Disease A B C D E F G H I J K L M N O P Q R S T U V W X Y Z [0-9]
Gene A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

ALOX5AP

Gene name: arachidonate 5-lipoxygenase activating protein
OMIM ID: 603700
Chromosome location: 13q12.3

Polymorphisms

Disease/PhenotypeIschemic stroke, susceptibility to
Reference transcriptNM_001204406.1
DNA Changec.241+2284A>T (SG13S114)
A.A. Change
Exon/Intronintron 2
Variation Typesubstitution
Reference SNPrs10507391
Cases175 patients
Controls201 controls
Frequency
Allele/GenotypeFrequency in casesFrequency in controlsOR (95%CI)P-value
A229 (65.4%)302 (75.1%)1
T121 (34.6%)100 (24.9%)1.59 (1.16-2.19) 0.004
AA89 (50.9%)119 (59.2%)1
AT51 (29.1%)64 (31.8%)1.06 (0.67-1.68)0.786
TT35 (20.0%)18 (9.0%)2.57 (1.49-4.83)0.003
ReferenceDiakite B, Hamzi K, Hmimech W, Nadifi S; GMRAVC. Genetic polymorphisms of T-1131C APOA5 and ALOX5AP SG13S114 with the susceptibility of ischaemic stroke in Morocco.
J Genet. 2016 Jun;95(2):303-9.