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Protein-coding gene in the species Homo sapiens
Zinc finger protein 469 is a protein that in humans is encoded by the ZNF469 gene. This gene encodes a zinc-finger protein. Low-percent homology to certain
ZNF469
Group of genetic connective tissues disorders
also often seen. It has two types. Type 1 occurs due to variations in the ZNF469 gene. Type 2 is due to variations in the PRDM5 gene. Cardiac-valvular EDS
Ehlers–Danlos_syndrome
C2H2 ZF Known motif – High-throughput in vitro [1,320] DGGGAGGGGGYGSNS ZNF469 ENSG00000225614 C2H2 ZF Likely sequence specific TF according to literature
List of human transcription factors
List_of_human_transcription_factors
Deformation of the eye's cornea into a conelike shape
been found to be associated with the condition. These genes include BANP-ZNF469, COL4A4, FOXO1, FNDC3B, IMMP2L and RXRA-COL5A1. Others likely also exist
Keratoconus
Breast cancer, somatic; 114480; RB1CC1 Brittle cornea syndrome; 229200; ZNF469 Brody myopathy; 601003; ATP2A1 Bronchiectasis with or without elevated sweat
List_of_OMIM_disorder_codes
Q96JM2 18927 ZNF467 HGNC:23154; Q7Z7K2 18928 ZNF468 HGNC:33105; Q5VIY5 18929 ZNF469 HGNC:23216; Q96JG9 18930 ZNF470 HGNC:22220; Q6ECI4 18931 ZNF471 HGNC:23226;
List of human protein-coding genes 9
List_of_human_protein-coding_genes_9
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