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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4q25-q26, PITX2 to 4q27, EXOSC9 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
4q25-q26 PITX2, IDG2, RIEG1, RGS, IGDS2 Paired-like homeodomain transcription factor-2   601542 Axenfeld-Rieger syndrome, type 1, 180500 (3); Iridogoniodysgenesis,type 2, 137600 (3); Ring dermoid of cornea, 180550 (3); Peters anomaly, 604229 (3)   Ch, Fd, RE  
4q25 PLA2G12A, GXII, ROSSY Phospholipase A2, Group XIIA   611652     REc  
4q25-q26 PRSS12, BSSP3, MRT1 Protease, serine, 12   606709 Mental retardation, autosomal recessive 1, 249500 (3)   A  
4q25-q27 ANK2, LQT4 Ankyrin-2, nonerythrocytic   106410 Long QT syndrome-4, 600919 (3); Cardiac arrhythmia,ankyrin-B-related, 600919 (3)   REa, A, Fd  
4q25-q27 DAPP1, BAM32 Dual adaptor of phosphotyrosine and 3-phosphoinositides 1   605768     A  
4q25-q27 FGF2, FGFB Fibroblast growth factor-2 (basic)   134920   many alternate names REa, A 3(Fgf2)
4q25-q34 GENEX3414 Genethonin 1   607406     R  
4q26 ARSJ Arylsulfatase J   610010     REc  
4q26 CAMK2D Calcium/calmodulin-dependent protein kinase II-delta   607708     R, REc  
4q26 CGT UDP-galactose ceramide galactosyltransferase (cerebroside synthase) 601291     Psh, A  
4q26 PDE5A Phosphodiesterase 5A   603310     A, REc  
4q26 PGRMC2 Progesterone receptor membrane component 2   607735     REc  
4q26-q27 IL2 Interleukin-2   147680 Severe combined immunodeficiency due to IL2 deficiency (1)   REa, A, F 3(Il2)
4q26-q27 IL21 Interleukin 21   605384     R 3(Il21)
4q26-q27 MYOZ2 Myozenin 2   605602     REc  
4q26-q28 ANXA5, ENX2 Annexin A5 (endonexin II)   131230     REa, A, D 3(Anx5)
4q27 BBS7 BBS7 gene   607590 Bardet-Biedl syndrome 7, 209900 (3)   REc, REn  
4q27 BBS12, FLJ35630, C4orf24 BBS12 gene   610683 Bardet-Biedl syndrome 12, 209900 (3) 1Mb centromeric to BBS Fd, REc  
4q27 CCNA, CCN1 Cyclin A   123835     A 3(Cyca)
4q27 CELIAC6, AIS5 Celiac disease, susceptibility to, 6   611598 {Celiac disease, susceptibility to, 6} (2); {Autoimmune disease,susceptibility to, 5} (2)   Fd  
4q27 EXOSC9, PMSCL1 Exosome component 9   606180     R, REc  
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