromosome
Chromosome 3 is one of the 23 pairs of chromosomes in humans . People normally have two copies of this chromosome. Chromosome 3 spans more than 201 million base pairs (the building material of DNA ) and represents about 6.5 percent of the total DNA in cells .
Genes
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:
ALAS1 : aminolevulinate, delta-, synthase 1
APEH : encoding enzyme Acylamino-acid-releasing enzyme
ARPP-21 : Cyclic AMP-regulated phosphoprotein, 21 kDa
AZI2 : encoding protein 5-azacytidine-induced protein 2
BRK1 : SCAR/WAVE actin nucleating complex subunit
BRPF1 : bromodomain and PHD finger containing 1
BTD : biotinidase
CEP15 : predicted DNA binding protein .
CFAP20DC : encoding protein Chromosome 3 open reading frame 67
C3orf62 : chromosome 3 open reading frame 62
CACNA2D3 : calcium channel, voltage-dependent, alpha 2/delta subunit 3
CCR5 : chemokine (C-C motif) receptor 5
CGGBP1 : CGG triplet repeat binding protein 1
CMTM7 : CKLF like MARVEL transmembrane domain containing 7
CNTN4 : Contactin 4
COL7A1 : Collagen, type VII, alpha 1 (epidermolysis bullosa, dystrophic, dominant and recessive)
CRBN : Cereblon protein
DCLK3 : Doublecortin like kinase 3
DLEC1 : encoding protein Deleted in lung and esophageal cancer 1
EAF1 : ELL associated factor 1
ENTPD3 : ectonucleoside triphosphate diphosphohydrolase 3
FAM107A : Family with sequence similarity 107 member A
FAM19A1 : Family with sequence similarity 19 member A1, C-C motif chemokine like
FBXL2 : F-box and leucine rich repeat protein 2
FOXP1 : Forkhead Box Protein P1
FRA3A encoding protein Fragile site, aphidicolin type, common, fra(3)(p24.2)
FRMD4B encoding protein FERM domain containing 4B
GHRLOS : non-coding RNA ghrelin opposite strand (non-protein coding)
GMPPB : GDP-mannose pyrophosphorylase B
HACL1 : encoding protein 2-hydroxyacyl-CoA lyase 1
HEMK1 : encoding protein HemK methyltransferase family member 1
HIGD1A : HIG1 domain family member 1A
HSN1B : Hereditary sensory neuropathy, type ib
HTD2 : encoding protein Hydroxyacyl-thioester dehydratase type 2
LARS2 : leucyl-tRNA synthetase, mitochondrial
LIMD1 : LIM domain-containing protein 1
LOC105377021 : encoding protein LOC105377021
LINC00312 : Long intergenic non-protein-coding RNA 312
LZTFL1 : Leucine zipper transcription factor like 1
MIR138-1 : encoding protein MicroRNA 138-1
MIR425 : MicroRNA 425
MIR885 : encoding protein MicroRNA 885
MITF : microphthalmia-associated transcription factor
MLH1 : mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
MYRIP : Myosin VIIA and Rab interacting protein
NBEAL2 : Neurobeachin-like 2
NDUFAF3 : encoding enzyme NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3
NKTR : NK-tumor recognition protein
NPRL2 : Nitrogen permease regulator 2-like protein
OXTR : oxytocin receptor
PCAF : acetyltransferase activity
PHF7 encoding protein PHD finger protein 7
PRICKLE2 : encoding protein Prickle planar cell polarity protein 2
PTHR1 : parathyroid hormone receptor 1
QRICH1 : encoding protein QRICH1, also known as Glutamine-rich protein 1,
RBM6 : RNA-binding protein 6
RPP14 : Ribonuclease P protein subunit p14
SCN5A : sodium channel , voltage-gated, type V, alpha (long QT syndrome 3)
SETD5 : SET domain containing 5
SFMBT1 : Scm-like with four mbt domains 1
SLC25A20 : solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
STT3B : catalytic subunit of the oligosaccharyltransferase complex
SYNPR : synaptoporin
TAFA4 : encoding protein Family with sequence similarity 19 member A4, C-C motif chemokine like
TCAIM : encoding protein T-cell activation inhibitor, mitochondrial
TDGF1 : Teratocarcinoma-derived growth factor 1
TMEM158 : Transmembrane protein 158
TMIE : transmembrane inner ear
TRAK1 : trafficking kinesin-binding protein 1
TRANK1 : encoding protein Tetratricopeptide repeat and ankyrin repeat containing 1
TTLL3 : encoding protein Tubulin tyrosine ligase-like family, member 3
TUSC2 : tumor suppressor candidate 2
UCN2 : Urocortin-2
ULK4 : UNC-51 like kinase 4
VGLL3 : vestigial-like family member 3
VHL : von Hippel-Lindau tumor suppressor
ZMYND10 : zinc finger MYND-type containing 10
ZNF197 : encoding protein Zinc finger protein 197
ZNF502 : encoding protein Zinc finger protein 502
ZNF620 : encoding protein Zinc finger protein 620
ZNF621 : encoding protein Zinc finger protein 621
ZNF717 : encoding protein Zinc finger protein 717
q-arm
Partial list of the genes located on q-arm (long arm) of human chromosome 3:
ADIPOQ : adiponectin
AMOTL2 : encoding protein Angiomotin-like protein 2
ARHGAP31 : Rho GRPase activating protein 31
BCHE : butyrylcholinesterase
C3orf70 chromosome 3 open reading frame 70
CAMPD1 : Camptodactyly
CCDC80 : Coiled-coil domain containing protein 80
CD200R1 : Cell surface glycoprotein CD200 receptor 1
CHST13 : encoding protein Carbohydrate (chondroitin 4) sulfotransferase 13
CLDND1 : Claudin domain containing 1
CPN2 : Carboxypeptidase N subunit 2
CPOX : coproporphyrinogen oxidase (coproporphyria, harderoporphyria)
DPPA2 : Developmental pluripotency associated 2
DTX3L : encoding protein Deltex e3 ubiquitin ligase 3l
DZIP3 : encoding protein DAZ interacting zinc finger protein 3
EAF2 : ELL associated factor 2
EFCC1 : EF-hand and coiled-coil domain containing 1
ETM1 : Essential tremor 1
ETV5 : ETS variant 5
FAM3D : family with sequence similarity 3, member D
FAM43A : family with sequence similarity 43 member A
FAM162A : family with sequence similarity 162 member A
FBXO40 : encoding protein F-box protein 40
FILIP1L : encoding protein Filamin A interacting protein 1 like
GYG1 : Glycogenin-1
HACD2 encoding protein 3-hydroxyacyl-CoA dehydratase 2
HGD : homogentisate 1,2-dioxygenase (homogentisate oxidase)
IFT122 : intraflagellar transport gene 122
KIAA1257 : KIAA1257
LINC01279 : encoding protein long intergenic non-protein coding RNA 1279
LNCR5 : encoding protein lung cancer susceptibility 5
LMLN : encoding protein Leishmanolysin-like (metallopeptidase M8 family)
LRRC15 : leucine rich repeat containing 15
LSG1 : large subunit GTPase 1 homolog
MB21D2 : encoding protein Mab-21 domain containing 2
MCCC1 : methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)
MORC1 : encoding protein Morc family cw-type zinc finger 1
MYLK : Telokin
NEPRO : encoding protein Nucleolus and neural progenitor protein
NFKBIZ : NF-kappa-B inhibitor zeta
OTOL1 : encoding glycoprotein Otolin
PARP14 encoding protein Poly(ADP-ribose) polymerase family member 14
PCCB : propionyl Coenzyme A carboxylase, beta polypeptide
PDCD10 : programmed cell death 10
PIK3CA : phosphoinositide-3-kinase, catalytic, alpha polypeptide
PISRT1 : long non-coding RNA
PROSER1 : Proline and serine rich protein 1
RAB7 : RAB7, member RAS oncogene family
RASA2 : encoding protein Ras p21 protein activator 2
RETNLB : resistin-like beta
RHO : rhodopsin visual pigment
RIOX2 : Ribosomal oxygenase 2
SELT : Selenoprotein T
SENP7 : Sentrin-specific protease 7
SERP1 : Stress-associated endoplasmic reticulum protein 1
SOX2 : transcription factor
SOX2OT : SOX2 overlapping transcript
SPG14 encoding protein Spastic paraplegia 14 (autosomal recessive)
SRPRB : Signal recognition particle receptor subunit beta
TEX55 : encoding protein Testis expressed 55
TIMMDC1 : TIMMDC1
TMEM44 : encoding protein Transmembrane protein 44
TM4SF1 : Transmembrane 4 L6 family member 1
TMPRSS7 : encoding protein Transmembrane serine protease 7
TP63 : Tumor protein p63
TRAT1 : T-cell receptor-associated transmembrane adapter 1
USH3A : Usher syndrome 3A
ZBED2 : encoding protein Zinc finger BED-type containing 2
ZNF9 : zinc finger protein 9 (a cellular retroviral nucleic acid binding protein)
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, type 1
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
3p14 microdeletion syndrome
Cytogenetic band
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 (e.g.
Ensembl ,
UCSC Genome Browser ).
G-banding patterns of human chromosome 3 in three different resolutions (400, 550 and 850). Band length in this diagram is based on the ideograms from ISCN (2013). This type of ideogram represents actual relative band length observed under a microscope at the different moments during the
mitotic process .
G-bands of human chromosome 3 in resolution 850 bphs
Chr.
Arm
Band
ISCN start
ISCN stop
Basepair start
Basepair stop
Stain
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
References
1 2 "Search results – 3[ CHR] AND "Homo sapiens"[ Organism] AND ("has ccds"[ Properties] AND alive[ prop] ) – Gene" . NCBI . CCDS Release 20 for Homo sapiens . 2016-09-08. Retrieved 2017-05-28 .
↑ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics . Garland Science. p. 45. ISBN 978-1-136-84407-2 .
1 2 3 Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3) . Last update 2014-06-03. Retrieved 2017-04-26.
↑ 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 .
↑ "Statistics & Downloads for chromosome 3" . HUGO Gene Nomenclature Committee . 2017-05-12. Archived from the original on 2017-06-29. Retrieved 2017-05-19 .
↑ "Chromosome 3: Chromosome summary – Homo sapiens" . Ensembl Release 88 . 2017-03-29. Retrieved 2017-05-19 .
↑ "Human chromosome 3: entries, gene names and cross-references to MIM" . UniProt . 2018-02-28. Retrieved 2018-03-16 .
↑ "Search results – 3[ CHR] AND "Homo sapiens"[ Organism] AND ("genetype protein coding"[ Properties] AND alive[ prop] ) – Gene" . NCBI . 2017-05-19. Retrieved 2017-05-20 .
↑ "Search results – 3[ 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. Retrieved 2017-05-20 .
↑ "Search results – 3[ CHR] AND "Homo sapiens"[ Organism] AND ("genetype pseudo"[ Properties] AND alive[ prop] ) – Gene" . NCBI . 2017-05-19. Retrieved 2017-05-20 .
↑ CRBN cereblon [Homo sapiens (human)] - Gene - NCBI
↑ "Scientists pinpoint genes common among people with severe coronavirus infections" . MSN .
↑ Severe Covid-19 GWAS Group; et al. (2020). "Genomewide Association Study of Severe Covid-19 with Respiratory Failure" . New England Journal of Medicine . 383 (16): 1522– 1534. doi :10.1056/NEJMoa2020283 . PMC 7315890 . PMID 32558485 . {{cite journal }}: CS1 maint: numeric names: authors list (link )
↑ 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 .
1 2 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.
External links
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 .
Basic concepts Types Processes and evolution Structures
See also