PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM
The OMIM Gene map presents the cytogenetic map location of disease genes and other expressed genes described in OMIM. See the OMIM Morbid Map for a list of disease genes organized by disease. For more refined maps of genes and DNA segments click on the Location to invoke NCBI Entrez Map Viewer.
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17q12, PPARBP to 17q12-q21, KRTAP1-3 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
17q12 PPARBP, PBP, TRAP220 Peroxisome proliferator-activated receptor-binding protein   604311     A  
17q12 RASL10B, RRP17 Ras-like, family 10, member B   612128     REc  
17q12 RFFL Ring finger and FYVE-like domain containing 1 (rififylin)   609735     R, REc 11(Rffl)
17q12 RNF110, ZNF144, MEL18 Ring finger protein 110 (zinc finger protein-144) 600346   previously assigned to 12q22 A, H, REc 10(Mel18)
17q12 SLC25A39, CGI69 Solute carrier family 25, member 39   610820     REc 11(Slc25a39)
17q12 SNIP, KIAA1684 SNAP25-interacting protein   610786     REc  
17q12 TBC1D3, PRC17, TBC1D3A TBC1D3 gene   607741     REc  
17q12 TBC1D3B, PRC17 TBC1 domain family, member 3B   610144     REc  
17q12 TBC1D3C TBC1 domain family, member 3C   610806     REc  
17q12 TCAP, LGMD2G, CMD1N Telethonin   604488 Muscular dystrophy, limb-girdle, type 2G, 601954 (3);Cardiomyopathy, dilated, 1N, 607487 (3)   Fd, REc  
17q12-q21 ARF4L ADP-ribosylation factor 4-like   600732     REc, Psh  
17q12-q21 COASY Coenzyme A synthase   609855     REc  
17q12-q21 HSD17B1, EDH17B2 Estradiol 17-beta-dehydrogenase-1   109684     A, REa  
17q12-q21 IGFBP4 Insulin-like growth factor-binding protein-4   146733     A  
17q12-q21 KRT9, EPPK Keratin 9   607606 Epidermolytic palmoplantar keratoderma, 144200 (3)   Fd, REa  
17q12-q21 KRT14 Keratin 14   148066 Epidermolysis bullosa simplex, Dowling-Meara type, 131760 (3);Epidermolysis bullosa simplex, Koebner type, 131900 (3); Epidermolysis bullosa simplex, recessive, 601001 (3); Naegeli-Franceschetti-Jadassohnsyndrome, 161000 (3); Dermatopathia pigmentosa reticularis, 125595 (3); Epidermolysis bullosa simplex, Weber-Cockayne type, 131800 (3)   REa  
17q12-q21 KRT16 Keratin 16   148067 Pachyonychia congenita, Jadassohn-Lewandowsky type, 167200 (3);Palmoplantar keratoderma, nonepidermolytic, 600962 (3); Palmoplantar verrucous nevus, unilateral, 144200 (3) probably 17q21-q22 REa, Fd  
17q12-q21 KRT17, PC2, PCHC1 Keratin 17   148069 Pachyonychia congenita, Jackson-Lawler type, 167210 (3);Steatocystoma multiplex, 184500 (3) ~5' to KRT16; probably 17q21-q22 REn, Fd  
17q12-q21 KRT20, CD20, KRT21 Keratin 20   608218     REn  
17q12-q21 KRTAP1-1, KAP1.1, KAP1.7, KAP1.6 Keratin-associated protein 1-1   608819     REc  
17q12-q21 KRTAP1-3, KAP1.3, KAP1.2, KAP1.9 Keratin-associated protein 1-3   608820     REc  
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