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".
  • You must capitalize X and Y to search for those chromosomes.
Xpter-p22.32, ARSC2 to Xp22.31, FAAP95 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
Xpter-p22.32 ARSC2 Arylsulfatase C, f form   301780   probably close to STS = ARSC1, or s form D  
Xpter-p22.32 ASMT, HIOMT Acetylserotonin methyltransferase   300015   pseudoautosomal REa, Fd  
Xpter-p22.32 ASMTLX, ASTML Acetylserotonin methyltransferase-like   300162     REc  
Xpter-p22.32 CD99, MIC2, MIC2X CD99 antigen (MIC2 (monoclonal antibody 12E7))   313470   distal to STS S, A, D  
Xpter-p22.32 SHOX, GCFX, SS, PHOG Short stature homeo box   312865 Short stature, idiopathic familial, 300582 (3); Leri-Weilldyschondrosteosis, 127300 (3); Langer mesomelic dysplasia, 249700 (3) pseudoautosomal; ?gene causing short stature in Turner syndrome Fd, D, REc  
Xpter-p22.32 HDPA Hodgkin disease, susceptibility, pseudoautosomal   300221 {Hodgkin disease susceptibility, pseudoautosomal} (2)   Fd  
Xpter-p22.32 XG Xg blood group   314700 [Blood group, XG system] (3) nonlyonizing; spans pseudoautosomal boundary; XGPY on Yq11.21 F, D  
Xp22.33 NLGN4, KIAA1260, AUTSX2, ASPGX2 Neuroligin 4   300427 {Autism, susceptibility to, X-linked-2}, 300495 (3); {Aspergersyndrome, susceptibility to, X-linked-2}, 300497 (3); Mental retardation, X-linked, 300495 (3)   R  
Xp22.33 PGPL Pseudoautosomal GTP-binding protein-like   300124     Psh, A, REc  
Xp22.33 VSPA Visuospatial/perceptual abilities   313000 Turner syndrome-associated neurocognitive phenotype (2);[Visuospatial/perceptual abilities] (2)   D  
Xp22.33 ZBED1, ALTE, KIAA0785, TRAMP Zinc finger, (BED-type)-containing protein 1   300178     REc  
Xp22.33-p22.32 FAM9A Family with sequence similarity 9, member A   300477   pseudogene on Xq28, Yp11.31, 1p36.12, 8p11.1 REc  
Xp22.32 CSF2RA Colony-stimulating factor-2 receptor, alpha, low-affinity, granulocyte-macrophage 306250 Pulmonary alveolar proteinosis, 300770 (3) order in PAR: pter-CSF2RA-IL3RA-ANT3-ASMT-MIC2-cen A 19(Csf2ra)
Xp22.32 FAM9B Family with sequence similarity 9, member B   300478     REc  
Xp22.32 HDHD1A, DXF68S1E, GS1 Haloacid dehalogenase-like hydrolase domain-containing 1A   306480   escapes X-inactivation; 100kb telomeric to STS REn  
Xp22.32 SLC25A6, ANT3 Solute carrier family 25 (mitochondrial carrier), member 6 (adenine nucleotide translocator-3, liver) 300151   1st intron ~1.3Mb from Xqter; nonlyonized Pcm, REc, REn  
Xp22.32 SFRS17A, DXYS155E, XE7 Splicing factor, arginine/serine-rich, 17A   312095   nonlyonizing REn  
Xp22.32 STS, ARSC1, ARSC, SSDD, XLI Steroid sulfatase, microsomal (arylsulfatase C, isozyme S)   300747 Ichthyosis, X-linked, 308100 (3) nonlyonizing F, S, D X,Y(Sts)
Xp22.32 XGR XG/MIC2 regulator   314705   ?between XG and MIC2 F  
Xp22.31 ASB11 Ankyrin repeat- and SOCS box-containing protein 11   300626     REc  
Xp22.31 FAAP95, FAAP90, FLJ34064, FANCB Fanconi anemia-associated polypeptide, 95kD   300515 Fanconi anemia, complementation group B, 300514 (3)   REn  
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