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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3p12-p11.1, CGGBP1 to 3q11-q12, TFG <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
3p12-p11.1 CGGBP1 CGG triplet repeat binding protein 1   603363     REc, REa, A  
3p12-q13 ARL6, BBS3 ADP-ribosylation factor-like 6   608845 Bardet-Biedl syndrome 3, 209900 (3); {Bardet-Biedl syndrome 1,modifier of}, 209900 (3)   Fd, REc  
3p12-q13 DYX5 Dyslexia, susceptibility to, 5   606896 {Dyslexia, susceptibility to, 5} (2) ?same locus as SSD Fd  
3p12-q13 ESRRBL1, HIPPI Estrogen-related receptor, beta-like 1 (HIP1 protein interactor) 606621     R, REc  
3p12-q13 SSD Speech-sound disorder   608445 {Speech-sound disorder} (2) ?same locus as DYX5 Fd  
3p12-q13.2 IL12A Interleukin-12A (natural killer cell stimulatory factor-1, cytotoxic lymphocyte maturation factor-1, p35) 161560     REa, Psh  
3p12-qter ZNF80 Zinc finger protein-80 (pT17)   194553     REa  
3p11.2 CHMP2B, DMT1, VPS2B CHMP family, member 2B   609512 Dementia, familial, nonspecific, 600795 (3); Amyotrophic lateralsclerosis, CHMP2B-related (3)   Fd, REc  
3p11.2 EPHA3, ETK1, HEK Ephrin receptor EphA3 (human embryo kinase 1)   179611     REa, A  
3p11 POU1F1, PIT1, CPHD1 POU domain, class 1, transcription factor 1 (Pit1, growth hormone factor 1) 173110 Pituitary hormone deficiency, combined, 1, 613038 (3)   Fd, A 16(Pit1,dw)
3p CRCL Creatinine clearance QTL   607135 Creatinine clearance QTL (2) in African Ambericans Fd  
3p MYL3, CMH8 Myosin, light polypeptide-3, alkali; ventricular, skeletal, slow   160790 Cardiomyopathy, familial hypertrophic, 8, 608751 (3)   REa, H 9(Mylc)
3p PRKCD Protein kinase C, delta   176977     REa, H 14(Pkcd)
3p RPL15 Ribosomal protein L15   604174     REa, R  
3q CBLB CAS-BR-M murine ecotropic retroviral transforming sequence B   604491     Psh, A  
3q COX17 Cytochrome c oxidase assembly protein COX17   604813   pseudogene on chr. 13? R  
3q DFNB15 Deafness, autosomal recessive 15   601869 Deafness, autosomal recessive 15 (2)   Fd  
3q PCYT1A, CTPCT, PCYT1 Phosphate cytidylyltransferase 1, choline, alpha isoform   123695     H, R 16(Ctpct)
3q RPL24 Ribosomal protein L24   604180     REa, R  
3q RPN1 Ribophorin I   180470     REa, Ch 6(Rpn1)
3q11-q12 TFG TRK-fused gene   602498 Chondrosarcoma, extraskeletal myxoid, 612237 (1) fused with NR4A3 or NTRK1 A  
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