acetyltransferase 6A (KAT6A), is an enzyme that, in humans, is encoded by the KAT6A gene. This gene is located on human chromosome 8, band 8p11.21. The KAT6A protein...
9 KB (1,071 words) - 14:58, 22 October 2022
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome (redirect from KAT6A syndrome)
viral infections. This condition is caused by heterozygous mutations in the KAT6A gene, in chromosome 8. These mutations are often sporadic, and are either...
7 KB (441 words) - 03:08, 24 July 2024
HGNC:4201 Q92830 7941 KAT2B HGNC:8638 Q92831 7942 KAT5 HGNC:5275 Q92993 7943 KAT6A HGNC:13013 Q92794 7944 KAT6B HGNC:17582 Q8WYB5 7945 KAT7 HGNC:17016 O95251...
277 KB (17 words) - 19:37, 1 October 2024
RNF213, FLCN, PDGFRB, AR (i.e. the androgen receptor gene), BTK, MLL3, KAT6A, BRD3, EP400, TET2, IL6, and IL7R. The PI3K/AKT/mTOR pathway promotes the...
22 KB (2,440 words) - 21:14, 6 January 2024
associated with neurodevelopment disabilities and autism, including NR4A2, KAT6A, PPP2R5D, CSNK2A1, PHIP, CDC42BPB, TKT, DHPS, PRUNE, EMC1, AHDC1, POGZ,...
37 KB (3,482 words) - 02:45, 4 April 2024