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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  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "CYP1", "5", "1pter", "Xq", or "alzheimer".
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22p12, RNR5 to 22q11, SMARCB1 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
22p12 RNR5 Ribosomal RNA-5   180454     A  
22p ZNF72 Zinc finger protein-72 (Cos8)   194546     REa  
22p ZNF73 Zinc finger protein-73 (Cos12)   194547     REa  
22cen-q12 UCRC Ubiquinol-cytochrome C reductase complex, 7.2kD subunit   610843     R, REc  
22q RPL3 Ribosomal protein L3   604163     REa, R  
22q11 ACF Asymmetric crying facies (Cayler cardiofacial syndrome)   125520 Cayler cardiofacial syndrome (2)   Fd  
22q11 ADRBK2, BARK2, GRK3 Adrenergic, beta, receptor kinase-2   109636     A  
22q11 ARVCF Armadillo repeat gene deleted in VCFS   602269   ?role in VCFS A, REc  
22q11 CECR, CES Cat eye syndrome   115470 Cat eye syndrome (2) partial tetrasomy of 22q11 Ch, A, D  
22q11 CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like   602007     A  
22q11 DGCR6 DiGeorge syndrome critical region 6   601279     REn  
22q11 DGCR6L DiGeorge syndrome critical region gene 6-like   609459     REc, REn  
22q11 DVL, DVL1 Dishevelled, Drosophila, homolog-like   601225     Ch, REc  
22q11 HCF2, HC2, SERPIND1 Heparin cofactor II   142360 Thrombophilia due to heparin cofactor II deficiency, 612356 (3) proximal to BCR REb, REa  
22q11 HIRA, TUPLE1 Histone cell cycle regulation defective, S. cerevisiae, homolog of, A (Tup-like enhancer of split 1) 600237   ?role in CATCH22 A 16(Tuple1)
22q11 NAGA Acetylgalactosaminidase, alpha-N- (alpha-galactosidase B)   104170 Schindler disease, type I, 609241 (3); Kanzaki disease, 609242 (3);Schindler disease, type III, 609241 (3) proximal to Ph1 break S, Ch  
22q11 NLVCF Nuclear localization signal deleted in velocardiofacial syndrome   605089     REc 16(Nlvcf)
22q11 P2RXL1, P2XM, P2X6 Purinergic receptor P2X-like 1   608077     A  
22q11 RTN4R, NOGOR NOGO receptor (reticulon 4 receptor)   605566 {Schizophrenia, susceptibility to}, 181500 (3)   REc  
22q11 SLC25A1, SLC20A3, CTP Solute carrier family 25 (mitochondrial citrate transporter), member 1   190315     REc, Psh, A  
22q11 SMARCB1, SNF5, INI1, RDT SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 601607 Rhabdoid tumors (3); Rhabdoid predisposition syndrome, familial (3)   Ch, REc  
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