HTRA1 wt Allele

Human HTRA1 wild-type allele is located in the vicinity of 10q26.3 and is approximately 53 kb in length. This allele, which encodes serine protease HTRA1 protein, is involved in the mediation of proteolysis. Variations in the promoter of the gene are associated with age-related macular degeneration type 7. Mutation of the gene is associated with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy. (NCI Thesaurus)

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HTRA1 Gene

This gene plays a role in proteolysis.

HTR3A wt Allele

Definition: Human HTR3A wild-type allele is located in the vicinity of 11q23.1 and is approximately 15 kb in length. This allele, which…

HTR3A Gene

This gene plays a role in neurotransmitter modulation and in chaperone activity.

HTR2A wt Allele

Human HTR2A wild-type allele is located within 13q14-q21 and is approximately 63 kb in length. This allele, which encodes 5-hydroxytryptamine 2A receptor…

HTR2A Gene

This gene plays a role in G protein-coupled receptor signal transduction and sterol metabolism.

HTR2A 2 Allele

HTR2A-T Allele is a variant form of 20-kb 3-exon human HTR2A Gene (GPCR1/5HT2 Family), which encodes Serotonin 5-HT-2A Receptor, a conserved integral…