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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6p12.1, RN7SK to 6p11, AITD1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
6p12.1 RN7SK, 7SK RNA, 7SK small nuclear   606515     REa  
6p12.1-p11.2 SLC35B2, PAPST1, SLL Solute carrier family 35 (3'-phosphoadenosine 5')-phosphosulfate transporter), member B2 610788     REc  
6p12 C6orf33, LMPB1, MPRB Membrane progestin receptor, beta   607780     REn  
6p12 CAPN11 Calpain 11   604822     REa, R  
6p12 CD2AP, CMS CD2-associated protein   604241 Glomerulosclerosis, focal segmental, 3, 607832 (3)   R, REc  
6p12 CRISP2, TPX1, TSP1 Cysteine-rich secretory protein 2   187430     REa 17(Tpx1)
6p12 ELOVL5, HELO1 Elongation of very long chain fatty acids-like 5   611805     REc  
6p12 GCLC, GLCLC Glutamate-cysteine ligase, catalytic subunit   606857 Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency,230450 (3); {Myocardial infarction, susceptibility to}, 608446 (3)   REa, Psh, A, Fd 9(Glclc)
6p12 GNMT Glycine N-methyltransferase   606628 Glycine N-methyltransferase deficiency, 606664 (3)   A  
6p12 IL17F, ML1 Interleukin 17F   606496     R  
6p12 KLHL31, KLHL Kelch-like 31   610749     REc, H 9(Klhl31)
6p12 MCM3 Minichromosome maintenance, S. cerevisiae, homolog of, 3   602693     A  
6p12 NYS2, NYSA Nystagmus-2, autosomal dominant   164100 Nystagmus-2, autosomal dominant (2)   Fd  
6p12 TFAP2B, CHAR Transcription factor AP-2 beta (activating enhancer-binding protein 2 beta) 601601 Char syndrome, 169100 (3)   A, Fd 1(Tfap2b)
6p12 VEGF, MVCD1 Vascular endothelial growth factor   192240 {Microvascular complications of diabetes 1}, 603933 (3)   A  
6p12-p11.2 TINAG, TIN1, TIN2 Tubulointerstitial nephritis antigen   606749     A  
6p12-p11.1 PRIM2A Primase polypeptide 2A, 58kD   176636     Psh, A 2(Prim2)
6p12-p11 DST, BPAG1, DMH, D6S1101 Dystonin (bullous pemphigoid antigen 1)   113810     A, REa 1(Bpag1)
6p12-p11 EFHC1, FLJ10466, EJM1, JAE, EJA1 EF hand domain (C-terminal)-containing 1   608815 {Myoclonic epilepsy, juvenile, susceptiblity to, 1}, 254770 (3);{Epilepsy, juvenile absence, susceptibility to, 1}, 607631 (3)   REc  
6p12-q12 ARCC1 Age-related cortical cataract 1   609026 {Cataract, age-related cortical, susceptibility to} (2)   Fd  
6p11 AITD1 Autoimmune thyroid disease, susceptibility to, 1   608173 {Autoimmune thyroid disease, susceptibility to, 1} (2)   Fd  
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