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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7pter-p22, PRKAR1B to 7p22, LFNG <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
7pter-p22 PRKAR1B Protein kinase, cAMP-dependent, regulatory, type I, beta   176911     Fd  
7p22.3 C7orf20, CEE Chromosome 7 open reading frame 20   612056     REc  
7p22.3 CENTA1 Centaurin, alpha-1   608114     REc  
7p22.3 UNC84A, KIAA0810, SUN1 UNC84, C. elegans, homolog of, A   607723     R, REc  
7p22.3 ZFAND2A, AIRAP Zinc finger, AN1-type, domain-containing protein 2A   610699     REc  
7p22.2 EIF3B, EIF3S9, PRT1 Eukaryotic translation initiation factor 3, subunit B   603917     REc  
7p22.2 GNA12 Guanine nucleotide-binding protein, alpha-12   604394     R, REc  
7p22.2 TMED4 Transmembrane EMP24 protein transport domain-containing protein 4   612038     REc  
7p22.1 CYTH3, PSCD3, ARNO3, GRP1 Cytohesin 3   605081     R, REc  
7p22.1 PAPOLB, TPAP Poly(A) polymerase, beta   607436     REc  
7p22.1 RADIL, KIAA1849 RAP GTPase interactor   611491     REc  
7p22.1 STBMS1 Strabismus, susceptibility to, 1   185100 {Strabismus, susceptibility to, 1} (2) max lod at marker 1911/1912 Fd  
7p22.1-p21.3 MEOX2 Mesenchyme homeo box 2   600535     A  
7p22 CARD11, CARMA1, BIMP3 Caspase recruitment domain-containing protein 11   607210     R, REc  
7p22 ERVK6 Endogenous retroviral sequence K, 6   605626     A  
7p22 FSCN1, SNL Fascin homolog 1, actin-bundling protein (singed, Drosophila, homolog-like) 602689     A  
7p22 FHII Hyperaldosteronism, familial, type II   605635 Hyperaldosteronism, familial, type II (2)   Fd  
7p22 FTSJ2, FJH1 FTSJ, E. coli, homolog of, 2   606906     R  
7p22 ICA1 Islet cell autoantigen 1, 69kD   147625     A 6(Ica1)
7p22 JTV1 JTV1 gene   600859     A  
7p22 LFNG, SCDO3 Lunatic fringe   602576 Spondylocostal dysostosis, autosomal recessive 3, 609813 (3)   REa, R, A 5(Lfng)
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