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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20p13, SLC24A3 to 20p12.1-p11.23, BFSP1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
20p13 SLC24A3, NCKX3 Solute carrier family 24 (sodium/potassium/calcium exchanger), member 3 609839     REc  
20p13 SNPH Syntaphilin   604942     R, REc  
20p13 STK35, CLIK1 Serine/threonine kinase 35   609370     REn  
20p13 TBC1D20, C20orf140 TBC1 domain family, member 20   611663     REc  
20p13 TCF15 Transcription factor-15 (basic helix-loop-helix)   601010     A 2(Meso1)
20p13 TMC2 Transmembrane cochlear-expressed gene 2   606707     REc  
20p13-p12.3 C20orf155, GCD10 Gcd10, S. cerevisiae, homolog of   608188     REc  
20p13-p12.3 MCM8 Minichromosome maintenance, S. cerevisiae, homolog of, 8   608187     REc  
20p13-p12.3 PANK2, NBIA1, PKAN, HARP Pantothenate kinase 2   606157 Neurodegeneration, pantothenate kinase-associated, 234200 (3);HARP syndrome, 607236 (3)   LD, Fd  
20p13-p12.3 SCA23 Spinocerebellar ataxia 23   610245 Spinocerebellar ataxia 23 (2) max lod at D20S199 Fd  
20p13-p12.1 RNF24, G1L Ring finger protein 24   612489     REc  
20p13-p12 SLC4A11, BTR1, NABC1, CHED2, CDPD Solute carrier family 4 (sodium borate cotransporter), member 11   610206 Corneal endothelial dystrophy 2, 217700 (3); Corneal endothelialdystrophy and perceptive deafness, 217400 (3)   REc, Fd  
20p13-p12 SLC23A2, SVCT2 Solute carrier family 23 (nucleobase transporters), member 2 (sodium-dependent vitamin C transporter 2) 603791     R, REc  
20p12.3 BMND7 Bone mineral density QTL 7   611738 {Osteoporosis}, 166710 (2) most significant association with haplotype C Fd  
20p12.3 CRCS11 Colorectal cancer, susceptibility to, 11   612592 {Colorectal cancer, susceptibility to, 11} (2) associated with rs961253 Fd  
20p12.3 MENOQ3 Menopause, natural, age at, QTL3   612885 {Menopause, natural, age at, QTL3} (2) associated with rs16991615 Fd  
20p12.3-p12.1 SPTLC3, SPTLC2L Serine palmitoyltransferase, long-chain base subunit 3   611120     REc  
20p12.1 C20orf7 Chromosome 20 open reading frame 7   612360 Mitochondrial complex 1 deficiency, 252010 (3)   REc  
20p12.1 DSTN, ADF Destrin   609114     R, REc  
20p12.1 TASP1, C20orf13 Threonine aspartase 1   608270     REc  
20p12.1-p11.23 BFSP1, CP115 Beaded filament structural protein-1 (filensin)   603307 Cataract, cortical, juvenile-onset, 611391 (3)   A  
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