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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3p23-p21, NKTR to 3p22-p21.3, CYP8B1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
3p23-p21 NKTR Natural tumor-killer recognition sequence   161565   mouse gene close to Cck REa 9(Nktr)
3p23-p21 SCLC1 Small-cell cancer of lung   182280 Small-cell cancer of lung (2) centromeric to ERBA2 Ch, D  
3p23-p21 SMARCC1, BAF155 SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily C, member 1 601732     R, Psh  
3p23-p21 TDGF1 Teratocarcinoma-derived growth factor-1   187395 Forebrain defects (3)   REa, A 9(Tdgf1)
3p22.3 GPD1L, KIAA0089 Glycerol-3-phosphate dehydrogenase 1-like   611778 Brugada syndrome 2, 611777 (3)   REc, Fd  
3p22.3 PDCD6IP, AIP1, ALIX, KIAA1375 Programmed cell death 6-interacting protein   608074     R  
3p22.2 CMYA1, XIN Cardiomyopathy-associated protein 1   609777     R, REc  
3p22.2 MIRN26A1, MIR26A Micro RNA 26A1   612151     REc  
3p22.2-p21.32 MHB Myopathy, hyaline body   255160 Myopathy, hyaline body (2) between D3S3572 and D3S3624 Fd  
3p22.1 SLC25A38 Solute carrier family 25, member 38   610819     REc 9(Slc25a38)
3p22 AXUD1 Axin1 upregulated   606458     R  
3p22 CCR8, CMKBR8, CMKBRL2, CKRL1 Chemokine (C-C) receptor 8   601834     Psh  
3p22 CRTAP, CASP Cartilage-associated protein   605497 Osteogenesis imperfecta, type IIB, 610854 (3); Osteogenesisimperfecta, type VII, 610682 (3)   A 9(Crtap)
3p22 MIRN128-2, MIR128B, MIR128-2 Micro RNA 128-2   611769     REc  
3p22 SLC4A7, NBC2, NBC3 Solute carrier family 4, sodium bicarbonate cotransporter, member 7   603353     A  
3p22 TGFBR2, HNPCC6, AAT3, MFS2, LDS1B, LDS2B Transforming growth factor, beta receptor II, 70-80kD   190182 Colorectal cancer, hereditary nonpolyposis, type 6 (3); Esophagealcancer, 133239 (3); Loeys-Dietz syndrome, type 1B, 610168 (3); Loeys-Dietz syndrome, type 2B, 610380 (3)   A, REa, Fd 9(Tgbfr2)
3p22 VIPR1 Vasoactive intestinal peptide receptor 1   192321   incorrectly assigned to 2q37 A 9(Vipr1)
3p22-p21.33 TGM4 Transglutaminase-4, prostate   600585     A  
3p22-p21.3 ACVR2B, ACTRIIB Activin A receptor, type IIB   602730 Heterotaxy, visceral, 4, autosomal (3)   REc, A  
3p22-p21.3 CTNNB1 Catenin (cadherin-associated protein), beta 1, 88kD   116806 Colorectal cancer (3); Hepatoblastoma (3); Pilomatricoma, 132600 (3);Ovarian carcinoma, endometrioid type (3); Hepatocellular carcinoma, 114550 (3)   A, REn, Psh 9(Catnb)
3p22-p21.3 CYP8B1, CYP12 Cytochrome P450, subfamily VIIIB, polypeptide 1   602172     A, R 9(Cyp8b1)
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