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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18p11.32, CETN1 to 18p11.3-p11.2, PTPN2 <<Move Up Move Down>>
Location Symbol Title MIM # Disorder Comments Method Mouse
18p11.32 CETN1, CEN1 Centrin-1   603187     REa, REc  
18pter-p11.21 ERV1 Oncogene ERV1; endogenous retrovirus-1   131150     REa, A  
18p11.32 COLEC12, SRCL, CLP1 Collectin 12   607621     REc  
18p11.32 TYMS, TS, TMS Thymidylate synthase   188350   <50 kb from YES1 S, A  
18p11.32 RTS Thymidylate synthase, antisense   607427     REn  
18p11.32 THOC1, HPR1 THO complex 1 (nuclear matrix protein p84)   606930     R, REc  
18p11.32-p11.31 DFNB46 Deafness, neurosensory, autosomal recessive 46   609647 Deafness, neurosensory, autosomal recessive 46 (2) between D18S59 and D18S391 Fd  
18p11.32-p11.23 HTS Hypotrichosis simplex   605389 Hypotrichosis simplex (2)   Fd  
18p11.31 ARHGAP28, KIAA1314 RHO GTPase-activating protein 28   610592     R, REc  
18p11.31 LAMA1 Laminin, alpha-1   150320     A 17(Lama)
18p11.31 MYL12B, MRLC2 Myosin, light chain 12B, regulatory   609211     R, REc  
18p11.31 MYP2 Myopia, high grade, autosomal dominant 1   160700 Myopia-2 (2)   Fd  
18p11.31-p11.2 NDUFV2 NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kD   600532 {Parkinson disease, susceptibility to}, 168600 (3) pseudogene on 19q13.3-qter REa, A  
18p11.31-q11.2 SCKL2 Seckel syndrome 2   606744 Seckel syndrome 2 (2) between D18S78 and D18S866 Fd  
18p11.3 DSAP4 Porokeratosis, disseminated superficial actinic, 4   612353 Porokeratosis, disseminated superficial actinic, 4 (2) between telomere and D18S391 Fd  
18p11.3 EPB41L3, DAL1 Erythrocyte membrane protein band 4.1-like 3   605331     REc  
18p11.3 RAB31 Ras-associated protein RAB31   605694     REa, REc  
18p11.3 TGIF, HPE4 TG-interacting factor   602630 Holoprosencephaly-4, 142946 (3); Hypotrichosis simplex, contiguousgene syndrome with, 605389 (2)   Ch, A  
18p11.3 YES1 Oncogene YES-1   164880   <50 kb from TYMS REa, REn, A  
18p11.3-p11.2 AA1 Alopecia areata 1   104000 Alopecia areata 1 (2) max lod at D18S967 Fd  
18p11.3-p11.2 PTPN2, PTPT Protein tyrosine phosphatase, nonreceptor-type, 2   176887     REc, A 18(Ptpt)
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