Chromosome 1


Chromosome 1 is the designation for the largest human chromosome. Humans have two copies of chromosome 1, as they do with all of the autosomes, which are the non-sex chromosomes. Chromosome 1 spans about 249 million nucleotide base pairs, which are the basic units of information for DNA. It represents about 8% of the total DNA in human cells.
It was the last completed chromosome, sequenced two decades after the beginning of the Human Genome Project.

Genes

Number of genes

The following are some of the gene count estimates of human chromosome 1. Because researchers use different approaches to genome annotation their predictions of the number of genes on each chromosome varies. Among various projects, the collaborative consensus coding sequence project takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes.
Estimated byProtein-coding genesNon-coding RNA genesPseudogenesSourceRelease date
CCDS1,9612016-09-08
HGNC1,9937071,1132017-05-12
Ensembl2,0441,9241,2232017-03-29
UniProt2,0642018-02-28
NCBI2,0931,7901,4262017-05-19

Gene list

The following is a partial list of genes on human chromosome 1. For complete list, see the link in the infobox on the right.
Partial list of the genes located on p-arm of human chromosome 1:

q-arm

Partial list of the genes located on q-arm of human chromosome 1:

Diseases and disorders

There are 890 known diseases related to this chromosome. Some of these diseases are hearing loss, Alzheimer's disease, glaucoma and breast cancer. Rearrangements and mutations of chromosome 1 are prevalent in cancer and many other diseases. Patterns of sequence variation reveal signals of recent selection in specific genes that may contribute to human fitness, and also in regions where no function is evident.
Complete monosomy is invariably lethal before birth. Complete trisomy is lethal within days after conception. Some partial deletions and partial duplications produce birth defects.
The following diseases are some of those related to genes on chromosome 1 :
Chr.ArmBandISCN
start
ISCN
stop
Basepair
start
Basepair
stop
StainDensity
1p36.330100gneg
1p36.32100244gpos25
1p36.31244344gneg
1p36.23344459gpos25
1p36.22459660gneg
1p36.21660861gpos50
1p36.138611206gneg
1p36.1212061321gpos25
1p36.1113211521gneg
1p35.315211651gpos25
1p35.216511780gneg
1p35.117801895gpos25
1p34.318952210gneg
1p34.222102411gpos25
1p34.124112770gneg
1p3327702986gpos75
1p32.329863273gneg
1p32.232733416gpos50
1p32.134163732gneg
1p31.337323976gpos50
1p31.239764206gneg
1p31.142064852gpos100
1p22.348525210gneg
1p22.252105440gpos75
1p22.154405741gneg
1p21.357415957gpos75
1p21.259576029gneg
1p21.160296244gpos100
1p13.362446459gneg
1p13.264596660gpos50
1p13.166606861gneg
1p1268617048gpos50
1p11.270487119gneg
1p11.171197335acen
1q1173357579acen
1q1275798483gvar
1q21.184838756gneg
1q21.287568957gpos50
1q21.389579244gneg
1q2292449459gpos50
1q23.194599832gneg
1q23.2983210048gpos50
1q23.31004810349gneg
1q24.11034910507gpos50
1q24.21050710679gneg
1q24.31067910894gpos75
1q25.11089411009gneg
1q25.21100911196gpos50
1q25.31119611598gneg
1q31.11159811827gpos100
1q31.21182711942gneg
1q31.31194212172gpos100
1q32.11217212617gneg
1q32.21261712803gpos25
1q32.31280313033gneg
1q411303313320gpos100
1q42.111332013406gneg
1q42.121340613607gpos25
1q42.131360713966gneg
1q42.21396614153gpos50
1q42.31415314397gneg
1q431439714756gpos75
1q441475615100gneg