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 198 million base pairs (the building material of DNA ) and represents about 6.5 percent of the total DNA in cells .
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.[ 4]
The following is a partial list of genes on human chromosome 3. For complete list, see the link in the infobox on the right.
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
C3orf14-Chromosome 3 open reading frame 14 : 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[ 11]
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
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 [ edit ]
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 [ 12] [ 13]
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
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,
[ 14] 550
[ 15] and 850
[ 3] ). Band length in this diagram is based on the ideograms from ISCN (2013).
[ 16] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the
mitotic process .
[ 17]
G-bands of human chromosome 3 in resolution 850 bphs[ 3]
Chr.
Arm[ 18]
Band[ 19]
ISCN start[ 20]
ISCN stop[ 20]
Basepair start
Basepair stop
Stain[ 21]
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
^ a b "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 .
^ a b c 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 .
^ a b 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.
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