PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM
The OMIM Morbid Map presents the cytogenetic map location of disease genes described in OMIM. For a map organized by chromosome, see the OMIM Gene Map. For more refined maps of genes and DNA segments, use NCBI Entrez Map Viewer and the Genome Database.
Search for: (from the current location)    
  • Enter gene symbol, chromosomal location, or disorder keyword to search for, e.g. "recessive", "CYP1","5", "1pter", or "Xq".
  • You must capitalize X and Y to search for those chromosomes.
  <<Move Up Move Down>>
DisorderSymbol(s)OMIMLocation
Mental retardation, X-linked nonspecific, type 19 (3)RPS6KA3, RSK2, MRX19300075 Xp22.2-p22.1
Mental retardation, X-linked nonspecific, type 46, 300436 (3)ARHGEF6, MRX46, COOL2300267 Xq26
Mental retardation, X-linked nonspecific, type 50 (2)MRX50300115 Xp11.3-p11.21
Mental retardation, X-linked nonsyndromic (3)FGD1, FGDY, AAS300546 Xp11.21
Mental retardation, X-linked syndromic (3)UBE2A, RAD6A312180 Xq24-q25
Mental retardation, X-linked syndromic 10, 300220 (3)HSD17B10, HADH2, ERAB, MRXS10, MRX17, MRX31, DUPXp11.22300256 Xp11.2
Mental retardation, X-linked syndromic, Christianson type, 300243 (3)SLC9A6, NHE6300231 Xq26.3
Mental retardation, X-linked syndromic, Turner type, 300706 (3)HUWE1, UREB1, KIAA0312, LASU1300697 Xp11.2
Mental retardation, X-linked, 1 (2)MRX1309530 Xp11.3-q21.1
Mental retardation, X-linked, 2 (2)MRX2300428 Xp22.3
Mental retardation, X-linked, 21/34, 300143 (3)IL1RAPL1, IL1R8, MRX21, MRX34300206 Xp22.1-p21.3
Mental retardation, X-linked, 300495 (3)NLGN4, KIAA1260, AUTSX2, ASPGX2300427 Xp22.33
Mental retardation, X-linked, FRAXE type, 309548 (3)AFF2, FMR2, FRAXE, MRX2300806 Xq28
Mental retardation, X-linked, Lubs type, 300260 (3)MECP2, RTT, PPMX, MRX16, MRX79, AUTSX3, MRXSL, MRXS13, MRX79, MRX16300005 Xq28
Mental retardation, X-linked, Shashi type (2)MRXS11, SMRXS300238 Xq26-q27
Mental retardation, X-linked, Snyder-Robinson type, 309583 (3)SMS, SRS, MRSR300105 Xp22.1
Mental retardation, X-linked, South African type (2)MRSA300243 Xq24-q27.3
Mental retardation, X-linked, ZDHHC9-related (3)ZDHHC9, DHHC9300646 Xq26.1
Mental retardation, X-linked, syndromic 12 (2) (?)MRXS12309545 Xp11
Mental retardation, X-linked, syndromic 13, 300055 (3)MECP2, RTT, PPMX, MRX16, MRX79, AUTSX3, MRXSL, MRXS13, MRX79, MRX16300005 Xq28
Copyright © 1966-2009 Johns Hopkins University <<Move Up Move Down>>

Disclaimer | Write to the Help Desk | Privacy Policy
NCBI | NLM | NIH