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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10q21, CTNNA3 to 10q21.1, PBLD <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
10q21 CTNNA3 Catenin, alpha-3   607667     A, Psh  
10q21 DDX21 DEAD/H box 21   606357     R, REc 10(Ddx21)
10q21 IBD15 Inflammatory bowel disease-15   612255 {Inflammatory bowel disease-15} (2) association with rs10761659 Fd  
10q21 IPMK Inositol polyphosphate multikinase   609851     REc  
10q21 MAFD8 Major affective disorder 8   612357 {Major affective disorder-8, susceptibility to} (2) associated with rs20994336 Fd  
10q21 NPFF1 Neuropeptide FF1   607448     R  
10q21 RNANC, NCRNA Retinal nonattachment, nonsyndromic congenital   221900 Retinal nonattachment, nonsyndromic congenital (2)   Fd  
10q21 SGPL1, SPL Sphingosine-1-phosphate lyase 1   603729     H 10(Spl)
10q21 TFAM, TCF6L2, TCF6L1, TCF6L3, MTTF1, TCF6 Transcription factor A, mitochondrial   600438     Psh, A 10(Tfam)
10q21-q22 CDH23, USH1D Cadherin-23 (otocadherin)   605516 Usher syndrome, type 1D, 601067 (3); Deafness, autosomal recessive12, 601386 (3); Usher syndrome, type 1D/F digenic, 601067 (3) between D10S529 and D10S573 Fd, REc 10(Cdh23, v)
10q21-q22 EIF4EBP2, 4EBP2 Eukaryotic translation initiation factor-4E binding protein-1   602224     A 10(Eif4ebp2)
10q21-q22 ERLIN1 Endoplasmic reticulum lipid raft-associated protein 1   611604     R, REc  
10q21-q22 PCDH15, DFNB23, USH1F Protocadherin 15   605514 Usher syndrome, type 1F, 602083 (3); Deafness, autosomal recessive23, 609533 (3); Usher syndrome, type 1D/F digenic, 601067 (3)   REc 10(av)
10q21-q22 PPP3CB, CALNB Protein phosphatase-3 (formerly 2B), catalytic subunit, beta isoform (calcineurin A beta) 114106     REa  
10q21-q23 CMD1C, CMPD3 Cardiomyopathy, dilated-1C, autosomal dominant   601493 Cardiomyopathy, dilated, 1C (2)   Fd  
10q21-q23 SPOCK2, KIAA0275 SPARC/osteonectin, CWCV, and KAZAL-like domains proteoglycan 2   607988     R, REc  
10q21-q24 HTR7 5-hydroxytryptamine (serotonin) receptor-7, adenylate cyclase-coupled   182137     REa, Fd  
10q21.1 CDC2, CDK1 Cell division cycle 2, G1 to S and G2 to M   116940     REa, A 10(Cdc2a)
10q21.1 CISD1, MITONEET CDGSH iron sulfur domain protein 1   611932     REc  
10q21.1 JDP1 J domain-containing protein 1   606060     REc  
10q21.1 PBLD, MAWBP, MAWDBP Phenazine biosynthesis-like protein domain-containing protein   612189     Psh, R  
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