Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.Īutosomal dominant Autosomal dominant form Autosomal dominant type In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. IKBKB IKBKB-DT HSALNG0064877 POLB KAT6A ENSG00000254165 RF00017-6594 PLAT RF00017-6593ĭeviation from the norm of height with respect to that which is expected according to age and gender norms.Ī mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. SP1 ATF2 POLR2A KLF17 CTCF ZNF600 ZIC2 BRCA1 HIC1 MAZ

RefSeq EPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas dbSUPER POLR2A KLF17 JUND ZNF184 CTCF ZNF600 ZNF10 REST ZNF207 MAZ PLAT HSALNG0064871 KAT6A POLB HGSNAT lnc-KAT6A-3 AP3M2 RF00017-6594 RF00017-6593ĮPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas KAT6A lnc-AP3M2-3 KAT6A-AS1 ENSG00000254165 IKBKB AP3M2 PLAT GPAT4 POLB LOC124900271ĮPDnew Ensembl ENCODE CraniofacialAtlas dbSUPERĭPF2 ATF2 NCOR1 JUND ZNF600 ZIC2 HIC1 NFIC MNT ZNF639 SP1 KLF6 ZNF580 POLR2A KLF17 JUND NCOR1 ZNF184 ZIC2 ZNF600 EPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas dbSUPER

Myst 3 windowed mode