Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Chromosome 4 likely contains between 700 and 1,100 genes.

Genes

The following are some of the genes located on chromosome 4:

• ANK2: ankyrin 2, neuronal
• CXCL1: chemokine (C-X-C motif) ligand 1, scyb1
• CXCL2: chemokine (C-X-C motif) ligand 2, scyb2
• CXCL3: chemokine (C-X-C motif) ligand 3, scyb3
• CXCL4: chemokine (C-X-C motif) ligand 4, Platelet factor-4, PF-4, scyb4
• CXCL5: chemokine (C-X-C motif) ligand 5, scyb5
• CXCL6: chemokine (C-X-C motif) ligand 6, scyb6
• CXCL7: chemokine (C-X-C motif) ligand 7, PPBP, scyb7
• CXCL8: chemokine (C-X-C motif) ligand 8, interleukin 8 (IL-8), scyb8
• CXCL9: chemokine (C-X-C motif) ligand 9, scyb9
• CXCL10: chemokine (C-X-C motif) ligand 10, scyb10
• CXCL11: chemokine (C-X-C motif) ligand 11, scyb11
• CXCL13: chemokine (C-X-C motif) ligand 13, scyb13
• EVC: Ellis van Creveld syndrome
• EVC2: Ellis van Creveld syndrome 2 (limbin)
• FGFR3: fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism, bladder cancer)
• FGFRL1: fibroblast growth factor receptor-like 1
• Complement Factor I: Complement Factor I
• HTT (Huntingtin): huntingtin protein (Huntington's disease)
• MMAA: methylmalonic aciduria (cobalamin deficiency) cblA type
• PKD2: polycystic kidney disease 2 (autosomal dominant)
• QDPR: quinoid dihydropteridine reductase
• SNCA: synuclein, alpha (non A4 component of amyloid precursor)
• UCHL1: ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
• WFS1: Wolfram syndrome 1 (wolframin)
• FGF2: Fibroblast growth factor 2 (basic fibroblast growth factor)
• KDR: Kinase insert domain receptor (Vascular endothelial growth factor receptor 2)

Diseases & disorders

The following are some of the diseases related to genes located on chromosome 4:

• achondroplasia
• bladder cancer
• Crouzonodermoskeletal syndrome
• Chronic Lymphocytic Leukemia
• Ellis-van Creveld syndrome
• Fibrodysplasia ossificans progessiva FOP
• Hemophilia C
• Huntington's disease
• Hemolytic Uremic Syndrome
• hypochondroplasia
• methylmalonic acidemia
• Muenke syndrome
• nonsyndromic deafness
• nonsyndromic deafness, autosomal dominant
• Parkinsons disease
• polycystic kidney disease
• Romano-Ward syndrome
• SADDAN
• tetrahydrobiopterin deficiency
• thanatophoric dysplasia
• thanatophoric dysplasia, type 1
• thanatophoric dysplasia, type 2
• Wolfram syndrome

References

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